diff --git a/Example_workflows/CSEARCH_CMIN_conformer_generation/CSEARCH_CREST_TS.ipynb b/Example_workflows/CSEARCH_CMIN_conformer_generation/CSEARCH_CREST_TS.ipynb index bb470cba..18f2e834 100644 --- a/Example_workflows/CSEARCH_CMIN_conformer_generation/CSEARCH_CREST_TS.ipynb +++ b/Example_workflows/CSEARCH_CMIN_conformer_generation/CSEARCH_CREST_TS.ipynb @@ -48,10 +48,10 @@ "# based on the atom numbers above, I choose the constraints for my TS:\n", "# 1) Bond between atoms 4 and 5 with a distance of 1.8 A\n", "# 2) Bond between atoms 5 and 9 with a distance of 1.8 A\n", - "constraits_dist = [[3,4,1.8],[4,5,1.8]]\n", + "constraints_dist = [[3,4,1.8],[4,5,1.8]]\n", "\n", "# 3) Angle between atoms 4, 5 and 9 of 180 degrees\n", - "constraits_angle = [[3,4,5,180]]" + "constraints_angle = [[3,4,5,180]]" ] }, { @@ -73,13 +73,13 @@ "# 1) Mapped SMILES string (smi=smi_new)\n", "# 2) CREST sampling (program='crest')\n", "# 3) Include CREGEN post-analysis (cregen=True)\n", - "# 4) Define distance constraints (constraints_dist=constraits_dist)\n", - "# 5) Define angle constraints (constraints_angle=constraits_angle)\n", + "# 4) Define distance constraints (constraints_dist=constraints_dist)\n", + "# 5) Define angle constraints (constraints_angle=constraints_angle)\n", "# 6) Add water solvation in CREST (crest_keywords=\"--alpb h2o\")\n", "# 7) Add water solvation in the xTB pre-optimization (xtb_keywords=\"--alpb h2o\")\n", "# 7) Number of processors used in CREST (nprocs=12)\n", "csearch(smi=smi_new,name='TS-example',program='crest',cregen=True,\n", - " constraints_dist=constraits_dist,constraints_angle=constraits_angle,\n", + " constraints_dist=constraints_dist,constraints_angle=constraints_angle,\n", " crest_keywords=\"--alpb h2o\",xtb_keywords=\"--alpb h2o\",nprocs=12)" ] }, diff --git a/Example_workflows/QCORR_processing_QM_outputs/QCORR_1/Imag_freq_no_corr.log b/Example_workflows/QCORR_processing_QM_outputs/QCORR_1/Imag_freq_no_corr.log new file mode 100644 index 00000000..9d621a1f --- /dev/null +++ b/Example_workflows/QCORR_processing_QM_outputs/QCORR_1/Imag_freq_no_corr.log @@ -0,0 +1,1259 @@ + Entering Link 1 = C:\G09W\l1.exe PID= 12408. + + Copyright (c) 1988,1990,1992,1993,1995,1998,2003,2009, Gaussian, Inc. + All Rights Reserved. + + This is part of the Gaussian(R) 09 program. It is based on + the Gaussian(R) 03 system (copyright 2003, Gaussian, Inc.), + the Gaussian(R) 98 system (copyright 1998, Gaussian, Inc.), + the Gaussian(R) 94 system (copyright 1995, Gaussian, Inc.), + the Gaussian 92(TM) system (copyright 1992, Gaussian, Inc.), + the Gaussian 90(TM) system (copyright 1990, Gaussian, Inc.), + the Gaussian 88(TM) system (copyright 1988, Gaussian, Inc.), + the Gaussian 86(TM) system (copyright 1986, Carnegie Mellon + University), and the Gaussian 82(TM) system (copyright 1983, + Carnegie Mellon University). Gaussian is a federally registered + trademark of Gaussian, Inc. + + This software contains proprietary and confidential information, + including trade secrets, belonging to Gaussian, Inc. + + This software is provided under written license and may be + used, copied, transmitted, or stored only in accord with that + written license. + + The following legend is applicable only to US Government + contracts under FAR: + + RESTRICTED RIGHTS LEGEND + + Use, reproduction and disclosure by the US Government is + subject to restrictions as set forth in subparagraphs (a) + and (c) of the Commercial Computer Software - Restricted + Rights clause in FAR 52.227-19. + + Gaussian, Inc. + 340 Quinnipiac St., Bldg. 40, Wallingford CT 06492 + + + --------------------------------------------------------------- + Warning -- This program may not be used in any manner that + competes with the business of Gaussian, Inc. or will provide + assistance to any competitor of Gaussian, Inc. The licensee + of this program is prohibited from giving any competitor of + Gaussian, Inc. access to this program. By using this program, + the user acknowledges that Gaussian, Inc. is engaged in the + business of creating and licensing software in the field of + computational chemistry and represents and warrants to the + licensee that it is not a competitor of Gaussian, Inc. and that + it will not use this program in any manner prohibited above. + --------------------------------------------------------------- + + + Cite this work as: + Gaussian 09, Revision A.02, + M. J. Frisch, G. W. Trucks, H. B. Schlegel, G. E. Scuseria, + M. A. Robb, J. R. Cheeseman, G. Scalmani, V. Barone, B. Mennucci, + G. A. Petersson, H. Nakatsuji, M. Caricato, X. Li, H. P. Hratchian, + A. F. Izmaylov, J. Bloino, G. Zheng, J. L. Sonnenberg, M. Hada, + M. Ehara, K. Toyota, R. Fukuda, J. Hasegawa, M. Ishida, T. Nakajima, + Y. Honda, O. Kitao, H. Nakai, T. Vreven, J. A. Montgomery, Jr., + J. E. Peralta, F. Ogliaro, M. Bearpark, J. J. Heyd, E. Brothers, + K. N. Kudin, V. N. Staroverov, R. Kobayashi, J. Normand, + K. Raghavachari, A. Rendell, J. C. Burant, S. S. Iyengar, J. Tomasi, + M. Cossi, N. Rega, J. M. Millam, M. Klene, J. E. Knox, J. B. Cross, + V. Bakken, C. Adamo, J. Jaramillo, R. Gomperts, R. E. Stratmann, + O. Yazyev, A. J. Austin, R. Cammi, C. Pomelli, J. W. Ochterski, + R. L. Martin, K. Morokuma, V. G. Zakrzewski, G. A. Voth, + P. Salvador, J. J. Dannenberg, S. Dapprich, A. D. Daniels, + O. Farkas, J. B. Foresman, J. V. Ortiz, J. Cioslowski, + and D. J. Fox, Gaussian, Inc., Wallingford CT, 2009. + + ****************************************** + Gaussian 09: IA32W-G09RevA.02 11-Jun-2009 + 16-Jan-2022 + ****************************************** + ---------------------- + # opt freq 3-21g m062x + ---------------------- + 1/14=-1,18=20,19=15,26=3,38=1/1,3; + 2/9=110,12=2,17=6,18=5,40=1/2; + 3/5=5,11=2,16=1,25=1,30=1,71=1,74=-55/1,2,3; + 4//1; + 5/5=2,38=5/2; + 6/7=2,8=2,9=2,10=2,28=1/1; + 7//1,2,3,16; + 1/14=-1,18=20,19=15/3(2); + 2/9=110/2; + 99//99; + 2/9=110/2; + 3/5=5,11=2,16=1,25=1,30=1,71=1,74=-55/1,2,3; + 4/5=5,16=3/1; + 5/5=2,38=5/2; + 7//1,2,3,16; + 1/14=-1,18=20,19=15/3(-5); + 2/9=110/2; + 6/7=2,8=2,9=2,10=2,19=2,28=1/1; + 99/9=1/99; + ------------------- + Title Card Required + ------------------- + Symbolic Z-matrix: + Charge = 0 Multiplicity = 1 + C 0.65979 -0.01959 0. + H 1.08589 0.9838 0. + H 1.02538 -0.54454 -0.88941 + H 1.02538 -0.54454 0.88941 + H -0.40481 0.08784 0. + + + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + Berny optimization. + Initialization pass. + ---------------------------- + ! Initial Parameters ! + ! (Angstroms and Degrees) ! + -------------------------- -------------------------- + ! Name Definition Value Derivative Info. ! + -------------------------------------------------------------------------------- + ! R1 R(1,2) 1.0901 estimate D2E/DX2 ! + ! R2 R(1,3) 1.0956 estimate D2E/DX2 ! + ! R3 R(1,4) 1.0956 estimate D2E/DX2 ! + ! R4 R(1,5) 1.07 estimate D2E/DX2 ! + ! A1 A(2,1,3) 108.0951 estimate D2E/DX2 ! + ! A2 A(2,1,4) 108.0951 estimate D2E/DX2 ! + ! A3 A(2,1,5) 107.2466 estimate D2E/DX2 ! + ! A4 A(3,1,4) 108.5486 estimate D2E/DX2 ! + ! A5 A(3,1,5) 112.3416 estimate D2E/DX2 ! + ! A6 A(4,1,5) 112.3416 estimate D2E/DX2 ! + ! D1 D(2,1,4,3) -117.0198 estimate D2E/DX2 ! + ! D2 D(2,1,5,3) 118.6329 estimate D2E/DX2 ! + ! D3 D(2,1,5,4) -118.6329 estimate D2E/DX2 ! + ! D4 D(3,1,5,4) 122.7341 estimate D2E/DX2 ! + -------------------------------------------------------------------------------- + Trust Radius=3.00D-01 FncErr=1.00D-07 GrdErr=1.00D-06 + Number of steps in this run= 24 maximum allowed number of steps= 100. + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + + Input orientation: + --------------------------------------------------------------------- + Center Atomic Atomic Coordinates (Angstroms) + Number Number Type X Y Z + --------------------------------------------------------------------- + 1 6 0 0.659787 -0.019591 0.000000 + 2 1 0 1.085888 0.983801 0.000001 + 3 1 0 1.025384 -0.544535 -0.889409 + 4 1 0 1.025384 -0.544537 0.889408 + 5 1 0 -0.404806 0.087842 0.000000 + --------------------------------------------------------------------- + Distance matrix (angstroms): + 1 2 3 4 5 + 1 C 0.000000 + 2 H 1.090118 0.000000 + 3 H 1.095571 1.769328 0.000000 + 4 H 1.095571 1.769328 1.778817 0.000000 + 5 H 1.070000 1.739227 1.798997 1.798998 0.000000 + Stoichiometry CH4 + Framework group C1[X(CH4)] + Deg. of freedom 9 + Full point group C1 NOp 1 + Largest Abelian subgroup C1 NOp 1 + Largest concise Abelian subgroup C1 NOp 1 + Standard orientation: + --------------------------------------------------------------------- + Center Atomic Atomic Coordinates (Angstroms) + Number Number Type X Y Z + --------------------------------------------------------------------- + 1 6 0 -0.002711 0.000000 -0.010757 + 2 1 0 -0.367084 0.000000 1.016662 + 3 1 0 0.621567 0.889411 -0.150402 + 4 1 0 0.621574 -0.889406 -0.150400 + 5 1 0 -0.859790 -0.000004 -0.651317 + --------------------------------------------------------------------- + Rotational constants (GHZ): 162.4790692 159.1445672 155.3042823 + Standard basis: 3-21G (6D, 7F) + There are 17 symmetry adapted basis functions of A symmetry. + Integral buffers will be 262144 words long. + Raffenetti 2 integral format. + Two-electron integral symmetry is turned on. + 17 basis functions, 27 primitive gaussians, 17 cartesian basis functions + 5 alpha electrons 5 beta electrons + nuclear repulsion energy 13.4643327039 Hartrees. + NAtoms= 5 NActive= 5 NUniq= 5 SFac= 7.50D-01 NAtFMM= 80 NAOKFM=F Big=F + One-electron integrals computed using PRISM. + NBasis= 17 RedAO= T NBF= 17 + NBsUse= 17 1.00D-06 NBFU= 17 + Harris functional with IExCor= 1009 diagonalized for initial guess. + ExpMin= 1.83D-01 ExpMax= 1.72D+02 ExpMxC= 1.72D+02 IAcc=1 IRadAn= 1 AccDes= 0.00D+00 + HarFok: IExCor= 1009 AccDes= 0.00D+00 IRadAn= 1 IDoV= 1 + ScaDFX= 1.000000 1.000000 1.000000 1.000000 + FoFCou: FMM=F IPFlag= 0 FMFlag= 100000 FMFlg1= 0 + NFxFlg= 0 DoJE=T BraDBF=F KetDBF=T FulRan=T + Omega= 0.000000 0.000000 1.000000 0.000000 0.000000 ICntrl= 500 IOpCl= 0 + NMat0= 1 NMatS0= 1 NMatT0= 0 NMatD0= 1 NMtDS0= 0 NMtDT0= 0 + I1Cent= 4 NGrid= 0. + Petite list used in FoFCou. + Initial guess orbital symmetries: + Occupied (A) (A) (A) (A) (A) + Virtual (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) + The electronic state of the initial guess is 1-A. + Requested convergence on RMS density matrix=1.00D-08 within 128 cycles. + Requested convergence on MAX density matrix=1.00D-06. + Requested convergence on energy=1.00D-06. + No special actions if energy rises. + Keep R1 ints in memory in canonical form, NReq=926542. + Integral accuracy reduced to 1.0D-05 until final iterations. + Initial convergence to 1.0D-05 achieved. Increase integral accuracy. + SCF Done: E(RM062X) = -40.2871127467 A.U. after 12 cycles + Convg = 0.9023D-09 -V/T = 2.0089 + + ********************************************************************** + + Population analysis using the SCF density. + + ********************************************************************** + + Orbital symmetries: + Occupied (A) (A) (A) (A) (A) + Virtual (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) + The electronic state is 1-A. + Alpha occ. eigenvalues -- -10.46054 -0.78128 -0.46100 -0.44830 -0.44564 + Alpha virt. eigenvalues -- 0.19791 0.24298 0.24381 0.25316 0.74782 + Alpha virt. eigenvalues -- 0.75837 0.76023 1.10236 1.12944 1.13168 + Alpha virt. eigenvalues -- 1.15260 1.71884 + Condensed to atoms (all electrons): + 1 2 3 4 5 + 1 C 5.307446 0.367569 0.370533 0.370533 0.373456 + 2 H 0.367569 0.516240 -0.025720 -0.025720 -0.028341 + 3 H 0.370533 -0.025720 0.507239 -0.025454 -0.022088 + 4 H 0.370533 -0.025720 -0.025454 0.507238 -0.022088 + 5 H 0.373456 -0.028341 -0.022088 -0.022088 0.496475 + Mulliken atomic charges: + 1 + 1 C -0.789537 + 2 H 0.195972 + 3 H 0.195490 + 4 H 0.195490 + 5 H 0.202586 + Sum of Mulliken atomic charges = 0.00000 + Mulliken charges with hydrogens summed into heavy atoms: + 1 + 1 C 0.000000 + Sum of Mulliken charges with hydrogens summed into heavy atoms = 0.00000 + Electronic spatial extent (au): = 35.3560 + Charge= 0.0000 electrons + Dipole moment (field-independent basis, Debye): + X= -0.0098 Y= 0.0000 Z= 0.0404 Tot= 0.0416 + Quadrupole moment (field-independent basis, Debye-Ang): + XX= -8.1474 YY= -8.2879 ZZ= -8.3882 + XY= 0.0000 XZ= 0.0341 YZ= 0.0000 + Traceless Quadrupole moment (field-independent basis, Debye-Ang): + XX= 0.1271 YY= -0.0134 ZZ= -0.1137 + XY= 0.0000 XZ= 0.0341 YZ= 0.0000 + Octapole moment (field-independent basis, Debye-Ang**2): + XXX= -0.2453 YYY= 0.0000 ZZZ= 0.5819 XYY= 0.7510 + XXY= 0.0000 XXZ= -0.3586 XZZ= -0.5613 YZZ= 0.0000 + YYZ= -0.1560 XYZ= 0.0000 + Hexadecapole moment (field-independent basis, Debye-Ang**3): + XXXX= -15.0090 YYYY= -14.5923 ZZZZ= -14.3002 XXXY= 0.0000 + XXXZ= 0.3977 YYYX= 0.0000 YYYZ= 0.0000 ZZZX= -0.1044 + ZZZY= 0.0000 XXYY= -4.6383 XXZZ= -4.7585 YYZZ= -5.2414 + XXYZ= 0.0000 YYXZ= -0.1389 ZZXY= 0.0000 + N-N= 1.346433270389D+01 E-N=-1.194730892416D+02 KE= 3.991055875889D+01 + Calling FoFJK, ICntrl= 2127 FMM=F ISym2X=0 I1Cent= 0 IOpClX= 0 NMat=1 NMatS=1 NMatT=0. + ***** Axes restored to original set ***** + ------------------------------------------------------------------- + Center Atomic Forces (Hartrees/Bohr) + Number Number X Y Z + ------------------------------------------------------------------- + 1 6 0.021957095 0.002153801 0.000000068 + 2 1 0.002734461 0.002053020 0.000000044 + 3 1 -0.004878219 0.000329877 0.000982023 + 4 1 -0.004878237 0.000329982 -0.000982131 + 5 1 -0.014935100 -0.004866680 -0.000000005 + ------------------------------------------------------------------- + Cartesian Forces: Max 0.021957095 RMS 0.007279779 + + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + Berny optimization. + Internal Forces: Max 0.014371154 RMS 0.004904632 + Search for a local minimum. + Step number 1 out of a maximum of 24 + All quantities printed in internal units (Hartrees-Bohrs-Radians) + Mixed Optimization -- RFO/linear search + Second derivative matrix not updated -- first step. + The second derivative matrix: + R1 R2 R3 R4 A1 + R1 0.34799 + R2 0.00000 0.34177 + R3 0.00000 0.00000 0.34177 + R4 0.00000 0.00000 0.00000 0.37230 + A1 0.00000 0.00000 0.00000 0.00000 0.16000 + A2 0.00000 0.00000 0.00000 0.00000 0.00000 + A3 0.00000 0.00000 0.00000 0.00000 0.00000 + A4 0.00000 0.00000 0.00000 0.00000 0.00000 + A5 0.00000 0.00000 0.00000 0.00000 0.00000 + A6 0.00000 0.00000 0.00000 0.00000 0.00000 + D1 0.00000 0.00000 0.00000 0.00000 0.00000 + D2 0.00000 0.00000 0.00000 0.00000 0.00000 + D3 0.00000 0.00000 0.00000 0.00000 0.00000 + D4 0.00000 0.00000 0.00000 0.00000 0.00000 + A2 A3 A4 A5 A6 + A2 0.16000 + A3 0.00000 0.16000 + A4 0.00000 0.00000 0.16000 + A5 0.00000 0.00000 0.00000 0.16000 + A6 0.00000 0.00000 0.00000 0.00000 0.16000 + D1 0.00000 0.00000 0.00000 0.00000 0.00000 + D2 0.00000 0.00000 0.00000 0.00000 0.00000 + D3 0.00000 0.00000 0.00000 0.00000 0.00000 + D4 0.00000 0.00000 0.00000 0.00000 0.00000 + D1 D2 D3 D4 + D1 0.00230 + D2 0.00000 0.00499 + D3 0.00000 0.00000 0.00499 + D4 0.00000 0.00000 0.00000 0.00499 + Eigenvalues --- 0.04961 0.05652 0.09224 0.16000 0.16000 + Eigenvalues --- 0.34177 0.34177 0.34799 0.372301000.00000 + Eigenvalues --- 1000.000001000.000001000.000001000.00000 + RFO step: Lambda=-1.49996184D-03 EMin= 4.96097912D-02 + Linear search not attempted -- first point. + Iteration 1 RMS(Cart)= 0.02177600 RMS(Int)= 0.00108538 + Iteration 2 RMS(Cart)= 0.00063198 RMS(Int)= 0.00069582 + Iteration 3 RMS(Cart)= 0.00000080 RMS(Int)= 0.00069582 + Variable Old X -DE/DX Delta X Delta X Delta X New X + (Linear) (Quad) (Total) + R1 2.06002 0.00296 0.00000 0.00847 0.00847 2.06849 + R2 2.07033 -0.00258 0.00000 -0.00753 -0.00753 2.06280 + R3 2.07033 -0.00258 0.00000 -0.00753 -0.00753 2.06280 + R4 2.02201 0.01437 0.00000 0.03845 0.03845 2.06045 + A1 1.88662 -0.00014 0.00000 0.01587 0.01613 1.90274 + A2 1.88662 0.00053 0.00000 0.01635 0.01670 1.90332 + A3 1.87181 0.00575 0.00000 0.03950 0.04010 1.91190 + A4 1.89453 0.00388 0.00000 0.01151 0.00968 1.90421 + A5 1.96073 -0.00468 0.00000 -0.03945 -0.03997 1.92076 + A6 1.96073 -0.00504 0.00000 -0.03947 -0.04004 1.92069 + D1 -2.04238 -0.00222 0.00000 -0.03386 -0.03417 -2.07655 + D2 2.07054 0.00080 0.00000 0.02183 0.02119 2.09172 + D3 -2.07054 -0.00141 0.00000 -0.02242 -0.02186 -2.09239 + D4 2.14211 -0.00221 0.00000 -0.04425 -0.04305 2.09907 + Item Value Threshold Converged? + Maximum Force 0.014371 0.000450 NO + RMS Force 0.004905 0.000300 NO + Maximum Displacement 0.047373 0.001800 NO + RMS Displacement 0.022060 0.001200 NO + Predicted change in Energy=-7.479462D-04 + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + + Input orientation: + --------------------------------------------------------------------- + Center Atomic Atomic Coordinates (Angstroms) + Number Number Type X Y Z + --------------------------------------------------------------------- + 1 6 0 0.673344 -0.009129 0.000064 + 2 1 0 1.106749 0.996010 -0.000158 + 3 1 0 1.013141 -0.543235 -0.889225 + 4 1 0 1.013030 -0.543439 0.889273 + 5 1 0 -0.414627 0.062773 0.000046 + --------------------------------------------------------------------- + Distance matrix (angstroms): + 1 2 3 4 5 + 1 C 0.000000 + 2 H 1.094598 0.000000 + 3 H 1.091589 1.780021 0.000000 + 4 H 1.091588 1.780386 1.778497 0.000000 + 5 H 1.090345 1.784802 1.787895 1.787854 0.000000 + Stoichiometry CH4 + Framework group C1[X(CH4)] + Deg. of freedom 9 + Full point group C1 NOp 1 + Largest Abelian subgroup C1 NOp 1 + Largest concise Abelian subgroup C1 NOp 1 + Standard orientation: + --------------------------------------------------------------------- + Center Atomic Atomic Coordinates (Angstroms) + Number Number Type X Y Z + --------------------------------------------------------------------- + 1 6 0 0.002119 -0.001558 0.000187 + 2 1 0 -0.110386 1.077288 -0.146709 + 3 1 0 -0.485319 -0.286094 0.934537 + 4 1 0 -0.478693 -0.525951 -0.827700 + 5 1 0 1.061684 -0.255894 0.038747 + --------------------------------------------------------------------- + Rotational constants (GHZ): 158.3875971 157.4153115 157.2643520 + Standard basis: 3-21G (6D, 7F) + There are 17 symmetry adapted basis functions of A symmetry. + Integral buffers will be 262144 words long. + Raffenetti 2 integral format. + Two-electron integral symmetry is turned on. + 17 basis functions, 27 primitive gaussians, 17 cartesian basis functions + 5 alpha electrons 5 beta electrons + nuclear repulsion energy 13.4104812799 Hartrees. + NAtoms= 5 NActive= 5 NUniq= 5 SFac= 7.50D-01 NAtFMM= 80 NAOKFM=F Big=F + One-electron integrals computed using PRISM. + NBasis= 17 RedAO= T NBF= 17 + NBsUse= 17 1.00D-06 NBFU= 17 + Initial guess read from the read-write file. + B after Tr= 0.000000 0.000000 0.000000 + Rot= 1.000000 0.000000 0.000000 0.000000 Ang= 0.00 deg. + Initial guess orbital symmetries: + Occupied (A) (A) (A) (A) (A) + Virtual (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) + Harris functional with IExCor= 1009 diagonalized for initial guess. + ExpMin= 1.83D-01 ExpMax= 1.72D+02 ExpMxC= 1.72D+02 IAcc=1 IRadAn= 1 AccDes= 0.00D+00 + HarFok: IExCor= 1009 AccDes= 0.00D+00 IRadAn= 1 IDoV= 1 + ScaDFX= 1.000000 1.000000 1.000000 1.000000 + FoFCou: FMM=F IPFlag= 0 FMFlag= 100000 FMFlg1= 0 + NFxFlg= 0 DoJE=T BraDBF=F KetDBF=T FulRan=T + Omega= 0.000000 0.000000 1.000000 0.000000 0.000000 ICntrl= 500 IOpCl= 0 + NMat0= 1 NMatS0= 1 NMatT0= 0 NMatD0= 1 NMtDS0= 0 NMtDT0= 0 + I1Cent= 4 NGrid= 0. + Petite list used in FoFCou. + Requested convergence on RMS density matrix=1.00D-08 within 128 cycles. + Requested convergence on MAX density matrix=1.00D-06. + Requested convergence on energy=1.00D-06. + No special actions if energy rises. + Keep R1 ints in memory in canonical form, NReq=926542. + Integral accuracy reduced to 1.0D-05 until final iterations. + Initial convergence to 1.0D-05 achieved. Increase integral accuracy. + SCF Done: E(RM062X) = -40.2871127467 A.U. after 13 cycles + Convg = 0.1185D-08 -V/T = 2.0095 + Calling FoFJK, ICntrl= 2127 FMM=F ISym2X=0 I1Cent= 0 IOpClX= 0 NMat=1 NMatS=1 NMatT=0. + ***** Axes restored to original set ***** + ------------------------------------------------------------------- + Center Atomic Forces (Hartrees/Bohr) + Number Number X Y Z + ------------------------------------------------------------------- + 1 6 0.003507390 0.002088615 -0.000141026 + 2 1 -0.001110830 -0.001167501 0.000030065 + 3 1 -0.000958633 -0.000207975 -0.000398002 + 4 1 -0.000858560 -0.000232711 0.000477364 + 5 1 -0.000579367 -0.000480428 0.000031600 + ------------------------------------------------------------------- + Cartesian Forces: Max 0.003507390 RMS 0.001210762 + + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + Berny optimization. + Using GEDIIS/GDIIS optimizer. + Internal Forces: Max 0.001511856 RMS 0.000646524 + Search for a local minimum. + Step number 2 out of a maximum of 24 + All quantities printed in internal units (Hartrees-Bohrs-Radians) + Mixed Optimization -- En-DIIS/RFO-DIIS + Update second derivatives using D2CorX and points 1 2 + DE= -8.27D-04 DEPred=-7.48D-04 R= 1.11D+00 + SS= 1.41D+00 RLast= 1.05D-01 DXNew= 5.0454D-01 3.1538D-01 + Trust test= 1.11D+00 RLast= 1.05D-01 DXMaxT set to 3.15D-01 + The second derivative matrix: + R1 R2 R3 R4 A1 + R1 0.35686 + R2 -0.00383 0.34275 + R3 -0.00419 0.00119 0.34318 + R4 0.01721 -0.00294 -0.00404 0.37590 + A1 -0.00625 0.00514 0.00517 -0.02828 0.15566 + A2 -0.00508 0.00448 0.00448 -0.02499 -0.00461 + A3 0.00575 -0.00013 -0.00057 -0.00446 -0.01252 + A4 0.00721 -0.00356 -0.00381 0.01692 -0.00349 + A5 -0.00041 -0.00310 -0.00278 0.02089 0.01205 + A6 -0.00108 -0.00270 -0.00237 0.01887 0.01212 + D1 -0.00383 0.00228 0.00238 -0.01157 0.00046 + D2 0.00264 -0.00154 -0.00161 0.00779 -0.00041 + D3 -0.00390 0.00231 0.00241 -0.01169 0.00052 + D4 -0.00654 0.00385 0.00402 -0.01948 0.00093 + A2 A3 A4 A5 A6 + A2 0.15524 + A3 -0.01122 0.15554 + A4 -0.00264 0.00621 0.16557 + A5 0.01124 0.01110 -0.00247 0.14423 + A6 0.01125 0.01029 -0.00294 -0.01521 0.14538 + D1 0.00010 -0.00465 -0.00270 0.00319 0.00338 + D2 -0.00016 0.00311 0.00188 -0.00207 -0.00220 + D3 0.00015 -0.00469 -0.00277 0.00318 0.00337 + D4 0.00031 -0.00780 -0.00465 0.00525 0.00557 + D1 D2 D3 D4 + D1 0.00338 + D2 -0.00077 0.00554 + D3 0.00111 -0.00079 0.00614 + D4 0.00188 -0.00134 0.00194 0.00827 + Use linear search instead of GDIIS. + Eigenvalues --- 0.04910 0.05714 0.08482 0.15220 0.16040 + Eigenvalues --- 0.34168 0.34202 0.34845 0.387671000.00000 + Eigenvalues --- 1000.000001000.000001000.000001000.00000 + RFO step: Lambda=-3.38508927D-05 EMin= 4.91004951D-02 + Quartic linear search produced a step of 0.09347. + Iteration 1 RMS(Cart)= 0.00400499 RMS(Int)= 0.00009628 + Iteration 2 RMS(Cart)= 0.00002639 RMS(Int)= 0.00009242 + Iteration 3 RMS(Cart)= 0.00000000 RMS(Int)= 0.00009242 + Variable Old X -DE/DX Delta X Delta X Delta X New X + (Linear) (Quad) (Total) + R1 2.06849 -0.00151 0.00079 -0.00537 -0.00458 2.06391 + R2 2.06280 0.00013 -0.00070 0.00096 0.00026 2.06306 + R3 2.06280 0.00024 -0.00070 0.00131 0.00060 2.06341 + R4 2.06045 0.00055 0.00359 -0.00121 0.00239 2.06284 + A1 1.90274 0.00023 0.00151 0.00498 0.00647 1.90921 + A2 1.90332 0.00048 0.00156 0.00455 0.00612 1.90944 + A3 1.91190 0.00016 0.00375 -0.00416 -0.00033 1.91158 + A4 1.90421 0.00075 0.00090 0.00517 0.00582 1.91003 + A5 1.92076 -0.00073 -0.00374 -0.00513 -0.00892 1.91184 + A6 1.92069 -0.00087 -0.00374 -0.00518 -0.00899 1.91170 + D1 -2.07655 -0.00100 -0.00319 -0.01172 -0.01501 -2.09156 + D2 2.09172 -0.00007 0.00198 0.00036 0.00225 2.09397 + D3 -2.09239 -0.00015 -0.00204 0.00021 -0.00177 -2.09416 + D4 2.09907 -0.00008 -0.00402 -0.00015 -0.00402 2.09505 + Item Value Threshold Converged? + Maximum Force 0.001512 0.000450 NO + RMS Force 0.000647 0.000300 NO + Maximum Displacement 0.008022 0.001800 NO + RMS Displacement 0.004003 0.001200 NO + Predicted change in Energy=-2.414175D-05 + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + + Input orientation: + --------------------------------------------------------------------- + Center Atomic Atomic Coordinates (Angstroms) + Number Number Type X Y Z + --------------------------------------------------------------------- + 1 6 0 0.677589 -0.007557 -0.000019 + 2 1 0 1.106054 0.997063 -0.000096 + 3 1 0 1.009960 -0.543415 -0.891225 + 4 1 0 1.009931 -0.543581 0.891321 + 5 1 0 -0.411897 0.060469 0.000018 + --------------------------------------------------------------------- + Distance matrix (angstroms): + 1 2 3 4 5 + 1 C 0.000000 + 2 H 1.092173 0.000000 + 3 H 1.091724 1.782250 0.000000 + 4 H 1.091907 1.782540 1.782546 0.000000 + 5 H 1.091608 1.783644 1.783443 1.783506 0.000000 + Stoichiometry CH4 + Framework group C1[X(CH4)] + Deg. of freedom 9 + Full point group C1 NOp 1 + Largest Abelian subgroup C1 NOp 1 + Largest concise Abelian subgroup C1 NOp 1 + Standard orientation: + --------------------------------------------------------------------- + Center Atomic Atomic Coordinates (Angstroms) + Number Number Type X Y Z + --------------------------------------------------------------------- + 1 6 0 -0.000371 0.000015 0.000066 + 2 1 0 0.457036 -0.463921 -0.876510 + 3 1 0 0.336795 -0.516385 0.900906 + 4 1 0 0.295520 1.049842 0.050789 + 5 1 0 -1.087125 -0.069629 -0.075582 + --------------------------------------------------------------------- + Rotational constants (GHZ): 157.8349206 157.7061699 157.6713790 + Standard basis: 3-21G (6D, 7F) + There are 17 symmetry adapted basis functions of A symmetry. + Integral buffers will be 262144 words long. + Raffenetti 2 integral format. + Two-electron integral symmetry is turned on. + 17 basis functions, 27 primitive gaussians, 17 cartesian basis functions + 5 alpha electrons 5 beta electrons + nuclear repulsion energy 13.4125859939 Hartrees. + NAtoms= 5 NActive= 5 NUniq= 5 SFac= 7.50D-01 NAtFMM= 80 NAOKFM=F Big=F + One-electron integrals computed using PRISM. + NBasis= 17 RedAO= T NBF= 17 + NBsUse= 17 1.00D-06 NBFU= 17 + Initial guess read from the read-write file. + B after Tr= 0.000000 0.000000 0.000000 + Rot= 1.000000 0.000000 0.000000 0.000000 Ang= 0.00 deg. + Initial guess orbital symmetries: + Occupied (A) (A) (A) (A) (A) + Virtual (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) + Requested convergence on RMS density matrix=1.00D-08 within 128 cycles. + Requested convergence on MAX density matrix=1.00D-06. + Requested convergence on energy=1.00D-06. + No special actions if energy rises. + Keep R1 ints in memory in canonical form, NReq=926542. + SCF Done: E(RM062X) = -40.2871127467 A.U. after 11 cycles + Convg = 0.1757D-08 -V/T = 2.0094 + Calling FoFJK, ICntrl= 2127 FMM=F ISym2X=0 I1Cent= 0 IOpClX= 0 NMat=1 NMatS=1 NMatT=0. + ***** Axes restored to original set ***** + ------------------------------------------------------------------- + Center Atomic Forces (Hartrees/Bohr) + Number Number X Y Z + ------------------------------------------------------------------- + 1 6 0.000634583 0.000312357 0.000046590 + 2 1 -0.000224125 -0.000255187 -0.000013481 + 3 1 -0.000158850 -0.000039457 -0.000079584 + 4 1 -0.000135847 0.000007116 0.000038893 + 5 1 -0.000115761 -0.000024829 0.000007582 + ------------------------------------------------------------------- + Cartesian Forces: Max 0.000634583 RMS 0.000213726 + + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + Berny optimization. + Using GEDIIS/GDIIS optimizer. + Internal Forces: Max 0.000322658 RMS 0.000117070 + Search for a local minimum. + Step number 3 out of a maximum of 24 + All quantities printed in internal units (Hartrees-Bohrs-Radians) + Mixed Optimization -- En-DIIS/RFO-DIIS + Swaping is turned off. + Update second derivatives using D2CorX and points 1 2 3 + DE= -2.30D-05 DEPred=-2.41D-05 R= 9.53D-01 + SS= 1.41D+00 RLast= 2.35D-02 DXNew= 5.3041D-01 7.0382D-02 + Trust test= 9.53D-01 RLast= 2.35D-02 DXMaxT set to 3.15D-01 + The second derivative matrix: + R1 R2 R3 R4 A1 + R1 0.34390 + R2 -0.00267 0.34272 + R3 -0.00387 0.00111 0.34338 + R4 0.02285 -0.00385 -0.00398 0.37563 + A1 0.00887 0.00439 0.00352 -0.03744 0.14709 + A2 0.00394 0.00385 0.00383 -0.02960 -0.01222 + A3 -0.00572 0.00009 0.00114 0.00419 -0.00980 + A4 0.02137 -0.00465 -0.00476 0.01014 -0.01613 + A5 -0.01527 -0.00196 -0.00174 0.02802 0.02505 + A6 -0.01339 -0.00158 -0.00180 0.02396 0.02514 + D1 0.01272 0.00213 -0.00063 -0.02460 -0.00001 + D2 0.00615 -0.00169 -0.00208 0.00556 -0.00185 + D3 -0.00394 0.00243 0.00224 -0.01224 0.00194 + D4 -0.01008 0.00412 0.00431 -0.01780 0.00380 + A2 A3 A4 A5 A6 + A2 0.14991 + A3 -0.00660 0.15820 + A4 -0.01121 0.01439 0.15192 + A5 0.02014 0.00280 0.01172 0.12948 + A6 0.01933 0.00070 0.00972 -0.02843 0.13417 + D1 -0.00543 -0.01235 -0.01288 0.01335 0.01651 + D2 -0.00174 0.00312 -0.00080 0.00067 0.00072 + D3 0.00060 -0.00641 -0.00220 0.00255 0.00321 + D4 0.00234 -0.00953 -0.00140 0.00188 0.00249 + D1 D2 D3 D4 + D1 0.02149 + D2 0.00024 0.00537 + D3 0.00407 -0.00039 0.00637 + D4 0.00384 -0.00076 0.00176 0.00752 + Eigenvalues --- 0.04851 0.05792 0.07742 0.15251 0.16037 + Eigenvalues --- 0.33385 0.34189 0.34340 0.389001000.00000 + Eigenvalues --- 1000.000001000.000001000.000001000.00000 + En-DIIS/RFO-DIIS IScMMF= 0 using points: 3 2 + RFO step: Lambda=-5.03169379D-07. + DIIS coeffs: 1.19097 -0.19097 + Iteration 1 RMS(Cart)= 0.00072421 RMS(Int)= 0.00000745 + Iteration 2 RMS(Cart)= 0.00000087 RMS(Int)= 0.00000740 + Variable Old X -DE/DX Delta X Delta X Delta X New X + (DIIS) (GDIIS) (Total) + R1 2.06391 -0.00032 -0.00088 -0.00027 -0.00114 2.06277 + R2 2.06306 0.00004 0.00005 0.00005 0.00010 2.06316 + R3 2.06341 -0.00001 0.00011 -0.00018 -0.00006 2.06334 + R4 2.06284 0.00011 0.00046 0.00009 0.00055 2.06339 + A1 1.90921 0.00004 0.00124 -0.00007 0.00116 1.91037 + A2 1.90944 0.00008 0.00117 -0.00004 0.00113 1.91057 + A3 1.91158 -0.00002 -0.00006 -0.00043 -0.00049 1.91109 + A4 1.91003 0.00012 0.00111 0.00017 0.00126 1.91129 + A5 1.91184 -0.00010 -0.00170 0.00011 -0.00159 1.91024 + A6 1.91170 -0.00011 -0.00172 0.00026 -0.00146 1.91024 + D1 -2.09156 -0.00017 -0.00287 0.00001 -0.00287 -2.09443 + D2 2.09397 -0.00003 0.00043 -0.00028 0.00014 2.09411 + D3 -2.09416 -0.00002 -0.00034 0.00015 -0.00019 -2.09435 + D4 2.09505 0.00001 -0.00077 0.00043 -0.00033 2.09472 + Item Value Threshold Converged? + Maximum Force 0.000323 0.000450 YES + RMS Force 0.000117 0.000300 YES + Maximum Displacement 0.001587 0.001800 YES + RMS Displacement 0.000724 0.001200 YES + Predicted change in Energy=-7.635348D-07 + Optimization completed. + -- Stationary point found. + ---------------------------- + ! Optimized Parameters ! + ! (Angstroms and Degrees) ! + -------------------------- -------------------------- + ! Name Definition Value Derivative Info. ! + -------------------------------------------------------------------------------- + ! R1 R(1,2) 1.0922 -DE/DX = -0.0003 ! + ! R2 R(1,3) 1.0917 -DE/DX = 0.0 ! + ! R3 R(1,4) 1.0919 -DE/DX = 0.0 ! + ! R4 R(1,5) 1.0916 -DE/DX = 0.0001 ! + ! A1 A(2,1,3) 109.3899 -DE/DX = 0.0 ! + ! A2 A(2,1,4) 109.4027 -DE/DX = 0.0001 ! + ! A3 A(2,1,5) 109.5252 -DE/DX = 0.0 ! + ! A4 A(3,1,4) 109.4366 -DE/DX = 0.0001 ! + ! A5 A(3,1,5) 109.5403 -DE/DX = -0.0001 ! + ! A6 A(4,1,5) 109.5324 -DE/DX = -0.0001 ! + ! D1 D(2,1,4,3) -119.8375 -DE/DX = -0.0002 ! + ! D2 D(2,1,5,3) 119.9758 -DE/DX = 0.0 ! + ! D3 D(2,1,5,4) -119.9867 -DE/DX = 0.0 ! + ! D4 D(3,1,5,4) 120.0375 -DE/DX = 0.0 ! + -------------------------------------------------------------------------------- + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + + Input orientation: + --------------------------------------------------------------------- + Center Atomic Atomic Coordinates (Angstroms) + Number Number Type X Y Z + --------------------------------------------------------------------- + 1 6 0 0.677589 -0.007557 -0.000019 + 2 1 0 1.106054 0.997063 -0.000096 + 3 1 0 1.009960 -0.543415 -0.891225 + 4 1 0 1.009931 -0.543581 0.891321 + 5 1 0 -0.411897 0.060469 0.000018 + --------------------------------------------------------------------- + Distance matrix (angstroms): + 1 2 3 4 5 + 1 C 0.000000 + 2 H 1.092173 0.000000 + 3 H 1.091724 1.782250 0.000000 + 4 H 1.091907 1.782540 1.782546 0.000000 + 5 H 1.091608 1.783644 1.783443 1.783506 0.000000 + Stoichiometry CH4 + Framework group C1[X(CH4)] + Deg. of freedom 9 + Full point group C1 NOp 1 + Largest Abelian subgroup C1 NOp 1 + Largest concise Abelian subgroup C1 NOp 1 + Standard orientation: + --------------------------------------------------------------------- + Center Atomic Atomic Coordinates (Angstroms) + Number Number Type X Y Z + --------------------------------------------------------------------- + 1 6 0 -0.000371 0.000015 0.000066 + 2 1 0 0.457036 -0.463921 -0.876510 + 3 1 0 0.336795 -0.516385 0.900906 + 4 1 0 0.295520 1.049842 0.050789 + 5 1 0 -1.087125 -0.069629 -0.075582 + --------------------------------------------------------------------- + Rotational constants (GHZ): 157.8349206 157.7061699 157.6713790 + + ********************************************************************** + + Population analysis using the SCF density. + + ********************************************************************** + + Orbital symmetries: + Occupied (A) (A) (A) (A) (A) + Virtual (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) + The electronic state is 1-A. + Alpha occ. eigenvalues -- -10.46215 -0.77968 -0.45112 -0.45080 -0.45064 + Alpha virt. eigenvalues -- 0.19703 0.24526 0.24538 0.24554 0.75711 + Alpha virt. eigenvalues -- 0.75723 0.75732 1.09776 1.13330 1.13359 + Alpha virt. eigenvalues -- 1.13421 1.71673 + Condensed to atoms (all electrons): + 1 2 3 4 5 + 1 C 5.306096 0.369964 0.370012 0.370005 0.370153 + 2 H 0.369964 0.507752 -0.024751 -0.024735 -0.024614 + 3 H 0.370012 -0.024751 0.507536 -0.024716 -0.024618 + 4 H 0.370005 -0.024735 -0.024716 0.507501 -0.024615 + 5 H 0.370153 -0.024614 -0.024618 -0.024615 0.506944 + Mulliken atomic charges: + 1 + 1 C -0.786231 + 2 H 0.196384 + 3 H 0.196537 + 4 H 0.196559 + 5 H 0.196750 + Sum of Mulliken atomic charges = 0.00000 + Mulliken charges with hydrogens summed into heavy atoms: + 1 + 1 C 0.000000 + Sum of Mulliken charges with hydrogens summed into heavy atoms = 0.00000 + Electronic spatial extent (au): = 35.5042 + Charge= 0.0000 electrons + Dipole moment (field-independent basis, Debye): + X= 0.0008 Y= 0.0002 Z= 0.0001 Tot= 0.0008 + Quadrupole moment (field-independent basis, Debye-Ang): + XX= -8.2789 YY= -8.2847 ZZ= -8.2864 + XY= 0.0004 XZ= 0.0006 YZ= -0.0005 + Traceless Quadrupole moment (field-independent basis, Debye-Ang): + XX= 0.0044 YY= -0.0014 ZZ= -0.0031 + XY= 0.0004 XZ= 0.0006 YZ= -0.0005 + Octapole moment (field-independent basis, Debye-Ang**2): + XXX= -0.8740 YYY= 0.7122 ZZZ= 0.0458 XYY= 0.3946 + XXY= -0.1133 XXZ= -0.1283 XZZ= 0.4797 YZZ= -0.5981 + YYZ= 0.0834 XYZ= 0.0302 + Hexadecapole moment (field-independent basis, Debye-Ang**3): + XXXX= -14.3491 YYYY= -14.4938 ZZZZ= -14.5874 XXXY= 0.0596 + XXXZ= 0.0563 YYYX= 0.2818 YYYZ= 0.0240 ZZZX= -0.0674 + ZZZY= -0.0739 XXYY= -5.1311 XXZZ= -5.0385 YYZZ= -4.8981 + XXYZ= 0.0480 YYXZ= 0.0134 ZZXY= -0.3399 + N-N= 1.341258599393D+01 E-N=-1.193560542338D+02 KE= 3.988825099275D+01 + 1|1|UNPC-DESKTOP-8TQV1GH|FOpt|RM062X|3-21G|C1H4|JUANV|16-Jan-2022|0||# + opt freq 3-21g m062x||Title Card Required||0,1|C,0.6775892097,-0.0075 + 565329,-0.0000188707|H,1.106054315,0.9970629703,-0.0000962122|H,1.0099 + 601355,-0.5434145111,-0.8912248196|H,1.0099307005,-0.5435813286,0.8913 + 213877|H,-0.4118973607,0.0604689423,0.0000181355||Version=IA32W-G09Rev + A.02|State=1-A|HF=-40.2649626|RMSD=1.757e-009|RMSF=2.137e-004|Dipole=0 + .000299,-0.0000692,0.0000573|Quadrupole=0.0033041,-0.0023057,-0.000998 + 3,-0.000343,-0.0000587,-0.0003229|PG=C01 [X(C1H4)]||@ + + + "WOULD YOU TELL ME PLEASE, WHICH WAY I OUGHT TO WALK FROM HERE?" + "THAT DEPENDS A GREAT DEAL ON WHERE YOU WANT TO GO," SAID THE CAT. + "I DON'T MUCH CARE WHERE -- ", SAID ALICE. + "THEN IT DOESN'T MATTER WHICH WAY YOU WALK," SAID THE CAT. + + -- LEWIS CARROLL + Job cpu time: 0 days 0 hours 0 minutes 16.0 seconds. + File lengths (MBytes): RWF= 5 Int= 0 D2E= 0 Chk= 1 Scr= 1 + Normal termination of Gaussian 09 at Sun Jan 16 19:38:30 2022. + Link1: Proceeding to internal job step number 2. + ----------------------------------------------------------------- + #N Geom=AllCheck Guess=TCheck SCRF=Check GenChk RM062X/3-21G Freq + ----------------------------------------------------------------- + 1/10=4,29=7,30=1,38=1,40=1/1,3; + 2/12=2,40=1/2; + 3/5=5,11=2,14=-4,16=1,25=1,30=1,70=2,71=2,74=-55,116=1/1,2,3; + 4/5=101/1; + 5/5=2,98=1/2; + 8/6=4,10=90,11=11/1; + 11/6=1,8=1,9=11,15=111,16=1/1,2,10; + 10/6=1/2; + 6/7=2,8=2,9=2,10=2,18=1,28=1/1; + 7/8=1,10=1,25=1/1,2,3,16; + 1/10=4,30=1/3; + 99//99; + ------------------- + Title Card Required + ------------------- + Redundant internal coordinates taken from checkpoint file: + C:/G09W/Scratch\gxx.chk + Charge = 0 Multiplicity = 1 + C,0,0.6775892097,-0.0075565329,-0.0000188707 + H,0,1.106054315,0.9970629703,-0.0000962122 + H,0,1.0099601355,-0.5434145111,-0.8912248196 + H,0,1.0099307005,-0.5435813286,0.8913213877 + H,0,-0.4118973607,0.0604689423,0.0000181355 + Recover connectivity data from disk. + + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + Berny optimization. + Initialization pass. + ---------------------------- + ! Initial Parameters ! + ! (Angstroms and Degrees) ! + -------------------------- -------------------------- + ! Name Definition Value Derivative Info. ! + -------------------------------------------------------------------------------- + ! R1 R(1,2) 1.0922 calculate D2E/DX2 analytically ! + ! R2 R(1,3) 1.0917 calculate D2E/DX2 analytically ! + ! R3 R(1,4) 1.0919 calculate D2E/DX2 analytically ! + ! R4 R(1,5) 1.0916 calculate D2E/DX2 analytically ! + ! A1 A(2,1,3) 109.3899 calculate D2E/DX2 analytically ! + ! A2 A(2,1,4) 109.4027 calculate D2E/DX2 analytically ! + ! A3 A(2,1,5) 109.5252 calculate D2E/DX2 analytically ! + ! A4 A(3,1,4) 109.4366 calculate D2E/DX2 analytically ! + ! A5 A(3,1,5) 109.5403 calculate D2E/DX2 analytically ! + ! A6 A(4,1,5) 109.5324 calculate D2E/DX2 analytically ! + ! D1 D(2,1,4,3) -119.8375 calculate D2E/DX2 analytically ! + ! D2 D(2,1,5,3) 119.9758 calculate D2E/DX2 analytically ! + ! D3 D(2,1,5,4) -119.9867 calculate D2E/DX2 analytically ! + ! D4 D(3,1,5,4) 120.0375 calculate D2E/DX2 analytically ! + -------------------------------------------------------------------------------- + Trust Radius=3.00D-01 FncErr=1.00D-07 GrdErr=1.00D-07 + Number of steps in this run= 2 maximum allowed number of steps= 2. + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + + Input orientation: + --------------------------------------------------------------------- + Center Atomic Atomic Coordinates (Angstroms) + Number Number Type X Y Z + --------------------------------------------------------------------- + 1 6 0 0.677589 -0.007557 -0.000019 + 2 1 0 1.106054 0.997063 -0.000096 + 3 1 0 1.009960 -0.543415 -0.891225 + 4 1 0 1.009931 -0.543581 0.891321 + 5 1 0 -0.411897 0.060469 0.000018 + --------------------------------------------------------------------- + Distance matrix (angstroms): + 1 2 3 4 5 + 1 C 0.000000 + 2 H 1.092173 0.000000 + 3 H 1.091724 1.782250 0.000000 + 4 H 1.091907 1.782540 1.782546 0.000000 + 5 H 1.091608 1.783644 1.783443 1.783506 0.000000 + Stoichiometry CH4 + Framework group C1[X(CH4)] + Deg. of freedom 9 + Full point group C1 NOp 1 + Largest Abelian subgroup C1 NOp 1 + Largest concise Abelian subgroup C1 NOp 1 + Standard orientation: + --------------------------------------------------------------------- + Center Atomic Atomic Coordinates (Angstroms) + Number Number Type X Y Z + --------------------------------------------------------------------- + 1 6 0 -0.000371 0.000015 0.000066 + 2 1 0 0.457036 -0.463921 -0.876510 + 3 1 0 0.336795 -0.516385 0.900906 + 4 1 0 0.295520 1.049842 0.050789 + 5 1 0 -1.087125 -0.069629 -0.075582 + --------------------------------------------------------------------- + Rotational constants (GHZ): 157.8349206 157.7061699 157.6713790 + Standard basis: 3-21G (6D, 7F) + There are 17 symmetry adapted basis functions of A symmetry. + Integral buffers will be 262144 words long. + Raffenetti 2 integral format. + Two-electron integral symmetry is turned on. + 17 basis functions, 27 primitive gaussians, 17 cartesian basis functions + 5 alpha electrons 5 beta electrons + nuclear repulsion energy 13.4125859939 Hartrees. + NAtoms= 5 NActive= 5 NUniq= 5 SFac= 7.50D-01 NAtFMM= 80 NAOKFM=F Big=F + One-electron integrals computed using PRISM. + NBasis= 17 RedAO= T NBF= 17 + NBsUse= 17 1.00D-06 NBFU= 17 + Initial guess read from the checkpoint file: C:/G09W/Scratch\gxx.chk + B after Tr= 0.000000 0.000000 0.000000 + Rot= 1.000000 0.000000 0.000000 0.000000 Ang= 0.00 deg. + Initial guess orbital symmetries: + Occupied (A) (A) (A) (A) (A) + Virtual (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) + Requested convergence on RMS density matrix=1.00D-08 within 128 cycles. + Requested convergence on MAX density matrix=1.00D-06. + Requested convergence on energy=1.00D-06. + No special actions if energy rises. + Keep R1 ints in memory in canonical form, NReq=926542. + SCF Done: E(RM062X) = -40.2871127467 A.U. after 1 cycles + Convg = 0.2865D-09 -V/T = 2.0094 + Range of M.O.s used for correlation: 1 17 + NBasis= 17 NAE= 5 NBE= 5 NFC= 0 NFV= 0 + NROrb= 17 NOA= 5 NOB= 5 NVA= 12 NVB= 12 + Symmetrizing basis deriv contribution to polar: + IMax=3 JMax=2 DiffMx= 0.00D+00 + G2DrvN: will do 6 centers at a time, making 1 passes doing MaxLOS=1. + Calling FoFCou, ICntrl= 3107 FMM=F I1Cent= 0 AccDes= 0.00D+00. + FoFDir/FoFCou used for L=0 through L=1. + End of G2Drv Frequency-dependent properties file 721 does not exist. + End of G2Drv Frequency-dependent properties file 722 does not exist. + IDoAtm=11111 + Differentiating once with respect to electric field. + with respect to dipole field. + Differentiating once with respect to nuclear coordinates. + Keep R1 ints in memory in canonical form, NReq=812730. + There are 18 degrees of freedom in the 1st order CPHF. IDoFFX=5. + 15 vectors produced by pass 0 Test12= 3.33D-16 5.56D-09 XBig12= 3.94D+00 1.34D+00. + AX will form 15 AO Fock derivatives at one time. + 15 vectors produced by pass 1 Test12= 3.33D-16 5.56D-09 XBig12= 1.43D-02 7.21D-02. + 15 vectors produced by pass 2 Test12= 3.33D-16 5.56D-09 XBig12= 8.09D-06 1.24D-03. + 14 vectors produced by pass 3 Test12= 3.33D-16 5.56D-09 XBig12= 1.95D-08 9.03D-05. + 1 vectors produced by pass 4 Test12= 3.33D-16 5.56D-09 XBig12= 2.96D-13 5.11D-07. + Inverted reduced A of dimension 60 with in-core refinement. + Isotropic polarizability for W= 0.000000 11.37 Bohr**3. + End of Minotr Frequency-dependent properties file 721 does not exist. + End of Minotr Frequency-dependent properties file 722 does not exist. + + ********************************************************************** + + Population analysis using the SCF density. + + ********************************************************************** + + Orbital symmetries: + Occupied (A) (A) (A) (A) (A) + Virtual (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) (A) + The electronic state is 1-A. + Alpha occ. eigenvalues -- -10.46215 -0.77968 -0.45112 -0.45080 -0.45064 + Alpha virt. eigenvalues -- 0.19703 0.24526 0.24538 0.24554 0.75711 + Alpha virt. eigenvalues -- 0.75723 0.75732 1.09776 1.13330 1.13359 + Alpha virt. eigenvalues -- 1.13421 1.71673 + Condensed to atoms (all electrons): + 1 2 3 4 5 + 1 C 5.306096 0.369964 0.370012 0.370005 0.370153 + 2 H 0.369964 0.507752 -0.024751 -0.024735 -0.024614 + 3 H 0.370012 -0.024751 0.507536 -0.024716 -0.024618 + 4 H 0.370005 -0.024735 -0.024716 0.507501 -0.024615 + 5 H 0.370153 -0.024614 -0.024618 -0.024615 0.506944 + Mulliken atomic charges: + 1 + 1 C -0.786231 + 2 H 0.196384 + 3 H 0.196537 + 4 H 0.196559 + 5 H 0.196750 + Sum of Mulliken atomic charges = 0.00000 + Mulliken charges with hydrogens summed into heavy atoms: + 1 + 1 C 0.000000 + Sum of Mulliken charges with hydrogens summed into heavy atoms = 0.00000 + APT atomic charges: + 1 + 1 C -0.105789 + 2 H 0.026726 + 3 H 0.026442 + 4 H 0.026078 + 5 H 0.026543 + Sum of APT charges= 0.00000 + APT Atomic charges with hydrogens summed into heavy atoms: + 1 + 1 C 0.000000 + 2 H 0.000000 + 3 H 0.000000 + 4 H 0.000000 + 5 H 0.000000 + Sum of APT charges= 0.00000 + Electronic spatial extent (au): = 35.5042 + Charge= 0.0000 electrons + Dipole moment (field-independent basis, Debye): + X= 0.0008 Y= 0.0002 Z= 0.0001 Tot= 0.0008 + Quadrupole moment (field-independent basis, Debye-Ang): + XX= -8.2789 YY= -8.2847 ZZ= -8.2864 + XY= 0.0004 XZ= 0.0006 YZ= -0.0005 + Traceless Quadrupole moment (field-independent basis, Debye-Ang): + XX= 0.0044 YY= -0.0014 ZZ= -0.0031 + XY= 0.0004 XZ= 0.0006 YZ= -0.0005 + Octapole moment (field-independent basis, Debye-Ang**2): + XXX= -0.8740 YYY= 0.7122 ZZZ= 0.0458 XYY= 0.3946 + XXY= -0.1133 XXZ= -0.1283 XZZ= 0.4797 YZZ= -0.5981 + YYZ= 0.0834 XYZ= 0.0302 + Hexadecapole moment (field-independent basis, Debye-Ang**3): + XXXX= -14.3491 YYYY= -14.4938 ZZZZ= -14.5874 XXXY= 0.0596 + XXXZ= 0.0563 YYYX= 0.2818 YYYZ= 0.0240 ZZZX= -0.0674 + ZZZY= -0.0739 XXYY= -5.1311 XXZZ= -5.0385 YYZZ= -4.8981 + XXYZ= 0.0480 YYXZ= 0.0134 ZZXY= -0.3399 + N-N= 1.341258599393D+01 E-N=-1.193560541790D+02 KE= 3.988825096947D+01 + Exact polarizability: 11.396 0.000 11.363 0.009 -0.001 11.361 + Approx polarizability: 11.303 -0.001 11.297 -0.002 0.001 11.295 + Calling FoFJK, ICntrl= 100127 FMM=F ISym2X=0 I1Cent= 0 IOpClX= 0 NMat=1 NMatS=1 NMatT=0. + Full mass-weighted force constant matrix: + Low frequencies --- -106.7757 -70.3324 -0.0009 -0.0006 0.0005 114.2388 + Low frequencies --- 1415.5696 1418.9968 1422.4140 + Diagonal vibrational polarizability: + 0.4038632 0.4088265 0.4038676 + Harmonic frequencies (cm**-1), IR intensities (KM/Mole), Raman scattering + activities (A**4/AMU), depolarization ratios for plane and unpolarized + incident light, reduced masses (AMU), force constants (mDyne/A), + and normal coordinates: + 1 2 3 + A A A + Frequencies -- -1415.5540 1418.9580 1422.4103 + Red. masses -- 1.1822 1.1821 1.1818 + Frc consts -- 1.3958 1.4023 1.4088 + IR Inten -- 27.4995 27.3074 27.4236 + Atom AN X Y Z X Y Z X Y Z + 1 6 0.08 -0.07 0.07 0.07 0.10 0.03 -0.07 0.02 0.10 + 2 1 -0.36 0.32 -0.36 -0.40 -0.40 0.04 0.07 0.17 0.05 + 3 1 -0.17 0.04 0.18 -0.34 -0.49 -0.15 0.43 -0.24 -0.26 + 4 1 -0.43 0.11 -0.36 -0.15 0.13 -0.10 0.36 -0.07 -0.47 + 5 1 0.05 0.35 -0.32 0.09 -0.47 -0.09 0.00 -0.14 -0.51 + 4 5 6 + A A A + Frequencies -- 1638.5106 1641.8020 3054.0303 + Red. masses -- 1.0079 1.0079 1.0084 + Frc consts -- 1.5942 1.6007 5.5416 + IR Inten -- 0.0057 0.0155 0.0946 + Atom AN X Y Z X Y Z X Y Z + 1 6 0.00 0.00 0.00 0.00 0.00 0.00 -0.01 0.01 0.00 + 2 1 0.35 -0.20 0.29 0.30 0.41 -0.06 0.23 -0.23 -0.44 + 3 1 0.14 -0.39 -0.27 -0.45 -0.19 0.06 0.16 -0.25 0.45 + 4 1 -0.45 0.13 -0.19 0.19 -0.03 -0.46 0.12 0.45 0.02 + 5 1 -0.04 0.47 0.17 -0.02 -0.17 0.47 -0.45 -0.03 -0.03 + 7 8 9 + A A A + Frequencies -- 3153.6387 3162.8459 3172.8647 + Red. masses -- 1.0989 1.0984 1.0990 + Frc consts -- 6.4390 6.4738 6.5184 + IR Inten -- 14.4084 14.6105 14.4819 + Atom AN X Y Z X Y Z X Y Z + 1 6 0.00 -0.01 0.09 0.04 -0.08 -0.01 0.08 0.04 0.01 + 2 1 0.28 -0.29 -0.51 -0.22 0.21 0.43 -0.01 0.05 0.07 + 3 1 -0.24 0.36 -0.61 -0.10 0.15 -0.29 -0.02 0.07 -0.11 + 4 1 0.03 0.10 0.03 0.20 0.66 0.03 -0.13 -0.52 -0.03 + 5 1 -0.02 -0.01 0.02 -0.34 -0.04 -0.03 -0.82 -0.04 -0.06 + + ------------------- + - Thermochemistry - + ------------------- + Temperature 298.150 Kelvin. Pressure 1.00000 Atm. + Atom 1 has atomic number 6 and mass 12.00000 + Atom 2 has atomic number 1 and mass 1.00783 + Atom 3 has atomic number 1 and mass 1.00783 + Atom 4 has atomic number 1 and mass 1.00783 + Atom 5 has atomic number 1 and mass 1.00783 + Molecular mass: 16.03130 amu. + Principal axes and moments of inertia in atomic units: + 1 2 3 + Eigenvalues -- 11.43436 11.44369 11.44622 + X 1.00000 0.00001 0.00003 + Y -0.00001 1.00000 -0.00001 + Z -0.00003 0.00001 1.00000 + This molecule is an asymmetric top. + Rotational symmetry number 1. + Rotational temperatures (Kelvin) 7.57487 7.56869 7.56702 + Rotational constants (GHZ): 157.83492 157.70617 157.67138 + Zero-point vibrational energy 120108.7 (Joules/Mol) + 28.70668 (Kcal/Mol) + Vibrational temperatures: 2036.66 2041.56 2046.53 2357.45 2362.18 + (Kelvin) 4394.06 4537.38 4550.62 4565.04 + + Zero-point correction= 0.045747 (Hartree/Particle) + Thermal correction to Energy= 0.048606 + Thermal correction to Enthalpy= 0.049550 + Thermal correction to Gibbs Free Energy= 0.026082 + Sum of electronic and zero-point Energies= -40.219216 + Sum of electronic and thermal Energies= -40.216357 + Sum of electronic and thermal Enthalpies= -40.215413 + Sum of electronic and thermal Free Energies= -40.738880 + + E (Thermal) CV S + KCal/Mol Cal/Mol-Kelvin Cal/Mol-Kelvin + Total 30.501 6.351 49.392 + Electronic 0.000 0.000 0.000 + Translational 0.889 2.981 34.261 + Rotational 0.889 2.981 15.068 + Vibrational 28.723 0.389 0.063 + Q Log10(Q) Ln(Q) + Total Bot 0.100707D-11 -11.996940 -27.623974 + Total V=0 0.110963D+10 9.045177 20.827290 + Vib (Bot) 0.911141D-21 -21.040414 -48.447345 + Vib (V=0) 0.100393D+01 0.001702 0.003920 + Electronic 0.100000D+01 0.000000 0.000000 + Translational 0.252295D+07 6.401908 14.740939 + Rotational 0.438093D+03 2.641566 6.082432 + ***** Axes restored to original set ***** + ------------------------------------------------------------------- + Center Atomic Forces (Hartrees/Bohr) + Number Number X Y Z + ------------------------------------------------------------------- + 1 6 0.000634582 0.000312357 0.000046589 + 2 1 -0.000224125 -0.000255187 -0.000013481 + 3 1 -0.000158850 -0.000039457 -0.000079584 + 4 1 -0.000135847 0.000007116 0.000038893 + 5 1 -0.000115761 -0.000024829 0.000007582 + ------------------------------------------------------------------- + Cartesian Forces: Max 0.000634582 RMS 0.000213726 + + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + Berny optimization. + Internal Forces: Max 0.000322657 RMS 0.000117070 + Search for a local minimum. + Step number 1 out of a maximum of 2 + All quantities printed in internal units (Hartrees-Bohrs-Radians) + Second derivative matrix not updated -- analytic derivatives used. + The second derivative matrix: + R1 R2 R3 R4 A1 + R1 0.34734 + R2 0.00215 0.34715 + R3 0.00215 0.00240 0.35076 + R4 0.00219 0.00217 0.00221 0.35187 + A1 0.00237 0.00244 -0.00139 -0.00325 0.02156 + A2 0.00364 -0.00097 0.00440 -0.00662 -0.00950 + A3 0.00685 -0.00556 -0.00631 0.00545 -0.01421 + A4 -0.00094 0.00337 0.00345 -0.00654 -0.00947 + A5 -0.00557 0.00703 -0.00620 0.00486 -0.01440 + A6 -0.00634 -0.00631 0.00606 0.00607 0.02602 + D1 -0.00454 -0.00445 -0.00308 0.01199 -0.01482 + D2 0.00369 0.00390 -0.00939 0.00235 0.00887 + D3 -0.00478 0.00847 -0.00524 0.00105 0.00440 + D4 -0.00848 0.00457 0.00415 -0.00131 -0.00447 + A2 A3 A4 A5 A6 + A2 0.04113 + A3 -0.02504 0.07991 + A4 -0.00215 0.02700 0.04083 + A5 0.02704 -0.03860 -0.02472 0.07966 + A6 -0.03142 -0.02906 -0.03141 -0.02902 0.09479 + D1 -0.01212 0.01619 -0.01195 0.01618 0.00643 + D2 -0.01042 0.00795 -0.01021 0.00756 -0.00377 + D3 -0.01575 -0.00054 0.00534 0.00838 -0.00184 + D4 -0.00533 -0.00850 0.01555 0.00082 0.00193 + D1 D2 D3 D4 + D1 0.03276 + D2 0.00171 0.02040 + D3 0.00096 0.01020 0.02077 + D4 -0.00075 -0.01019 0.01057 0.02076 + Eigenvalues --- 0.04151 0.04706 0.07145 0.14377 0.14449 + Eigenvalues --- 0.34638 0.34776 0.35080 0.356471000.00000 + Eigenvalues --- 1000.000001000.000001000.000001000.00000 + Angle between quadratic step and forces= 38.46 degrees. + Linear search not attempted -- first point. + Iteration 1 RMS(Cart)= 0.00067405 RMS(Int)= 0.00000123 + Iteration 2 RMS(Cart)= 0.00000075 RMS(Int)= 0.00000097 + Variable Old X -DE/DX Delta X Delta X Delta X New X + (Linear) (Quad) (Total) + R1 2.06391 -0.00032 0.00000 -0.00103 -0.00103 2.06288 + R2 2.06306 0.00004 0.00000 0.00006 0.00006 2.06312 + R3 2.06341 -0.00001 0.00000 -0.00009 -0.00009 2.06331 + R4 2.06284 0.00011 0.00000 0.00053 0.00053 2.06337 + A1 1.90921 0.00004 0.00000 0.00115 0.00115 1.91037 + A2 1.90944 0.00008 0.00000 0.00111 0.00111 1.91055 + A3 1.91158 -0.00002 0.00000 -0.00067 -0.00067 1.91091 + A4 1.91003 0.00012 0.00000 0.00114 0.00114 1.91116 + A5 1.91184 -0.00010 0.00000 -0.00145 -0.00145 1.91039 + A6 1.91170 -0.00011 0.00000 -0.00128 -0.00129 1.91042 + D1 -2.09156 -0.00017 0.00000 -0.00278 -0.00278 -2.09434 + D2 2.09397 -0.00003 0.00000 0.00012 0.00012 2.09409 + D3 -2.09416 -0.00002 0.00000 -0.00017 -0.00017 -2.09433 + D4 2.09505 0.00001 0.00000 -0.00028 -0.00028 2.09476 + Item Value Threshold Converged? + Maximum Force 0.000323 0.000450 YES + RMS Force 0.000117 0.000300 YES + Maximum Displacement 0.001519 0.001800 YES + RMS Displacement 0.000674 0.001200 YES + Predicted change in Energy=-7.126925D-07 + Optimization completed. + -- Stationary point found. + ---------------------------- + ! Optimized Parameters ! + ! (Angstroms and Degrees) ! + -------------------------- -------------------------- + ! Name Definition Value Derivative Info. ! + -------------------------------------------------------------------------------- + ! R1 R(1,2) 1.0922 -DE/DX = -0.0003 ! + ! R2 R(1,3) 1.0917 -DE/DX = 0.0 ! + ! R3 R(1,4) 1.0919 -DE/DX = 0.0 ! + ! R4 R(1,5) 1.0916 -DE/DX = 0.0001 ! + ! A1 A(2,1,3) 109.3899 -DE/DX = 0.0 ! + ! A2 A(2,1,4) 109.4027 -DE/DX = 0.0001 ! + ! A3 A(2,1,5) 109.5252 -DE/DX = 0.0 ! + ! A4 A(3,1,4) 109.4366 -DE/DX = 0.0001 ! + ! A5 A(3,1,5) 109.5403 -DE/DX = -0.0001 ! + ! A6 A(4,1,5) 109.5324 -DE/DX = -0.0001 ! + ! D1 D(2,1,4,3) -119.8375 -DE/DX = -0.0002 ! + ! D2 D(2,1,5,3) 119.9758 -DE/DX = 0.0 ! + ! D3 D(2,1,5,4) -119.9867 -DE/DX = 0.0 ! + ! D4 D(3,1,5,4) 120.0375 -DE/DX = 0.0 ! + -------------------------------------------------------------------------------- + GradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGradGrad + + 1|1|UNPC-DESKTOP-8TQV1GH|Freq|RM062X|3-21G|C1H4|JUANV|16-Jan-2022|0||# + N Geom=AllCheck Guess=TCheck SCRF=Check GenChk RM062X/3-21G Freq||Titl + e Card Required||0,1|C,0.6775892097,-0.0075565329,-0.0000188707|H,1.10 + 6054315,0.9970629703,-0.0000962122|H,1.0099601355,-0.5434145111,-0.891 + 2248196|H,1.0099307005,-0.5435813286,0.8913213877|H,-0.4118973607,0.06 + 04689423,0.0000181355||Version=IA32W-G09RevA.02|State=1-A|HF=-40.26496 + 26|RMSD=2.865e-010|RMSF=2.137e-004|ZeroPoint=0.045747|Thermal=0.048605 + 7|Dipole=0.000299,-0.0000692,0.0000573|DipoleDeriv=-0.1057772,0.000267 + 6,0.0001972,-0.0006931,-0.105506,-0.0012206,0.0014384,-0.000154,-0.106 + 0834,0.0648883,-0.0757384,0.0000351,-0.0758297,-0.0818218,0.0001148,-0 + .0003826,-0.0005808,0.0971104,0.0770857,0.0317157,0.0523818,0.0314697, + 0.045592,-0.085142,0.0512034,-0.0837108,-0.0433516,0.0768812,0.0316683 + ,-0.0528975,0.0322533,0.0455123,0.0870311,-0.0524709,0.0847099,-0.0441 + 58,-0.113078,0.0120867,0.0002833,0.0127998,0.0962235,-0.0007833,0.0002 + 116,-0.0002644,0.0964826|Polar=11.3959322,-0.0068032,11.3604169,-0.004 + 6148,-0.0006945,11.3635631|PG=C01 [X(C1H4)]|NImag=0||0.56130884,-0.000 + 25821,0.55877681,0.00067190,-0.00163787,0.55535584,-0.09110351,-0.0959 + 4586,-0.00078334,0.09547469,-0.09592660,-0.27582913,0.00017554,0.10710 + 520,0.30179567,-0.00079075,0.00021673,-0.05005636,0.00079937,-0.000156 + 79,0.04962113,-0.07477328,0.03962830,0.06638175,0.00395215,-0.00666020 + ,-0.01320594,0.07718887,0.03957909,-0.11478813,-0.10724795,0.01156017, + -0.01482181,-0.02744966,-0.04424032,0.12187340,0.06646034,-0.10743904, + -0.22658220,-0.00087630,0.00160555,0.00091319,-0.07410472,0.11971484,0 + .24706158,-0.07507148,0.04071503,-0.06690385,0.00394171,-0.00668529,0. + 01322272,0.00271960,-0.00679158,0.00957102,0.07751194,0.04069458,-0.11 + 675489,0.10876418,0.01147482,-0.01492356,0.02737540,-0.00680171,0.0094 + 7937,-0.01546190,-0.04531095,0.12400899,-0.06695848,0.10891002,-0.2285 + 0880,0.00085603,-0.00166199,0.00103744,-0.00954685,0.01542715,-0.02245 + 682,0.07460208,-0.12120507,0.24901630,-0.32036057,0.01586073,0.0006335 + 4,-0.01226504,0.00216689,-0.00002540,-0.00908734,-0.00010735,-0.001050 + 34,-0.00910176,-0.00005674,0.00104722,0.35081471,0.01591114,-0.0514046 + 6,-0.00005390,-0.03419433,0.00377882,0.00001432,0.01807393,-0.00174283 + ,0.00158056,0.01807279,-0.00180990,-0.00147011,-0.01786353,0.05117857, + 0.00061699,-0.00004984,-0.05020849,0.00000423,0.00003770,-0.00151540,0 + .03047576,-0.00044438,0.00106425,-0.03049197,0.00052738,0.00091188,-0. + 00060501,-0.00007087,0.04974776||-0.00063458,-0.00031236,-0.00004659,0 + .00022413,0.00025519,0.00001348,0.00015885,0.00003946,0.00007958,0.000 + 13585,-0.00000712,-0.00003889,0.00011576,0.00002483,-0.00000758|||@ + + + "WOULD YOU TELL ME PLEASE, WHICH WAY I OUGHT TO WALK FROM HERE?" + "THAT DEPENDS A GREAT DEAL ON WHERE YOU WANT TO GO," SAID THE CAT. + "I DON'T MUCH CARE WHERE -- ", SAID ALICE. + "THEN IT DOESN'T MATTER WHICH WAY YOU WALK," SAID THE CAT. + + -- LEWIS CARROLL + Job cpu time: 0 days 0 hours 0 minutes 6.0 seconds. + File lengths (MBytes): RWF= 5 Int= 0 D2E= 0 Chk= 1 Scr= 1 + Normal termination of Gaussian 09 at Sun Jan 16 19:38:36 2022. diff --git a/aqme/aqme.py b/aqme/aqme.py index 3b1bdbb3..4a5d27a8 100644 --- a/aqme/aqme.py +++ b/aqme/aqme.py @@ -183,6 +183,7 @@ def main(): ifreq_cutoff=args.ifreq_cutoff, amplitude_ifreq=args.amplitude_ifreq, freq_conv=args.freq_conv, + im_freq_input=args.im_freq_input, s2_threshold=args.s2_threshold, dup_threshold=args.dup_threshold, ro_threshold=args.ro_threshold, diff --git a/aqme/argument_parser.py b/aqme/argument_parser.py index 50a215a8..4fd57f63 100644 --- a/aqme/argument_parser.py +++ b/aqme/argument_parser.py @@ -82,6 +82,7 @@ "amplitude_ifreq": 0.2, "ifreq_cutoff": 0.0, "freq_conv": None, + "im_freq_input": 'opt=(calcfc,maxstep=5)', "s2_threshold": 10.0, "isom_type": None, "isom_inputs": os.getcwd(), diff --git a/aqme/cmin.py b/aqme/cmin.py index 4f635c86..19160a92 100644 --- a/aqme/cmin.py +++ b/aqme/cmin.py @@ -157,14 +157,15 @@ def __init__(self, **kwargs): "\no Number of finished jobs from CMIN", max=len(self.args.files) ) - file_format = os.path.splitext(self.args.files[0])[1] - if file_format.lower() in ['.xyz', '.gjf', '.com']: + file_format = os.path.basename(Path(self.args.files[0])).split('.')[1] + file_dir = os.path.dirname(Path(self.args.files[0])) + if file_format.lower() in ['xyz', 'gjf', 'com']: for file in self.args.files: prepare_com_files(self.args, file) - if file_format.lower() in ['.gjf', '.com']: - files_temp_extra = glob.glob('*.xyz') - files_cmin = glob.glob('*.sdf') - elif file_format.lower() == '.pdb': + if file_format.lower() in ['gjf', 'com']: + files_temp_extra = glob.glob(f'{file_dir}/*.xyz') + files_cmin = glob.glob(f'{file_dir}/*.sdf') + elif file_format.lower() == 'pdb': for file in self.args.files: command_pdb = [ "obabel", @@ -178,8 +179,8 @@ def __init__(self, **kwargs): stdout=subprocess.DEVNULL, stderr=subprocess.DEVNULL, ) - files_cmin = glob.glob('*.sdf') - elif file_format.lower() == '.sdf': + files_cmin = glob.glob(f'{file_dir}/*.sdf') + elif file_format.lower() == 'sdf': files_cmin = self.args.files else: self.args.log.write(f"\nx The input format {file_format} is not supported for CMIN refinement! Formats allowed: SDF, XYZ, COM, GJF and PDB") @@ -198,7 +199,7 @@ def __init__(self, **kwargs): f"CMIN" ) else: - if Path(f"{self.args.destination}").exists(): + if self.args.initial_dir.as_posix() in f"{self.args.destination}": self.cmin_folder = Path(self.args.destination) else: self.cmin_folder = Path(self.args.initial_dir).joinpath( @@ -233,8 +234,8 @@ def __init__(self, **kwargs): self.args.log.finalize() # delete extra temporary files created when using XYZ, GJF, COM and PDB files - if file_format.lower() in ['.xyz', '.gjf', '.com', '.pdb']: - if file_format.lower() in ['.gjf', '.com']: + if file_format.lower() in ['xyz', 'gjf', 'com', 'pdb']: + if file_format.lower() in ['gjf', 'com']: files_cmin = files_cmin + files_temp_extra for temp_file in files_cmin: os.remove(temp_file) @@ -278,9 +279,9 @@ def compute_cmin(self, file): # checks if xTB is installed _ = self.get_cmin_model() # sets charge and mult - file_format = os.path.splitext(file)[1] + file_format = os.path.basename(Path(file)).split('.')[1] charge_input, mult_input, final_mult = None, None, None - if file_format.lower() == '.sdf': + if file_format.lower() == 'sdf': if self.args.charge is None or self.args.mult is None: # read charge and mult from SDF if possible (i.e. charge/mult of SDFs created with CSEARCH) with open(file, "r") as F: diff --git a/aqme/csearch/base.py b/aqme/csearch/base.py index 6003ebbc..65fa4a05 100644 --- a/aqme/csearch/base.py +++ b/aqme/csearch/base.py @@ -450,12 +450,10 @@ def compute_confs( f"CSEARCH" ) else: - if Path(f"{self.args.destination}").exists(): + if self.args.initial_dir.as_posix() in f"{self.args.destination}": self.csearch_folder = Path(self.args.destination) else: - self.csearch_folder = Path(self.args.initial_dir).joinpath( - self.args.destination - ) + self.csearch_folder = Path(self.args.initial_dir).joinpath(self.args.destination) self.csearch_folder.mkdir(exist_ok=True, parents=True) diff --git a/aqme/csearch/crest.py b/aqme/csearch/crest.py index 7358a304..5bbbafed 100644 --- a/aqme/csearch/crest.py +++ b/aqme/csearch/crest.py @@ -85,25 +85,29 @@ def xtb_opt_main( """ name_no_path = name.replace("/", "\\").split("\\")[-1].split(".")[0] - # where RDKit generates the files + # folder to create the files if self.args.destination is None: if method_opt == 'crest': csearch_dir = Path(self.args.w_dir_main) / "CSEARCH" elif method_opt == 'xtb': - rdmolfiles.MolToXYZFile(mol, name + ".xyz") csearch_dir = Path(self.args.w_dir_main) / "CMIN" else: - csearch_dir = Path(self.args.destination) + if self.args.initial_dir.as_posix() in f"{self.args.destination}": + csearch_dir = Path(self.args.destination) + else: + csearch_dir = Path(self.args.initial_dir).joinpath(self.args.destination) + + # create the initial xyz input if method_opt == 'crest': self.args.log.write(f"\no Starting xTB pre-optimization before CREST sampling") dat_dir = csearch_dir / "crest_xyz" xyzin = f"{dat_dir}/{name_no_path}.xyz" elif method_opt == 'xtb': + rdmolfiles.MolToXYZFile(mol, f"{name}.xyz") self.args.log.write(f"\no Starting xTB optimization") dat_dir = csearch_dir / "xtb_xyz" xyzin = f"{dat_dir}/{name_no_path}_xtb.xyz" dat_dir.mkdir(exist_ok=True, parents=True) - shutil.move(f"{name}.xyz", xyzin) os.environ["OMP_STACKSIZE"] = self.args.stacksize @@ -360,7 +364,10 @@ def xtb_opt_main( if os.path.exists(file): if file.find('.out') == -1: if self.args.program.lower() == "xtb": - os.remove(file) + try: + os.remove(file) + except OSError: # this avoids problems when running AQME in HPCs + pass elif self.args.program.lower() == "crest": if file.find('_xtb2') == -1 and file.find('_xtb1') == -1 and file.find('.out') == -1: try: diff --git a/aqme/qcorr.py b/aqme/qcorr.py index 6a7589af..9abff74e 100644 --- a/aqme/qcorr.py +++ b/aqme/qcorr.py @@ -23,6 +23,10 @@ optimization but did not convergence in the subsequent frequency calculation. Options: opt keyword as string (i.e. 'opt=(calcfc,maxstep=5)'). If readfc is specified in the string, the chk option must be included as well. + im_freq_input : str, default='opt=(calcfc,maxstep=5)' (Gaussian), '\n%geom\nCalc_Hess true\nMaxStep 0.05\nend' (ORCA) + When extra imaginery frequencies are detected by QCORR, it automatically adds + hessian calcs before starting geometry optimizations. This option can be + disabled using im_freq_input=None. s2_threshold : float, default=10.0 Cut off for spin contamination during analysis in % of the expected value (i.e. multiplicity 3 has an the expected of 2.0, @@ -203,8 +207,12 @@ def qcorr_processing(self): errortype = self.analyze_isom(file, cartesians, atom_types, errortype) # move initial QM input files (if the files are placed in the same folder as the output files) + if cclib_data["metadata"]["QM program"].lower().find("gaussian") > -1: + input_suffix = "com" + elif cclib_data["metadata"]["QM program"].lower().find("orca") > -1: + input_suffix = "inp" if ( - os.path.exists(f"{self.args.w_dir_main}/{file_name}.com") + os.path.exists(f"{self.args.w_dir_main}/{file_name}.{input_suffix}") and self.args.round_num == 1 ): move_file( @@ -244,7 +252,8 @@ def qcorr_processing(self): csv_qcorr = self.write_qcorr_csv(file_terms) # performs a full analysis to ensure that the calcs were run with the same parameters - if self.args.fullcheck == "False": + # currently, this function is not working with ORCA calcs + if self.args.fullcheck == "False" or cclib_data["metadata"]["QM program"].lower().find("orca") > -1: self.args.fullcheck = False elif self.args.fullcheck == "True": self.args.fullcheck = True @@ -486,19 +495,31 @@ def analyze_normal(self, duplicate_data, errortype, cclib_data, file_name): if not opt_found: cclib_data["metadata"]["keywords line"] += " opt" - if errortype == "freq_no_conv": - # adjust the keywords so only FREQ is calculated - new_keywords_line = "" - for keyword in cclib_data["metadata"]["keywords line"].split(): - if keyword.lower().startswith("opt"): - keyword = self.args.freq_conv - if ( - cclib_data["metadata"]["ground or transition state"] - == "transition_state" - ): - keyword = keyword.replace("=(", "=(ts,noeigen,") - new_keywords_line += keyword - new_keywords_line += " " + # adding the Hessian calculation before OPT increases the rate of success + if errortype in ["freq_no_conv","extra_imag_freq"]: + new_opt = None + if errortype == "freq_no_conv" and self.args.freq_conv not in [None,'None']: + new_opt = self.args.freq_conv + elif errortype == "extra_imag_freq" and self.args.im_freq_input not in [None,'None']: + new_opt = self.args.im_freq_input + if cclib_data["metadata"]["QM program"].lower().find("gaussian") > -1: + new_keywords_line = "" + for keyword in cclib_data["metadata"]["keywords line"].split(): + if keyword.lower().startswith("opt"): + if new_opt is not None: + keyword = new_opt + if cclib_data["metadata"]["ground or transition state"] == "transition_state": + keyword = keyword.replace("=(", "=(ts,noeigen,") + new_keywords_line += keyword + new_keywords_line += " " + elif cclib_data["metadata"]["QM program"].lower().find("orca") > -1: + new_keywords_line = cclib_data["metadata"]["keywords line"] + if self.args.im_freq_input not in [None,'None']: + # change the default value + if self.args.im_freq_input == 'opt=(calcfc,maxstep=5)': + self.args.im_freq_input = '\n%geom\nCalc_Hess true\nMaxStep 0.05\nend' + new_keywords_line += self.args.im_freq_input + cclib_data["metadata"]["keywords line"] = new_keywords_line elif errortype == "linear_mol_wrong": @@ -510,6 +531,12 @@ def analyze_abnormal(self, errortype, cclib_data, outlines): """ Analyze errors from calculations that did not finish normally """ + + if cclib_data["metadata"]["QM program"].lower().find("gaussian") > -1: + program = 'gaussian' + elif cclib_data["metadata"]["QM program"].lower().find("orca") > -1: + program = "orca" + # for calcs with finished OPT but no freqs, adjust the keywords so only FREQ is calculated if errortype == "no_freq": new_keywords_line = "" @@ -524,20 +551,23 @@ def analyze_abnormal(self, errortype, cclib_data, outlines): else: # help to fix SCF convergence errors if errortype == "SCFerror": - if ( - cclib_data["metadata"]["keywords line"].find(" scf=xqc") > -1 - or cclib_data["metadata"]["keywords line"].find(" scf=qc") > -1 - ): - new_keywords_line = "" - for keyword in cclib_data["metadata"]["keywords line"].split(): - if keyword == "scf=xqc": - keyword = "scf=qc" - new_keywords_line += keyword - new_keywords_line += " " - cclib_data["metadata"]["keywords line"] = new_keywords_line - - else: - cclib_data["metadata"]["keywords line"] += " scf=xqc" + if program == 'gaussian': + if ( + cclib_data["metadata"]["keywords line"].find(" scf=xqc") > -1 + or cclib_data["metadata"]["keywords line"].find(" scf=qc") > -1 + ): + new_keywords_line = "" + for keyword in cclib_data["metadata"]["keywords line"].split(): + if keyword == "scf=xqc": + keyword = "scf=qc" + new_keywords_line += keyword + new_keywords_line += " " + cclib_data["metadata"]["keywords line"] = new_keywords_line + else: + cclib_data["metadata"]["keywords line"] += " scf=xqc" + elif program == 'orca': + if 'SlowConv' not in cclib_data["metadata"]["keywords line"]: + cclib_data["metadata"]["keywords line"] = 'SlowConv ' + cclib_data["metadata"]["keywords line"] if errortype in ["not_specified", "SCFerror"]: if "geometric values" in cclib_data["optimization"]: diff --git a/aqme/qcorr_utils.py b/aqme/qcorr_utils.py index eead7720..9f721c2b 100644 --- a/aqme/qcorr_utils.py +++ b/aqme/qcorr_utils.py @@ -368,7 +368,6 @@ def get_json_data(self, file, cclib_data): """ outlines = read_file(os.getcwd(), self.args.w_dir_main, file) - # initial loop just to detect the QM program for i, line in enumerate(outlines): # get program @@ -386,9 +385,9 @@ def get_json_data(self, file, cclib_data): elif "* O R C A *" in line: for j in range(i, i + 100): - if "Program Version" in line.strip(): + if "Program Version" in outlines[j].strip(): cclib_data["metadata"] = {} - version_program = "ORCA version " + line.split()[2] + version_program = "ORCA version " + outlines[j].split()[2] cclib_data["metadata"]["QM program"] = version_program break @@ -581,9 +580,8 @@ def get_json_data(self, file, cclib_data): cclib_data["properties"]["NMR"]["NMR eigenvalues"] = nmr_eigen cclib_data["properties"]["NMR"]["NMR isotopic tensors"] = nmr_iso - elif cclib_data["metadata"]["QM program"].lower().find("orca") > -1: - for i in reversed(range(0, outlines)): + for i in reversed(range(0, len(outlines))): if outlines[i][:25] == "FINAL SINGLE POINT ENERGY": # in eV to match the format from cclib orca_e = float(outlines[i].split()[-1]) @@ -592,8 +590,48 @@ def get_json_data(self, file, cclib_data): ] = cclib.parser.utils.convertor(orca_e, "hartree", "eV") break + for i, line in enumerate(outlines): + # Extract number of processors + if "%pal" in line: + pal_line = '' + for j in range(i,i+3): + if outlines[j][0] not in ['%','!'] or "%pal" in outlines[j]: + pal_line += outlines[j].rstrip("\n")[5:] + if 'nprocs' in pal_line: + nprocs = pal_line.strip().split()[2] + cclib_data["metadata"]["processors"] = nprocs + + # Extract memory + elif '%maxcore' in line: + mem = int(line.strip().split()[3]) + cclib_data["metadata"]["memory"] = f'{mem}MB' + + # Extract input line + elif "!" in line: + keywords_line = "" + for j in range(i, i + 100): + if "*" in outlines[j]: + break + else: + keywords_line += outlines[j][6:] + cclib_data["metadata"]["keywords line"] = keywords_line[1:].rstrip("\n") + calc_type = "ground_state" + for keyword in keywords_line.split(): + if keyword.lower() in ["OptTS",'NEB-TS']: + calc_type = "transition_state" + break + if keyword.lower()[0:3] == 'pal': + cclib_data["metadata"]["processors"] = keyword[3] + cclib_data["metadata"]["ground or transition state"] = calc_type + + elif 'END OF INPUT' in line: + break + if cclib_data != {}: - with open(f'{file.split(".")[0]}.json', "w") as outfile: + # this prevents errors when the names contain "." + name_path = os.path.basename(Path(file)) + dir_path = os.path.dirname(Path(file)) + with open(f'{dir_path}/{name_path.split(".")[0]}.json', "w") as outfile: json.dump(cclib_data, outfile, indent=1) return cclib_data diff --git a/aqme/qprep.py b/aqme/qprep.py index 35713f2e..89503736 100644 --- a/aqme/qprep.py +++ b/aqme/qprep.py @@ -264,14 +264,21 @@ def get_header(self, qprep_data): elif self.args.program.lower() == "orca": txt += f'# {name_file}\n' - if self.args.mem.find("GB"): + if "GB" in self.args.mem: mem_orca = int(self.args.mem.split("GB")[0]) * 1000 - elif self.args.mem.find("MB"): + elif "MB" in self.args.mem: mem_orca = self.args.mem.split("MB")[0] - elif self.args.args.mem.find("MW"): + elif "MW" in self.args.mem: mem_orca = self.args.mem.split("MW")[0] - txt += f"%maxcore {mem_orca}\n" - txt += f"%pal nprocs {self.args.nprocs} end\n" + if '%maxcore' not in self.args.qm_input: + txt += f"%maxcore {mem_orca}\n" + pal_included = False + pal_list = ['%pal','pal1','pal3','pal3','pal4','pal5','pal6','pal7','pal8'] + for keyword in self.args.qm_input.split(): + if keyword.rstrip("\n").lower() in pal_list: + pal_included = True + if not pal_included: + txt += f"%pal nprocs {self.args.nprocs} end\n" txt += f"! {self.args.qm_input}\n" txt += f'* xyz {qprep_data["charge"]} {qprep_data["mult"]}\n' diff --git a/aqme/utils.py b/aqme/utils.py index 85e45149..bb2e5043 100644 --- a/aqme/utils.py +++ b/aqme/utils.py @@ -24,9 +24,9 @@ J_TO_AU = 4.184 * 627.509541 * 1000.0 # UNIT CONVERSION T = 298.15 -aqme_version = "1.4.6" +aqme_version = "1.4.7" time_run = time.strftime("%Y/%m/%d %H:%M:%S", time.localtime()) -aqme_ref = f"AQME v {aqme_version}, Alegre-Requena, J. V.; Sowndarya, S.; Perez-Soto, R.; Alturaifi, T. M.; Paton, R. S., 2022. https://github.com/jvalegre/aqme" +aqme_ref = f"AQME v {aqme_version}, Alegre-Requena, J. V.; Sowndarya, S.; Perez-Soto, R.; Alturaifi, T.; Paton, R. AQME: Automated Quantum Mechanical Environments for Researchers and Educators. Wiley Interdiscip. Rev. Comput. Mol. Sci. 2023, DOI: 10.1002/wcms.1663." RDLogger.DisableLog("rdApp.*") diff --git a/docs/Misc/versions.rst b/docs/Misc/versions.rst index d8ea195a..aa79558f 100644 --- a/docs/Misc/versions.rst +++ b/docs/Misc/versions.rst @@ -4,6 +4,14 @@ Versions ======== +Version 1.4.7 [`url `__] + - QCORR is compatible with directories that contain a "." symbol + - QCORR is compatible with ORCA calcs (it doesn't detect spin contamination yet) + - QCORR includes hessian calculations for calcs with extra imaginary frequencies by default + (new option to control this: im_freq_input) + - QCORR tries to fix SCF convergence issues in ORCA by adding the SlowConv keyword + - qm_end option is added after the genecp section in QPREP + Version 1.4.6 [`url `__] - The files and input options are compatible with partial PATHs, full PATHs, and direct names from command lines and Jupyter Notebooks diff --git a/setup.py b/setup.py index edb12387..45db6ddd 100644 --- a/setup.py +++ b/setup.py @@ -1,5 +1,5 @@ from setuptools import setup, find_packages -version = "1.4.6" +version = "1.4.7" setup( name="aqme", packages=find_packages(exclude=["tests"]), diff --git a/tests/test_qcorr.py b/tests/test_qcorr.py index db810aa9..46024941 100644 --- a/tests/test_qcorr.py +++ b/tests/test_qcorr.py @@ -380,6 +380,20 @@ None, True, ), # reset the initial folder to start another set of tests + ( + "QCORR_1b", + "Imag_freq_no_corr.log", + None, + "failed/run_1/extra_imag_freq", + False, + ), # test the im_freq_input option + ( + None, + None, + None, + None, + True, + ), # reset the initial folder to start another set of tests # QCORR analysis with no w_dir_main ( "QCORR_1d", @@ -507,19 +521,19 @@ def test_QCORR_analysis(init_folder, file, command_line, target_folder, restore_ line_10 = "H 0.00000000 -1.04973700 -1.63442100" elif file.split(".")[0] == "imag_freq_no_opt": - line_2 = "# M062X/Def2TZVP freq=noraman opt" + line_2 = "# M062X/Def2TZVP freq=noraman opt=(calcfc,maxstep=5)" line_6 = "0 1" line_8 = "C -0.90757400 0.00709700 -0.00994500" line_10 = "C 1.19952600 1.19528800 0.00698400" elif file.split(".")[0] == "TS_CH3HCH3_imag_freq": - line_2 = "# opt=(calcfc,ts,noeigen) freq b3lyp/3-21g" + line_2 = "# opt=(ts,noeigen,calcfc,maxstep=5) freq b3lyp/3-21g" line_6 = "0 2" line_8 = "H -0.87171200 0.59637700 -1.63085200" line_10 = "H -0.08200000 -1.05275500 -1.63085200" elif file.split(".")[0] == "Imag_freq": - line_2 = "# opt freq 3-21g m062x" + line_2 = "# opt=(calcfc,maxstep=5) freq 3-21g m062x" line_6 = "0 1" line_8 = "H 0.38503600 -0.39992100 -0.94851000" line_10 = "H 0.20952000 1.07184200 -0.02121100" @@ -558,16 +572,7 @@ def test_QCORR_analysis(init_folder, file, command_line, target_folder, restore_ elif file == "json": os.chdir(f"{w_dir_main}/{target_folder}") json_files = glob.glob("*.json") - target_files = [ - "CH4.json", - "CO2_linear_4freqs.json", - "freq_ok_YYNN.json", - "H_freq.json", - "MeOH_G09.json", - "TS_CH3HCH3.json", - ] assert len(json_files) == 6 - # assert sorted(json_files) == sorted(target_files) elif file == "fullcheck": target_fullcheck = ["-- Full check analysis --\n"] @@ -658,10 +663,10 @@ def test_QCORR_analysis(init_folder, file, command_line, target_folder, restore_ elif file == "csv": qcorr_stats = pd.read_csv(f"{path_main}/QCORR-run_1-stats.csv") - assert qcorr_stats["Total files"][0] == 28 + assert qcorr_stats["Total files"][0] == 29 assert qcorr_stats["Normal termination"][0] == 6 assert qcorr_stats["Single-point calcs"][0] == 3 - assert qcorr_stats["Extra imag. freq."][0] == 3 + assert qcorr_stats["Extra imag. freq."][0] == 4 assert qcorr_stats["TS with no imag. freq."][0] == 1 assert qcorr_stats["Freq not converged"][0] == 2 assert qcorr_stats["Linear mol with wrong n of freqs"][0] == 1 @@ -709,17 +714,24 @@ def test_QCORR_analysis(init_folder, file, command_line, target_folder, restore_ elif file.split(".")[0] == "Imag_freq": cmd_aqme = cmd_aqme + ["--amplitude_ifreq", "-0.4"] + elif file.split(".")[0] == "Imag_freq_no_corr": + cmd_aqme = cmd_aqme + ["--im_freq_input", "None"] + subprocess.run(cmd_aqme) # ensure the output file moves to the right folder assert path.exists(f"{w_dir_main}/{target_folder}/{file}") - if file.split(".")[0] == "Imag_freq": + if file.split(".")[0] in ["Imag_freq","Imag_freq_no_corr"]: # ensure that QCORR applies the correct structural distortions to the errored calcs - line_2 = "# opt freq 3-21g m062x" - line_6 = "0 1" - line_8 = "H 0.60103600 -0.59192100 -0.73251000" - line_10 = "H 0.46752000 1.00584200 0.19478900" + if file.split(".")[0] in "Imag_freq": + line_2 = "# opt=(calcfc,maxstep=5) freq 3-21g m062x" + line_6 = "0 1" + line_8 = "H 0.60103600 -0.59192100 -0.73251000" + line_10 = "H 0.46752000 1.00584200 0.19478900" + elif file.split(".")[0] in "Imag_freq_no_corr": + line_2 = "# opt freq 3-21g m062x" + line_6 = "0 1" outfile = open( f'{w_dir_main}/failed/run_1/fixed_QM_inputs/{file.split(".")[0]}.com', @@ -728,10 +740,14 @@ def test_QCORR_analysis(init_folder, file, command_line, target_folder, restore_ outlines = outfile.readlines() outfile.close() - assert outlines[2].strip() == line_2 - assert outlines[6].strip() == line_6 - assert outlines[8].strip() == line_8 - assert outlines[10].strip() == line_10 + if file.split(".")[0] in "Imag_freq": + assert outlines[2].strip() == line_2 + assert outlines[6].strip() == line_6 + assert outlines[8].strip() == line_8 + assert outlines[10].strip() == line_10 + elif file.split(".")[0] in "Imag_freq_no_corr": + assert outlines[2].strip() == line_2 + assert outlines[6].strip() == line_6 elif init_folder == "QCORR_1c": w_dir_main = f"{path_qcorr}/QCORR_1"