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|
************************************************************************
*************** Dalton - An Electronic Structure Program ***************
************************************************************************
This is output from DALTON (Release Dalton2013 patch 0)
----------------------------------------------------------------------------
NOTE:
Dalton is an experimental code for the evaluation of molecular
properties using (MC)SCF, DFT, CI, and CC wave functions.
The authors accept no responsibility for the performance of
the code or for the correctness of the results.
The code (in whole or part) is provided under a licence and
is not to be reproduced for further distribution without
the written permission of the authors or their representatives.
See the home page "http://daltonprogram.org" for further information.
If results obtained with this code are published,
the appropriate citations would be both of:
K. Aidas, C. Angeli, K. L. Bak, V. Bakken, R. Bast,
L. Boman, O. Christiansen, R. Cimiraglia, S. Coriani,
P. Dahle, E. K. Dalskov, U. Ekstroem, T. Enevoldsen,
J. J. Eriksen, P. Ettenhuber, B. Fernandez, L. Ferrighi,
H. Fliegl, L. Frediani, K. Hald, A. Halkier, C. Haettig,
H. Heiberg, T. Helgaker, A. C. Hennum, H. Hettema,
E. Hjertenaes, S. Hoest, I.-M. Hoeyvik, M. F. Iozzi,
B. Jansik, H. J. Aa. Jensen, D. Jonsson, P. Joergensen,
J. Kauczor, S. Kirpekar, T. Kjaergaard, W. Klopper,
S. Knecht, R. Kobayashi, H. Koch, J. Kongsted, A. Krapp,
K. Kristensen, A. Ligabue, O. B. Lutnaes, J. I. Melo,
K. V. Mikkelsen, R. H. Myhre, C. Neiss, C. B. Nielsen,
P. Norman, J. Olsen, J. M. H. Olsen, A. Osted,
M. J. Packer, F. Pawlowski, T. B. Pedersen, P. F. Provasi,
S. Reine, Z. Rinkevicius, T. A. Ruden, K. Ruud, V. Rybkin,
P. Salek, C. C. M. Samson, A. Sanchez de Meras, T. Saue,
S. P. A. Sauer, B. Schimmelpfennig, K. Sneskov,
A. H. Steindal, K. O. Sylvester-Hvid, P. R. Taylor,
A. M. Teale, E. I. Tellgren, D. P. Tew, A. J. Thorvaldsen,
L. Thoegersen, O. Vahtras, M. A. Watson, D. J. D. Wilson,
M. Ziolkowski and H. Aagren,
"The Dalton quantum chemistry program system",
WIREs Comput. Mol. Sci. 2013. (doi: 10.1002/wcms.1172)
and
Dalton, a Molecular Electronic Structure Program,
Release DALTON2013.1 (2013), see http://daltonprogram.org
----------------------------------------------------------------------------
Authors in alphabetical order (major contribution(s) in parenthesis):
Kestutis Aidas, Vilnius University, Lithuania (QM/MM)
Celestino Angeli, University of Ferrara, Italy (NEVPT2)
Keld L. Bak, UNI-C, Denmark (AOSOPPA, non-adiabatic coupling, magnetic properties)
Vebjoern Bakken, University of Oslo, Norway (DALTON; geometry optimizer, symmetry detection)
Radovan Bast, KTH Stockholm, Sweden (DALTON installation and execution frameworks)
Linus Boman, NTNU, Norway (Cholesky decomposition and subsystems)
Ove Christiansen, Aarhus University, Denmark (CC module)
Renzo Cimiraglia, University of Ferrara, Italy (NEVPT2)
Sonia Coriani, University of Trieste, Italy (CC module, MCD in RESPONS)
Paal Dahle, University of Oslo, Norway (Parallelization)
Erik K. Dalskov, UNI-C, Denmark (SOPPA)
Thomas Enevoldsen, Univ. of Southern Denmark, Denmark (SOPPA)
Janus J. Eriksen, Aarhus University, Denmark (PE-MP2/SOPPA, TDA)
Berta Fernandez, U. of Santiago de Compostela, Spain (doublet spin, ESR in RESPONS)
Lara Ferrighi, Aarhus University, Denmark (PCM Cubic response)
Heike Fliegl, University of Oslo, Norway (CCSD(R12))
Luca Frediani, UiT The Arctic U. of Norway, Norway (PCM)
Bin Gao, UiT The Arctic U. of Norway, Norway (Gen1Int library)
Christof Haettig, Ruhr-University Bochum, Germany (CC module)
Kasper Hald, Aarhus University, Denmark (CC module)
Asger Halkier, Aarhus University, Denmark (CC module)
Hanne Heiberg, University of Oslo, Norway (geometry analysis, selected one-electron integrals)
Trygve Helgaker, University of Oslo, Norway (DALTON; ABACUS, ERI, DFT modules, London, and much more)
Alf Christian Hennum, University of Oslo, Norway (Parity violation)
Hinne Hettema, University of Auckland, New Zealand (quadratic response in RESPONS; SIRIUS supersymmetry)
Eirik Hjertenaes, NTNU, Norway (Cholesky decomposition)
Maria Francesca Iozzi, University of Oslo, Norway (RPA)
Brano Jansik Technical Univ. of Ostrava Czech Rep. (DFT cubic response)
Hans Joergen Aa. Jensen, Univ. of Southern Denmark, Denmark (DALTON; SIRIUS, RESPONS, ABACUS modules, London, and much more)
Dan Jonsson, UiT The Arctic U. of Norway, Norway (cubic response in RESPONS module)
Poul Joergensen, Aarhus University, Denmark (RESPONS, ABACUS, and CC modules)
Joanna Kauczor, Linkoeping University, Sweden (Complex polarization propagator (CPP) module)
Sheela Kirpekar, Univ. of Southern Denmark, Denmark (Mass-velocity & Darwin integrals)
Wim Klopper, KIT Karlsruhe, Germany (R12 code in CC, SIRIUS, and ABACUS modules)
Stefan Knecht, ETH Zurich, Switzerland (Parallel CI and MCSCF)
Rika Kobayashi, Australian National Univ., Australia (DIIS in CC, London in MCSCF)
Henrik Koch, NTNU, Norway (CC module, Cholesky decomposition)
Jacob Kongsted, Univ. of Southern Denmark, Denmark (Polarizable embedding, QM/MM)
Andrea Ligabue, University of Modena, Italy (CTOCD, AOSOPPA)
Ola B. Lutnaes, University of Oslo, Norway (DFT Hessian)
Juan I. Melo, University of Buenos Aires, Argentina (LRESC, Relativistic Effects on NMR Shieldings)
Kurt V. Mikkelsen, University of Copenhagen, Denmark (MC-SCRF and QM/MM)
Rolf H. Myhre, NTNU, Norway (Cholesky, subsystems and ECC2)
Christian Neiss, Univ. Erlangen-Nuernberg, Germany (CCSD(R12))
Christian B. Nielsen, University of Copenhagen, Denmark (QM/MM)
Patrick Norman, Linkoeping University, Sweden (Cubic response and complex response in RESPONS)
Jeppe Olsen, Aarhus University, Denmark (SIRIUS CI/density modules)
Jogvan Magnus H. Olsen, Univ. of Southern Denmark, Denmark (Polarizable embedding, PE library, QM/MM)
Anders Osted, Copenhagen University, Denmark (QM/MM)
Martin J. Packer, University of Sheffield, UK (SOPPA)
Filip Pawlowski, Kazimierz Wielki University, Poland (CC3)
Thomas B. Pedersen, University of Oslo, Norway (Cholesky decomposition)
Patricio F. Provasi, University of Northeastern, Argentina (Analysis of coupling constants in localized orbitals)
Zilvinas Rinkevicius, KTH Stockholm, Sweden (open-shell DFT, ESR)
Elias Rudberg, KTH Stockholm, Sweden (DFT grid and basis info)
Torgeir A. Ruden, University of Oslo, Norway (Numerical derivatives in ABACUS)
Kenneth Ruud, UiT The Arctic U. of Norway, Norway (DALTON; ABACUS magnetic properties and much more)
Pawel Salek, KTH Stockholm, Sweden (DALTON; DFT code)
Claire C. M. Samson University of Karlsruhe Germany (Boys localization, r12 integrals in ERI)
Alfredo Sanchez de Meras, University of Valencia, Spain (CC module, Cholesky decomposition)
Trond Saue, Paul Sabatier University, France (direct Fock matrix construction)
Stephan P. A. Sauer, University of Copenhagen, Denmark (SOPPA(CCSD), SOPPA prop., AOSOPPA, vibrational g-factors)
Bernd Schimmelpfennig, Forschungszentrum Karlsruhe, Germany (AMFI module)
Kristian Sneskov, Aarhus University, Denmark (QM/MM, PE-CC)
Arnfinn H. Steindal, UiT The Arctic U. of Norway, Norway (parallel QM/MM)
K. O. Sylvester-Hvid, University of Copenhagen, Denmark (MC-SCRF)
Peter R. Taylor, VLSCI/Univ. of Melbourne, Australia (Symmetry handling ABACUS, integral transformation)
Andrew M. Teale, University of Nottingham, England (DFT-AC, DFT-D)
David P. Tew, University of Bristol, England (CCSD(R12))
Olav Vahtras, KTH Stockholm, Sweden (triplet response, spin-orbit, ESR, TDDFT, open-shell DFT)
David J. Wilson, La Trobe University, Australia (DFT Hessian and DFT magnetizabilities)
Hans Agren, KTH Stockholm, Sweden (SIRIUS module, RESPONS, MC-SCRF solvation model)
--------------------------------------------------------------------------------
Date and time (Linux) : Fri Feb 27 06:11:17 2015
Host name : wn701
* Work memory size : 207360000 = 1.545 gigabytes.
* Directories for basis set searches:
1) /home/langner
2) /usr/local/dalton/intel-13.1/2013/dalton/basis
Compilation information
-----------------------
Who compiled | root
Host | supernova.services.kdm.wcss.pl
System | Linux-2.6.18-348.3.1.el5
CMake generator | Unix Makefiles
Processor | x86_64
64-bit integers | OFF
MPI | ON
Fortran compiler | /usr/local/openmpi/intel-13.1/1.6.5/bin/mpif90
C compiler | /usr/local/openmpi/intel-13.1/1.6.5/bin/mpicc
C++ compiler | /usr/local/openmpi/intel-13.1/1.6.5/bin/mpicxx
C++ compiler version | unknown
Static linking | OFF
Last Git revision | 653a3c9fdcde6b463c7e208ddf10abd66f7c54f6
Configuration time | 2014-01-15 11:00:36.908921
* Sequential calculation using 1 CPU
Content of the .dal input file
----------------------------------
BASIS
STO-3G
Water
AtomTypes=2
Charge=8.0 Atoms=1
O 0.0 0.0 0.0
Charge=1.0 Atoms=2
H 0.99 0.0 0.0
H -0.272881 0.951649 0.0
**DALTON INPUT
.RUN WAVE FUNCTIONS
**WAVE FUNCTIONS
.CC
*CC INPUT
.CC(T)
**END OF DALTON INPUT
*******************************************************************
*********** Output from DALTON general input processing ***********
*******************************************************************
--------------------------------------------------------------------------------
Overall default print level: 0
Print level for DALTON.STAT: 1
HERMIT 1- and 2-electron integral sections will be executed
"Old" integral transformation used (limited to max 255 basis functions)
Wave function sections will be executed (SIRIUS module)
--------------------------------------------------------------------------------
****************************************************************************
*************** Output of molecule and basis set information ***************
****************************************************************************
The two title cards from your ".mol" input:
------------------------------------------------------------------------
1: Water
2:
------------------------------------------------------------------------
Atomic type no. 1
--------------------
Nuclear charge: 8.00000
Number of symmetry independent centers: 1
Number of basis sets to read; 2
Basis set file used for this atomic type with Z = 8 :
"/usr/local/dalton/intel-13.1/2013/dalton/basis/STO-3G"
Atomic type no. 2
--------------------
Nuclear charge: 1.00000
Number of symmetry independent centers: 2
Number of basis sets to read; 2
Basis set file used for this atomic type with Z = 1 :
"/usr/local/dalton/intel-13.1/2013/dalton/basis/STO-3G"
SYMADD: Requested addition of symmetry
--------------------------------------
Symmetry test threshold: 5.00E-06
- molecule centered at center of mass and rotated so
principal axes of inertia are along coordinate axes.
Symmetry class found: C(2v)
Symmetry Independent Centres
----------------------------
8 : 0.00000000 0.00000000 -0.06667852 Isotope 1
1 : 0.00000000 0.79064922 0.52911825 Isotope 1
The following elements were found: X Y
SYMGRP: Point group information
-------------------------------
Full point group is: C(2v)
Represented as: C2v
* The point group was generated by:
Reflection in the yz-plane
Reflection in the xz-plane
* Group multiplication table
| E C2z Oxz Oyz
-----+--------------------
E | E C2z Oxz Oyz
C2z | C2z E Oyz Oxz
Oxz | Oxz Oyz E C2z
Oyz | Oyz Oxz C2z E
* Character table
| E C2z Oxz Oyz
-----+--------------------
A1 | 1 1 1 1
B1 | 1 -1 1 -1
B2 | 1 -1 -1 1
A2 | 1 1 -1 -1
* Direct product table
| A1 B1 B2 A2
-----+--------------------
A1 | A1 B1 B2 A2
B1 | B1 A1 A2 B2
B2 | B2 A2 A1 B1
A2 | A2 B2 B1 A1
Isotopic Masses
---------------
O 15.994915
H _1 1.007825
H _2 1.007825
Total mass: 18.010565 amu
Natural abundance: 99.730 %
Center-of-mass coordinates (a.u.): 0.000000 0.000000 -0.000000
Atoms and basis sets
--------------------
Number of atom types : 2
Total number of atoms: 3
Basis set used is "STO-3G" from the basis set library.
label atoms charge prim cont basis
----------------------------------------------------------------------
O 1 8.0000 15 5 [6s3p|2s1p]
H 2 1.0000 3 1 [3s|1s]
----------------------------------------------------------------------
total: 3 10.0000 21 7
----------------------------------------------------------------------
Threshold for neglecting AO integrals: 1.00D-12
Cartesian Coordinates (a.u.)
----------------------------
Total number of coordinates: 9
O : 1 x 0.0000000000 2 y 0.0000000000 3 z -0.0666785241
H / 1 : 4 x 0.0000000000 5 y 0.7906492179 6 z 0.5291182519
H / 2 : 7 x 0.0000000000 8 y -0.7906492179 9 z 0.5291182519
Symmetry Coordinates
--------------------
Number of coordinates in each symmetry: 3 2 3 1
Symmetry A1 ( 1)
1 O z 3
2 H y [ 5 - 8 ]/2
3 H z [ 6 + 9 ]/2
Symmetry B1 ( 2)
4 O x 1
5 H x [ 4 + 7 ]/2
Symmetry B2 ( 3)
6 O y 2
7 H y [ 5 + 8 ]/2
8 H z [ 6 - 9 ]/2
Symmetry A2 ( 4)
9 H x [ 4 - 7 ]/2
Interatomic separations (in Angstrom):
--------------------------------------
O H _1 H _2
------ ------ ------
O : 0.000000
H _1: 0.523885 0.000000
H _2: 0.523885 0.836787 0.000000
Max interatomic separation is 0.8368 Angstrom ( 1.5813 Bohr)
between atoms 3 and 2, "H _2" and "H _1".
Min HX interatomic separation is 0.5239 Angstrom ( 0.9900 Bohr)
WARNING: Number of short HX and YX bond lengths: 2 0
WARNING: If not intentional, maybe your coordinates were in Angstrom,
WARNING: but "Angstrom" was not specified in .mol file
Bond distances (Angstrom):
--------------------------
atom 1 atom 2 distance
------ ------ --------
bond distance: H _1 O 0.523885
bond distance: H _2 O 0.523885
bond distance: H _2 H _1 0.836787
Bond angles (degrees):
----------------------
atom 1 atom 2 atom 3 angle
------ ------ ------ -----
bond angle: H _1 O H _2 106.000
bond angle: O H _1 H _2 37.000
bond angle: O H _2 H _1 37.000
Principal moments of inertia (u*A**2) and principal axes
--------------------------------------------------------
IA 0.177938 0.000000 1.000000 0.000000
IB 0.352846 0.000000 0.000000 1.000000
IC 0.530784 1.000000 0.000000 0.000000
Rotational constants
--------------------
The molecule is planar.
A B C
2840199.9224 1432293.8163 952137.3312 MHz
94.738872 47.776179 31.759883 cm-1
@ Nuclear repulsion energy : 16.794007988674 Hartree
Symmetry Orbitals
-----------------
Number of orbitals in each symmetry: 4 1 2 0
Symmetry A1 ( 1)
1 O 1s 1
2 O 1s 2
3 O 2pz 5
4 H 1s 6 + 7
Symmetry B1 ( 2)
5 O 2px 3
Symmetry B2 ( 3)
6 O 2py 4
7 H 1s 6 - 7
No orbitals in symmetry A2 ( 4)
Symmetries of electric field: B1 (2) B2 (3) A1 (1)
Symmetries of magnetic field: B2 (3) B1 (2) A2 (4)
.---------------------------------------.
| Starting in Integral Section (HERMIT) |
`---------------------------------------'
*************************************************************************
****************** Output from HERMIT input processing ******************
*************************************************************************
************************************************************************
************************** Output from HERINT **************************
************************************************************************
Threshold for neglecting two-electron integrals: 1.00D-12
Number of two-electron integrals written: 138 ( 34.0% )
Megabytes written: 0.007
>>>> Total CPU time used in HERMIT: 0.01 seconds
>>>> Total wall time used in HERMIT: 0.05 seconds
.----------------------------------.
| End of Integral Section (HERMIT) |
`----------------------------------'
.--------------------------------------------.
| Starting in Wave Function Section (SIRIUS) |
`--------------------------------------------'
*** Output from Huckel module :
Using EWMO model: F
Using EHT model: T
Number of Huckel orbitals each symmetry: 4 1 2 0
Huckel EHT eigenvalues for symmetry : 1
-20.815540 -1.721112 -0.642474 -0.119190
Huckel EHT eigenvalues for symmetry : 2
-0.616200
Huckel EHT eigenvalues for symmetry : 3
-0.704737 -0.160647
**********************************************************************
*SIRIUS* a direct, restricted step, second order MCSCF program *
**********************************************************************
Date and time (Linux) : Fri Feb 27 06:11:17 2015
Host name : wn701
Title lines from ".mol" input file:
Water
Print level on unit LUPRI = 2 is 0
Print level on unit LUW4 = 2 is 5
@ (Integral direct) CC calculation.
@ This is a combination run starting with
@ a restricted, closed shell Hartree-Fock calculation
Initial molecular orbitals are obtained according to
".MOSTART EHT " input option
Wave function specification
============================
For the specification of the Coupled Cluster: see later.
@ For the wave function of type : >>> CC <<<
@ Number of closed shell electrons 10
@ Number of electrons in active shells 0
@ Total charge of the molecule 0
@ Spin multiplicity and 2 M_S 1 0
Total number of symmetries 4
@ Reference state symmetry 1
Orbital specifications
======================
Abelian symmetry species All | 1 2 3 4
--- | --- --- --- ---
Total number of orbitals 7 | 4 1 2 0
Number of basis functions 7 | 4 1 2 0
** Automatic occupation of RHF orbitals **
-- Initial occupation of symmetries is determined from extended Huckel guess.
-- Initial occupation of symmetries is :
@ Occupied SCF orbitals 5 | 3 1 1 0
Maximum number of Fock iterations 0
Maximum number of DIIS iterations 60
Maximum number of QC-SCF iterations 60
Threshold for SCF convergence 1.00D-06
Changes of defaults for CC:
---------------------------
>>>>> DIIS optimization of Hartree-Fock <<<<<
C1-DIIS algorithm; max error vectors = 4
Automatic occupation of symmetries with 10 electrons.
Iter Total energy Error norm Delta(E) SCF occupation
-----------------------------------------------------------------------------
(Precalculated two-electron integrals are transformed to P-supermatrix elements.
Threshold for discarding integrals : 1.00D-12 )
@ 1 -73.2273758179 2.90D+00 -7.32D+01 3 1 1 0
Virial theorem: -V/T = 1.963073
@ MULPOP O -0.21; H _1 0.10; H _2 0.10;
-----------------------------------------------------------------------------
@ 2 -73.4315094723 2.41D-01 -2.04D-01 3 1 1 0
Virial theorem: -V/T = 1.956319
@ MULPOP O -1.12; H _1 0.56; H _2 0.56;
-----------------------------------------------------------------------------
@ 3 -73.4345390541 2.85D-02 -3.03D-03 3 1 1 0
Virial theorem: -V/T = 1.955089
@ MULPOP O -1.19; H _1 0.59; H _2 0.59;
-----------------------------------------------------------------------------
@ 4 -73.4345878930 7.71D-04 -4.88D-05 3 1 1 0
Virial theorem: -V/T = 1.954969
@ MULPOP O -1.19; H _1 0.60; H _2 0.60;
-----------------------------------------------------------------------------
@ 5 -73.4345879508 1.61D-04 -5.78D-08 3 1 1 0
Virial theorem: -V/T = 1.954972
@ MULPOP O -1.19; H _1 0.60; H _2 0.60;
-----------------------------------------------------------------------------
@ 6 -73.4345879538 1.15D-05 -2.93D-09 3 1 1 0
Virial theorem: -V/T = 1.954972
@ MULPOP O -1.19; H _1 0.60; H _2 0.60;
-----------------------------------------------------------------------------
@ 7 -73.4345879538 9.23D-09 -1.40D-11 3 1 1 0
@ *** DIIS converged in 7 iterations !
@ Converged SCF energy, gradient: -73.434587953781 9.23D-09
- total time used in SIRFCK : 0.00 seconds
*** SCF orbital energy analysis ***
Only the five lowest virtual orbital energies printed in each symmetry.
Number of electrons : 10
Orbital occupations : 3 1 1 0
Sym Hartree-Fock orbital energies
1 -20.42778715 -1.65908298 -0.57144538 0.99627162
2 -0.53360989
3 -0.93412130 1.46415730
E(LUMO) : 0.99627162 au (symmetry 1)
- E(HOMO) : -0.53360989 au (symmetry 2)
------------------------------------------
gap : 1.52988151 au
>>> Writing SIRIFC interface file <<<
>>>> CPU and wall time for SCF : 0.017 0.044
.-----------------------------------.
| >>> Final results from SIRIUS <<< |
`-----------------------------------'
@ Spin multiplicity: 1
@ Spatial symmetry: 1
@ Total charge of molecule: 0
@ Final HF energy: -73.434587953781
@ Nuclear repulsion: 16.794007988674
@ Electronic energy: -90.228595942455
@ Final gradient norm: 0.000000009227
Date and time (Linux) : Fri Feb 27 06:11:17 2015
Host name : wn701
(Only coefficients >0.0100 are printed.)
Molecular orbitals for symmetry species 1
------------------------------------------
Orbital 1 2 3 4
1 O :1s 0.9931 -0.2395 0.1032 0.1464
2 O :1s 0.0454 0.8469 -0.4521 -2.3372
3 O :2pz 0.0113 0.3537 0.9032 -0.8302
4 H :1s -0.0146 0.0636 0.0325 1.4608
Molecular orbitals for symmetry species 2
------------------------------------------
Orbital 1
1 O :2px 1.0000
Molecular orbitals for symmetry species 3
------------------------------------------
Orbital 1 2
1 O :2py 0.7075 -1.5190
2 H :1s 0.3774 1.8283
>>>> Total CPU time used in SIRIUS : 0.03 seconds
>>>> Total wall time used in SIRIUS : 0.06 seconds
Date and time (Linux) : Fri Feb 27 06:11:17 2015
Host name : wn701
.---------------------------------------.
| End of Wave Function Section (SIRIUS) |
`---------------------------------------'
.------------------------------------------.
| Starting in Coupled Cluster Section (CC) |
`------------------------------------------'
*******************************************************************************
*******************************************************************************
* *
* *
* START OF COUPLED CLUSTER CALCULATION *
* *
* *
*******************************************************************************
*******************************************************************************
CCR12 ANSATZ = 0
CCR12 APPROX = 0
*******************************************************************
* *
*<<<<<<<<<< >>>>>>>>>>*
*<<<<<<<<<< OUTPUT FROM COUPLED CLUSTER ENERGY PROGRAM >>>>>>>>>>*
*<<<<<<<<<< >>>>>>>>>>*
* *
*******************************************************************
The Direct Coupled Cluster Energy Program
-----------------------------------------
Number of t1 amplitudes : 4
Number of t2 amplitudes : 22
Total number of amplitudes in ccsd : 26
Iter. 1: Coupled cluster MP2 energy : -73.4463732668616984
Iter. 1: Coupled cluster CCSD energy : -73.4485237988900792
Iter. 2: Coupled cluster CCSD energy : -73.4490946600287629
Iter. 3: Coupled cluster CCSD energy : -73.4490970435479653
Iter. 4: Coupled cluster CCSD energy : -73.4490966774766463
Iter. 5: Coupled cluster CCSD energy : -73.4490966984833307
Iter. 6: Coupled cluster CCSD energy : -73.4490967046535701
CCSD energy converged to within 0.10D-07 is -73.449096704654
Final 2-norm of the CC vector function: 1.75572243D-06
+-------------------------------------------------------+
! Final results from the Coupled Cluster energy program !
+-------------------------------------------------------+
Total SCF energy: -73.4345879538
Total MP2 energy: -73.4463732669
Total CCSD energy: -73.4490967047
Perturbative triples corrections
--------------------------------
The E4 doubles and triples: -0.0000178781
The E5 singles and triples: 0.0000008570
Total energy CCSD(T): -73.4491137258
*******************************************************************************
*******************************************************************************
* *
* *
* SUMMARY OF COUPLED CLUSTER CALCULATION *
* *
* *
*******************************************************************************
*******************************************************************************
Total SCF energy: -73.4345879538
Total MP2 energy: -73.4463732669
Total CCSD energy: -73.4490967047
Perturbative triples corrections
--------------------------------
The E4 doubles and triples: -0.0000178781
The E5 singles and triples: 0.0000008570
Total energy CCSD(T): -73.4491137258
*******************************************************************************
*******************************************************************************
* *
* *
* END OF COUPLED CLUSTER CALCULATION *
* *
* *
*******************************************************************************
*******************************************************************************
>>>> CPU and wall time for CC : 0.055 0.121
Date and time (Linux) : Fri Feb 27 06:11:17 2015
Host name : wn701
.-------------------------------------.
| End of Coupled Cluster Section (CC) |
`-------------------------------------'
>>>> Total CPU time used in DALTON: 0.12 seconds
>>>> Total wall time used in DALTON: 0.40 seconds
Date and time (Linux) : Fri Feb 27 06:11:17 2015
Host name : wn701
|
