MOLPRO. Users Manual Version

Transcription

1 MOLPRO Users Manual Version H.-J. Werner Institut für Theoretische Chemie Universität Stuttgart Pfaffenwaldring 55 D Stuttgart Federal Republic of Germany P. J. Knowles School of Chemistry Cardiff University Main Building, Park Place, Cardiff CF10 3AT United Kingdom SHA1 d8c bb69708c8ce8541a11fe4fd2a76ec (Copyright c 2010 University College Cardiff Consultants Limited)

2 i Introduction to MOLPRO MOLPRO is a complete system of ab initio programs for molecular electronic structure calculations, designed and maintained by H.-J. Werner and P. J. Knowles, and containing contributions from a number of other authors. As distinct from other commonly used quantum chemistry packages, the emphasis is on highly accurate computations, with extensive treatment of the electron correlation problem through the multiconfiguration-reference CI, coupled cluster and associated methods. The recently developed explicitly correlated coupled-cluster methods yield CCSD(T) results with near basis set limit accuracy already with double ζ or triple ζ basis sets, thus reducing the computational effort for calculations of this quality by two orders of magnitude. Using local electron correlation methods, which significantly reduce the increase of the computational cost with molecular size, accurate ab initio calculations can be performed for much larger molecules than with most other programs. These methods have recently been augmented by explicitly correlated terms, which strongly reduce both the basis set truncation errors and the errors of the local approximations. The heart of the program consists of the multiconfiguration SCF, multireference CI, and coupledcluster routines, and these are accompanied by a full set of supporting features. The package comprises Integral generation for generally contracted symmetry adapted gaussian basis functions (spd f ghi). There are two programs with identical functionality: the preferred code is SEWARD (R. Lindh) which is the best on most machines; ARGOS (R. M. Pitzer) is available as an alternative, and in some cases is optimum for small memory scalar machines. Also two different gradient integral codes, namely CADPAC (R. Amos) and ALASKA (R. Lindh) are available. Only the latter allows the use of generally contracted symmetry adapted gaussian basis functions. Effective Core Potentials (contributions from H. Stoll). Many one-electron properties. Some two-electron properties, e.g. L 2 x, L 2 y, L 2 z, L x L y etc.. Closed-shell and open-shell (spin restricted and unrestricted) self consistent field. Density-functional theory in the Kohn-Sham framework with various gradient corrected exchange and correlation potentials. Multiconfiguration self consistent field. This is the quadratically convergent MCSCF procedure described in J. Chem. Phys. 82 (1985) The program can optimize a weighted energy average of several states, and is capable of treating both completely general configuration expansions and also long CASSCF expansions as described in Chem. Phys. Letters 115 (1985) 259. Multireference CI. As well as the usual single reference function approaches (MP2, SDCI, CEPA), this module implements the internally contracted multireference CI method as described in J. Chem. Phys. 89 (1988) 5803 and Chem. Phys. Lett. 145 (1988) 514. Non variational variants (e.g. MR-ACPF), as described in Theor. Chim. Acta 78 (1990) 175, are also available. Electronically excited states can be computed as described in Theor. Chim. Acta, (1992). Multireference second-order and third-order perturbation theory (MRPT2, CASPT2, MRPT3) as described in Mol. Phys. 89, 645 (1996) and J. Chem. Phys. 112, 5546 (2000).

3 ii Møller-Plesset perturbation theory (MPPT), Coupled-Cluster (CCSD), Quadratic configuration interaction (QCISD), and Brueckner Coupled-Cluster (BCCD) for closed shell systems, as described in Chem. Phys. Lett. 190 (1992) 1. Perturbative corrections for triple excitations can also be calculated (Chem. Phys. Letters 227 (1994) 321). Open-shell coupled cluster theories as described in J. Chem. Phys. 99 (1993) 5219, Chem. Phys. Letters 227 (1994) 321. An interface to the MRCC program of M. Kallay, allowing coupled-cluster calculations with arbitrary excitation level. Full Configuration Interaction. This is the determinant based benchmarking program described in Comp. Phys. Commun. 54 (1989) 75. Analytical energy gradients for SCF, DFT, state-averaged MCSCF/CASSCF, MRPT2/CASPT2, MP2 and QCISD(T) methods. Analytical non-adiabatic coupling matrix elements for MCSCF. Valence-Bond analysis of CASSCF wavefunction, and energy-optimized valence bond wavefunctions as described in Int. J. Quant. Chem. 65, 439 (1997). One-electron transition properties for MCSCF, MRCI, and EOM-CCSD wavefunctions, CASSCF and MRCI transition properties also between wavefunctions with different orbitals, as described in Mol. Phys. 105, 1239, (2007). Spin-orbit coupling, as described in Mol. Phys., 98, 1823 (2000). More recently, a new spin-orbit integral program for generally contracted basis sets has been implemented. Douglas-Kroll-Hess Hamiltonian up to arbitrary order. Density-functional theory symmetry-adapted intermolecular perturbation theory (with density fitting), DFT-SAPT, as described in J. Chem. Phys. 122, (2005). Some two-electron transition properties for MCSCF wavefunctions (e.g., L 2 x etc.). Mulliken population analysis and Natural Population Analysis (NPA) Orbital localization. Natural bond orbitals (NBOs). Distributed Multipole Analysis (A. J. Stone). Automatic geometry optimization as described in J. Comp. Chem. 18, (1997), Constrained optimization is also possible. Automatic calculation of vibrational frequencies, intensities, and thermodynamic properties. Reaction path following, as described in Theor. Chem. Acc. 100, (1998), 21. Efficient facilities to treat large lattices of point charges for QM/MM calculations, including lattice gradients. Various utilities allowing other more general optimizations, looping and branching (e.g., for automatic generation of complete potential energy surfaces), general housekeeping operations.

4 iii Geometry output in XYZ, MOLDEN and Gaussian formats; molecular orbital and frequency output in MOLDEN format. Integral-direct implementation of all Hartree-Fock, DFT and pair-correlated methods (MP, CCSD, MRCI etc.), as described in Mol. Phys., 96, (1999), 719. At present, perturbative triple excitation methods are not implemented. Local second-order Møller-Plesset perturbation theory (LMP2) and local coupled cluster methods, as described in in J. Chem. Phys. 104, 6286 (1996), Chem. Phys. Lett. 290, 143 (1998), J. Chem. Phys. 111, 5691 (1999), J. Chem. Phys. 113, 9443 (2000), J. Chem. Phys. 113, 9986 (2000), Chem. Phys. Letters 318, 370 (2000), J. Chem. Phys. 114, 661 (2001), Phys. Chem. Chem. Phys. 4, 3941 (2002), J. Chem. Phys. 116, 8772 (2002). Local density fitting methods, as described in J. Chem. Phys. 118, 8149 (2003), Phys. Chem. Chem. Phys. 5, 3349 (2003), Mol. Phys. 102, 2311 (2004). Analytical energy gradients for LMP2, DF-LMP2, and LQCISD as described in J. Chem. Phys. 108, 5185, (1998), Phy. Chem. Chem. Phys. 3, 4853 (2001), J. Chem. Phys. 121, 737 (2004). Explicitly correlated MP2-F12 and CCSD(T)-F12 methods, as described in J. Chem. Phys. 119, 4607 (2003), J. Chem. Phys. 121, 4479 (2004), J. Chem. Phys. 124, (2006), J. Chem. Phys. 124, (2006), J. Chem. Phys. 127, (2007), J. Chem. Phys. 130, (2009). Explicitly correlated local methods, as described in J. Chem. Phys. 129, (2009), J. Chem. Phys. 130, (2009), J. Chem. Phys. 130, (2009). Parallel execution on distributed memory machines, as described in J. Comp. Chem. 19, (1998), At present, SCF, DFT, MRCI, MP2, LMP2, CCSD(T), LCCSD(T) energies and SCF, DFT gradients are parallelized. Most density fitted codes such as DF-HF, DF- KS, DF-LMP2, DF-LMP2 gradients, DF-LCCSD(T), DF-MP2-F12, DF-DFT-SAPT, and GIAO-DF-HF NMR shieldings are also parallelized. Automatic embarrassingly parallel computation of numerical gradients and Hessians (mppx Version). The program is written mostly in standard Fortran 90. Those parts which are machine dependent are maintained through the use of a supplied preprocessor, which allows easy interconversion between versions for different machines. Each release of the program is ported and tested on a number of systems. A large library of commonly used orbital basis sets is available, which can be extended as required. There is a comprehensive users manual, which includes installation instructions. The manual is available in PDF and also in HTML for mounting on a Worldwide Web server. More recent methods and enhancements include: 1. Explicitly correlated MP2-F12 (closed-shell) and RMP2-F12 (open-shell) methods with many many different ansätze, as described in H.-J. Werner, T. B. Adler, and F. R. Manby, J. Chem. Phys. 126, (2007) and G. Knizia and H.-J. Werner, J. Chem. Phys. 128, (2008). 2. Explicitly correlated CCSD(T)-F12 methods as described in T. B. Adler, G. Knizia, and H.-J. Werner, J. Chem. Phys. 127, (2007) (closed-shell) and G. Knizia, T. B. Adler, and H.-J. Werner, J. Chem. Phys. 130, (2009) (open-shell).

5 iv 3. Explicitly correlated LMP2-F12 and LCCSD-F12 methods as described in H.-J. Werner, J. Chem. Phys. 129, (2009), T. B. Adler, H.-J. Werner, and F. R. Manby, J. Chem. Phys. 130, (2009), and T. B. Adler and H.-J. Werner, J. Chem. Phys. 130, (2009). 4. Natural localized orbitals, NPA and NBO analysis and improved methods for domain selection in local correlation calculations as described in R. A. Mata and H.-J. Werner, Mol. Phys. 105, 2753 (2007); see also R. A. Mata and H.-J. Werner, J. Chem. Phys. 125, (2006). 5. Correlation regions in local correlation calculations as described in R. A. Mata, H.-J. Werner and M. Schütz, J. Chem. Phys. 128, (2008). 6. Automated calculation of anharmonic vibrational frequencies and zero-point energies using VCI methods as described in T. Hrenar, H.-J. Werner, and G. Rauhut, J. Chem. Phys. 126, (2007) and references therein. 7. Dynamical state weighting as described in M. P. Deskevich and D. J. Nesbitt, and H.-J. Werner, J. Chem. Phys. 120, 7281 (2004). 8. Coupling of DFT and coupled cluster methods as described in E. Goll, T. Leininger, F. R. Manby, A. Mitrushchenkov, H.-J. Werner, and H. Stoll, Phys. Chem. Chem. Phys. 10, 3353 (2008) and references therein. 9. NMR chemical shifts using London atomic orbitals for density-fitted Hartree-Fock, as described in S. Loibl, F.R. Manby, M. Schütz, Mol. Phys. 108, 1362 (2010). 10. Local response methods (LCC2) for computing excitation energies and transition properties in large molecule as described in D. Kats, T. Korona, M. Schütz, J. Chem. Phys. 125, (2006), D. Kats, T. Korona, M. Schütz, J. Chem. Phys. 127, (2007), and D. Kats, M. Schütz, J. Chem. Phys. 131, (2009). 11. Automatic basis set extrapolation. 12. Enhanced connections to other programs, including graphical display of output and 3- dimensional structures. 13. Support for Mac OS X Future enhancements presently under development include Explicitly correlated local coupled cluster methods (closed and open-shell) Explicitly correlated CASPT2-F12 and MRCI-F12 methods. Analytical energy gradients for CCSD(T) and CCSD(T)-F12. Analytic second derivatives for DFT. New, more efficient MRCI methods for larger molecules. NMR chemical shifts using London atomic orbitals for local MP2. These features will be included in the base version at later stages. The above list is for information only, and no representation is made that any of the above will be available within any particular time.

6 v MOLPRO on the WWW The latest information on MOLPRO, including program updates, can be found on the worldwide web at location References All publications resulting from use of this program must acknowledge the following. MOLPRO, version , a package of ab initio programs, H.-J. Werner, P. J. Knowles, G. Knizia, F. R. Manby, M. Schütz, P. Celani, T. Korona, R. Lindh, A. Mitrushenkov, G. Rauhut, K. R. Shamasundar, T. B. Adler, R. D. Amos, A. Bernhardsson, A. Berning, D. L. Cooper, M. J. O. Deegan, A. J. Dobbyn, F. Eckert, E. Goll, C. Hampel, A. Hesselmann, G. Hetzer, T. Hrenar, G. Jansen, C. Köppl, Y. Liu, A. W. Lloyd, R. A. Mata, A. J. May, S. J. McNicholas, W. Meyer, M. E. Mura, A. Nicklass, D. P. O Neill, P. Palmieri, K. Pflüger, R. Pitzer, M. Reiher, T. Shiozaki, H. Stoll, A. J. Stone, R. Tarroni, T. Thorsteinsson, M. Wang, and A. Wolf,, see Some journals insist on a shorter list of authors; in such a case, the following should be used instead. MOLPRO, version , a package of ab initio programs, H.-J. Werner, P. J. Knowles, G. Knizia, F. R. Manby, M. Schütz, and others, see Depending on which programs are used, the following references should be cited. Integral evaluation (SEWARD) R. Lindh, U. Ryu, and B. Liu, J. Chem. Phys. 95, 5889 (1991). Integral-direct Implementation M. Schütz, R. Lindh, and H.-J. Werner, Mol. Phys. 96, 719 (1999). MCSCF/CASSCF: H.-J. Werner and P. J. Knowles, J. Chem. Phys. 82, 5053 (1985); P. J. Knowles and H.-J. Werner, Chem. Phys. Lett. 115, 259 (1985). See also: H.-J. Werner and W. Meyer, J. Chem. Phys. 73, 2342 (1980); H.-J. Werner and W. Meyer, J. Chem. Phys. 74, 5794 (1981); H.-J. Werner, Adv. Chem. Phys. LXIX, 1 (1987). Internally contracted MRCI: H.-J. Werner and P.J. Knowles, J. Chem. Phys. 89, 5803 (1988); P.J. Knowles and H.-J. Werner, Chem. Phys. Lett. 145, 514 (1988). See also: H.-J. Werner and E.A. Reinsch, J. Chem. Phys. 76, 3144 (1982); H.-J. Werner, Adv. Chem. Phys. LXIX, 1 (1987). Excited states with internally contracted MRCI: P. J. Knowles and H.-J. Werner, Theor. Chim. Acta 84, 95 (1992). Internally contracted MR-ACPF, QDVPT, etc: H.-J. Werner and P. J. Knowles, Theor. Chim Acta 78, 175 (1990).

7 vi The original reference to uncontracted MR-ACPF, QDVPT, MR-AQCC are: R. J. Gdanitz and R. Ahlrichs, Chem. Phys. Lett. 143, 413 (1988); R. J. Cave and E. R. Davidson, J. Chem. Phys. 89, 6798 (1988); P. G. Szalay and R. J. Bartlett, Chem. Phys. Lett. 214, 481 (1993). Multireference perturbation theory (CASPT2/CASPT3): H.-J. Werner, Mol. Phys. 89, 645 (1996); P. Celani and H.-J. Werner, J. Chem. Phys. 112, 5546 (2000). Coupling of multi-reference configuration interaction and multi-reference perturbation theory, P. Celani, H. Stoll, H.-J. Werner and P. J. Knowles, Mol. Phys. 102, 2369 (2004). Analytical energy gradients and geometry optimization Gradient integral evaluation (ALASKA): R. Lindh, Theor. Chim. Acta 85, 423 (1993); MCSCF gradients: T. Busch, A. Degli Esposti, and H.-J. Werner, J. Chem. Phys. 94, 6708 (1991); MP2 and LMP2 gradients: A. El Azhary, G. Rauhut, P. Pulay, and H.-J. Werner, J. Chem. Phys. 108, 5185 (1998); DF-LMP2 gradients: M. Schütz, H.-J. Werner, R. Lindh and F. R. Manby, J. Chem. Phys. 121, 737 (2004). QCISD and LQCISD gradients: G. Rauhut and H.-J. Werner, Phys. Chem. Chem. Phys. 3, 4853 (2001); CASPT2 gradients: P. Celani and H.-J. Werner, J. Chem. Phys. 119, 5044 (2003). Geometry optimization: F. Eckert, P. Pulay and H.-J. Werner, J. Comp. Chemistry 18, 1473 (1997); Reaction path following: F. Eckert and H.-J. Werner, Theor. Chem. Acc. 100, 21, Harmonic frequencies G. Rauhut, A. El Azhary, F. Eckert, U. Schumann, and H.-J. Werner, Spectrochimica Acta 55, 651 (1999). T. Hrenar, G. Rauhut, H.-J. Werner, J. Phys. Chem. A 110, 2060 (2006). Anharmonic frequencies (SURF, VSCF, VCI): G. Rauhut, J. Chem. Phys. 121, 9313 (2004); T. Hrenar, H.-J. Werner, G. Rauhut, J. Chem. Phys. 126, (2007); G. Rauhut, T. Hrenar, Chem. Phys. 346, 160 (2008); M. Neff, G. Rauhut, J. Chem. Phys. 131, (2009). Møller-Plesset Perturbation theory (MP2, MP3, MP4): Closed-shell Møller-Plesset Perturbation theory up to fourth order [MP4(SDTQ)] is part of the coupled cluster code, see CCSD. Open-shell Møller-Plesset Perturbation theory (RMP2): R. D. Amos, J. S. Andrews, N. C. Handy, and P. J. Knowles, Chem. Phys. Lett. 185, 256 (1991). Coupled-Cluster treatments (QCI, CCSD, BCCD): C. Hampel, K. Peterson, and H.-J. Werner, Chem. Phys. Lett. 190, 1 (1992) and references therein. The program to compute the perturbative triples corrections has been developed by M. J. O. Deegan and P. J. Knowles, Chem. Phys. Lett. 227, 321 (1994). Equation-of-Motion Coupled Cluster Singles and Doubles (EOM-CCSD): T. Korona and H.-J. Werner, J. Chem. Phys. 118, 3006 (2003). Open-shell coupled-cluster (RCCSD, UCCSD): P. J. Knowles, C. Hampel and H.-J. Werner, J. Chem. Phys. 99, 5219 (1993); Erratum: J. Chem. Phys. 112, 3106 (2000).

8 vii Local MP2 (LMP2): G. Hetzer, P. Pulay, and H.-J. Werner, Chem. Phys. Lett. 290, 143 (1998) M. Schütz, G. Hetzer, and H.-J. Werner, J. Chem. Phys. 111, 5691 (1999) G. Hetzer, M. Schütz, H. Stoll, and H.-J. Werner, J. Chem. Phys. 113, 9443 (2000) See also references on energy gradients and density fitting. Local Coupled Cluster methods (LCCSD, LQCISD, LMP4): C. Hampel and H.-J. Werner, J. Chem. Phys (1996) M. Schütz and H.-J. Werner, J. Chem. Phys. 114, 661 (2001) M. Schütz, Phys. Chem. Chem.Phys. 4, 3941 (2002) See also references on energy gradients and density fitting. Local triple excitations: M. Schütz and H.-J. Werner, Chem. Phys. Lett. 318, 370 (2000); M. Schütz, J. Chem. Phys. 113, 9986 (2000). M. Schütz, J. Chem. Phys. 116, 8772 (2002). Density fitting methods: DFT, Poisson fitting: DF-MP2, DF-LMP2: DF-LCCSD: DF-HF: DF-LMP2 gradients: DF-LCCSD(T): F. R. Manby, P. J. Knowles, and A. W. Lloyd, J. Chem. Phys. 115, 9144 (2001). H.-J. Werner, F. R. Manby, and P. J. Knowles, J. Chem. Phys. 118, 8149 (2003). M. Schütz and F. R. Manby, Phys. Chem. Chem. Phys. 5, 3349 (2003) R. Polly, H.-J. Werner, F. R. Manby, and Peter J. Knowles, Mol. Phys. 102, 2311 (2004). M. Schütz, H.-J. Werner, R. Lindh and F. R. Manby, J. Chem. Phys. 121, 737 (2004). H.-J. Werner and M. Schütz, in prepation. Explicitly correlated methods with density fitting: DF-MP2-R12: F. R. Manby, J. Chem. Phys. 119, 4807 (2003). DF-MP2-F12/2A: A. J. May and F. R. Manby, J. Chem. Phys. 121, 4479 (2004). DF-MP2-F12: H.-J. Werner, T. B. Adler, and F. R. Manby, J. Chem. Phys. 126, (2007). DF-RMP2-F12: G. Knizia and H.-J. Werner, J. Chem. Phys. 128, (2008). DF-LMP2-F12: H.-J. Werner and F. R. Manby, J. Chem. Phys., 124, (2006); F. R. Manby H.-J. Werner, T. B. Adler, and A. J. May, J. Chem. Phys. 124, (2006); H.-J. Werner, T. B. Adler, and F. R. Manby, J. Chem. Phys. 126, (2007); T. B. Adler, H.-J. Werner, and F. R. Manby, J. Chem. Phys. 130, (2009). CCSD(T)-F12: T. B. Adler, G. Knizia, and H.-J. Werner, J. Chem. Phys. 127, (2007). UCCSD(T)-F12: G. Knizia, T. B. Adler, and H.-J. Werner, J. Chem. Phys. 130, (2009).

9 viii Rangehybrid methods: T. Leininger, H. Stoll, H.-J. Werner, and A. Savin, Chem. Phys. Lett. 275, 151 (1997). J.G. Ángyán, I.C. Gerber, A. Savin, and J. Toulouse, Phys. Rev. A 72, (2005). E. Goll, H.-J. Werner, and H. Stoll, Phys. Chem. Chem. Phys. 7, 3917 (2005). Full CI (FCI): P. J. Knowles and N. C. Handy, Chem. Phys. Letters 111, 315 (1984); P. J. Knowles and N. C. Handy, Comp. Phys. Commun. 54, 75 (1989). Distributed Multipole Analysis (DMA): A. J. Stone, Chem. Phys. Letters 83, 233 (1981). Valence bond: D. L. Cooper, T. Thorsteinsson, and J. Gerratt, Int. J. Quant. Chem. 65, 439 (1997); D. L. Cooper, T. Thorsteinsson, and J. Gerratt, Adv. Quant. Chem. 32, (1998). See also An overview of the CASVB approach to modern valence bond calculations, T. Thorsteinsson and D. L. Cooper, in Quantum Systems in Chemistry and Physics. Volume 1: Basic problems and models systems, eds. A. Hernndez-Laguna, J. Maruani, R. McWeeny, and S. Wilson (Kluwer, Dordrecht, 2000); pp Relativistic corrections using the Douglas-Kroll Hamiltonian: M. Reiher, A. Wolf, JCP 121, (2004); M. Reiher, A. Wolf, JCP 121, (2004); A. Wolf, M. Reiher, B. A. Hess, JCP 117, (2002). Spin-orbit coupling: A. Berning, M. Schweizer, H.-J. Werner, P. J. Knowles, and P. Palmieri, Mol. Phys., 98, 1823 (2000). Diabatization procedures: H.-J. Werner and W. Meyer, J. Chem. Phys. 74, 5802 (1981); H.-J. Werner, B. Follmeg, and M. H. Alexander, J. Chem. Phys. 89, 3139 (1988); D. Simah, B. Hartke, and H.-J. Werner, J. Chem. Phys. 111, 4523 (1999). DF-DFT-SAPT: A. Heßelmann, G. Jansen and M. Schütz, J. Chem. Phys. 122, (2005). NMR shielding tensors: S. Loibl, F.R. Manby, M. Schütz, Mol. Phys. 108, 1362 (2010).

10 CONTENTS ix Contents 1 HOW TO READ THIS MANUAL 1 2 RUNNING MOLPRO Options Running MOLPRO on parallel computers Specifying parallel execution DEFINITION OF MOLPRO INPUT LANGUAGE Input format Commands Directives Global directives Options Data Expressions Intrinsic functions Variables Setting variables String variables Procedures Procedure definition Procedure calls GENERAL PROGRAM STRUCTURE Input structure Files Records Restart Data set manipulation Memory allocation Multiple passes through the input Symmetry Defining the wavefunction Defining orbital subspaces Selecting orbitals and density matrices (ORBITAL, DENSITY)

11 CONTENTS x 4.12 Summary of keywords known to the controlling program MOLPRO help INTRODUCTORY EXAMPLES Using the molpro command Simple SCF calculations Geometry optimizations CCSD(T) CASSCF and MRCI Tables Procedures Do loops PROGRAM CONTROL Starting a job (***) Ending a job (---) Restarting a job (RESTART) Including secondary input files (INCLUDE) Allocating dynamic memory (MEMORY) DO loops (DO/ENDDO) Examples for do loops Branching (IF/ELSEIF/ENDIF) IF statements GOTO commands Labels (LABEL) Procedures (PROC/ENDPROC) Text cards (TEXT) Checking the program status (STATUS) Global Thresholds (GTHRESH) Global Print Options (GPRINT/NOGPRINT) One-electron operators and expectation values (GEXPEC) Example for computing expectation values Example for computing relativistic corrections

12 CONTENTS xi 7 FILE HANDLING FILE DELETE ERASE DATA Assigning punch files (PUNCH) MOLPRO system parameters (GPARAM) VARIABLES Setting variables Indexed variables String variables System variables Macro definitions using string variables Indexed Variables (Vectors) Vector operations Special variables Variables set by the program Variables recognized by the program Displaying variables The SHOW command Clearing variables Reading variables from an external file TABLES AND PLOTTING Tables Plotting Diatomic potential curve analysis MOLECULAR GEOMETRY Geometry specifications Z-matrix input XYZ input Symmetry specification Writing Gaussian, XMol or MOLDEN input (PUT) Visualization of results using Molden

13 CONTENTS xii 10.4 Geometry Files Lattice of point charges Redefining and printing atomic masses Dummy centres Counterpoise calculations Example: interaction energy of OH-Ar BASIS INPUT Overview: sets and the basis library Cartesian and spherical harmonic basis functions The basis set library Default basis sets Default basis sets for individual atoms Basis blocks Auxiliary basis sets for density fitting or resolution of the identity Primitive set definition Contracted set definitions Examples EFFECTIVE CORE POTENTIALS Input from ECP library Explicit input for ECPs Example for explicit ECP input Example for ECP input from library CORE POLARIZATION POTENTIALS Input options Example for ECP/CPP INTEGRATION Sorted integrals INTEGRAL-DIRECT CALCULATIONS (GDIRECT) Example for integral-direct calculations

14 CONTENTS xiii 15 DENSITY FITTING Options for density fitting Options to select the fitting basis sets Screening thresholds Parameters to enable local fitting Parameters for fitting domains Miscellaneous control options THE SCF PROGRAM Options Options to control HF convergence Options for the diagonalization method Options for convergence acceleration methods (DIIS) Options for integral direct calculations Special options for UHF calculations Options for local density-fitting calculations Options for polarizabilities Printing options Defining the wavefunction Defining the number of occupied orbitals in each symmetry Specifying closed-shell orbitals Specifying open-shell orbitals Saving the final orbitals Starting orbitals Initial orbital guess Starting with previous orbitals Starting with a previous density matrix Rotating pairs of orbitals Using additional point-group symmetry Expectation values Polarizabilities Miscellaneous directives Level shifts Maximum number of iterations Convergence threshold

15 CONTENTS xiv Sanity check on the energy Print options Interpolation Reorthonormalization of the orbitals Direct SCF THE DENSITY FUNCTIONAL PROGRAM Options Directives Density source (DENSITY, ODENSITY) Thresholds (DFTTHRESH) Exact exchange computation (EXCHANGE) Rangehybrid methods (RANGEHYBRID) Exchange-correlation potential (POTENTIAL) Grid blocking factor (DFTBLOCK) Dump integrand values(dftdump) Numerical integration grid control (GRID) Target quadrature accuracy (GRIDTHRESH) Radial integration grid (RADIAL) Angular integration grid (ANGULAR) Atom partitioning of integration grid (VORONOI) Grid caching (GRIDSAVE, NOGRIDSAVE) Grid symmetry (GRIDSYM,NOGRIDSYM) Grid printing (GRIDPRINT) Density Functionals Alias density functionals Implementing new functionals Implementing new hybrid-functionals Empirical damped dispersion correction Examples ORBITAL LOCALIZATION Defining the input orbitals (ORBITAL) Saving the localized orbitals (SAVE) Choosing the localization method (METHOD) Delocalization of orbitals (DELOCAL)

16 CONTENTS xv 18.5 Localizing AOs(LOCAO) Selecting the orbital space Defining the occupied space (OCC) Defining the core orbitals (CORE) Defining groups of orbitals (GROUP, OFFDIAG) Localization between groups (OFFDIAG) Ordering of localized orbitals No reordering (NOORDER) Ordering using domains (SORT) Defining reference orbitals (REFORB) Selecting the fock matrix (FOCK) Selecting a density matrix (DENSITY) Localization thresholds (THRESH) Options for PM localization (PIPEK) Printing options (PRINT) THE MCSCF PROGRAM MULTI Structure of the input Defining the orbital subspaces Occupied orbitals Frozen-core orbitals Closed-shell orbitals Freezing orbitals Defining the optimized states Defining the state symmetry Defining the number of states in the present symmetry Specifying weights in state-averaged calculations Dynamical weighting Defining the configuration space Occupation restrictions Selecting configurations Specifying orbital configurations Selecting the primary configuration set Projection to specific Λ states in linear molecules Restoring and saving the orbitals and CI vectors

17 CONTENTS xvi Defining the starting guess Rotating pairs of initial orbitals Saving the final orbitals Saving the CI vectors and information for a gradient calculation Natural orbitals Pseudo-canonical orbitals Localized orbitals Diabatic orbitals Selecting the optimization methods Selecting the CI method Selecting the orbital optimization method Disabling the optimization Disabling the extra symmetry mechanism Calculating expectation values Matrix elements over one-electron operators Matrix elements over two-electron operators Saving the density matrix Miscellaneous options Print options Convergence thresholds Maximum number of iterations Test options Special optimization parameters Saving wavefunction information for CASVB Saving transformed integrals Coupled-perturbed MCSCF Gradients for SA-MCSCF Difference gradients for SA-MCSCF Non-adiabatic coupling matrix elements for SA-MCSCF MCSCF hessians Optimizing valence bond wavefunctions Hints and strategies Examples

18 CONTENTS xvii 20 THE CI PROGRAM Introduction Specifying the wavefunction Occupied orbitals Frozen-core orbitals Closed-shell orbitals Defining the orbitals Defining the state symmetry Additional reference symmetries Selecting configurations Occupation restrictions Explicitly specifying reference configurations Defining state numbers Defining reference state numbers Specifying correlation of orbital pairs Restriction of classes of excitations Options Coupled Electron Pair Approximation Coupled Pair Functional (ACPF, AQCC) Projected excited state calculations Transition matrix element options Convergence thresholds Level shifts Maximum number of iterations Restricting numbers of expansion vectors Selecting the primary configuration set Canonicalizing external orbitals Saving the wavefunction Starting wavefunction One electron properties Transition moment calculations Saving the density matrix Natural orbitals Miscellaneous options Miscellaneous parameters

19 CONTENTS xviii 20.4 Miscellaneous thresholds Print options Examples Cluster corrections for multi-state MRCI MULTIREFERENCE RAYLEIGH SCHRÖDINGER PERTURBATION THEORY Introduction Excited state calculations Multi-State CASPT Performing SS-SR-CASPT2 calculations Performing MS-MR-CASPT2 calculations Modified Fock-operators in the zeroth-order Hamiltonian Level shifts Integral direct calculations CASPT2 gradients Coupling MRCI and MRPT2: The CIPT2 method Further options for CASPT2 and CASPT NEVPT2 calculations General considerations Input description MØLLER PLESSET PERTURBATION THEORY Expectation values for MP Polarizabilities and second-order properties for MP CPHF for gradients, expectation values and polarizabilities Density-fitting MP2 (DF-MP2, RI-MP2) Spin-component scaled MP2 (SCS-MP2) THE CLOSED SHELL CCSD PROGRAM Coupled-cluster, CCSD Quadratic configuration interaction, QCI Brueckner coupled-cluster calculations, BCCD The BRUECKNER directive Singles-doubles configuration interaction, CISD The DIIS directive Examples

20 CONTENTS xix Single-reference correlation treatments for H 2 O Single-reference correlation treatments for N 2 F Saving the density matrix Natural orbitals Dual basis set calculations EXCITED STATES WITH EQUATION-OF-MOTION CCSD (EOM-CCSD) Options for EOM Options for EOMPAR card Options for EOMPRINT card Examples PES for lowest excited states for hydrogen fluride EOM-CCSD transition moments for hydrogen fluoride Calculate an EOM-CCSD state most similar to a given CIS state Excited states with CIS First- and second-order properties for CCSD OPEN-SHELL COUPLED CLUSTER THEORIES The MRCC program of M. Kallay (MRCC) Installing MRCC Running MRCC SMILES INTERNAL BASIS SETS EXTERNAL BASIS SETS Example LOCAL CORRELATION TREATMENTS Introduction Getting started Summary of options Summary of directives General Options Options for selection of domains Standard domains Extended domains

21 CONTENTS xx Manually Defining orbital domains (DOMAIN) Options for selection of pair classes Directives The LOCAL directive The MULTP directive Saving the wavefunction (SAVE) Restarting a calculation (START) Correlating subsets of electrons (REGION) Domain Merging (MERGEDOM) Energy partitioning for molecular cluster calculations (ENEPART) Doing it right Basis sets Symmetry and Orientation Localization Orbital domains Freezing domains Pair Classes Gradients and frequency calculations Intermolecular interactions Density-fitted LMP2 (DF-LMP2) and coupled cluster (DF-LCCSD(T0)) LOCAL METHODS FOR EXCITED STATES Local CC2 and ADC(2) Options for EOM Parameters on LAPLACE card Print options Examples EXPLICITLY CORRELATED METHODS Reference functions Wave function Ansätze The general ansatz The diagonal ansatz (D) The fixed amplitude ansatz (FIX) RI Approximations Basis sets

22 CONTENTS xxi 31.5 Symmetry Options Choosing the ansatz and the level of approximation CABS Singles correction Pair specific geminal exponents CCSD(T)-F DF-LMP2-F12 calculations with local approximations Variables set by the F12 programs THE FULL CI PROGRAM Defining the orbitals Occupied orbitals Frozen-core orbitals Defining the state symmetry Printing options Interface to other programs SYMMETRY-ADAPTED INTERMOLECULAR PERTURBATION THEORY Introduction First example DFT-SAPT High order terms Density fitting SAPT with ECP s Examples HF-SAPT calculation of the H 2 O dimer using the δ(hf) correction DFT-SAPT calculation of the NeAr dimer using the δ(hf) correction DF-DFT-SAPT calculation of the NeAr dimer using the δ(hf) correction Options PROPERTIES AND EXPECTATION VALUES The property program Calling the property program (PROPERTY) Expectation values (DENSITY) Orbital analysis (ORBITAL) Specification of one-electron operators

23 CONTENTS xxii Printing options Examples Distributed multipole analysis Calling the DMA program (DMA) Specifying the density matrix (DENSITY) Linear molecules (LINEAR, GENERAL) Maximum rank of multipoles (LIMIT) Omitting nuclear contributions (NONUCLEAR) Specification of multipole sites (ADD, DELETE) Defining the radius of multipole sites (RADIUS) Notes and references Examples Mulliken population analysis Calling the population analysis program (POP) Defining the density matrix (DENSITY) Populations of basis functions (INDIVIDUAL) Example Natural Bond Orbital Analysis Calling the Natural Bond Orbital analysis program (NBO) Saving the NLMO orbitals (SAVE) Finite field calculations Dipole fields (DIP) Quadrupole fields (QUAD) General fields (FIELD) Examples Relativistic corrections Example CUBE dump density or orbital values STEP setting the point spacing DENSITY source of density ORBITAL source of orbitals AXIS direction of grid axes BRAGG spatial extent of grid ORIGIN centroid of grid TITLE user defined title

24 CONTENTS xxiii DESCRIPTION user defined description Format of cube file GOPENMOL calculate grids for visualization in gopenmol RELATIVISTIC CORRECTIONS Using the Douglas Kroll Hess Hamiltonian Example for computing relativistic corrections DIABATIC ORBITALS NON ADIABATIC COUPLING MATRIX ELEMENTS The DDR procedure QUASI-DIABATIZATION THE VB PROGRAM CASVB Structure of the input Defining the CASSCF wavefunction The VBDUMP directive Other wavefunction directives Defining the valence bond wavefunction Specifying orbital configurations Selecting the spin basis Recovering CASSCF CI vector and VB wavefunction Saving the VB wavefunction Specifying a guess Orbital guess Guess for structure coefficients Read orbitals or structure coefficients Permuting orbitals Optimization control Optimization criterion Number of iterations CASSCF-projected structure coefficients Saddle-point optimization Defining several optimizations Multi-step optimization