PQS (chemical)

PQS (chemical)
Developer(s) Parallel Quantum Solutions
Stable release PQS ab initio v. 4.0
Operating system Linux, Microsoft Windows, Mac OS
License Commercial
Website www.pqs-chem.com

PQS is a general purpose quantum chemistry program. Its roots go back to the first ab initio gradient program developed in Professor Peter Pulay's group but now it is developed and distributed commercially by Parallel Quantum Solutions. There is a reduction in cost for academic users and a site license. Its strong points are geometry optimization, NMR chemical shift calculations, and large MP2 calculations, and high parallel efficiency on computing clusters. It includes many other capabilities including Density functional theory, the semiempirical methods, MINDO/3, MNDO, AM1 and PM3, Molecular mechanics using the SYBYL 5.0 Force Field, the quantum mechanics/molecular mechanics mixed method using the ONIOM method, natural bond orbital (NBO) analysis and COSMO solvation models. Recently, a highly efficient arallel CCSD(T) code for closed shell systems has been developed. This code includes many other post Hartree–Fock methods: MP2, MP3, MP4, CISD, CEPA, QCISD and so on.

History

The origin of PQS program was developed by Meyer and Pulay in the late 1960s. They both were at the Max-Planck Institute for Physics and Astrophysics in Munich when they began to write a new ab initio program.[1] The main propose was to establish new ab initio techniques. Pulay and Meyer had slightly different interests.[1] Pulay was interested in implementing gradient geometry optimization, analytical energy derivatives (force), and force constant calculations via the numerical differentiation of analytical forces, while Meyer enthused about the coupled-electron pair approximation (CEPA), spin density calculation, and extremely accurate correlation methods like pseudonatural orbital-configuration interaction (PNO-CI).[1] At that time, analytical gradients were limited to closed-shell Hartree-Fork wavefunctions. However, they were able to do it for unrestricted (UHF) and restricted open-shell (ROHF) methods in 1970. The first version of the code was completed in 1969 at Max-Plank institute and University of Stuttgart. Then, Meyer named it “MOLPRO” and used Gaussian lobe basis sets.[1] In the 1970s, the current version of MOLPRO added a number of advanced methods such as multiconfiguration self-consistentfield (MC-SCF) and internally contracted multireference configuration interaction (MR-CI). Simultaneously, in the 1980s, MOLPRO was extended and mostly rewritten by Werner, Knowles and Meyer’s coworkers.[1]

Meanwhile in 1976, Puley was visiting Boggs at the University of Texas, Austin and Schaefer at the University of California. They wrote a new program called TEXAS based on the original MOLPRO and replaced Gaussian lobe functions with the standard Gaussian functions.[1] TEXAS emphasized large molecules, SCF convergence, geometry optimization techniques, and vibrational spectroscopy-related calculations. From 1982 onward, the program was further developed at the University of Arkansas.[1]

The primary significant expansion was the usage of a few new electron correlation methods by Saebo and a first- order MC-SCF program by Hamilton. A critical option was the implementation of the first practical gauge-invariant atomic orbital (GIAO) NMR program by Wolinski, who additionally included a highly efficient integral package.[1] Bofill executed an unhindered natural orbital-complete active space (UNO-CAS) program including analytical gradients; this is a minimal-cost alternative to MC-SCF and works just as well in most cases. TEXAS was initially parallelized in 1995–1996 on a cluster of 10 IBM RS6000 workstations.[1]

In 1996, Baker joined Pulay and, around the same time, Intel brought out the Pentium Pro, a processor for PC that was competitive with low-end workstations and less costly by around an order of magnitude. Understanding the capability of this improvement for computational chemistry, PQS was formed and a SBIR grant application was submitted in July 1997 for the commercial development of PC clusters for parallel ab initio calculations.[1] In the meantime, the Pulay group, financed by a National Science Foundation grant, set about constructing a Linux cluster using 300 MHz Pentium II processors. By a fortunate circumstance, a few capable and PC proficient graduate students were available, specifically Magyarfalvi and Shirel.[1] The PC cluster was a complete success, and significantly outperformed the IBM Workstation cluster that was the group's computational mainstay at a small amount of its expense.[1]

The PQS programming was demonstrated on the TEXAS code and parts of it, chiefly the NMR code, were authorized to PQS from the University of Arkansas.[1] Much of the code was widely changed to comply with the twin points of (a) having all major functionality fully parallel; and (b) having the capacity to routinely perform calculations on extensive systems.[1] They aimed primarily for a modest level of parallelism (from 8 to 32 CPUs), as this is the most widely recognized size for an individual or group resource. Indeed, even on very large clusters it is normal for any given user to be allocated only a percentage of the available processors.[1]

Features

The basis capabilities in high-level correlated energies for PQS ab initio v. 4.0 include MP3, MP4, CID, CISD, CEPA-0, CEPA-2, QCISD, QCISD(T), CCD, CCSD and CCSD(T) wavefunctions; enforced geometry optimization (used, among other things, to simulate the results of Atomic Force Microscopy (AFM) experiments); full-accuracy, canonical UMP2 energies and analytical polarizabilities and hyperpolarizabilities for HF and DFT wavefunctions.[2]

See also

Reference

  1. 1 2 3 4 5 6 7 8 9 10 11 12 13 14 15 Baker, Jon; Wolinski, Krzysztof; Malagoli, Massimo; Kinghorn, Don; Wolinski, Pawel; Magyarfalvi, Gábor; Saebo, Svein; Janowski, Tomasz; Pulay, Peter (2008). "Quantum chemistry in parallel with PQS". Journal of Computational Chemistry 30 (2): 317–335. doi:10.1002/jcc.21052.
  2. ↑ "PQS ab initio v. 4.0". Parallel Quantum Solutions. Turnkey Computational Chemistry.
  3. 1 2 "PQS Ab Initio Program Package" (PDF). Parallel Quantum Solution.
  4. ↑ Leszczynski, Jerzy; Kaczmarek-Kędziera, Anna; G. Papadopoulos, Manthos; Reis, Heribert; J. Sadlej, Andrzej; K. Shukla, Manoj. Handbook of Computational Chemistry (2012 ed.). Springer.

External links

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