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PSI is an ab initio computational chemistry package originally written by the research group of Henry F. Schaefer, III (University of Georgia). It performs high-accuracy quantum computations on small to medium-sized molecules. PSI4 is the latest release of the program package - it is open source, released as free under the GPL through SourceForge. Primary development is currently conducted by Daniel Crawford (Virginia Tech), David Sherrill (Georgia Tech), Edward Valeev (Virginia Tech), and Rollin King (Bethel University).〔Justin M. Turney, Andrew C. Simmonett, Robert M. Parrish, Edward G. Hohenstein, Francesco A. Evangelista, Justin T. Fermann, Benjamin J. Mintz, Lori A. Burns, Jeremiah J. Wilke, Micah L. Abrams, Nicholas J. Russ, Matthew L. Leininger, Curtis L. Janssen, Edward T. Seidl, Wesley D. Allen, Henry F. Schaefer, Rollin A. King, Edward F. Valeev, C. David Sherrill, T. Daniel Crawford. Wiley Interdisciplinary Reviews: Computational Molecular Science, Vol 2 Issue 4, pages 556–565., 2012. DOI: 10.1002/wcms.93.〕 The earlier PSI3 is widely available in many Linux releases such as Ubuntu. ==Features== The basic capabilities of PSI are concentrated around the following methods of quantum chemistry: * Hartree–Fock method * Coupled cluster * CASSCF * multireference configuration interaction methods. Several methods are available for computing excited electronic states, including configuration interaction singles (CIS), the random phase approximation (RPA), and equation-of-motion coupled cluster (EOM-CCSD). PSI3 also includes the explicitly-correlated MP2-R12 method and the ability to compute the Born–Oppenheimer diagonal correction using configuration interaction wave functions. 抄文引用元・出典: フリー百科事典『 ウィキペディア（Wikipedia）』 ■ウィキペディアで「PSI (computational chemistry)」の詳細全文を読む スポンサード リンク
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