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Focus is on the practical implementation of the classical description in quantum chemistry codes (in particular, HONDO8.1). Expressions are given for the self\u2010consistent coupling between the classical partitions (dipole polarizabilities and boundary surface dipoles and charges) and for the coupling between classical and quantum partitions. The latter is mediated through expanded, rather than exact, potentials and fields. In this way, the computation of only a limited number of formal interactions between unit charge distributions located at the expansion centers suffices to evaluate the reaction field contributions. The electronic part of the coupling can be included in the Hamiltonian via the Fock matrix. The field operators, as well as the one\u2010 and two\u2010electron matrix elements over the basis functions, are simple. The expressions for these are given explicitly.<\/jats:p><jats:p>Nonequilibrium potentials and Monte Carlo sampling over classical degrees of freedom have been added to better mimic experimental conditions. \u00a9 1995 by John Wiley &amp; Sons, Inc.<\/jats:p>","DOI":"10.1002\/jcc.540160105","type":"journal-article","created":{"date-parts":[[2005,1,2]],"date-time":"2005-01-02T01:06:43Z","timestamp":1104628003000},"page":"37-55","source":"Crossref","is-referenced-by-count":98,"title":["Implementation of reaction field methods in quantum chemistry computer codes"],"prefix":"10.1002","volume":"16","author":[{"given":"A. H.","family":"De Vries","sequence":"first","affiliation":[]},{"given":"P. Th.","family":"Van Duijnen","sequence":"additional","affiliation":[]},{"given":"A. H.","family":"Juffer","sequence":"additional","affiliation":[]},{"given":"J. A. C.","family":"Rullmann","sequence":"additional","affiliation":[]},{"given":"J. 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