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Relationship between the energy of donor–acceptor bond and the reorganization energy in molecular complexes
Author(s) -
Timoshkin A. Y.,
Davydova E. I.,
Sevastianova T. N.,
Suvorov A. V.,
Schaefer H. F.
Publication year - 2002
Publication title -
international journal of quantum chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.484
H-Index - 105
eISSN - 1097-461X
pISSN - 0020-7608
DOI - 10.1002/qua.10073
Subject(s) - chemistry , acceptor , bond dissociation energy , dissociation (chemistry) , pyridine , halide , bond energy , binding energy , computational chemistry , molecule , crystallography , photochemistry , atomic physics , inorganic chemistry , medicinal chemistry , organic chemistry , physics , condensed matter physics
Donor–acceptor complexes of silicon halides with ammonia, pyridine, and 2,2′bipyridine SiX 4 · n D (X = F, Cl, Br) have been studied at the B3LYP/pVDZ level of theory. Energies of the donor–acceptor bond have been estimated taking into account the reorganization energy of the donor and acceptor fragments and basis set superposition error correction. Despite of the very low (or even negative) dissociation energy of SiX 4 · n D into free fragments, the Si–N bonding in all complexes is rather strong (75–220 kJ mol −1 ). It is the reorganization energy of the acceptor SiX 4 (75–280 kJ mol −1 ) that governs the dissociation energy of the complex. Thus, in contrast to the complexes of group 13 halides, the reorganization effects are crucial for the complexes of group 14 halides, and their neglecting leads to erroneous conclusions about the strength of the donor–acceptor bond in these systems. © 2002 Wiley Periodicals, Inc. Int J Quantum Chem, 2002