Abstract
We present a new quantum-mechanical resonance theory based on the first-order reduced density matrix and its representation in terms of natural bond orbitals (NBOs). This “natural” resonance theory (NRT) departs in important respects from the classical Pauling-Wheland formulation, yet it leads to quantitative resonance weights that are in qualitative accord with conventional resonance theory and chemical intuition. The NRT variational functional leads to an optimal resonance-weighted approximation to the full density matrix, combining the “single reference” limit of weak delocalization (incorporating diagonal population changes only) with the full “multireference” limit of strong delocalization (incorporating off-diagonal couplings between resonance structures. The NRT variational functional yields an error measure that serves as an intrinsic criterion of accuracy of the resonance-theoretic description. The NRT program structure, algorithms, and numerical characteristics are described in supplementary material, and detailed chemical applications are presented in two companion papers. © 1998 John Wiley & Sons, Inc. J Comput Chem 19: 593–609, 1998
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