Simulating trends in reaction path geometry as a function of external fields. A generalized electronic diabatic model for two‐dimensional energy surfaces

Abstract

AbstractWe introduce a protocol to represent quantum states as a linear superposition of model electronic diabatic basis states coupled in an external (static) electric field. By considering an entire family of these models, we uncover trends in reaction‐path geometry and the topology of potential‐energy surfaces, including all those that can be realized in a two‐dimensional configurational space. Our approach can be used as a tool to model the key parameters (e.g., diabatic basis states, external field intensity) that yield desired geometrical characteristics in an actual potential energy surface. In this work, external agents such as laser fields, or a group of neighboring charges, are regarded as essential requirements to prompt, or trigger, the occurrence of a chemical process. In these cases, reaction path geometry can be modulated externally so as to yield processes that would appear to occur far from gas‐phase geometries. This phenomenology is intrinsically nonadiabatic. Our present approach accounts for the possibility of such features, i.e., the occurrence of quantum states whose electronic structures resemble products, while at geometries that are more similar to those of reactants. © 2008 Wiley Periodicals, Inc. Int J Quantum Chem, 2008