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Electron noncovalent models

The material model consists of a large assembly of molecules, each well characterized and interacting according to the theory of noncovalent molecular interactions. Within this framework, no dissociation processes, such as those inherently present in water, nor other covalent processes are considered. This material model may be described at different mathematical levels. We start by considering a full quantum mechanical (QM) description in the Born-Oppenheimer approximation and limited to the electronic ground state. The Hamiltonian in the interaction form may be written as ... [Pg.2]

J. L. Sessler, B. Wang, A. Harriman, Long-Range Photoinduced Electron Transfer in an Associated But Noncovalently Linked Photosynthetic Model System , J. Am. Chem. Soc., 115, 10418 (1993)... [Pg.169]

System 1 is a benchmark in D—[H]—A electron-transfer studies because it provides the first direct experimental validation to the hypothesis that donor-acceptor coupling is affected by the presence and nature of the noncovalent interaction. Comparison of 1 with Wasielewski s covalently linked model system 2 [71], which... [Pg.2077]

A general method, proposed by Politzer and coworkers, to estimate physico-chemical properties depending on noncovalent interactions [Brinck et ai, 1993 Murray et al., 1993 Politzer etal., 1993 Murray et al., 1994]. This is based on molecular surface area in conjunction with some statistically-based quantities related to the - molecular electrostatic potential (MEP) at the - molecular surface. The electron isodensity contour surface [0.001 a.u. contour of Q(r)j is taken as the molecular surface model. [Pg.189]

Among the systems proposed as models for the photosynthetic reaction center, supramolecular assemblies in which Ru(II)-polypyridine complexes and 4,4 -bipyridinium units are held together noncovalently in threaded and interlocked structures have been extensively studied [43, 82-88]. In such assemblies, connections between the molecular components rely on charge transfer interactions between the electron acceptor bipyridinium units and aromatic electron donor groups (Fig. 3). For instance, in the various pseudorotaxanes formed in acetonitrile solution at 298 K by the threading of cyclophane 4 + by the dioxybenzene-containing tethers of 192+ (Fig. 17) [84], an efficient photoinduced electron... [Pg.8]


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