Molecular methyl probe model

In recent years, there have been many significant advances in our models for the dynamics for proton transfer. However, only a limited number of experimental studies have served to probe the validity of these models for bimolecular systems. The proton-transfer process within the benzophenone-AL A -di methyl aniline contact radical IP appears to be the first molecular system that clearly illustrates non-adiabatic proton transfer at ambient temperatures in the condensed phase. The studies of Pines and Fleming on napthol photoacids-carboxylic base pairs appear to provide evidence for adiabatic proton transfer. Clearly, from an experimental perspective, the examination of the predictions of the various theoretical models is still in the very early stages of development. 

T. Yamazaki, Y.-F. Zhu, A. ProbstI, R. K. Chadha, and M. Goodman, J. Org. Chem., 56, 6644 (1991). Probing a Molecular Model of Taste Utilizing Peptidomimetic Stereoisomers of 2-Aminocyclopentanecarboxylic Acid Methyl Ester. 

ABSTRACT. Excimer fluorescence is developed as a quantitative probe of isolated chain statistics and intermolecular segment density for miscible and immiscible blends of polystyrene (PS) with poly(vinyl methyl ether) (PVME). Rotational isomeric state calculations combined with a one-dimensional random walk model are used to explain the dependence of the excimer to monomer intensity ratio on PS molecular weight for 5% PS/PVME blends. A model for a three-dimensional random walk on a spatially periodic lattice is presented to explain the fluorescence of miscible PS/PVME blends at high concentrations. Finally, a simple two-phase morphological model is employed to analyze the early stages of phase separation kinetics. 

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