Department of Chemistry, Stanford University, Stanford, California 94305, USA.
J Chem Phys. 2012 Aug 14;137(6):064109. doi: 10.1063/1.4742762.
The theory of vibrational excitation transfer, which causes spectral diffusion and is also influenced by structural spectral diffusion, is developed and applied to systems consisting of vibrational chromophores. Excitation transfer induced spectral diffusion is the time-dependent change in vibrational frequency induced by an excitation on an initially excited molecule jumping to other molecules that have different vibrational frequencies within the inhomogeneously broadened vibrational absorption line. The excitation transfer process is modeled as Förster resonant transfer, which depends on the overlap of the homogeneous spectra of the donating and accepting vibrational chromophores. Because the absorption line is inhomogeneously broadened, two molecules in close proximity can have overlaps of their homogeneous lines that range from substantial to very little. In the absence of structural dynamics, the overlap of the homogeneous lines of the donating and accepting vibrational chromophores would be fixed. However, dynamics of the medium that contains the vibrational chromophores, e.g., a liquid solvent or a surrounding protein, produce spectral diffusion. Spectral diffusion causes the position of a molecule's homogeneous line within the inhomogeneous spectrum to change with time. Therefore, the overlap of donating and accepting molecules' homogeneous lines is time dependent, which must be taken into account in the excitation transfer theory. The excitation transfer problem is solved for inhomogeneous lines with fluctuating homogeneous line frequencies. The method allows the simultaneous treatment of both excitation transfer induced spectral diffusion and structural fluctuation induced spectral diffusion. It is found that the excitation transfer process is enhanced by the stochastic fluctuations in frequencies. It is shown how a measurement of spectral diffusion can be separated into the two types of spectral diffusion, which permits the structural spectral diffusion to be determined in the presence of excitation transfer spectral diffusion. Various approximations and computational methodologies are explored.
振动激发转移理论,它会引起光谱扩散,并且也受到结构光谱扩散的影响,被开发并应用于由振动发色团组成的系统中。激发转移诱导的光谱扩散是最初被激发的分子上的激发跃迁到具有不同振动频率的其他分子时,引起的振动频率的时变变化,这些分子在非均匀展宽的振动吸收线内。激发转移过程被建模为Förster 共振转移,它取决于供体和受体振动发色团的均匀光谱的重叠。由于吸收线是非均匀展宽的,因此两个近距离的分子可以具有从很大到很小的均匀线重叠。在没有结构动力学的情况下,供体和受体振动发色团的均匀线重叠是固定的。然而,包含振动发色团的介质的动力学,例如液体溶剂或周围的蛋白质,会产生光谱扩散。光谱扩散导致分子的均匀线在非均匀光谱中的位置随时间变化。因此,供体和受体分子的均匀线重叠是时间相关的,这在激发转移理论中必须考虑。对于具有波动均匀线频率的非均匀线,解决了激发转移问题。该方法允许同时处理激发转移诱导的光谱扩散和结构波动诱导的光谱扩散。结果表明,随机频率波动会增强激发转移过程。展示了如何将光谱扩散的测量分离为两种类型的光谱扩散,这允许在存在激发转移光谱扩散的情况下确定结构光谱扩散。探索了各种近似和计算方法。