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Spin and Molecular Dynamics in Acyl-Containing Biradicals: Time-Resolved Electron Paramagnetic Resonance and Laser Flash Photolysis Study

机译:含酰基双自由基中的自旋和分子动力学:时间分辨电子顺磁共振和激光闪光光解研究

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摘要

A combination of time-resolved electron paramagnetic resonance (TREPR) and laser flash photolysis (LFP) studies of flexible acyl-containing biradicals over a wide temperature range is reported. In contrast to previous reports, it is shown that the main channel of intersystem crossing in these biradicals is the electron spin relaxation of the acyl moiety rather than spin-orbit interaction in the biradical. This relaxation determines the decay rate of the electron spin polarization at low temperatures and the biradical lifetime at high temperatures. The relaxation mechanism is attributed to the spin-rotation interaction, associated with the rotation of the carbonyl group about the neighboring C-C bond axis. From a model simulation of the time profile of the spin-polarized TREPR signal based on the numerical solution of the stochastic Liouville equation of the spin density matrix in frame of realistic model of biradical, the Arrhenius parameters for correlation times of spin rotation interaction and activation energies for molecular and spin dynamics were determined in two solvents, 2-propanol and hexane.
机译:报告了时间分辨电子顺磁共振(TREPR)和激光闪光光解(LFP)在宽温度范围内对含酰基柔性双自由基的研究。与以前的报告相反,表明这些双自由基中系统间交叉的主要通道是酰基部分的电子自旋弛豫,而不是双自由基中的自旋-轨道相互作用。这种弛豫确定了低温下电子自旋极化的衰减率以及高温下的双自由基寿命。弛豫机理归因于自旋-旋转相互作用,其与羰基围绕相邻的C-C键轴的旋转有关。从基于双密度现实模型框架中自旋密度矩阵的随机Liouville方程数值解的自旋极化TREPR信号时间分布的模型仿真中,自旋旋转相互作用和激活相关时间的阿伦尼乌斯参数在2-丙醇和己烷这两种溶剂中确定了分子动力学和自旋动力学的能量。

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