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首页> 外文期刊>Chimia >Intramolecular Electron-Transfer Studies as a Function of Bridge Topology: The Importance of Solvent-Mediated Donor-Acceptor Electronic Coupling
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Intramolecular Electron-Transfer Studies as a Function of Bridge Topology: The Importance of Solvent-Mediated Donor-Acceptor Electronic Coupling

机译:分子内电子转移研究作为桥拓扑的函数:溶剂介导的供体-受体电子偶联的重要性

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The donor-acceptor electronic coupling matrix elements, |V|, for photoin-duced, intramolecular electron-transfer (ET) reactions in one linear and three C-shaped molecules have been determined from the temperature dependence of ET rate constants. The coupling matrix element in the linear molecule was found to be solvent-independent. By contrast, the coupling matrix elements in two of the three C-shaped molecules exhibit significant solvent dependence. Donor-acceptor coupling matrix elements were calculated for the linear and C-shaped molecules in the absence and presence of solvent molecules using the generalized Mulliken-Hush theory. Together, the experimental and theoretical results indicate that solvent molecules, and not the covalent bridge, mediate the electronic coupling in the C-shaped molecules. Preliminary studies of ET rate constants as a function of solvent bulk are also described.
机译:从ET速率常数的温度依赖性,已经确定了一个线性分子和三个C形分子中用于光致诱导的分子内电子转移(ET)反应的供体-受体电子耦合矩阵元素| V |。发现线性分子中的偶联基质元素是溶剂无关的。相比之下,三个C形分子中的两个中的偶联基质元素表现出显着的溶剂依赖性。使用广义Mulliken-Hush理论,在不存在和存在溶剂分子的情况下,计算线性和C形分子的供体-受体偶联基质元素。总之,实验和理论结果表明,溶剂分子而非共价桥介导了C形分子中的电子偶联。还描述了ET速率常数作为溶剂体积的函数的初步研究。

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