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Ultrafast charge transfer dynamics in supramolecular Pt(II) donor-bridge-acceptor assemblies: the effect of vibronic coupling

机译:超分子pt(II)供体 - 桥 - 受体组件中的超快电荷转移动力学:电子振动耦合的影响

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摘要

Thanks to major advances in laser technologies, recent investigations of the ultrafast coupling of nuclear and electronic degrees of freedom (vibronic coupling) have revealed that such coupling plays a crucial role in a wide range of photoinduced reactions in condensed phase supramolecular systems. This paper investigates several new donor–bridge–acceptor charge-transfer molecular assemblies built on a trans-Pt(II) acetylide core. We also investigate how targeted vibrational excitation with low-energy IR light post electronic excitation can perturb vibronic coupling and affect the efficiency of electron transfer (ET) in solution phase. We compare and contrast properties of a range of donor–bridge–acceptor Pt(II) trans-acetylide assemblies, where IR excitation of bridge vibrations during UV-initiated charge separation in some cases alters the yields of light-induced product states. We show that branching to multiple product states from a transition state with appropriate energetics is the most rigid condition for the type of vibronic control we demonstrate in our study.
机译:由于激光技术的重大进步,最近对核和电子自由度的超快速耦合(振动耦合)的研究表明,这种耦合在凝聚相超分子系统中广泛的光致反应中起着至关重要的作用。本文研究了建立在反式Pt(II)乙炔核心上的几种新的供体-桥-受体电荷转移分子组件。我们还研究了在电子激发后用低能红外光进行有针对性的振动激发如何扰动振动耦合并影响溶液相中电子转移(ET)的效率。我们比较和对比了一系列供体-桥-受体Pt(II)反乙炔化合物的性质,在某些情况下,其中UV引发的电荷分离过程中,桥振动的IR激发会改变光诱导产物态的产率。我们表明,从过渡态到具有适当能量的多个产品状态分支是我们在研究中证明的振动控制类型的最严格条件。

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