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Ultrafast photoresponsive materials for all-optical light modulation by polymer thin films

机译:超快光学光学薄膜全光调制材料

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摘要

Ultrafast and single exponential responsive materials were achieved by encapsulating donor-acceptor linked molecules into cucurbitunitl[8], CB[8], as nanocavity hosts. Various aromatic groups were linked with various types of 4,4'-bipyridinium groups through propyloxy linker. They showed characteristic charge-transfer (CT) absorption with specific colors in aqueous solutions. Upon addition of CB[8], they showed remarkably different colors due to intramolecular CT complex formation in CB[8]. Upon femtosecond laser excitation of CT band extremely fast electron transfer occurred from a donor to an acceptor unit accompanying new absorption in the visible to near-infrared region due mainly to photoreduced bipyridinium derivatives. Thermal back electron transfer reactions in CB[8] were found to follow a single exponential decay with rate constants ranging more than two orders depending on the combination of a donor and an acceptor unit. Their rate constants vs. free energy changes for oxidized donors and reduced acceptors in linked molecules were expressed by the Marcus theory. (C) 2017 Elsevier Ltd. All rights reserved.
机译:通过将供体 - 受体连接的分子包封到CucurbitUnitl [8],Cb [8]中,以超速度和单指数响应材料作为纳米蜂巢宿主来实现。各种芳族基团通过丙氧基接头与各种类型的4,4'-双吡啶基团连接。它们显示出特征电荷转移(CT)在水溶液中具有特定颜色的吸收。加入Cb [8]后,由于CB [8]中的分子内CT复合物形成,它们显示出显着不同的颜色。在Femtosecond激光激发到CT带的激光激发极快的电子传递从供体到受到近红外区域的可见的新吸收的受体单元,主要是光指向光吡啶鎓衍生物。发现CB [8]中的热背电子转移反应遵循单个指数衰减,其常数常数根据供体和受体单元的组合而定的速率常数。它们的速率常数与无氧化供体的自由能量变化,并且链接分子中的减少的受体被Marcus理论表达。 (c)2017 Elsevier Ltd.保留所有权利。

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