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SUPRAMOLECULAR COMPLEXES OF PHOTOEXCITED FUNCTIONALIZED FULLERENES AND SPIN LABELED ALKYL AMMONIUM DERIVATIVES

机译:光激发功能性富勒烯和自旋标记烷基铵衍生物的超分子络合物

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The formation of host-guest complexes of triplet excited fullerene derivatives and nitroxide radicals was monitored by TR-EPR. C_(60) functionalized with crown ethers and nitroxide radicals bearing an ammonium group have been investigated. The TR-EPR spectra of these systems, which are able to form host-guest complexes have been compared with those obtained with different fullerene derivatives and nitroxide radicals not expected to associate. The spectra of the host-guest complexes showed features peculiar of the quartet state of the coupled radical triplet system. The species with no supramolecular association gave the simple superposition of the triplet and the nitroxide radical spectra. For both cases simulations have been performed on the spectra obtained at different temperatures. The spectral changes have been related to the kinetics of the association-dissociation process.
机译:用TR-EPR监测三重激发的富勒烯衍生物和氮氧自由基的主体-客体复合物的形成。研究了冠醚和带有铵基的硝基自由基官能化的C_(60)。这些系统能够形成客体-客体配合物的TR-EPR光谱已与使用不同富勒烯衍生物和预计不会缔合的氮氧自由基进行比较。客体-客体配合物的光谱显示出偶合的自由基三重态系统的四重态特有的特征。没有超分子缔合的物种给出了三重态和氮氧化物自由基光谱的简单叠加。对于这两种情况,已经对在不同温度下获得的光谱进行了模拟。光谱变化与缔合-解离过程的动力学有关。

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