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首页> 外文期刊>Angewandte Chemie >Nuclear Spin Singlet States in Photoactive Molecules: From Fluorescence/NMR Bimodality to a Bimolecular Switch for Spin Singlet States
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Nuclear Spin Singlet States in Photoactive Molecules: From Fluorescence/NMR Bimodality to a Bimolecular Switch for Spin Singlet States

机译:核自旋单态在光活性分子中的状态:从荧光/ NMR双极性到旋转单态的双分子开关

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摘要

Nuclear spin singlet states are silent states in nuclear magnetic resonance (NMR). However, they can be probed indirectly and offer great potential for the development of contrast agents for magnetic resonance imaging (MRI). Introduced here are two novel concepts: Firstly, the bimodal NMR/fluorescence properties of C-13(2)-tetraphenylethylene. It possesses a long-lived singlet state in organic solvents, and it shortens upon the addition of water. This simultaneously increases the aggregation-induced emission (AIE) of the molecule, resulting in a substantial enhancement of fluorescence. Secondly, introduced is a bimolecular switch for singlet states based on 3-H-2-coumarin containing an isolated proton. Upon UV-light exposure, a dimer forms, leading to a coupling between two previously isolated protons. A nuclear spin singlet state can now be populated. Excitation with a wavelength of 254 nm results in partial ring cleavage of the molecule back to its monomer.
机译:核自旋单态状态是核磁共振(NMR)中的静音状态。 然而,它们可以间接探测,并为磁共振成像(MRI)的造影剂的开发提供巨大潜力。 这里介绍的是两种新颖的概念:首先,C-13(2)-Tα乙烯的双峰NMR /荧光性能。 它具有在有机溶剂中具有长寿命的单线状态,并且在加入水时缩短。 这同时增加分子的聚集诱导的发射(AIE),导致荧光的显着增强。 其次,介绍的是基于含有分离质子的3-H-2-香豆素的单态状态的双分子开关。 在紫外线曝光时,二聚体形式,导致两个先前分离的质子之间的耦合。 现在可以填充核自旋单态状态。 波长为254nm的激发导致分子的部分环裂解回其单体。

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