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3-巯基吡喃-4-酮中超快激发态分子内质子转移诱导的快速系间窜越

Rapid Intersystem Crossing Induced by Ultrafast Excited-State Intramolecular Proton Transfer in 3-Mercaptopyran-4-one.

作者信息

Nag Probal, Bera Anshuman, Vennapusa Sivaranjana Reddy

机构信息

School of Chemistry, Indian Institute of Science Education and Research Thiruvananthapuram, Maruthamala P.O., Vithura, Thiruvananthapuram, Kerala 695551, India.

出版信息

J Phys Chem A. 2022 Sep 22;126(37):6407-6415. doi: 10.1021/acs.jpca.2c04205. Epub 2022 Sep 7.

Abstract

Investigation into the photoinduced processes of 3-mercaptopyran-4-one is carried out using trajectory-based surface hopping simulations. Excitation into the near-degenerate higher singlet excited states reveals rapid internal conversion (IC) into S on a sub-50 fs timescale. Excited-state intramolecular proton transfer (ESIPT) also takes place simultaneously with IC. We observe that following tautomerization, the molecule has multiple relaxation pathways. A channel exists for it to nonradiatively decay into the tautomer ground-state or undergo rapid intersystem crossing (ISC) into the close-lying higher triplet state, which ultimately decays into T. The simulations show that ISC is significantly enhanced after ESIPT, which is studied by tracking the changes in energy gaps and associated spin-orbit coupling elements.

摘要

利用基于轨迹的表面跳跃模拟对3-巯基吡喃-4-酮的光诱导过程进行了研究。激发到近简并的较高单重激发态显示在亚50飞秒时间尺度上快速内转换(IC)到S态。激发态分子内质子转移(ESIPT)也与IC同时发生。我们观察到,互变异构后,分子有多种弛豫途径。存在一个通道使其无辐射衰变回互变异构基态或快速系间窜越(ISC)到紧邻的较高三重态,最终衰变回T态。模拟表明,ESIPT后ISC显著增强,通过跟踪能隙和相关自旋-轨道耦合元素的变化对此进行了研究。

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