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Photogeneration of N-Heterocyclic Carbenes: Application in Photoinduced Ring-Opening Metathesis Polymerization
Published on: November 29, 2018
Significantly Boosted and Inversed Circularly Polarized Luminescence from Photogenerated Radical Anions in Dipeptide
Yuan Wang1,2, Yuqian Jiang3, Xuefeng Zhu1
1Beijing National Laboratory for Molecular Science, CAS Key Laboratory of Colloid Interface and Chemical Thermodynamics , Institute of Chemistry, Chinese Academy of Sciences , Beijing 100190 , P.R. China.
Abstract:
Circularly polarized luminescence (CPL) reflects the excited-state properties of the chiral system. However, compared to the singlet and triplet excited states, there are still many unknowns about CPL from the double excited state. Here, using the self-assembly strategy of a dipeptide substituted naphthalenediimide (NDI-GE) and the photogenerated radical anions, we have explored the ground-state (CD) and excited-state (CPL) chiral characteristics of neutral NDI and NDI•- radical anion assemblies. The neutral gelator assemblies showed CPL with the dissymmetry factor glum on the order of 10-3; the radical anion exhibited an inversed CPL signal with a significantly enhanced glum of 10-1. Time-dependent density functional theory calculation revealed that upon formation of the radical anions, the direction of the dipole moment changed, thus leading to the inversion of CD and CPL. The present work reveals a new platform for developing CPL materials based on the doublet excited state.
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