通过动态轴向手性控制手性双(二氟化硼)配合物与 Salen 配体实现圆极化发光的切换

IF 3 4区 化学 Q3 CHEMISTRY, PHYSICAL ChemPhotoChem Pub Date : 2024-05-22 DOI:10.1002/cptc.202400110
Dr. Masahiro Ikeshita, Ayumu Kuroda, Seika Suzuki, Prof. Dr. Yoshitane Imai, Prof. Dr. Takashi Tsuno
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引用次数: 0

摘要

圆偏振发光(CPL)的强度和手性已被溶液状态下的动态分子运动成功控制。我们合成了带有手性沙伦配体的双(二氟化硼)配合物,并研究了它们的光物理特性。虽然这些配合物在室温下的溶液中显示出围绕 C-N 键轴的快速分子旋转,但在低温下的核磁共振光谱中却观察到了两种被归类为非对映异构体的构象。此外,研究还发现这些异构体的平衡状态会随着溶剂和温度等外部环境的变化而改变,因此可以精确控制 CPL 的强度和手性,而不会发生发光颜色偏移。基于密度泛函理论(DFT)的理论计算显示,分子内手性激子耦合是 CPL 性能变化的关键。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

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Switching of Circularly Polarized Luminescence via Dynamic Axial Chirality Control of Chiral Bis(Boron Difluoride) Complexes with Salen Ligands

The intensity and handedness of circularly polarized luminescence (CPL) were successfully controlled by dynamic molecular motion in solutions. Bis(boron difluoride) complexes with chiral salen ligands were synthesized and their photophysical properties were investigated. Although these complexes showed rapid molecular rotation about the C−N bond axis in solution at room temperature, two conformers assigned as atropisomers were observed in the NMR spectra at low temperature. Furthermore, the equilibrium of these atropisomers was found to change depending on the external environment, such as the solvent and temperature, allowing precise control of the intensity and handedness of CPL without luminescence color shifts. Theoretical calculations based on density functional theory (DFT) revealed that intramolecular chiral exciton coupling is the key to changes in CPL properties.

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来源期刊
ChemPhotoChem
ChemPhotoChem Chemistry-Physical and Theoretical Chemistry
CiteScore
5.80
自引率
5.40%
发文量
165
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