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含1,1'-联萘骨架的平面和轴向手性聚亚甲基拱顶铂(II)配合物的手性光响应控制

Chiroptical Response Control of Planar and Axially Chiral Polymethylene-Vaulted Platinum(II) Complexes Bearing 1,1'-Binaphthyl Frameworks.

作者信息

Ikeshita Masahiro, Hara Nobuyuki, Imai Yoshitane, Naota Takeshi

机构信息

Department of Chemistry, Graduate School of Engineering Science, Osaka University, Machikaneyama, Toyonaka, Osaka 560-8531, Japan.

Department of Applied Molecular Chemistry, College of Industrial Technology, Nihon University, Narashino, Chiba 275-8575, Japan.

出版信息

Inorg Chem. 2023 Aug 28;62(34):13964-13976. doi: 10.1021/acs.inorgchem.3c01935. Epub 2023 Aug 15.

Abstract

In this study, the synthesis, structure, and chiroptical response control of planar chiral polymethylene-vaulted -bis[(β-iminomethyl)aryloxy]platinum(II) complexes bearing axially chiral 1,1'-binaphthyl ligands are described. A series of enantiopure polymethylene ( = 4-10)-vaulted complexes were prepared in 6 steps using commercially available ()- or ()-BINOL as the starting material without an optical resolution process. The -coordination and three-dimensional vaulted structures of the platinum complexes were elucidated from X-ray diffraction (XRD) studies. The complexes were found to show structural dependence of chiroptical responses in the dilute solution state such that the absolute values of [α], dissymmetry factors in circular dichroism (CD), and in circularly polarized luminescence (CPL) increased upon shortening the length of the polymethylene bridges. The enhanced chiroptical responses were theoretically investigated using density functional theory (DFT) and time-dependent DFT (TD-DFT) calculations, and the results are discussed in terms of the molecular structures and transition dipole moments of the ground states. The structural dependence of the chiroptical responses was ascribed to the distortion of the coordination platforms caused by restriction of the vaulting methylene linkers.

摘要

在本研究中,描述了带有轴向手性1,1'-联萘配体的平面手性聚亚甲基拱顶双[(β-亚氨基甲基)芳氧基]铂(II)配合物的合成、结构及手性光响应控制。以市售的()-或()-联萘酚为起始原料,通过6步反应制备了一系列对映体纯的聚亚甲基(= 4 - 10)拱顶配合物,无需光学拆分过程。通过X射线衍射(XRD)研究阐明了铂配合物的配位情况和三维拱顶结构。发现这些配合物在稀溶液状态下呈现出手性光响应的结构依赖性,即随着聚亚甲基桥长度的缩短,比旋光度[α]的绝对值、圆二色性(CD)中的不对称因子以及圆偏振发光(CPL)中的不对称因子均增大。利用密度泛函理论(DFT)和含时密度泛函理论(TD - DFT)计算对手性光响应增强进行了理论研究,并根据基态的分子结构和跃迁偶极矩对结果进行了讨论。手性光响应的结构依赖性归因于拱顶亚甲基连接基团的限制导致配位平台的扭曲。

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