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一维无限链的形成由水溶性铂(II)2,6-双(苯并咪唑-2'-基)吡啶双配合物盐的金属-金属和/或π-π堆积相互作用导向。

Formation of 1D Infinite Chains Directed by Metal-Metal and/or π-π Stacking Interactions of Water-Soluble Platinum(II) 2,6-Bis(benzimidazol-2'-yl)pyridine Double Complex Salts.

机构信息

Institute of Molecular Functional Materials (Areas of Excellence Scheme, University Grants Committee (Hong Kong)), and Department of Chemistry, The University of Hong Kong Pokfulam Road, Hong Kong, P. R. China.

Department of Physics, The University of Hong Kong Pokfulam Road, Hong Kong, P. R. China.

出版信息

J Am Chem Soc. 2018 Jan 17;140(2):657-666. doi: 10.1021/jacs.7b09770. Epub 2018 Jan 5.

Abstract

A new class of water-soluble double complex salts (DCSs), [Pt{bzimpy(TEG)}Cl][Pt{bzimpy(PrSO)}Cl] and its alkylplatinum(II) bzimpy derivatives (bzimpy = 2,6-bis(benzimidazol-2'-yl)pyridine, has been demonstrated to exhibit strong aggregation in water through Pt···Pt and π-π stacking interactions to give a variety of distinctive nanostructures based on the formation of one-dimensional (1D) infinite chains. The self-association process can be systemically controlled by varying the solvent composition and temperature and has been studied by H NMR, 2D NOESY NMR, mass spectrometry, electron and confocal fluorescence microscopy, UV-vis absorption, and emission spectroscopy.

摘要

一类新型水溶性双配合盐(DCS),[Pt{bzimpy(TEG)}Cl][Pt{bzimpy(PrSO)}Cl]及其烷基铂(II) bzimpy 衍生物(bzimpy = 2,6-双(苯并咪唑-2'-基)吡啶),已被证明通过 Pt···Pt 和 π-π 堆积相互作用在水中强烈聚集,形成基于一维(1D)无限链的各种独特纳米结构。通过改变溶剂组成和温度,可以系统地控制自组装过程,并通过 H NMR、2D NOESY NMR、质谱、电子和共聚焦荧光显微镜、紫外-可见吸收和发射光谱进行研究。

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