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通过虚拟组合文库筛选鉴定异双核 PdLL' 配位笼。

Identification of a Heteroleptic PdLL' Coordination Cage by Screening of a Virtual Combinatorial Library.

机构信息

Institut des Sciences et Ingénierie Chimiques, Ecole Polytechnique Fédérale de Lausanne (EPFL), 1015 Lausanne, Switzerland.

Fakultät für Chemie und Chemische Biologie, Technische Universität Dortmund, 44227 Dortmund, Germany.

出版信息

J Am Chem Soc. 2021 Feb 3;143(4):1773-1778. doi: 10.1021/jacs.0c12793. Epub 2021 Jan 21.

Abstract

The design of structurally defined heteroleptic coordination cages is a challenging task, and only few examples are known to date. Here we describe a selection approach that allowed the identification of a novel hexanuclear Pd cage containing two types of dipyridyl ligands. A virtual combinatorial library of PdL complexes was prepared by mixing six different dipyridyl ligands with substoichiometric amounts of Pd(CHCN). Analysis of the equilibrated reaction mixture revealed the preferential formation of a heteroleptic PdLL' assembly. The complex was prepared on a preparative scale by a targeted synthesis, and its structure was elucidated by single-crystal X-ray diffraction. It features an unprecedented trigonal-antiprismatic cage structure with two triangular PdL macrocycles bridged by six L' ligands. A related but significantly larger PdLL' cage was obtained by using metalloligands instead of organic dipyridyl ligands.

摘要

结构明确的杂配位笼的设计是一项具有挑战性的任务,迄今为止已知的例子很少。在这里,我们描述了一种选择方法,该方法可以鉴定出一种新型的包含两种类型二吡啶基配体的六核 Pd 笼。通过将六种不同的二吡啶基配体与亚化学计量的Pd(CHCN)混合,制备了PdL配合物的虚拟组合文库。对平衡反应混合物的分析表明,优先形成了杂配位PdLL'组装体。该配合物通过靶向合成在制备规模上进行了制备,并通过单晶 X 射线衍射对其结构进行了阐明。它具有前所未有的三角反棱柱笼状结构,由两个三角形的 PdL 大环通过六个 L'配体桥接。通过使用金属配体而不是有机二吡啶基配体,获得了一种相关但明显更大的PdLL'笼。

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