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在离散超分子自组装中能够形成可变键角的双齿配体。

Bidentate ligands capable of variable bond angles in the self-assembly of discrete supramolecules.

作者信息

Chi Ki-Whan, Addicott Chris, Arif Atta M, Das Neeladri, Stang Peter J

机构信息

Department of Chemistry, University of Utah, 315 South 1400 East, Salt Lake City, Utah 84112, USA.

出版信息

J Org Chem. 2003 Dec 12;68(25):9798-801. doi: 10.1021/jo0353785.

DOI:10.1021/jo0353785
PMID:14656109
Abstract

Flexible donor ligands like 1,2-bis(3-pyridyl)ethyne or 1,4-bis(3-pyridyl)-1,3-butadiyne self-assemble into discrete supramolecules instead of infinite networks upon combination with organoplatinum 90, 120, and 180 degree acceptor units. These systems are unique examples of versatile pyridine donors adjusting their bonding directionality to accommodate rigid platinum acceptors in the formation of closed macrocycles.

摘要

像1,2-双(3-吡啶基)乙炔或1,4-双(3-吡啶基)-1,3-丁二炔这样的柔性供体配体,与有机铂90度、120度和180度受体单元结合时,会自组装成离散的超分子,而不是无限网络。这些体系是多功能吡啶供体的独特例子,它们调整其键合方向性以在形成封闭大环时容纳刚性铂受体。

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