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溶液中的双硫族元素键合识别阵列

Double Chalcogen Bonding Recognition Arrays in Solution.

作者信息

Romito Deborah, Kählig Hanspeter, Tecilla Paolo, Sosso Gabriele C, Bonifazi Davide

机构信息

Department of Organic Chemistry, Faculty of Chemistry, University of Vienna, Währinger Straße 38, 1090, Vienna, Austria.

Dipertimento di Scienze Chimiche e Farmaceutiche, Università degli Studi di Trieste, Via Giorgieri 1, 34127, Trieste, Italy.

出版信息

Chemistry. 2024 Oct 28;30(60):e202401346. doi: 10.1002/chem.202401346. Epub 2024 Oct 16.

Abstract

N-substituted pyridino-based congeners of Ebselen, named here as Pyrselen, incorporating proximal Se and N atoms, undergo dimerization in solution and the solid state through a dual donor-acceptor arrangement of chalcogen bonding sites. Dimerization constants were measured within the 5-50 M range. Computational studies on the dimers depict a notable charge-transfer contribution to the association, validating Pyrselen as an effective scaffold for designing chalcogen-bonding-based recognition motifs.

摘要

依布硒啉的 N-取代吡啶基类似物,在此命名为 Pyrselen,其含有相邻的硒和氮原子,通过硫族元素键合位点的双供体-受体排列在溶液和固态中发生二聚化。二聚化常数在 5 - 50 M 范围内测定。对二聚体的计算研究表明电荷转移对缔合有显著贡献,证实 Pyrselen 是设计基于硫族元素键合的识别基序的有效支架。

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