Anion recognition based on halogen, chalcogen, pnictogen and tetrel bonding

被引:176
|
作者
Taylor, Mark S. [1 ]
机构
[1] Univ Toronto, Dept Chem, 80 St George St, Toronto, ON M5S 3H6, Canada
基金
加拿大创新基金会; 加拿大自然科学与工程研究理事会;
关键词
Supramolecular chemistry; Noncovalent interactions; Anion recognition; Halogen bonding; Chalcogen bonding; Pnictogen bonding; Tetrel bonding; BIDENTATE LEWIS-ACIDS; CHARGE-TRANSFER INTERACTIONS; DONOR-ACCEPTOR COMPLEXES; ORGANIC SELENOCYANATES; IMIDAZOLIUM RECEPTORS; STRUCTURAL CHEMISTRY; MOLECULAR-STRUCTURES; CARBON TETRABROMIDE; CRYSTAL-STRUCTURES; DYNAMIC-BEHAVIOR;
D O I
10.1016/j.ccr.2020.213270
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Compounds incorporating Group 14-17 elements as electron-deficient sites are capable of attractive, directional interactions with Lewis bases. These noncovalent interactions are known as tetrel, pnictogen, chalcogen and halogen bonding, respectively. When the Lewis base is a negatively charged species, such interactions can be employed as the basis for the development of anion receptors, which are of interest from a fundamental standpoint and in applications ranging from chemical sensing to catalysis and medicinal chemistry. Halogen bonding and related interactions offer intriguing features in this context, including distinctive patterns of anion selectivity and solvent effects, along with unique opportunities for structural variation and synthetic access. This review article summarizes advances in anion recognition using halogen, chalcogen, pnictogen and tetrel bonding, with a focus on examples for which solution-phase thermodynamic data have been obtained. (C) 2020 Elsevier B.V. All rights reserved.
引用
收藏
页数:25
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