Boronic acid building blocks: tools for self assembly

被引:425
作者
Nishiyabu, Ryuhei [1 ]
Kubo, Yuji [1 ]
James, Tony D. [2 ]
Fossey, John S. [1 ,3 ]
机构
[1] Tokyo Metropolitan Univ, Grad Sch Urban Environm Sci, Dept Appl Chem, Tokyo 1920397, Japan
[2] Univ Bath, Dept Chem, Bath BA2 7AY, Avon, England
[3] Univ Birmingham, Sch Chem, Birmingham B15 2TT, W Midlands, England
基金
英国工程与自然科学研究理事会;
关键词
CHIRAL DERIVATIZATION PROTOCOLS; INDUCED CONFORMATIONAL-CHANGES; COVALENT ORGANIC FRAMEWORKS; B-N BOND; NMR ANALYSIS; AFFINITY-CHROMATOGRAPHY; ENANTIOMERIC PURITY; PHENYLBORONIC ACID; HYDROGEN STORAGE; APPENDED POLY(L-LYSINE);
D O I
10.1039/c0cc02921a
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Dynamic covalent functionality has been acknowledged as a powerful tool for the construction of organised architectures, the reversible nature thermodynamically facilitates self-control and self-correction. The use of boronic acids complexation with diols and their congeners has already shown great promise in realising and developing reversible boron-containing multicomponent systems with dynamic covalent functionality. The structure-directing potential has lead to the development of a variety of self-organisation involving not only macrocycles, cages and capsules, but also porous covalent organic frameworks and polymers. Structure controls as well as remarkable synthesis are highlighted in this feature article.
引用
收藏
页码:1124 / 1150
页数:27
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