Selective sensing of saccharides using simple boronic acids and their aggregates
Xiamen University · Collaborative Innovation Center of Chemistry for Energy Materials · +2 more institutions
Abstract
The reversible boronic acid-diol interaction empowers boronic acid receptors' saccharide binding capacities, rendering them a class of lectin mimetic, termed "boronlectins". Boronic acids follow lectin functions not just in being able to bind saccharides, but in multivalent saccharide binding that enhances both affinity and selectivity. For almost a decade, efforts have been made to achieve and improve selectivity for given saccharide targets, most notably glucose, by using properly positioned boronic acids, offering multivalent interactions. Incorporation of several boronic acid groups into a covalent framework or non-covalent assembly of boronic acid are two general methods used to create such smart sensors,…
Citation impact
- FWCI
- 17.95
- Percentile
- 100%
- References
- 83
Authors
6- XWXin Wu
Xiamen University, Collaborative Innovation Center of Chemistry for Energy Materials
- ZLZhao Li
Collaborative Innovation Center of Chemistry for Energy Materials, Xiamen University
- XCXuan‐Xuan Chen
Collaborative Innovation Center of Chemistry for Energy Materials, Xiamen University
- JFJohn Fossey
University of Birmingham
- TDTony D. James
University of Bath
Topics & keywords
- Boronic acid
- Chemistry
- Supramolecular chemistry
- Lectin
- Selectivity
- Covalent bond
- Combinatorial chemistry
- Organic chemistry