| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 1366436 | Bioorganic & Medicinal Chemistry Letters | 2007 | 4 Pages |
Abstract
The phenylboronic acids substituted with an azo group on the ortho-position show a significant change in UV–vis spectra upon sugar binding. A new mechanism for the spectral change of the dyes is proposed based on the formation and cleavage of B–N dative bond between boronic acid group and azo group.
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Related Topics
Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Yuya Egawa, Ryota Gotoh, Satoshi Niina, Jun-ichi Anzai,