| Literature DB >> 25313715 |
Ashley R Longstreet1, Minyoung Jo, Rebecca R Chandler, Kenneth Hanson, Naiqian Zhan, Jeremy J Hrudka, Hedi Mattoussi, Michael Shatruk, D Tyler McQuade.
Abstract
Ylidenemalononitrile enamines undergo rapid amine exchange followed by a cyclization with primary amines to yield fluorescent products with emission intensities as high as 900 times greater than the starting materials. After identifying the fluorescent species by X-ray crystallography, we demonstrate that the rate of amine exchange is substrate dependent and that by simple structural variation the fluorescence can be tuned over the entire visible spectrum. We further demonstrate their potential application in biomolecule labeling.Entities:
Year: 2014 PMID: 25313715 DOI: 10.1021/ja509058u
Source DB: PubMed Journal: J Am Chem Soc ISSN: 0002-7863 Impact factor: 15.419