A Rationally Designed Fluorescence Turn-On Probe for the Gold(III) Ion
Organic Letters2010Vol. 12(5), pp. 932–934
Citations Over TimeTop 10% of 2010 papers
Abstract
A latent fluorophore (1) was rationally designed to give rise to strong fluorescence through a selective gold ion-mediated hydroarylation reaction by a catalytic amount of the gold(III) ion. It is a highly selective and sensitive fluorescence turn-on probe for gold(III) ions and is operative even in protic solvents.
Related Papers
- → The first ratiometric fluorescent probes for aminopeptidase N cell imaging(2012)52 cited
- → Complete suppression of the fluorophore fluorescence by combined effect of multiple fluorescence quenching groups: A fluorescent sensor for Cu2+ with zero background signals(2015)36 cited
- → Acridones and Quinacridones: Novel Fluorophores for Fluorescence Lifetime Studies(2004)51 cited
- → The quantification of fluorescent emission from biological samples using analysis of polarization(1992)22 cited
- → Development of Novel Fluorophores Based on Fluorescent Natural Products(2022)1 cited