| Literature DB >> 28836042 |
Norman Scholz1, Amol Jadhav2, Milind Shreykar2, Thomas Behnke1, Nithiya Nirmalananthan1, Ute Resch-Genger1, Nagaiyan Sekar3.
Abstract
A comprehensive systematic study of absorption and fluorescence properties in solvents of varying viscosity and polarity of three novel and red-emitting coumarin-rhodamine hybrid derivatives with differences in the rigidity of their substituents is presented. This includes ethanol-polyethylene glycol, toluene-polyethylene glycol, and toluene-paraffin mixtures. Moreover, protonation-induced effects on the spectroscopic properties are studied. A viscosity-induced emission enhancement was observed for all coumarin-rhodamine hybrid derivatives. MCR2 bearing a julolidine donor showed the expected low sensitivity to viscosity whereas MCR3 with its freely rotatable diphenylamino substituent revealed a particularly pronounced sensitivity to this parameter. Moreover, MCR2 shows an enhancement in emission in the open, i.e., protonated form in conjunction with a largely Stokes shift fluorescence in the deep red spectral region. This enables the application of these dyes as viscosity sensors and as far red emitting pH-sensitive probes.Entities:
Keywords: Coumarin-rhodamine hybrids; Fluorescence quantum yield; Polarity; Viscosity
Year: 2017 PMID: 28836042 DOI: 10.1007/s10895-017-2165-4
Source DB: PubMed Journal: J Fluoresc ISSN: 1053-0509 Impact factor: 2.217