Fluorescence energy transfer studies in a cross-linked polyurethane network

1995 ◽  
Vol 73 (11) ◽  
pp. 1823-1830 ◽  
Author(s):  
Jie Yang ◽  
Mitchell A. Winnik

A series of cross-linked polyurethane samples, labeled with dyes suitable for fluorescence energy transfer experiments, were prepared (donor, phenanthrene; acceptor, anthracene). Fluorescence decay profiles for these samples were measured as a function of acceptor concentration. These decays obey Förster nonradiative energy transfer kinetics, with an energy transfer critical distance (R0) of 26.7 Å. Fluorescence intensities, calculated from the decays by integrating the decay profiles, also fit the Perrin model, with a quenching radius (Rs) of 25.6 Å. The fluorescence decay profiles were further examined with a distribution analysis method, which also revealed uniformly distributed donors and acceptors in the polymer matrices. Keywords: fluorescence quenching, fluorescence decay, phenanthrene, anthracene, polyurethane.

2001 ◽  
Vol 05 (08) ◽  
pp. 633-644 ◽  
Author(s):  
GRAHAM HUNGERFORD ◽  
MARK VAN DER AUWERAER ◽  
DAVID B. AMABILINO

The fluorescence quenching of a Zn(II) porphyrin linked to Cu(I) catenates relative to a model compound without Cu(I) was attributed to energy transfer from the Zn(II) porphyrin to the metal-to-ligand charge transfer (MLCT) state of the Cu(I) (phenanthroline)2 center at the core of the molecules. The similarity of the fluorescence spectra and fluorescence decays of a Zn(II) porphyrin linked to an Au(III) porphyrin, a Zn(II) porphyrin or a benzoate moiety through the catenate framework suggested that no fluorescence quenching by electron transfer to the Au(III) porphyrin occurred and that the copper(I) (phenanthroline)2 center acts as an energy sink. The value of the critical distance for Förster type energy transfer, determined from spectral data is compatible with the observed rate constants for energy transfer and dimensions of the macrocycle. The multi-exponential nature of the fluorescence decay is attributed to the presence of different slowly interconverting conformations of the macrocycle to which the porphyrins are attached.


2000 ◽  
Vol 280 (2) ◽  
pp. 272-277 ◽  
Author(s):  
Bernhard Oswald ◽  
Frank Lehmann ◽  
Lydia Simon ◽  
Ewald Terpetschnig ◽  
Otto S. Wolfbeis

2013 ◽  
Vol 8 (1) ◽  
pp. 452 ◽  
Author(s):  
Yulia A Gromova ◽  
Anna O Orlova ◽  
Vladimir G Maslov ◽  
Anatoly V Fedorov ◽  
Alexander V Baranov

Sign in / Sign up

Export Citation Format

Share Document