Influence of Entanglements on the Time Dependence of Mixing in Nonradiative Energy Transfer Studies of Polymer Diffusion in Latex Films

2001 ◽  
Vol 34 (17) ◽  
pp. 6029-6038 ◽  
Author(s):  
Ewa Odrobina ◽  
Mitchell A. Winnik
2003 ◽  
Vol 36 (23) ◽  
pp. 8749-8760 ◽  
Author(s):  
Xiaodong Ye ◽  
J. P. S. Farinha ◽  
Jung Kwon Oh ◽  
Mitchell A. Winnik ◽  
Chi Wu

Polymer ◽  
2008 ◽  
Vol 49 (8) ◽  
pp. 2055-2064 ◽  
Author(s):  
J. Pablo Tomba ◽  
Xiaodong Ye ◽  
Fugang Li ◽  
Mitchell A. Winnik ◽  
Willie Lau

1993 ◽  
Vol 58 (10) ◽  
pp. 2266-2271 ◽  
Author(s):  
Herbert Morawetz

Recent studies of polymers in solution and in bulk by energy transfer between two fluorescent labels are reviewed. Such studies are concerned with the equilibrium and dynamics of polymer chain expansion, molecular cluster formation in solution, the miscibility of polymers in bulk, and the interdiffusion of polymer latex particles.


1992 ◽  
Vol 46 (9) ◽  
pp. 1376-1381 ◽  
Author(s):  
Huei-Yang D. Ke ◽  
Gary D. Rayson

The emission spectra and fluorescence decay curves of solid UO2+2- Datura at liquid nitrogen temperature have been measured. The linewidth of the emission peaks of UO2+2 ions in UO2+2- Datura decreases with the UO2+2 concentration. This linewidth broadening phenomenon can be explained by the existence of resonance interactions between adjacent UO2+2- Datura species. The analysis of the emission peak position of the bound ions has been used to provide a measure of the electronic factors contributing to the interaction between the uranyl ion and phosphoryl and dicarboxyl moieties on the cell wall material. An observed blue shift of the uranyl fluorescence spectrum as a function of solution pH has been ascribed to a distortion of the normally linear O-U-O bond. An inter- and intra-molecular nonradiative energy transfer model has been successfully used to interpret the measured lifetime data of UO2+2- Datura.


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