## Abstract The time‐resolved fluorescence behavior of polystyrene and a series of styrene–methyl methacrylate copolymers has been examined by using pulsed laser excitation. Although the photophysical characteristics of styrene‐ and naphthalene‐containing polymers may be described by the same gener
Transient decay studies of photophysical processes in aromatic polymers. V. Temperature dependence of excimer formation and dissociation in copolymers of 1-vinylnaphthalene and methyl methacrylate
✍ Scribed by Phillips, D. ;Roberts, A. J. ;Soutar, I.
- Publisher
- Wiley (John Wiley & Sons)
- Year
- 1982
- Tongue
- English
- Weight
- 468 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0098-1273
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✦ Synopsis
Abstract
The use of pulsed laser excitation upon a series of 1‐vinylnaphthalene/methyl methacrylate co‐polymers in which the intramolecular chromophore concentration is varied over a wide composition range has allowed the individual rate constants governing intramolecular excimer formation to be determined at various temperatures between 205 and 295 K. Triple exponential functions are necessary for adequate description of the photophysical kinetics over the entire temperature range. It is proposed that the kinetic and temperature behavior is consistent with a kinetic scheme involving two kinetically distinct monomeric species and an excimer in which energy may be transferred from the second monomer M^*^~2~ to the first monomer M^*^~1~ which can interact with the excimer by a conventional migration mechanism.
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The fluorescence behaviour of a series of acenaphthylene/methyl methacrylate copolymers covering a wide range of intramolecular chromophore compositions has been examined using pulsed laser excitation. The decay of emission intensity in the region of monomer fluorescence could be described only by t