TY  - JOUR
  - Nickel*, B.,Ruth, A. A.
  - 1994
  - June
  - Chemical Physics
  - Dual Phosphorescence from 2-(2'-Hydroxyphenyl)Benzoxazole in Amorphous Solid-Solution - Temperature-Dependence of Dispersive Kinetics of Nonexponential Triplet Decay
  - Validated
  - ()
  - 184
  - 1-3
  - 261
  - 271
  - 2-(2'-hydroxyphenyl)benzoxazole (HBO) can exist in two tautomeric forms, in an enol form (E) and a keto form (K). In the metastable triplet state of HBO in liquid alkanes, both tautomers have roughly the same energy, and a dual phosphorescence, -3K* --> 1K and 3E* --> 1E, is observed; both components of the dual phosphorescence exhibit the same monoexponential decay. In solid solution, the keto phosphorescence decays faster than the enol phosphorescence, and both decays are nonexponential. The dispersive kinetics of the dual phosphorescence from a solid solution can be described by a simple model with a minimum of parameters: The rate constants k(K) and k(E) for the decay of 3K* and 3E* to the respective electronic ground state and a distribution function for the energy difference between 3K* and 3E* in solid solution. The true distribution function seems to be better approximated by a Lorentzian than by a Gaussian. k(K) and k(E) are virtually independent of temperature.2-(2'-hydroxyphenyl)benzoxazole (HBO) can exist in two tautomeric forms, in an enol form (E) and a keto form (K). In the metastable triplet state of HBO in liquid alkanes, both tautomers have roughly the same energy, and a dual phosphorescence, -3K* --> 1K and 3E* --> 1E, is observed; both components of the dual phosphorescence exhibit the same monoexponential decay. In solid solution, the keto phosphorescence decays faster than the enol phosphorescence, and both decays are nonexponential. The dispersive kinetics of the dual phosphorescence from a solid solution can be described by a simple model with a minimum of parameters: The rate constants k(K) and k(E) for the decay of 3K* and 3E* to the respective electronic ground state and a distribution function for the energy difference between 3K* and 3E* in solid solution. The true distribution function seems to be better approximated by a Lorentzian than by a Gaussian. k(K) and k(E) are virtually independent of temperature.
  - 0301-01040301-0104
  - ://A1994NU73100024 ://A1994NU73100024
DA  - 1994/06
ER  - 

@article{V67924378,
   = {Nickel*,  B. and Ruth,  A. A. },
   = {1994},
   = {June},
   = {Chemical Physics},
   = {Dual Phosphorescence from 2-(2'-Hydroxyphenyl)Benzoxazole in Amorphous Solid-Solution - Temperature-Dependence of Dispersive Kinetics of Nonexponential Triplet Decay},
   = {Validated},
   = {()},
   = {184},
   = {1-3},
  pages = {261--271},
   = {{2-(2'-hydroxyphenyl)benzoxazole (HBO) can exist in two tautomeric forms, in an enol form (E) and a keto form (K). In the metastable triplet state of HBO in liquid alkanes, both tautomers have roughly the same energy, and a dual phosphorescence, -3K* --> 1K and 3E* --> 1E, is observed; both components of the dual phosphorescence exhibit the same monoexponential decay. In solid solution, the keto phosphorescence decays faster than the enol phosphorescence, and both decays are nonexponential. The dispersive kinetics of the dual phosphorescence from a solid solution can be described by a simple model with a minimum of parameters: The rate constants k(K) and k(E) for the decay of 3K* and 3E* to the respective electronic ground state and a distribution function for the energy difference between 3K* and 3E* in solid solution. The true distribution function seems to be better approximated by a Lorentzian than by a Gaussian. k(K) and k(E) are virtually independent of temperature.2-(2'-hydroxyphenyl)benzoxazole (HBO) can exist in two tautomeric forms, in an enol form (E) and a keto form (K). In the metastable triplet state of HBO in liquid alkanes, both tautomers have roughly the same energy, and a dual phosphorescence, -3K* --> 1K and 3E* --> 1E, is observed; both components of the dual phosphorescence exhibit the same monoexponential decay. In solid solution, the keto phosphorescence decays faster than the enol phosphorescence, and both decays are nonexponential. The dispersive kinetics of the dual phosphorescence from a solid solution can be described by a simple model with a minimum of parameters: The rate constants k(K) and k(E) for the decay of 3K* and 3E* to the respective electronic ground state and a distribution function for the energy difference between 3K* and 3E* in solid solution. The true distribution function seems to be better approximated by a Lorentzian than by a Gaussian. k(K) and k(E) are virtually independent of temperature.}},
  issn = {0301-01040301-0104},
   = {://A1994NU73100024 ://A1994NU73100024},
  source = {IRIS}
}