Accession Number:

ADA011908

Title:

Valence Photoisomerization of 1-Ethoxycarbonyl-1H-Azepine and Its Thermal Reversion. Quantitative Aspects

Descriptive Note:

Technical rept. 2, 1 Jul 1974-31 May 1975

Corporate Author:

BOSTON UNIV MA DEPT OF CHEMISTRY

Report Date:

1975-06-15

Pagination or Media Count:

29.0

Abstract:

Photolysis of 1-ethoxycarbonyl-1H-azepine in solution at 325 - 385 nm gives a valence isomer with a chemical efficiency of 95 and a quantum efficiency of 0.013. The valence isomer reverts cleanly to azepine at 112 - 145C in an uncatalyzed reaction which is exothermic. The valence isomerization can be driven by sunlight and laser emission at 458 nm and cycled in sequential photochemical and thermal steps. The azepine does not luminesce but the energies of S1 reactive and T1 unreactive excited states can be estimated from sensitization and quenching experiments.

Subject Categories:

  • Radiation and Nuclear Chemistry

Distribution Statement:

APPROVED FOR PUBLIC RELEASE