Organic photochemical storage of solar energy. Progress report, February 1, 1979-January 31, 1980
Study of valence isomerization of organic compounds has focused on two mechanisms of photosensitization involving either electron donor-acceptor interaction or energy transfer. The quenching of fluorescent sensitizers by isomerizable substrates results in the formation of excited complexes. These sensitizer-substrate pairs are highly polarized, leading to changes in bond order for the substrates. For several substrates such as quadricyclene, hexamethyldewarbenzene, and a nonbornadiene derivative, this perturbation results in efficient valence isomerization. Isomerization observed on irradiation of charge transfer complexes of isomerizable substrates is consistent with a similar exciplex - template mechanism. The energy transfer mechanism of photosensitization has been studied by measuring the temperature dependence of quantum yield for isomerization of dimethyl norbornadiene-2,3-dicarboxylate sensitized by benzanthrone. From temperature and quencher concentration profiles quenching constants have been obtained which are consistent with an endoergic triplet energy transfer mechanism. The thermal upconversion of the low energy triplet of benzanthrone results in a threefold increase in isomerization quantum yield over a 90/sup 0/ temperature range.
- Research Organization:
- Boston Univ., MA (USA). Dept. of Chemistry
- DOE Contract Number:
- EG-77-S-02-4380
- OSTI ID:
- 5654397
- Report Number(s):
- COO-4380-3
- Country of Publication:
- United States
- Language:
- English
Similar Records
Organic photochemical storage of solar energy. Progress report, July 1, 1977--Feburary 28, 1978
Organic photochemical storage of solar energy. Progress report, March 1, 1978-January 31, 1979
Radical ion/triplet mechanism for sensitized valence photoisomerization of a norbornadiene
Technical Report
·
Tue Feb 28 23:00:00 EST 1978
·
OSTI ID:5012614
Organic photochemical storage of solar energy. Progress report, March 1, 1978-January 31, 1979
Technical Report
·
Wed Jan 31 23:00:00 EST 1979
·
OSTI ID:6084358
Radical ion/triplet mechanism for sensitized valence photoisomerization of a norbornadiene
Journal Article
·
Thu Dec 31 23:00:00 EST 1981
· J. Phys. Chem.; (United States)
·
OSTI ID:5422855
Related Subjects
14 SOLAR ENERGY
140505* -- Solar Energy Conversion-- Photochemical
Photobiological
& Thermochemical Conversion-- (1980-)
ALKENES
AROMATICS
CHARGE TRANSPORT
CHEMICAL REACTIONS
CHEMISTRY
CYCLOALKENES
ENERGY
ENERGY SOURCES
ENERGY STORAGE
ENERGY TRANSFER
HYDROCARBONS
ISOMERIZATION
NORBORNADIENE
ORGANIC COMPOUNDS
PHOTOCHEMICAL ENERGY STORAGE
PHOTOCHEMISTRY
QUADRICYCLENE
REAGENTS
RENEWABLE ENERGY SOURCES
RESEARCH PROGRAMS
SENSITIZERS
SOLAR ENERGY
STORAGE
SUBSTRATES
TEMPERATURE DEPENDENCE
TOLUENE
140505* -- Solar Energy Conversion-- Photochemical
Photobiological
& Thermochemical Conversion-- (1980-)
ALKENES
AROMATICS
CHARGE TRANSPORT
CHEMICAL REACTIONS
CHEMISTRY
CYCLOALKENES
ENERGY
ENERGY SOURCES
ENERGY STORAGE
ENERGY TRANSFER
HYDROCARBONS
ISOMERIZATION
NORBORNADIENE
ORGANIC COMPOUNDS
PHOTOCHEMICAL ENERGY STORAGE
PHOTOCHEMISTRY
QUADRICYCLENE
REAGENTS
RENEWABLE ENERGY SOURCES
RESEARCH PROGRAMS
SENSITIZERS
SOLAR ENERGY
STORAGE
SUBSTRATES
TEMPERATURE DEPENDENCE
TOLUENE