Use this URL to cite or link to this record in EThOS: http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.475083
Title: Organic photochemistry
Author: Thompson, Michael
ISNI:       0000 0001 2448 2145
Awarding Body: University of Oxford
Current Institution: University of Oxford
Date of Award: 1978
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Abstract:
The photochemistry of a number of aromatic systems has been studied; - (i) Irradiation of 1,3, 5-tri-t-butylbenzene in neutral methanol yielded 4-methoxy-2, 4,6-exo -tri-t-butylbicyclo [3.1.0] hex-2-ene, together with a previously unreported compound, tentatively identified as a stereoisomer of 4-methoxy-2,4, 6-exo -tri-t-butylbicyclo [3.1.0] hex-2-ene. (ii) Irradiation of 1,3, 5-tri-t-butylbenzene in acidic methanol yielded 1, 2,4-tri-t-butylbenzene and 1, 2, 5-tri-t-butyl-Dewarbenzene only, as primary and secondary photoproducts respectively. The primary rearrangement process is considered in detail and is shown to be intramolecular by 13C-labelling techniques; a mechanism involving the protonation of a benzvalene is proposed. (iii) The photorearrangement in the gas phase of the six dimethylpyridine isomers has also been investigated. It is shown that the six isomers may be divided into two groups of three, 2, 5-, 2,4- and 3, 5-dimethylpyridine and 2, 6-, 2,3-, and 3,4 dimethylpyridine. Within each group, photolysis of one isomer leads to the formation of the other two isomers as major products. The rearrangement is shown to be intramolecular and a mechanism is proposed in which the nitrogen atom effectively inserts itself between any two carbon atoms in the aromatic nucleus. (iv) The photochemistry of the six N-methyl-dimethylpyridinium chlorides is also considered. Preliminary data suggests that photorearrangement of these compounds may occur by a mechanism analogous to that for the dimethylpyridines.
Supervisor: Not available Sponsor: Not available
Qualification Name: Thesis (Ph.D.) Qualification Level: Doctoral
EThOS ID: uk.bl.ethos.475083  DOI: Not available
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