A series of 9-substituted methylacridinium salts have been devised, chemiluminescent in alkaline hydrogen peroxide solutions.
Their relative light intensities correspond to the expected order of reactivity with the nucleophilic hydroperoxide anion, and the mechanistic evidence is consistent with the requirement for a four-membered cyclic peroxide intermediate as the direct precursor to
chemiluminescence. In every case, the actual emitter is N-methyl-acridone, λ max 442 mμ
The brightest compounds are a series of substituted phenyl esters. They have large rate differences (with a Hammett dependence) but have equal quantum yields, equivalent to that of the closely-related "classical" light producer, lucigenin. / Science, Faculty of / Chemistry, Department of / Graduate
| Identifer | oai:union.ndltd.org:UBC/oai:circle.library.ubc.ca:2429/35150 |
| Date | January 1969 |
| Creators | Richardson, Donald George |
| Publisher | University of British Columbia |
| Source Sets | University of British Columbia |
| Language | English |
| Detected Language | English |
| Type | Text, Thesis/Dissertation |
| Rights | For non-commercial purposes only, such as research, private study and education. Additional conditions apply, see Terms of Use https://open.library.ubc.ca/terms_of_use. |
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