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Phenylation of azobenzene

descriptionPublicationkeyboard_double_arrow_right Article 01 Jan 1970 Malaysia English Publisher:Royal Society of Chemistry (RSC)Journal:Journal of the Chemical Society B: Physical Organic (issn: 0045-6470, Copyright policy )
Authors: Miller, Joseph; Paul, D.B.; Wong, L.Y.; Kelso, A.G.;

doi: 10.1039/j29700000062

Phenylation of azobenzene

Abstract

The substituent effect of the phenylazo-group in homolytic phenylation has been measured with azobenzene as substrate and nitrobenzene as reference compound. Even after allowance for the large number of sites of substitution the phenylazo-group was shown to equal the nitro-group in its activating power. Isomer ratios and partial rate factors have been determined and are discussed.

Country
Malaysia
Related Organizations
Keywords

Q Science (General), QD Chemistry

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selected citations
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This is an alternative to the "Influence" indicator, which also reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
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popularity
This indicator reflects the "current" impact/attention (the "hype") of an article in the research community at large, based on the underlying citation network.
BIP!Popularity provided by BIP!
influence
This indicator reflects the overall/total impact of an article in the research community at large, based on the underlying citation network (diachronically).
BIP!Influence provided by BIP!
impulse
This indicator reflects the initial momentum of an article directly after its publication, based on the underlying citation network.
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