Transformations of Diphenyl Sulfide and Diphenylamine on Aluminum Chloride; Petroleum Chemistry; Vol. 57, iss. 3
| Parent link: | Petroleum Chemistry.— , 2006- Vol. 57, iss. 3.— 2017.— [P. 272–277] |
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| Ente Autore: | |
| Altri autori: | , , , , , , , |
| Riassunto: | Title screen Thianthrene has been synthesized by reacting diphenyl sulfide with AlCl3 in heptane at 98°C for 8 h at a diphenyl sulfide : AlCl3 molar ratio of 2 : 1; the thianthrene yield is 58%. The reaction mechanism proposed previously has been confirmed by quantum-chemical calculations; the reaction is characterized by a low negative value of Gibbs free energy, a low heat of reaction, and a high activation energy of the first step. Diphenyl ether and diphenylamine do not enter the test reaction because of low nucleophilicity of the heteroatoms; diphenylamine dimerizes under the reaction conditions to form N,N'-diphenylbenzidine. Режим доступа: по договору с организацией-держателем ресурса |
| Lingua: | inglese |
| Pubblicazione: |
2017
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| Soggetti: | |
| Accesso online: | http://dx.doi.org/10.1134/S0965544117020207 |
| Natura: | Elettronico Capitolo di libro |
| KOHA link: | https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=654604 |