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101 0 _aeng
135 _adrcn ---uucaa
181 0 _ai
182 0 _ab
200 1 _aTransformations of Diphenyl Sulfide and Diphenylamine on Aluminum Chloride
_fV. P. Nekhoroshev [et al.]
203 _aText
_celectronic
300 _aTitle screen
320 _a[References: p. 277 (10 tit.)]
330 _aThianthrene 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.
333 _aРежим доступа: по договору с организацией-держателем ресурса
461 _tPetroleum Chemistry
_d2006-
463 _tVol. 57, iss. 3
_v[P. 272–277]
_d2017
610 1 _aэлектронный ресурс
610 1 _aтруды учёных ТПУ
610 1 _adiphenylamine
610 1 _athianthrene
610 1 _aдифениламин
610 1 _aдифенил
610 1 _aхлорид алюминия
701 1 _aNekhoroshev
_bV. P.
_gViktor Petrovich
701 1 _aGubayddulin
_bR. R.
_gRustem Rinatovich
701 1 _aYarkova
_bA. G.
_gAnna Gennadjevna
701 1 _aNekhorosheva
_bA. V.
_gAleksandra Viktorovna
701 1 _aNifantjev
_bI. E.
_gIljya Eduardovich
701 1 _aVoronkov
_bE. O.
_gEvgeny Olegovich
701 1 _aPoleshchuk
_bO. Kh.
_cchemist
_cProfessor-consultant of Yurga technological Institute of Tomsk Polytechnic University, Doctor of chemical sciences
_f1947-
_gOleg Khemovich
_2stltpush
_3(RuTPU)RU\TPU\pers\31825
701 1 _aTarasova
_bO. I.
_gOksana Igorevna
712 0 2 _aНациональный исследовательский Томский политехнический университет (ТПУ)
_bЮргинский технологический институт (филиал) (ЮТИ)
_bКафедра сварочного производства (КСП)
_h355
_2stltpush
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801 2 _aRU
_b63413507
_c20170505
_gRCR
856 4 0 _uhttp://dx.doi.org/10.1134/S0965544117020207
942 _cCF