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Relation Between Catalyst Structure and Selectivity of the Oxidative Coupling of 2,6-dimethylphenol in the Presence of Copper Complexes: Studies Using EPR and NMR Научная публикация

Журнал Journal of Molecular Catalysis
ISSN: 0304-5102
Вых. Данные Год: 1990, Том: 57, Номер: 3, Страницы: 325-351 Страниц : 27 DOI: 10.1016/0304-5102(90)85007-5
Авторы Talsi E.P. 1 , Shaikhutdinova N.I. 1 , Shubin A.A. 1 , Chinakov V.D. 1 , Khlebnikov B.M. 1 , Yudkin B.I. 1 , Nekipelov V.M. 1 , Zamaraev K.I. 1
Организации
1 Institute of Catalysis, Novosibirsk 630090 (U.S.S.R.)
Реферат: Relation between catalyst structure and selectivity of the oxidative coupling of 2,6-dimethylphenol, I, into poly[oxy-(2,6-dimethyl)-1,4-phenylene], II, an important industrial polymer, in the presence of copper(II) complexes with acetate or formate and pyridine or piperidine in chloroform and chloroform + toluene solutions has been studied. Variations in the structure of the catalyst during various steps of the catalytic process have been elucidated using EPR and NMR. Six different types of Cu(II) complexes have been observed and their roles in the catalytic process have been identified. Intermediates that control reaction selectivity towards the desired polymeric product II seem to be mixed Cu(II) complexes with monomeric and oligomeric phenolate ions, acetic or formic ion and amines. The rate-determining step of oxidative coupling in steady-state conditions seems to be electron transfer from phenolate ions to the Cu(II) atom in these complexes. The selectivity is enhanced at high concentrations of these complexes, since in these conditions the monomeric phenoxyl radicals formed in the reaction mixture react mainly with coordinated phenolate and polyphenolate ligands to yield finally II, rather than recombining to form 3,3',5,5'-tetramethyldiphenoquinone, III, which is the main side product of the reaction. Complexes with oligomeric phenolate ligands seem to provide better selectivity than complexes with monomeric ones, since for the former complexes intramolecular electron transfer does not produce the monomeric phenol radicals necessary to make compound III.
Библиографическая ссылка: Talsi E.P. , Shaikhutdinova N.I. , Shubin A.A. , Chinakov V.D. , Khlebnikov B.M. , Yudkin B.I. , Nekipelov V.M. , Zamaraev K.I.
Relation Between Catalyst Structure and Selectivity of the Oxidative Coupling of 2,6-dimethylphenol in the Presence of Copper Complexes: Studies Using EPR and NMR
Journal of Molecular Catalysis. 1990. V.57. N3. P.325-351. DOI: 10.1016/0304-5102(90)85007-5 WOS Scopus РИНЦ CAPlusCA OpenAlex Sciact
Даты:
Поступила в редакцию: 22 дек. 1988 г.
Принята к публикации: 16 янв. 1989 г.
Опубликована в печати: 1 янв. 1990 г.
Опубликована online: 2 окт. 2001 г.
Идентификаторы БД:
Web of science: WOS:A1990CL41700007
Scopus: 2-s2.0-0025228156
РИНЦ: 31091563
Chemical Abstracts: 1990:217591
Chemical Abstracts (print): 112:217591
OpenAlex: W1980158749
Sciact: 12845
Цитирование в БД:
БД Цитирований
Scopus 25
OpenAlex 26
Альметрики: