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Coupling of Phenol with Ketones in the Presence of Heteropoly Acids with Different Structures and Compositions Full article

Journal Kinetics and Catalysis
ISSN: 0023-1584 , E-ISSN: 1608-3210
Output data Year: 2000, Volume: 41, Number: 6, Pages: 767-770 Pages count : 4 DOI: 10.1023/A:1026616902020
Tags Physical Chemistry; Phenol; Activation Energy; Toluene; Ketone
Authors Timofeeva M.N. 1 , Maksimov G.M. 1 , Utkin V.A. 1 , Likholobov V.A. 1
Affiliations
1 Boreskov Institute of Catalysis, Siberian Division, Russian Academy of Sciences, Novosibirsk, 630090, Russia

Abstract: The reactions of phenol coupling with ketones MeCOR (R = CH3, C2H5, C3H7, and C4H9) are studied in the presence of heteropoly acids with different structures and compositions in toluene solutions ([PhOH]/[MeCOR] = (2–8)/1 mol/mol; 50–70°C) with thioglycolic acid added as a promoter. The reaction rate depends on ketone and heteropoly acid, and the yield of bisphenols is as high as 24–72%. The reaction orders are 0.68, 0.77, and 0.97 with respect to H6P2W21O71, H3PW12O40, and H4SiW12O40, respectively, and the activation energies are 25.1, 21.0, and 20.6 kcal/mol, respectively. Heteropoly acids of the Dawson structure exhibited the highest activity.
Cite: Timofeeva M.N. , Maksimov G.M. , Utkin V.A. , Likholobov V.A.
Coupling of Phenol with Ketones in the Presence of Heteropoly Acids with Different Structures and Compositions
Kinetics and Catalysis. 2000. V.41. N6. P.767-770. DOI: 10.1023/A:1026616902020 WOS Scopus РИНЦ ANCAN OpenAlex
Original: Тимофеева М.Н. , Максимов Г.М. , Уткин В.А. , Лихолобов В.А.
Конденсация фенола с кетонами в присутствии гетерополикислот различных структур и составов
Кинетика и катализ. 2000. Т.41. №6. С.846-849. РИНЦ
Dates:
Submitted: Apr 30, 1999
Published print: Nov 1, 2000
Identifiers:
Web of science: WOS:000166250600009
Scopus: 2-s2.0-0034318943
Elibrary: 13349173
Chemical Abstracts: 2001:30612
Chemical Abstracts (print): 134:207455
OpenAlex: W300558716
Citing:
DB Citing
Web of science 3
Scopus 3
Elibrary 3
OpenAlex 4
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