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One-Step Solvent-Free Synthesis of Cyclic Carbonates by Oxidativecarboxylation of Styrenes over a Recyclable Ti-Containing Catalyst Full article

Journal Applied Catalysis B: Environmental
ISSN: 0926-3373 , E-ISSN: 1873-3883
Output data Year: 2016, Volume: 181, Pages: 363-370 Pages count : 8 DOI: 10.1016/j.apcatb.2015.08.010
Tags Carbon dioxide, Cyclic carbonate, Mesoporous titanium-silicate, Oxidative carboxylation, Styrene
Authors Maksimchuk Nataliya V. 1,2 , Ivanchikova Irina D. 1,3 , Ayupov Artem B. 1 , Kholdeeva Oxana A. 1,2
Affiliations
1 Boreskov Institute of Catalysis, Pr. Lavrentieva 5, Novosibirsk 630090, Russia
2 Novosibirsk State University, Pirogova str. 2, Novosibirsk 630090, Russia
3 Tomsk State University, Pr. Lenina 36, Tomsk 634050, Russia

Funding (3)

1 Russian Foundation for Basic Research 15-33-20225
2 Russian Foundation for Basic Research 13-03-00413
3 The Ministry of Education and Science of the Russian Federation

Abstract: A mesoporous titanium-silicate prepared by evaporation-induced self-assembly is an efficient hetero-geneous catalyst for the one-step oxidative carboxylation of styrenes with tert-butyl hydroperoxide andcarbon dioxide in the presence of tetrabutylammonium bromide as cocatalyst under mild solvent-freeconditions (50–70◦C, 8 bar CO2). The selectivity to cyclic carbonates reaches 69–70% at 92–98.5% sub-strate conversion. The catalyst can be easily recovered by filtration and reused several times without asignificant deterioration of the catalytic performance. The volume yield of SC as high as 1.1 kg/L could beachieved after seven reuses.
Cite: Maksimchuk N.V. , Ivanchikova I.D. , Ayupov A.B. , Kholdeeva O.A.
One-Step Solvent-Free Synthesis of Cyclic Carbonates by Oxidativecarboxylation of Styrenes over a Recyclable Ti-Containing Catalyst
Applied Catalysis B: Environmental. 2016. V.181. P.363-370. DOI: 10.1016/j.apcatb.2015.08.010 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Mar 27, 2015
Accepted: Aug 4, 2015
Published online: Aug 8, 2015
Published print: Feb 1, 2016
Identifiers:
Web of science: WOS:000364256000033
Scopus: 2-s2.0-84939864686
Elibrary: 24934002
Chemical Abstracts: 2015:1396349
Chemical Abstracts (print): 163:374220
OpenAlex: W1451751334
Citing:
DB Citing
Web of science 51
Scopus 57
Elibrary 49
OpenAlex 54
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