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Alcohol Acylation by Acetic Acid over Novel Lanthanide-Grafted Catalytic Systems Full article

Journal Reaction Kinetics, Mechanisms and Catalysis
ISSN: 1878-5190 , E-ISSN: 1878-5204
Output data Year: 2019, Volume: 127, Number: 1, Pages: 149–160 Pages count : 12 DOI: 10.1007/s11144-019-01574-0
Tags Alcohol acylation; Esterification; Lanthanide-containing catalysts; Lanthanide grafting; Nafion; Nafion composite
Authors Koskin A.P. 1 , Borodin A.O. 2,3 , Vedyagin A.A. 1,4
Affiliations
1 Boreskov Institute of Catalysis SB RAS
2 National Research Novosibirsk State University
3 Nikolaev Institute of Inorganic Chemistry SB RAS
4 National Research Tomsk Polytechnic University

Funding (1)

1 Federal Agency for Scientific Organizations 0303-2016-0014

Abstract: In the present study, novel heterogeneous analogues of lanthanide triflates [trifluoromethanesulfonates; Ln(SO3CF3)3 or Ln(OTf)3] were proposed as acidic catalysts for fine organic synthesis. A series of supported Ln3+ and Ln3+SFP systems (SFP—sulfonated fluoropolymer; Ln = La, Pr, Eu, Tm, Yb) were synthesized and tested in the acylation of alcohols with acetic acid. The synthesized systems were found to be stable under the reaction conditions and showed the ability for catalytic recycling. It was shown that high texture characteristics of the SFP/CNF samples have also a great impact on the efficiency of the catalytic process. For example, Ln3+SFP/CNF systems exhibit significantly higher catalytic activity if compare with the unsupported samples (Ln3+SFP) or the sample without sulfated fluoropolymer (CNF-SO3−Ln3+). It was found that Ln-composite contains blocks of SFP and thin SFP layer over the surface of CNF fibers. The lanthanide ions are evenly distributed within the polymer structure. Among the studied lanthanides, Yb-containing systems were found to be the most active one.
Cite: Koskin A.P. , Borodin A.O. , Vedyagin A.A.
Alcohol Acylation by Acetic Acid over Novel Lanthanide-Grafted Catalytic Systems
Reaction Kinetics, Mechanisms and Catalysis. 2019. V.127. N1. P.149–160. DOI: 10.1007/s11144-019-01574-0 WOS Scopus РИНЦ AN OpenAlex
Dates:
Submitted: Dec 29, 2018
Accepted: Apr 9, 2019
Published online: Apr 15, 2019
Published print: Jun 1, 2019
Identifiers:
Web of science: WOS:000468213500012
Scopus: 2-s2.0-85064720504
Elibrary: 41785393
Chemical Abstracts: 2019:875415
OpenAlex: W2937660594
Citing: Пока нет цитирований
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