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Kinetic Study of Alcohol-Catalyzed Substitution of tris(Dibenzoylmethanato) Fe(III) Ligands by Acetylacetone Full article

Journal Reaction Kinetics and Catalysis Letters
ISSN: 0133-1736 , E-ISSN: 1588-2837
Output data Year: 1986, Volume: 32, Number: 2, Pages: 263-267 Pages count : 5 DOI: 10.1007/BF02068321
Tags Physical Chemistry; Catalysis; Phenyl; Exchange Reaction; Kinetic Study
Authors Ivanchenko V.A. 1 , Nekipelov V.M. 1
Affiliations
1 Institute of Catalysis, Novosibirsk 630090, USSR

Abstract: It is shown that substitution of the CH3 group by phenyl group in the β-diketonato ring does not change the general mechanism of the exchange reaction. The reaction rate fall observed may be due either to a greater stability of tris(di-benzoylmethanato) Fe(III) (Fe(dbm) compared to tris(benzoylacetonato) Fe(III) (Fe(ba)3) or to a decrease in the stability of the Fe(dbm)3·ROH complex, which is a precursor of the rate-determining step, in comparison with Fe(ba)3·ROH.
Cite: Ivanchenko V.A. , Nekipelov V.M.
Kinetic Study of Alcohol-Catalyzed Substitution of tris(Dibenzoylmethanato) Fe(III) Ligands by Acetylacetone
Reaction Kinetics and Catalysis Letters. 1986. V.32. N2. P.263-267. DOI: 10.1007/BF02068321 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: Jul 2, 1985
Accepted: Jan 8, 1986
Published print: Sep 1, 1986
Identifiers:
Web of science: WOS:A1986H257200003
Scopus: 2-s2.0-34250126431
Elibrary: 30844228
Chemical Abstracts: 1988:112669
Chemical Abstracts (print): 108:112669
OpenAlex: W2576270120
Citing:
DB Citing
Web of science 1
Scopus 1
Elibrary 1
OpenAlex 1
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