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Dramatic Effect of Carboxylic Acid on the Electronic Structure of the Active Species in Fe(PDP)-Catalyzed Asymmetric Epoxidation Full article

Journal ACS Catalysis
ISSN: 2155-5435
Output data Year: 2016, Volume: 6, Number: 8, Pages: 5399-5404 Pages count : 6 DOI: 10.1021/acscatal.6b01473
Tags asymmetric epoxidation, bioinspired catalysis, enantioselectivity, EPR, iron, mechanism
Authors Zima Alexandra M. 1,2 , Lyakin Oleg Y. 2 , Ottenbacher Roman V. 1 , Bryliakov Konstantin P. 2 , Talsi Evgenii P. 2
Affiliations
1 Novosibirsk State University, Pirogova 2, Novosibirsk 630090, Russian Federation
2 Boreskov Institute of Catalysis, Pr. Lavrentieva 5, Novosibirsk 630090, Russian Federation

Funding (2)

1 Federal Agency for Scientific Organizations V.44.2.4.
2 Russian Science Foundation 14-13-00158

Abstract: The electronic structure of the iron–oxygen intermediates responsible for catalytic transformations in the biomimetic catalyst systems [((S,S)-PDP)FeII(OTf)2]/H2O2/RCOOH has been found to be strongly dependent on the structure of the carboxylic acid RCOOH. For carboxylic acids with primary and secondary α-carbon atoms (acetic acid, butyric acid, caproic acid), the active species exhibit electron paramagnetic resonance (EPR) spectra with large g-factor anisotropy (g1 = 2.7, g2 = 2.4, g3 = 1.7), whereas for those with tertiary α-carbon atoms (2-ethylhexanoic acid, valproic acid, 2-ethylbutyric acid), the active species display EPR spectra with small g-factor anisotropy (g1 = 2.07, g2 = 2.01, g3 = 1.96). The EPR spectra of the latter intermediates are very similar to those of the intermediates previously assigned to oxoiron(V) species. The systems featuring intermediates of the second type ensure higher enantioselection in the epoxidation of electron-deficient olefins.
Cite: Zima A.M. , Lyakin O.Y. , Ottenbacher R.V. , Bryliakov K.P. , Talsi E.P.
Dramatic Effect of Carboxylic Acid on the Electronic Structure of the Active Species in Fe(PDP)-Catalyzed Asymmetric Epoxidation
ACS Catalysis. 2016. V.6. N8. P.5399-5404. DOI: 10.1021/acscatal.6b01473 WOS Scopus РИНЦ ANCAN OpenAlex
Dates:
Submitted: May 25, 2016
Accepted: Jul 7, 2016
Published online: Jul 21, 2016
Published print: Aug 5, 2016
Identifiers:
Web of science: WOS:000381236700066
Scopus: 2-s2.0-84981357582
Elibrary: 27135297
Chemical Abstracts: 2016:1150162
Chemical Abstracts (print): 166:217700
OpenAlex: W2469624310
Citing:
DB Citing
Web of science 52
Scopus 52
Elibrary 52
OpenAlex 56
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