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  • 1 L.M. Litvinenko Institute of physico-organic and coal chemistry of NASU, R. Luxemburg Street 70, Donetsk 83114, Ukraine
  • | 2 Department of chemistry, Donetsk national university, Donetsk, Ukraine
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Abstract

A series of substituted N-hydroxyphthalimides (NHPI) with electron-withdrawing groups (4-C(O)OH, C=O) and an electron-donating group (4-C(CH3)3) were investigated as catalysts for cumene oxidation. The initial reaction rates, measured by the oxygen uptake, conversion of substrate and yield of oxidation products are discussed. The catalytic activity of oxidation rate enhancement of NHPI derivatives in acetonitrile follows the order 4-tert-BuNHPI > NHPI > 4-carb-NHPI > NDHPI > NAPI. NMPT, trityl-NPI and NHPLI are inactive.

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  • Impact Factor (2019): 1.520
  • Scimago Journal Rank (2019): 0.345
  • SJR Hirsch-Index (2019): 39
  • SJR Quartile Score (2019): Q3 Physical and Theoretical Chemistry
  • SJR Quartile Score (2019): Q4 Catalysis
  • Impact Factor (2018): 1.142
  • Scimago Journal Rank (2018): 0.374
  • SJR Hirsch-Index (2018): 37
  • SJR Quartile Score (2018): Q3 Physical and Theoretical Chemistry
  • SJR Quartile Score (2018): Q3 Catalysis

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Reaction Kinetics, Mechanisms and Catalysis
Language English
Size B5
Year of
Foundation
1974
Volumes
per Year
3
Issues
per Year
6
Founder Akadémiai Kiadó
Founder's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
Publisher Akadémiai Kiadó
Springer Nature Switzerland AG
Publisher's
Address
H-1117 Budapest, Hungary 1516 Budapest, PO Box 245.
CH-6330 Cham, Switzerland Gewerbestrasse 11.
Responsible
Publisher
Chief Executive Officer, Akadémiai Kiadó
ISSN 1878-5190 (Print)
ISSN 1878-5204 (Online)