Standard

Alcohol acylation by acetic acid over novel lanthanide-grafted catalytic systems. / Koskin, A. P.; Borodin, A. O.; Vedyagin, A. A.

в: Reaction Kinetics, Mechanisms and Catalysis, Том 127, № 1, 15.06.2019, стр. 149-160.

Результаты исследований: Научные публикации в периодических изданияхстатьяРецензирование

Harvard

Koskin, AP, Borodin, AO & Vedyagin, AA 2019, 'Alcohol acylation by acetic acid over novel lanthanide-grafted catalytic systems', Reaction Kinetics, Mechanisms and Catalysis, Том. 127, № 1, стр. 149-160. https://doi.org/10.1007/s11144-019-01574-0

APA

Koskin, A. P., Borodin, A. O., & Vedyagin, A. A. (2019). Alcohol acylation by acetic acid over novel lanthanide-grafted catalytic systems. Reaction Kinetics, Mechanisms and Catalysis, 127(1), 149-160. https://doi.org/10.1007/s11144-019-01574-0

Vancouver

Koskin AP, Borodin AO, Vedyagin AA. Alcohol acylation by acetic acid over novel lanthanide-grafted catalytic systems. Reaction Kinetics, Mechanisms and Catalysis. 2019 июнь 15;127(1):149-160. doi: 10.1007/s11144-019-01574-0

Author

Koskin, A. P. ; Borodin, A. O. ; Vedyagin, A. A. / Alcohol acylation by acetic acid over novel lanthanide-grafted catalytic systems. в: Reaction Kinetics, Mechanisms and Catalysis. 2019 ; Том 127, № 1. стр. 149-160.

BibTeX

@article{37b795ca34db4aaf82dbaf44a3489286,
title = "Alcohol acylation by acetic acid over novel lanthanide-grafted catalytic systems",
abstract = " In the present study, novel heterogeneous analogues of lanthanide triflates [trifluoromethanesulfonates; Ln(SO 3 CF 3 ) 3 or Ln(OTf) 3 ] were proposed as acidic catalysts for fine organic synthesis. A series of supported Ln 3+ and Ln 3+ 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, Ln 3+ SFP/CNF systems exhibit significantly higher catalytic activity if compare with the unsupported samples (Ln 3+ SFP) or the sample without sulfated fluoropolymer (CNF-SO 3 − Ln 3+ ). 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. ",
keywords = "Alcohol acylation, Esterification, Lanthanide grafting, Lanthanide-containing catalysts, Nafion, Nafion composite, NANOCOMPOSITES",
author = "Koskin, {A. P.} and Borodin, {A. O.} and Vedyagin, {A. A.}",
note = "Publisher Copyright: {\textcopyright} 2019, Akad{\'e}miai Kiad{\'o}, Budapest, Hungary.",
year = "2019",
month = jun,
day = "15",
doi = "10.1007/s11144-019-01574-0",
language = "English",
volume = "127",
pages = "149--160",
journal = "Reaction Kinetics, Mechanisms and Catalysis",
issn = "1878-5190",
publisher = "Springer Netherlands",
number = "1",

}

RIS

TY - JOUR

T1 - Alcohol acylation by acetic acid over novel lanthanide-grafted catalytic systems

AU - Koskin, A. P.

AU - Borodin, A. O.

AU - Vedyagin, A. A.

N1 - Publisher Copyright: © 2019, Akadémiai Kiadó, Budapest, Hungary.

PY - 2019/6/15

Y1 - 2019/6/15

N2 - In the present study, novel heterogeneous analogues of lanthanide triflates [trifluoromethanesulfonates; Ln(SO 3 CF 3 ) 3 or Ln(OTf) 3 ] were proposed as acidic catalysts for fine organic synthesis. A series of supported Ln 3+ and Ln 3+ 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, Ln 3+ SFP/CNF systems exhibit significantly higher catalytic activity if compare with the unsupported samples (Ln 3+ SFP) or the sample without sulfated fluoropolymer (CNF-SO 3 − Ln 3+ ). 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.

AB - In the present study, novel heterogeneous analogues of lanthanide triflates [trifluoromethanesulfonates; Ln(SO 3 CF 3 ) 3 or Ln(OTf) 3 ] were proposed as acidic catalysts for fine organic synthesis. A series of supported Ln 3+ and Ln 3+ 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, Ln 3+ SFP/CNF systems exhibit significantly higher catalytic activity if compare with the unsupported samples (Ln 3+ SFP) or the sample without sulfated fluoropolymer (CNF-SO 3 − Ln 3+ ). 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.

KW - Alcohol acylation

KW - Esterification

KW - Lanthanide grafting

KW - Lanthanide-containing catalysts

KW - Nafion

KW - Nafion composite

KW - NANOCOMPOSITES

UR - http://www.scopus.com/inward/record.url?scp=85064720504&partnerID=8YFLogxK

U2 - 10.1007/s11144-019-01574-0

DO - 10.1007/s11144-019-01574-0

M3 - Article

AN - SCOPUS:85064720504

VL - 127

SP - 149

EP - 160

JO - Reaction Kinetics, Mechanisms and Catalysis

JF - Reaction Kinetics, Mechanisms and Catalysis

SN - 1878-5190

IS - 1

ER -

ID: 19623399