Commercial gold(III) complex supported on functionalized carbon materials as catalyst for cyclohexane hydrocarboxylation

Bibliographic Details
Parent link:Catalysis Today
Vol. 357.— 2020.— [P. 39-45]
Corporate Author: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий (ИШХБМТ)
Other Authors: Pakrieva E. G. Ekaterina Germanovna, Ribeiro A. P. C. Ana, Martins L. M.D.R.S. Luнsa, Matias I. A.S. Inкs, Carabineiro S. A.C. Sonia, Kolobova E. N. Ekaterina Nikolaevna, Pombeiro A. J.L. P Armando, Figueiredo J. L. Jose, Pestryakov A. N. Aleksey Nikolaevich
Summary:Title screen
The commercial dichloro(2-pyridinecarboxylato)gold(III) complex (1), anchored on different carbon materials, is reported for the first time as a catalyst in the cyclohexane hydrocarboxylation to cyclohexanecarboxylic acid. The reaction was carried out in the presence of CO and water, peroxodisulfate, at ca. 50?°C, with 1 in solution and anchored on carbon nanotubes, carbon xerogel or activated carbon, with three different surface chemistries: original forms (CNT, CX or AC, respectively), oxidized with HNO3 (-ox) or oxidized with HNO3 and subsequently treated with NaOH (-ox-Na). 1@CNT-ox-Na was the best catalyst, yielding up to 78% of cyclohexanecarboxylic with a selectivity of 99%. Recycling studies showed that the catalyst was stable up to 4 cycles, the first decrease (11%) on the hydrocarboxylation yield being observed on the 5th cycle. No leaching of gold was found into the solution. The hydrocarboxylation of other cycloalkanes (cyclopentane, cycloheptane and cyclooctane) was also tested in the best conditions found for cyclohexane, but the respective carboxylic acids were obtained in considerably lower yields, which can be explained by different stabilities of cycloalkyl radicals.
Режим доступа: по договору с организацией-держателем ресурса
Published: 2020
Subjects:
Online Access:https://doi.org/10.1016/j.cattod.2019.05.050
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=660508

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200 1 |a Commercial gold(III) complex supported on functionalized carbon materials as catalyst for cyclohexane hydrocarboxylation  |f E. G. Pakrieva, A. P. C. Ribeiro, L. M.D.R.S. Martins [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 41 tit.] 
330 |a The commercial dichloro(2-pyridinecarboxylato)gold(III) complex (1), anchored on different carbon materials, is reported for the first time as a catalyst in the cyclohexane hydrocarboxylation to cyclohexanecarboxylic acid. The reaction was carried out in the presence of CO and water, peroxodisulfate, at ca. 50?°C, with 1 in solution and anchored on carbon nanotubes, carbon xerogel or activated carbon, with three different surface chemistries: original forms (CNT, CX or AC, respectively), oxidized with HNO3 (-ox) or oxidized with HNO3 and subsequently treated with NaOH (-ox-Na). 1@CNT-ox-Na was the best catalyst, yielding up to 78% of cyclohexanecarboxylic with a selectivity of 99%. Recycling studies showed that the catalyst was stable up to 4 cycles, the first decrease (11%) on the hydrocarboxylation yield being observed on the 5th cycle. No leaching of gold was found into the solution. The hydrocarboxylation of other cycloalkanes (cyclopentane, cycloheptane and cyclooctane) was also tested in the best conditions found for cyclohexane, but the respective carboxylic acids were obtained in considerably lower yields, which can be explained by different stabilities of cycloalkyl radicals. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Catalysis Today 
463 |t Vol. 357  |v [P. 39-45]  |d 2020 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a dichloro(2-pyridinecarboxylato)gold(III) complex 
610 1 |a cyclohexane hydrocarboxylationC?H activation 
610 1 |a carbon materials functionalization 
610 1 |a cyclohexanecarboxylic acid 
610 1 |a циклогексан 
610 1 |a углеродные материалы 
701 1 |a Pakrieva  |b E. G.  |c Chemical Engineer  |c Engineer of Tomsk Polytechnic University  |f 1989-  |g Ekaterina Germanovna  |3 (RuTPU)RU\TPU\pers\33273  |9 17018 
701 1 |a Ribeiro  |b A. P. C.  |g Ana 
701 1 |a Martins  |b L. M.D.R.S.  |g Luнsa 
701 1 |a Matias  |b I. A.S.  |g Inкs 
701 1 |a Carabineiro  |b S. A.C.  |g Sonia 
701 1 |a Kolobova  |b E. N.  |c Chemical Engineer  |c design engineer of Tomsk Polytechnic University  |f 1989-  |g Ekaterina Nikolaevna  |3 (RuTPU)RU\TPU\pers\34488  |9 17871 
701 1 |a Pombeiro  |b A. J.L. P  |g Armando 
701 1 |a Figueiredo  |b J. L.  |g Jose 
701 1 |a Pestryakov  |b A. N.  |c Chemist  |c Professor of Tomsk Polytechnic University, Doctor of Chemical Science  |f 1963-  |g Aleksey Nikolaevich  |3 (RuTPU)RU\TPU\pers\30471  |9 14796 
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