Efficient N-Heterocyclic Carbene/Ruthenium Catalytic Systems for the Alcohol Amidation with Amines: Involvement of Poly-Carbene Complexes?; ChemCatChem; Vol. 10, iss. 19

Dettagli Bibliografici
Parent link:ChemCatChem
Vol. 10, iss. 19.— 2018.— [P. 4338-4345]
Ente Autore: Национальный исследовательский Томский политехнический университет Исследовательская школа химических и биомедицинских технологий (ИШХБМТ)
Altri autori: Cheng Hua, Xiong Mao-Qian, Zhang Ni, Wang Hua-Jing, Miao Yang, Su Wei, Yuan Ye, Chen Cheng, Verpoort F. V. K. Frensis Valter Kornelius
Riassunto:Title screen
The atom-economic direct amidation of alcohols with amines has been recently highlighted as an attractive and promising transformation. Among the versatile reported catalytic systems, in situ generated N-heterocyclic carbene (NHC)/ruthenium (Ru) catalytic systems have demonstrated their advantages such as easy operation and use of commercial Ru compounds. However, the existing catalyst loadings are relatively high, and additional insights for the in situ catalyst generation are still not well-documented. In this work, a variety of benzimidazole-based NHC precursors were initially synthesized. Through the screening of various NHC precursors and other reaction conditions, active in situ catalytic systems were discovered for the efficient amide synthesis. Notably, the catalyst loading is as low as 0.5 mol?%. Furthermore, additional experiments were performed to validate the rationale for the superiority of the current catalytic systems over our previous system. It was observed that the ligand structure is one of the reasons for the higher activity. In addition, the higher ratio of the NHC precursor/[Ru] is another important factor for the improvement. Further HR-MS analysis identified the formation of two mono-NHC-Ru species as major species and two Ru species bearing multiple NHC ligands as minor species. Hopefully, the efficient and readily-accessible catalytic systems reported herein could demonstrate great potential for further practical applications.
Режим доступа: по договору с организацией-держателем ресурса
Lingua:inglese
Pubblicazione: 2018
Soggetti:
Accesso online:https://doi.org/10.1002/cctc.201800945
Natura: xMaterials Elettronico Capitolo di libro
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=660088

MARC

LEADER 00000naa0a2200000 4500
001 660088
005 20250328162644.0
035 |a (RuTPU)RU\TPU\network\29035 
090 |a 660088 
100 |a 20190424d2018 k||y0rusy50 ba 
101 0 |a eng 
102 |a DE 
135 |a drcn ---uucaa 
181 0 |a i  
182 0 |a b 
200 1 |a Efficient N-Heterocyclic Carbene/Ruthenium Catalytic Systems for the Alcohol Amidation with Amines: Involvement of Poly-Carbene Complexes?  |f Cheng Hua [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 22 tit.] 
330 |a The atom-economic direct amidation of alcohols with amines has been recently highlighted as an attractive and promising transformation. Among the versatile reported catalytic systems, in situ generated N-heterocyclic carbene (NHC)/ruthenium (Ru) catalytic systems have demonstrated their advantages such as easy operation and use of commercial Ru compounds. However, the existing catalyst loadings are relatively high, and additional insights for the in situ catalyst generation are still not well-documented. In this work, a variety of benzimidazole-based NHC precursors were initially synthesized. Through the screening of various NHC precursors and other reaction conditions, active in situ catalytic systems were discovered for the efficient amide synthesis. Notably, the catalyst loading is as low as 0.5 mol?%. Furthermore, additional experiments were performed to validate the rationale for the superiority of the current catalytic systems over our previous system. It was observed that the ligand structure is one of the reasons for the higher activity. In addition, the higher ratio of the NHC precursor/[Ru] is another important factor for the improvement. Further HR-MS analysis identified the formation of two mono-NHC-Ru species as major species and two Ru species bearing multiple NHC ligands as minor species. Hopefully, the efficient and readily-accessible catalytic systems reported herein could demonstrate great potential for further practical applications. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t ChemCatChem 
463 |t Vol. 10, iss. 19  |v [P. 4338-4345]  |d 2018 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a ruthenium 
610 1 |a N-heterocyclic carbene (s) 
610 1 |a atom-economic 
610 1 |a amide synthesis 
610 1 |a рутений 
610 1 |a гетероциклический ряд 
610 1 |a карбены 
610 1 |a синтез 
701 0 |a Cheng Hua 
701 0 |a Xiong Mao-Qian 
701 0 |a Zhang Ni 
701 0 |a Wang Hua-Jing 
701 0 |a Miao Yang 
701 0 |a Su Wei 
701 0 |a Yuan Ye 
701 0 |a Chen Cheng 
701 1 |a Verpoort  |b F. V. K.  |c Chemical Engineer  |c Professor of Tomsk Polytechnic University, doctor of chemical Sciences  |f 1963-  |g Frensis Valter Kornelius  |3 (RuTPU)RU\TPU\pers\35059  |9 18334 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Исследовательская школа химических и биомедицинских технологий (ИШХБМТ)  |c (2017- )  |3 (RuTPU)RU\TPU\col\23537 
801 2 |a RU  |b 63413507  |c 20210312  |g RCR 
856 4 |u https://doi.org/10.1002/cctc.201800945 
942 |c CF