Chemical and Photochemical Water Oxidation by [RuCl(NCNHCO)(DMSO)(py)]-Type Complexes

Bibliographic Details
Parent link:ChemCatChem.— , 2009-
Vol. 9, iss. 13.— 2017.— [С. 2565–2573]
Corporate Author: Национальный исследовательский Томский политехнический университет (ТПУ) Институт природных ресурсов (ИПР) Кафедра технологии органических веществ и полимерных материалов (ТОВПМ)
Other Authors: Wei Su, Younus H. A. Hussein, Chaemchuen S. Somboon, Cheng Chen, Verpoort F. V. K. Frensis Valter Kornelius
Summary:Title screen
In this work, the effects of substitutions in the backbone of imidazolylidene and axial ligands on the reactivity and stability of water-oxidation catalysts were investigated. Three pincer-type asymmetric imidazolium salts NCNHCO, NCNHC-4BrO, and NCNHC-BO (NHC: N-heterocyclic carbene), of which the donating ability of the corresponding imidazolylidene decreases in the same sequence, were prepared. Their application in metalation afforded the corresponding Ru complexes 1 a, 1 b, 2, and 3. It was found that the complexes incorporating the stronger donor displayed lower potential for each redox couple and longer lifetimes, but relatively low reaction rates. Under acidic conditions, water oxidation driven by cerium ammonium nitrate resulted in turnover numbers (TONs) of 2322, 1728, 1928, and 2208 for 1 a, 1 b, 2, and 3, respectively. Complex 2 exhibited a good match of reactivity and stability with a TON of 136 in a typical three-component photocatalysis. Importantly, NHCs could be another powerful tool for tuning the reactivity and stability of water-oxidation catalysts, in addition to substituted pyridines. Rational orchestration of modified NHCs and pyridines could eventually result in water-oxidation catalysts exhibiting appreciable effectiveness and considerable robustness.
Режим доступа: по договору с организацией-держателем ресурса
Published: 2017
Subjects:
Online Access:http://dx.doi.org/10.1002/cctc.201700049
Format: Electronic Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=656751

MARC

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200 1 |a Chemical and Photochemical Water Oxidation by [RuCl(NCNHCO)(DMSO)(py)]-Type Complexes  |f Wei Su [et al.] 
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300 |a Title screen 
320 |a [References: p. 2572-2573 (20 tit.)] 
330 |a In this work, the effects of substitutions in the backbone of imidazolylidene and axial ligands on the reactivity and stability of water-oxidation catalysts were investigated. Three pincer-type asymmetric imidazolium salts NCNHCO, NCNHC-4BrO, and NCNHC-BO (NHC: N-heterocyclic carbene), of which the donating ability of the corresponding imidazolylidene decreases in the same sequence, were prepared. Their application in metalation afforded the corresponding Ru complexes 1 a, 1 b, 2, and 3. It was found that the complexes incorporating the stronger donor displayed lower potential for each redox couple and longer lifetimes, but relatively low reaction rates. Under acidic conditions, water oxidation driven by cerium ammonium nitrate resulted in turnover numbers (TONs) of 2322, 1728, 1928, and 2208 for 1 a, 1 b, 2, and 3, respectively. Complex 2 exhibited a good match of reactivity and stability with a TON of 136 in a typical three-component photocatalysis. Importantly, NHCs could be another powerful tool for tuning the reactivity and stability of water-oxidation catalysts, in addition to substituted pyridines. Rational orchestration of modified NHCs and pyridines could eventually result in water-oxidation catalysts exhibiting appreciable effectiveness and considerable robustness. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t ChemCatChem  |d 2009- 
463 |t Vol. 9, iss. 13  |v [С. 2565–2573]  |d 2017 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a carbene ligands 
610 1 |a electrochemistry 
610 1 |a photocatalysis 
610 1 |a ruthenium 
610 1 |a water oxidation 
610 1 |a лиганды 
610 1 |a карбены 
610 1 |a электрохимия 
610 1 |a фотокатализ 
610 1 |a рутений 
610 1 |a окисление 
610 1 |a вода 
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