Redox Non-Innocent Ligands: Versatile New Tools to Control Catalytic Reactions
Тип публикации: Journal Article
Дата публикации: 2012-01-23
scimago Q1
wos Q1
БС1
SJR: 3.847
CiteScore: 20.8
Impact factor: 13.1
ISSN: 21555435
General Chemistry
Catalysis
Краткое описание
In this (tutorial overview) perspective we highlight the use of “redox non-innocent” ligands in catalysis. Two main types of reactivity in which the redox non-innocent ligand is involved can be specified: (A) The redox active ligand participates in the catalytic cycle only by accepting/donating electrons, and (B) the ligand actively participates in the formation/breaking of substrate covalent bonds. On the basis of these two types of behavior, four main application strategies of redox-active ligands in catalysis can be distinguished: The first strategy (I) involves oxidation/reduction of the ligand to tune the electronic properties (i.e., Lewis acidity/basicity) of the metal. In the second approach (II) the ligand is used as an electron reservoir. This allows multiple-electron transformations for metal complexes that are reluctant to such transformations otherwise (e.g., because the metal would need to accommodate an uncommon, high-energy oxidation state). This includes examples of (first row) transition ...
Найдено
Ничего не найдено, попробуйте изменить настройки фильтра.
Для доступа к списку цитирований публикации необходимо авторизоваться.
Для доступа к списку профилей, цитирующих публикацию, необходимо авторизоваться.
Топ-30
Журналы
|
20
40
60
80
100
120
140
160
|
|
|
Inorganic Chemistry
149 публикаций, 14.64%
|
|
|
Dalton Transactions
99 публикаций, 9.72%
|
|
|
Chemistry - A European Journal
68 публикаций, 6.68%
|
|
|
Journal of the American Chemical Society
59 публикаций, 5.8%
|
|
|
Organometallics
46 публикаций, 4.52%
|
|
|
Angewandte Chemie - International Edition
42 публикации, 4.13%
|
|
|
Angewandte Chemie
42 публикации, 4.13%
|
|
|
Chemical Communications
40 публикаций, 3.93%
|
|
|
European Journal of Inorganic Chemistry
33 публикации, 3.24%
|
|
|
ACS Catalysis
29 публикаций, 2.85%
|
|
|
Chemical Science
25 публикаций, 2.46%
|
|
|
Coordination Chemistry Reviews
17 публикаций, 1.67%
|
|
|
ChemCatChem
17 публикаций, 1.67%
|
|
|
New Journal of Chemistry
12 публикаций, 1.18%
|
|
|
Inorganica Chimica Acta
12 публикаций, 1.18%
|
|
|
Inorganic Chemistry Frontiers
12 публикаций, 1.18%
|
|
|
Chemical Society Reviews
11 публикаций, 1.08%
|
|
|
RSC Advances
10 публикаций, 0.98%
|
|
|
Polyhedron
9 публикаций, 0.88%
|
|
|
Chemical Reviews
8 публикаций, 0.79%
|
|
|
Journal of Organic Chemistry
8 публикаций, 0.79%
|
|
|
Organic Letters
8 публикаций, 0.79%
|
|
|
Molecules
7 публикаций, 0.69%
|
|
|
Journal of Organometallic Chemistry
7 публикаций, 0.69%
|
|
|
ChemistrySelect
7 публикаций, 0.69%
|
|
|
ACS Omega
7 публикаций, 0.69%
|
|
|
Topics in Organometallic Chemistry
7 публикаций, 0.69%
|
|
|
Russian Chemical Bulletin
6 публикаций, 0.59%
|
|
|
Russian Journal of Coordination Chemistry/Koordinatsionnaya Khimiya
6 публикаций, 0.59%
|
|
|
20
40
60
80
100
120
140
160
|
Издатели
|
50
100
150
200
250
300
350
|
|
|
American Chemical Society (ACS)
343 публикации, 33.69%
|
|
|
Wiley
269 публикаций, 26.42%
|
|
|
Royal Society of Chemistry (RSC)
226 публикаций, 22.2%
|
|
|
Elsevier
91 публикация, 8.94%
|
|
|
Springer Nature
26 публикаций, 2.55%
|
|
|
MDPI
16 публикаций, 1.57%
|
|
|
Pleiades Publishing
9 публикаций, 0.88%
|
|
|
Oxford University Press
6 публикаций, 0.59%
|
|
|
International Union of Crystallography (IUCr)
5 публикаций, 0.49%
|
|
|
Taylor & Francis
5 публикаций, 0.49%
|
|
|
Georg Thieme Verlag KG
3 публикации, 0.29%
|
|
|
Autonomous Non-profit Organization Editorial Board of the journal Uspekhi Khimii
2 публикации, 0.2%
|
|
|
World Scientific
2 публикации, 0.2%
|
|
|
American Association for the Advancement of Science (AAAS)
2 публикации, 0.2%
|
|
|
European Journal of Chemistry
2 публикации, 0.2%
|
|
|
The Society of Synthetic Organic Chemistry, Japan
1 публикация, 0.1%
|
|
|
OOO Zhurnal "Mendeleevskie Soobshcheniya"
1 публикация, 0.1%
|
|
|
Institute of Experimental Botany
1 публикация, 0.1%
|
|
|
Walter de Gruyter
1 публикация, 0.1%
|
|
|
Hindawi Limited
1 публикация, 0.1%
|
|
|
Proceedings of the National Academy of Sciences (PNAS)
1 публикация, 0.1%
|
|
|
IntechOpen
1 публикация, 0.1%
|
|
|
Canadian Science Publishing
1 публикация, 0.1%
|
|
|
The Electrochemical Society
1 публикация, 0.1%
|
|
|
Annual Reviews
1 публикация, 0.1%
|
|
|
50
100
150
200
250
300
350
|
- Мы не учитываем публикации, у которых нет DOI.
- Статистика публикаций обновляется еженедельно.
Вы ученый?
Создайте профиль, чтобы получать персональные рекомендации коллег, конференций и новых статей.
Метрики
1k
Всего цитирований:
1018
Цитирований c 2025:
64
(6.29%)
Цитировать
ГОСТ |
RIS |
BibTex |
MLA
Цитировать
ГОСТ
Скопировать
Lyaskovskyy V., de Bruin B. Redox Non-Innocent Ligands: Versatile New Tools to Control Catalytic Reactions // ACS Catalysis. 2012. Vol. 2. No. 2. pp. 270-279.
ГОСТ со всеми авторами (до 50)
Скопировать
Lyaskovskyy V., de Bruin B. Redox Non-Innocent Ligands: Versatile New Tools to Control Catalytic Reactions // ACS Catalysis. 2012. Vol. 2. No. 2. pp. 270-279.
Цитировать
RIS
Скопировать
TY - JOUR
DO - 10.1021/cs200660v
UR - https://doi.org/10.1021/cs200660v
TI - Redox Non-Innocent Ligands: Versatile New Tools to Control Catalytic Reactions
T2 - ACS Catalysis
AU - Lyaskovskyy, Volodymyr
AU - de Bruin, B.
PY - 2012
DA - 2012/01/23
PB - American Chemical Society (ACS)
SP - 270-279
IS - 2
VL - 2
SN - 2155-5435
ER -
Цитировать
BibTex (до 50 авторов)
Скопировать
@article{2012_Lyaskovskyy,
author = {Volodymyr Lyaskovskyy and B. de Bruin},
title = {Redox Non-Innocent Ligands: Versatile New Tools to Control Catalytic Reactions},
journal = {ACS Catalysis},
year = {2012},
volume = {2},
publisher = {American Chemical Society (ACS)},
month = {jan},
url = {https://doi.org/10.1021/cs200660v},
number = {2},
pages = {270--279},
doi = {10.1021/cs200660v}
}
Цитировать
MLA
Скопировать
Lyaskovskyy, Volodymyr, and B. de Bruin. “Redox Non-Innocent Ligands: Versatile New Tools to Control Catalytic Reactions.” ACS Catalysis, vol. 2, no. 2, Jan. 2012, pp. 270-279. https://doi.org/10.1021/cs200660v.