Very strong trans effect in ruthenacyclic carbamoyl complexes leads to ligand redistribution in phosphine derivatives-Reference-Cited by-同舟云学术

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Very strong trans effect in ruthenacyclic carbamoyl complexes leads to ligand redistribution in phosphine derivatives

Published:2019-05 Issue: Volume:887 Page:5-11
ISSN:0022-328X
Container-title:Journal of Organometallic Chemistry
language:en
Short-container-title:Journal of Organometallic Chemistry

Author:

Barik Chandan Kr,Ganguly Rakesh^ORCID,Li Yongxin,Leong Weng Kee^ORCID

Funder

Nanyang Technological University

Ministry of Education

Agency for Science, Technology and Research (A*STAR

SERC

Publisher

Elsevier BV

Subject

Materials Chemistry,Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry,Biochemistry

Reference43 articles.

1. A third type of hydrogenase catalyzing H2 activation

2. Reactions with Molecular Hydrogen in Microorganisms: Evidence for a Purely Organic Hydrogenation Catalyst

3. Structural and Functional Analogues of the Active Sites of the [Fe]-, [NiFe]-, and [FeFe]-Hydrogenases

4. Mössbauer Studies of the Iron−Sulfur Cluster-Free Hydrogenase: The Electronic State of the Mononuclear Fe Active Site

Cited by 3 articles. 订阅此论文施引文献订阅此论文施引文献，注册后可以免费订阅5篇论文的施引文献，订阅后可以查看论文全部施引文献

1. Follow-Up Study of Trans-C to Cis-C Thermally or Photochemically Induced Isomerization of Terpyridine Adducts of Cycloruthenated 2-Aryl-2′-pyridine Compounds;Inorganic Chemistry;2024-03-07

2. Ruthenacyclic carbamoyl mimics of the [Fe]-hydrogenase active site: Derivatisation at the 4-position of the pyridinyl ring;Polyhedron;2021-01

3. Ruthenium‐Based Structural Mimics of the Cofactor of [Fe]‐Hydrogenase: Replacement of the Acyl Moiety with an N‐Heterocyclic Carbene;ChemistrySelect;2020-09-10

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