Understanding the Preference for the Coplanarity of Alkenyl and Carbonyl Ligands in η1-Alkenyl Transition-Metal Complexes: A Simple Molecular Orbital Approach and ab Initio Calculations-Reference-Cited by-同舟云学术

Understanding the Preference for the Coplanarity of Alkenyl and Carbonyl Ligands in η1-Alkenyl Transition-Metal Complexes: A Simple Molecular Orbital Approach and ab Initio Calculations

Published:1998-08-01 Issue:18 Volume:17 Page:3974-3980
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Choi Sai-Heung¹,Bytheway Ian¹,Lin Zhenyang¹,Jia Guochen¹

Affiliation:

1. Department of Chemistry, The Hong Kong University of Science and Technology, Clear Water Bay, Kowloon, Hong Kong

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om9803669

Reference45 articles.

1. Reactions of Cationic Palladium(II) Methyl and Vinyl Complexes with Alkynes

2. Selective hydrogenation of 1-alkynes to alkenes catalyzed by an iron(II) cis-hydride .eta.2-dihydrogen complex. A case of intramolecular reaction between .eta.2-H2 and .sigma.-vinyl ligands

3. Mechanistic Study of Ruthenium-Catalyzed Hydrosilation of 1-(Trimethylsilyl)-1-buten-3-yne

4. Fünf‐ und sechsfach koordinierte Vinylruthenium‐ und ‐osmium‐Komplexe durch Alkin‐Insertion in Hydridometall‐Vorstufen

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