Stepwise Bromination of Two Acetylene Molecules on a Butterfly-Type Tetrairon Core and Reactivity of the Resulting Bromoacetylene Fragment toward Nucleophiles-Reference-Cited by-同舟云学术

Stepwise Bromination of Two Acetylene Molecules on a Butterfly-Type Tetrairon Core and Reactivity of the Resulting Bromoacetylene Fragment toward Nucleophiles

Published:2004-07-10 Issue:30 Volume:126 Page:9190-9191
ISSN:0002-7863
Container-title:Journal of the American Chemical Society
language:en
Short-container-title:J. Am. Chem. Soc.

Author:

Takano Masato¹,Okazaki Masaaki¹,Tobita Hiromi¹

Affiliation:

1. Department of Chemistry, Graduate School of Science, Tohoku University, Sendai 980-8578, Japan

Publisher

American Chemical Society (ACS)

Subject

Colloid and Surface Chemistry,Biochemistry,General Chemistry,Catalysis

Link

https://pubs.acs.org/doi/pdf/10.1021/ja047569a

Reference14 articles.

1. Reductive Coupling of Carbonyl Ligands on a Cubane-Type Tetrairon Cluster [Cp4Fe4(CO)4] or [(MeC5H4)4Fe4(CO)4] To Give an Acetylene-Coordinated Cluster [Cp4Fe4(HC⋮CH)2] or [(MeC5H4)4Fe4(HC⋮CH)2]

2. Synthesis and Structures of One- and Two-Electron Oxidized Forms of Bis(acetylene)tetrairon Clusters Cp‘4Fe4(HCCH)2 (Cp‘ = Cp, η5-C5H4Me)

3. Reversible Cleavage and Recombination of an Acetylenic Carbon−Carbon Bond on a Tetrairon Cluster Coupled with a Two-Electron Redox Reaction

4. (b) Patai, S.Supplement C2: The Chemistry ofTriple-bonded Functional Groups; John Wiley & Sons: New York, 1991; Chapter 6.

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