Novel Carbon Monochalcogenide Coordination Mode: [Rh2{μ-SeCMo(CO)2(Tp*)}2(η4-cod)2] (Tp* = hydrotris(3,5-dimethylpyrazol-1-yl)borate; cod = cyclo-octa-1,5-diene)-Reference-Cited by-同舟云学术

Novel Carbon Monochalcogenide Coordination Mode: [Rh2{μ-SeCMo(CO)2(Tp*)}2(η4-cod)2] (Tp* = hydrotris(3,5-dimethylpyrazol-1-yl)borate; cod = cyclo-octa-1,5-diene)

Published:2012-03-09 Issue:6 Volume:31 Page:2482-2485
ISSN:0276-7333
Container-title:Organometallics
language:en
Short-container-title:Organometallics

Author:

Hill Anthony F.¹,McQueen Caitlin M. A.¹

Affiliation:

1. Research School of Chemistry, The Australian National University, Canberra, ACT 0200, Australia

Publisher

American Chemical Society (ACS)

Subject

Inorganic Chemistry,Organic Chemistry,Physical and Theoretical Chemistry

Link

https://pubs.acs.org/doi/pdf/10.1021/om3000086

Reference63 articles.

1. Iridium−Molybdenum Carbido Complex via C−Se Activation of a Selenocarbonyl Ligand: (μ-Se2)[Ir2{C≡Mo(CO)2(Tp*)}2(CO)2(PPh3)2] (Tp* = hydrotris(dimethylpyrazolyl)borate)

2. THE ODD BIT OF CARBON

3. Formation of η2-aroyl, η1-halogenocarbyne or sterically crowded aryldiazenide ligands in the reactions of ring-substituted tricarbonyl[hydrotris(pyrazolyl)borato]-molybdate and -tungstate anions with arenediazonium cations and related oxidants

4. Facile Generation of Lithiocarbyne Complexes: [M(≡CLi)(CO)2{HB(pzMe2)3}] (M = Mo, W; pz = Pyrazol-1-yl)

5. The iridium(I) cation, [Ir(CO)(CH3CN)(PPh3)2]+ and its substitution reactions

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