Reduction–oxidation properties of organotransition-metal complexes. Part 32. One-electron oxidation of [Co(η4-cot)-(η-C5Me5)](cot = cyclooctatetraene): redox-induced polycyclic ring transformations of the resulting dimer, and crystal structure of [Co2(η4:η′4-C16H16)(η-C5Me5)2]
Author:
Publisher
Royal Society of Chemistry (RSC)
Subject
General Chemistry
Link
http://pubs.rsc.org/en/content/articlepdf/1991/DT/DT9910000001
Reference33 articles.
1. Reduction–oxidation properties of organotransition-metal complexes. Part 31. Reductive elimination, oxidative addition and substitution, and migratory insertion in pentaphenylcyclopentadienylruthenium nitrosyl chemistry
2. N. G. Connelly , in Paramagnetic Organometallic Species in Activation/Selectivity, Catalysis, eds. M. Chanon, M. Julliard and J. C. Poite, Kluwer Academic Publishers, Dordrecht, 1989, p. 71.
3. Synthetic applications of organotransition-metal redox reactions
4. Reduction-oxidation properties of organotransition-metal complexes. Part 12. Formation of carbon–carbon bonds via the oxidative dimerisation of [Fe(CO)3(η4-C8H8)] and the reduction of [Fe2(CO)6(η5:η′5-C16H16)]2+; X-ray crystal structures of [Fe2(CO)4{P(OPh)3}2(η5:η′5-C16H16)][PF6]2and [Fe(CO)3(η4-C16H16)]
5. Reduction–oxidation properties of organotransition-metal complexes. Part 20. Oxidative and thermolytic cyclopropane ring-opening reactions; X-ray crystal structure of [Fe2(CO)6(η4:η′4-C16H18)]
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