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Issue 9, 1971
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Reaction of a diazepine with chlorodicarbonylrhodium(I) dimer; the molecular structure of chloro-cis-dicarbonyl-(3,5,7-triphenyl-4H-1,2-diazepine)rhodium(I)

Abstract

Chlorodicarbonylrhodium(I) dimer reacts with 3,5,7-triphenyl-4H-1,2-diazepine without cleavage of the N–N bond of the diazepine to yield chloro-cis-dicarbonyl (3,5,7-triphenyl-4H-1,2-diazepine)rhodium(I) in which the diazepine (in a twisted boat conformation) is co-ordinated to the rhodium(I) atom via only one nitrogen atom.

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Article type: Paper
DOI: 10.1039/C29710000427
Citation: J. Chem. Soc. D, 1971,0, 427-428
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    Reaction of a diazepine with chlorodicarbonylrhodium(I) dimer; the molecular structure of chloro-cis-dicarbonyl-(3,5,7-triphenyl-4H-1,2-diazepine)rhodium(I)

    R. A. Smith, D. P. Madden, A. J. Carty and G. J. Palenik, J. Chem. Soc. D, 1971, 0, 427
    DOI: 10.1039/C29710000427

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