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Issue 37, 2016
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Dinitrogen binding, P4-activation and aza-Büchner ring expansions mediated by an isocyano analogue of the CpCo(CO) fragment

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Abstract

Synthetic studies targeting an m-terphenyl isocyanide analogue of the unstable 16e, S = 1 complex CpCo(CO) are reported (Cp = η5-C5H5). The m-terphenyl isocyanide CNArDipp2 (ArDipp2 = 2,6-(2,6-(i-Pr)2C6H3)2C6H3) is shown to readily bind to both CpCoI2 and Cp*CoI2 fragments (Cp* = η5-C5Me5) and provide mono-isocyanide starting materials that are suitable for chemical reduction. Treatment of CpCoI2(CNArDipp2) with KC8 produces the bridging isocyanide dimer, [CpCo(μ-CNArDipp2)]2, thereby indicating that the steric combination of Cp and CNArDipp2 ligands does not allow for the production of mononuclear complexes. However, Cp*CoI2(CNArDipp2) with KC8 under an N2 atmosphere results in the formation of the complex, Cp*Co(N2)(CNArDipp2), which is a unique two-legged piano stool complex featuring a coordinated dinitrogen ligand. The N2 ligand in Cp*Co(N2)(CNArDipp2) is shown to be labile and, upon removal by application of vacuum, leads to the production of an η4-coordinated 1-azabenz[b]azulene complex by aza-Büchner cyclization of the CNArDipp2 ligand. This cyclization reaction is rationalized via the intermediacy of the unobserved 16e species [Cp*Co(CNArDipp2)]. While this intramolecular aza-Büchner cyclization prevents isolation of [Cp*Co(CNArDipp2)], the dinitrogen complex Cp*Co(N2)(CNArDipp2) is shown to serve as a reliable synthon for this 16e species upon reaction with small molecule substrates. Both free CNArDipp2 and diphenylacetylene react with Cp*Co(N2)(CNArDipp2) to form two-legged piano stool complexes. In addition, Cp*Co(N2)(CNArDipp2) reacts readily with 0.5 and 1.0 equivalents of P4 to produce poly-phosphorus products resulting from P–P single bond cleavage.

Graphical abstract: Dinitrogen binding, P4-activation and aza-Büchner ring expansions mediated by an isocyano analogue of the CpCo(CO) fragment

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Publication details

The article was received on 14 Jul 2016, accepted on 21 Jul 2016 and first published on 21 Jul 2016


Article type: Paper
DOI: 10.1039/C6DT02789J
Citation: Dalton Trans., 2016,45, 14561-14569
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    Dinitrogen binding, P4-activation and aza-Büchner ring expansions mediated by an isocyano analogue of the CpCo(CO) fragment

    C. C. Mokhtarzadeh, A. L. Rheingold and J. S. Figueroa, Dalton Trans., 2016, 45, 14561
    DOI: 10.1039/C6DT02789J

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