Formal [2 + 2 + 2] Cycloaddition Reaction of a Metal–Carbyne Complex with Nitriles: Synthesis of a Metallapyrazine Complex

Although alkynes have been extensively exploited in [2 + 2 + 2] cycloadditions with nitriles to form N-heterocyclic aromatics, the “alkyne-like” metal–carbon triple bond has never been used in [2 + 2 + 2] cycloadditions with nitriles. We demonstrate the synthesis of the first metallapyrazine through...

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Veröffentlicht in:Organometallics 2019-05, Vol.38 (9), p.2264-2271
Hauptverfasser: Lin, Jianfeng, Ding, Linting, Zhuo, Qingde, Zhang, Hong, Xia, Haiping
Format: Artikel
Sprache:eng
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Zusammenfassung:Although alkynes have been extensively exploited in [2 + 2 + 2] cycloadditions with nitriles to form N-heterocyclic aromatics, the “alkyne-like” metal–carbon triple bond has never been used in [2 + 2 + 2] cycloadditions with nitriles. We demonstrate the synthesis of the first metallapyrazine through [2 + 2 + 2] cycloaddition reactions of a metal–carbyne complex with nitriles. Experimental observations and density functional theory calculations are evidence for the aromatic character of the metallapentalenopyrazine.
ISSN:0276-7333
1520-6041
DOI:10.1021/acs.organomet.9b00213