A Coordination-Induced 1,4→1,2-Quinonediimine Isomerization

Hitherto unused in coordination compounds, the para‐quinonoid azophenine (p‐ap) has now been applied for the synthesis of [Cu(PPh3)2(o‐ap)](BF4) (1), in which the ligand exists as its ortho‐quinonoid tautomer. Additional stabilization of this metal–π donor/ligand–π acceptor arrangement occurs throug...

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Veröffentlicht in:Angewandte Chemie International Edition 1998-10, Vol.37 (19), p.2681-2682
Hauptverfasser: Rall, Jochen, Stange, Andreas F., Hübler, Klaus, Kaim, Wolfgang
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Sprache:eng
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Zusammenfassung:Hitherto unused in coordination compounds, the para‐quinonoid azophenine (p‐ap) has now been applied for the synthesis of [Cu(PPh3)2(o‐ap)](BF4) (1), in which the ligand exists as its ortho‐quinonoid tautomer. Additional stabilization of this metal–π donor/ligand–π acceptor arrangement occurs through chelate‐like hydrogen bonding between the NH functionalities, which are both now ortho‐positioned, and the BF4− counterion.
ISSN:1433-7851
1521-3773
DOI:10.1002/(SICI)1521-3773(19981016)37:19<2681::AID-ANIE2681>3.0.CO;2-9