Metal-induced tautomerization of p- to o-quinone compounds: experimental evidence from CuI and ReI complexes of azophenine and DFT studies.

Azophenine (7,8-diphenyl-2,5-bis(phenylamino)-p-quinonediimine, L(p)) reacts with [Cu(PPh3)4](BF4) or [Re(CO)(5)Cl] to yield the (Ph3P)(2)Cu(+) or [(OC)(3)ClRe] complex of the tautomeric form 7,8-diphenyl-4,5-bis(phenylamino)-o-quinonediimine, L(o), as evident from structure determinations and from very intense metal-to-ligand charge transfer (MLCT) transitions in the visible region. Time-dependent DFT (TD-DFT) calculations on model complexes [(N intersection N)Re(CO)(3)Cl] confirm the spectroscopic results, showing considerably higher oscillator strengths of the MLCT transition for the o-quinonediimine complexes in comparison to compounds with N intersection N=1,4-dialkyl-1,4-diazabutadiene. The complexes are additionally stabilized through hydrogen bonding between two now ortho-positioned NHPh substituents and one fluoride of the BF(4) (-) anion (Cu complex) or the chloride ligand (Re complex). DFT Calculations on the model ligands p-quinonediimine or 2,5-diamino-p-quinonediimine and their ortho-quinonoid forms with and without Li(+) or Cu(+) are presented to discuss the relevance for metal-dependent quinoproteins.

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 through chelate-like hydrogen bonding between the NH functionalities, which are both now ortho-positioned, and the BF4- counterion.