Diphenoquinhydrones and Related Hydrogen-Bonded Charge-Transfer Complexes

Benzoquinone and hydroquinone cocrystallize to form quinhydrone, a 1:1 complex with a characteristic structure in which the components are positioned by hydrogen bonds and charge-transfer interactions. We have found that analogous diphenoquinhydrones can be made by combining 4,4'-diphenoquinones with the corresponding 4,4'-dihydroxybiphenyls. In addition, mixed diphenoquinhydrones can be assembled from components with different substituents, and mismatched quinhydrones can be made from benzoquinones and dihydroxybiphenyls. In all cases, the components of the resulting structures are linked in alternation by O-H center dot center dot center dot O hydrogen bonds to form essentially planar chains, which stack to produce layers in which pi-donors and pi-acceptors are aligned by charge-transfer interactions. Geometric parameters, computational studies, and spectroscopic properties of diphenoquinhydrones show that the key intermolecular interactions are stronger than those in simple quinhydrone analogues. These findings demonstrate that the principles of modular construction underlying the formation of classical quinhydrones can be generalized to produce a broad range of hydrogen-bonded charge-transfer materials in which the components are positioned by design.