Abstract
A new family of double salts has been developed that can display infinite one-dimensional chains of metallophilic interactions in the solid state. These salts are composed of cationic and anionic components that are designed to participate in metallophilic interactions with one another. These building blocks incorporate Au(III), Au(I), and Pt(II) atoms in the forms [L3PtX]+, [L2AuX2]+, [AuX4]−, and [AuX2]−. Five different metallophilic structural motifs have been observed in these double salts and their monomeric precursors. The particular structure observed is affected by metal oxidation state, the electronic nature of the neutral (L) and anionic (X) substituents, the synthetic conditions employed, as well as the solvent present.
ACKNOWLEDGEMENTS
I would like to thank all my students and colleagues whose names appear in the references and whose enthusiasm, hard work, and dedication made these results possible. We are particularly grateful to the Rheingold group at UC San Diego for indefatigable crystallographic collaborations. For financial support we are indebted to NSF (CAREER to LHD CHE-0134817 and NSEC CHE-0117752 to Columbia University), the Dreyfus Foundation (New Faculty Award and Henry Dreyfus Teacher-Scholar Awards to LHD), Barnard College, and Boston University.