Heteroleptic platinum(II) and palladium(II) complexes with thiacrown and diimine ligands

We wish to report the synthesis, crystal structures, spectroscopic and electrochemical properties of several new Pt(II) heteroleptic complexes containing the thiacrown, 9S3 (1,4,7-trithiacyclononane) with a series of substituted phenanthroline ligands and related diimine systems. These five ligands are 5,6-dimethyl-1,10-phenanthroline(5,6-Me2-phen), 4,7-dimethyl-1,10-phenanthroline(4,7-Me2-phen), 4,7-diphenyl-1,10-phenanthroline(4,7-Ph2-phen), 2,2′-bipyrimidine(bpm), and pyrazino[2,3-f]quinoxaline or 1,4,5,8-tetraazaphenanthrene(tap). All complexes have the general formula [Pt(9S3)(N2)](PF6)2 (N2 = diimine ligand) and form similar structures in which the Pt(II) center is surrounded by a cis arrangement of the two N donors from the diimine chelate and two sulfur atoms from the 9S3 ligand. The third 9S3 sulfur in each structure forms a longer interaction with the platinum resulting in an elongated square pyramidal structure, and this distance is sensitive to the identity of the diimine ligand. In addition, we report the synthesis, structural, electrochemical, and spectroscopic properties of related Pd(II) 9S3 complex with tap. The 195Pt NMR chemical shifts for the six Pt(II) complexes show a value near −3290 ppm, consistent with a cis-PtS2N2 coordination sphere although more electron-withdrawing ligands such as tap show resonances shifted by almost 100 ppm downfield. The physicochemical properties of the complexes generally follow the electron-donating or withdrawing properties of the phenanthroline substituents.

Substituted phenanthroline ligands form elongated square pyramidal Pt(II) complexes with the thiacrown 9S3.Figure optionsDownload as PowerPoint slide