Syntheses and structural studies of heterobimetallic thiocarboxylate complexes containing zinc and silver

• Attempts were made to synthesize heterobimetallic complexes of Zn(II) and Ag(I).
• [(PPh3)2Ag(μ-SCOPh)2Zn(SCOPh)] & [(PPh3)2Ag(μ-SCOPh)2Zn(SCOPh)H2O] co-crystallize.
• TD-DFT calculations were done to explain electronic spectra.
• Luminescence properties of both complexes have been studied in solid state.

Novel heterobimetallic complexes, [(PPh3)2Ag(μ-SCOth)2Zn(SCOth)(H2O)] (1) and {[(PPh3)2Ag(μ-SCOPh)2Zn(SCOPh)(H2O)][(PPh3)2Ag(μ-SCOPh)Zn(SCOPh)2]} (2) have been prepared and characterized by FTIR, 1H, 13C and 31P NMR spectroscopy. Molecular structures of the complexes have been determined by single crystal X-ray diffraction technique. In these complexes the two metal atoms (Ag and Zn) are held together by bridging (μ-S or μ-O,S) thiocaboxylate groups. The terminal thiocarboxylate ligand binds monodentately (through S) in 1. Structure of 2 is unique as two different molecules, [(PPh3)2Ag(μ-SCOPh)Zn(SCOPh)2] and [(PPh3)2Ag(μ-SCOPh)2Zn(SCOPh)H2O] co-crystallize in the same lattice. The terminal thiocarboxylate ligand is monodentate (S) in the latter while bidentate (O,S) in the former molecule. Electronic spectral behaviors of the complexes have been explained by TDDFT calculations. Luminescence properties of both have been studied in solid state.

New heterobimetallic complexes, [(PPh3)2Ag(μ-SCOR)2Zn(SCOR)(H2O)] [R = th (1) and Ph (2)] have been prepared. Molecular structures of the complexes have been determined by single crystal X-ray diffraction and electronic spectral behaviors of the complexes have been explained by TDDFT calculations.Figure optionsDownload as PowerPoint slide