Abstract
Selenosalicylic acid (ortho-HSeC6H4CO2H), the heavy element congener of the widely studied thiosalicylic acid, was prepared by reaction of 2-carboxybenzenediazonium chloride (HO2CC6H4N2+Cl-) with Na2Se2, followed by reduction of the resulting diselenide (SeC6H4CO2H)2 with zinc and acetic acid. The coordination chemistry of the selenosalicylate ligand towards a variety of platinum(ii), palladium(ii), nickel(ii), gold(iii), gold(i), rhodium(iii), iridium(iii) and ruthenium(ii) centres was explored. X-ray crystal structure determinations were carried out on the complexes [Pt(SeC6H4CO2)(PPh3)2], [{(p-cym)Ru(SeC6H4CO2)}2] (p-cym = η6-p-cymene, CH3C6H4CH(CH3)2), [{Cp*Rh(SeC6H4CO2)}2] (Cp* = η5-C5Me5) and [Cp*Ir(SeC6H4CO2)(PPh3)], and comparisons are made with corresponding thiosalicylate complexes. The complexes were characterised by NMR spectroscopy as well as ESI mass spectrometry, which indicated a greater propensity for fragmentation including by selenium loss, compared to the thiosalicylate analogues. Hirshfeld surface analysis to visualise and quantify intermolecular interactions revealed the dominance of H⋯H contacts in [{(p-cym)Ru(SeC6H4CO2)}2] and [Cp*Ir(SeC6H4CO2)(PPh3)].