State Key Laboratory of Coordination Chemistry, School of Chemistry and Chemical Engineering, Nanjing University, Nanjing 210093, China.
Dalton Trans. 2013 Nov 28;42(44):15625-36. doi: 10.1039/c3dt52331d.
Eight metal complexes of the type M(tpy)2 (tpy = 2,2':6',2''-terpyridine) featuring four pendant pyridine rings are reported and characterised by NMR, MS, absorption spectroscopy and electrochemical methods. Palladium-mediated Suzuki and Sonogashira cross-coupling reactions were performed on both free 4'-(3,5-dibromophenyl)-tpy and its Ru(II) complex in good yields. The ready N-alkylation of the pendant pyridyl units has significant influence on the absorption and electrochemical reduction of the complexes, processes which are localised on the periphery and leaves the Ru(tpy)2 core essentially unaffected. The binding of metal ions by the free pyridines is also demonstrated as means of assembling larger ordered non-covalent structures.
