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Updated: Jan 10, 2026

Amide Coupling Reaction for the Synthesis of Bispyridine-based Ligands and Their Complexation to Platinum as Dinuclear Anticancer Agents
Published on: May 28, 2014
Introduction of a 4-Hexyl-2-thienyl Substituent on Pyridine Rings as a Route for Brightly Luminescent
Alessia Colombo1, Claudia Dragonetti1, Francesco Fagnani1
1UdR INSTM di Milano, Dipartimento di Chimica, Università degli Studi di Milano, via C. Golgi 19, 20133 Milan, Italy.
Abstract:
The synthesis and characterization of two new complexes, namely Pt(1,3-bis(4-(4-hexyl-2-thienyl)-pyridin-2-yl)-5-mesitylbenzene)Cl and Pt(1,3-bis(4-(4-hexyl-2-thienyl)-pyridin-2-yl)-5-(2-thienyl)benzene)Cl, are reported. Both exhibit luminescence quantum yields approaching unity (Φlum = 0.96-0.99) in the green region of the visible spectrum (534-554 nm) in diluted degassed dichloromethane solution. Similarly to other N^C^N platinum(II) complexes, a broad emission band grows in the deep red region (738-752 nm) upon increasing the concentration, due to the creation of bi-molecular emissive excited states. Interestingly, it appears that the introduction of a 2-thienyl group on the pyridine rings is a route to maintain excellent quantum yields even in concentrated solution. In order to have an insight into the electronic properties of the novel compounds, density functional theory (DFT) and time-dependent (TD)DFT approaches were employed to calculate the molecular geometry, the ground state, the electronic structure and the excited electronic states of the complexes, both as a monomers and dimers in solution.
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