Abstract

Mononuclear and dinuclear zinc(II) and cadmium(II) complexes, [ZnLCl2] (1) and [Cd2L2Cl4] (2), with a chiral pentacyclic dihydrophenanthroline ligand L bearing a natural monoterpene (–)-α-pinene fragment were synthesized. DFT calculations of the specific rotation [α] and an NMR study show that the molecules of ligand L, complex 1 and the monomeric form of complex 2 exist in CDCl3 solutions with the P-helix conformation for the dihydrophenanthroline moiety. The dihydrophenanthroline fragments of L and mononuclear complex 1 also exists as a P-helix in the solid state, whereas the crystalline dinuclear complex 2 exists as an asymmetric dimer, [Cd2Cl4LPLM], where LP and LM are the ligand with P-helix and M-helix conformations of the dihydrophenanthroline fragment respectively. Full sets of photophysical parameters for L and complexes 1 and 2 have been determined. Compounds L, 1 and 2 display blue luminescence (λmax=427, 405 and 415nm in the solid state, respectively). The ligand L and complex 2 show moderate-to high quantum yields of 44% and 24%, respectively. The quantum yield for complex 1 is 6%. The emission lifetimes increase on going along the spectrum of luminescence, and in the deep red region, a rise of luminescence with times of 200–500ps is observed. These processes can be explained by the migration of excitons and the capture of excitation by “defective” centers.

Full Text
Published version (Free)

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call