Nature of the lowest energy excited state of a bis-phenanthroline [2]-catenand and its Cu(I), Ag(I) and Co(II) complexes

• Published in: Chemical physics letters Vol. 241; no. 5; pp. 555 - 558
• Main Authors: Armaroli, Nicola, Rodgers, Michael A.J., Ceroni, Paola, Balzani, Vincenzo, Dietrich-Buchecker, Christine O., Kern, Jean-Marc, Bailal, Abdelhakim, Sauvage, Jean-Pierre
• Format: Journal Article
• Language: English
• Published: Elsevier B.V 04.08.1995
• ISSN: 0009-2614; 1873-4448
• DOI: 10.1016/0009-2614(95)00666-R

The excited state absorption and emission spectra and lifetimes of a [2]-catenand made of two interlocked 30-membered rings (containing 2,9-dianisyl-1,10-phenanthroline-type coordinating moietes) and its Co 2+, Cu +, and Ag + complexes have been investigated in CH 2Cl 2 solution. The lowest energy excited state is established to be a triplet ligand-centered level for the Ag + complex and a triplet metal-to-ligand charge-transfer level for the Cu + complex. For the Co 2+ complex, where no emission or transient absorption can be observed, the lowest excited state is most likely to be a distorted triplet metal-centered level. No transient absorption can be observed for the lowest energy triplet excited state of the [2]-catenand in CH 2Cl 2 solution because of a fast reaction with solvent molecules.