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Tuning of the CT excited state and validity of the energy gap law in mixed ligand complexes of Ru(II) containing 4,4′-dicarboxy-2,2′-bipyridine

✍ Scribed by K. Kalyanasundaram; Md.K. Nazeeruddin


Publisher
Elsevier Science
Year
1992
Tongue
English
Weight
577 KB
Volume
193
Category
Article
ISSN
0009-2614

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✦ Synopsis


Using a series of electron-donating ligands (non-chromophoric or substituted bpy/phen type) the energy of the charge transfer (CT) transition has been varied systematically in mixed ligand complexes of Ru(II), [ Ru(dcbpy),(LL)

  1. In all cases the lowest energy transition is Ruddcbpy CT. The lowering of the CT state energy is caused mainly by increased charge density at the Ru center (tZg level). A comparison of the spectral shift with redox potentials shows that nearly 25% of the increased charge density at the Ru-center is transferred to the dcbpy ligand via mixing of the dn-n* orbitals. The variation in the emission lifetimes and quantum yields in this graded series of complexes is quantitatively interpreted in terms of the energy gap law.