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Zeolite-entrapped ruthenium(II) complexes with bipyridine and related ligands. Elimination of ligand-field-state deactivation and increase in [sup 3]MLCT state lifetimes

Journal Article · · Journal of the American Chemical Society; (United States)
DOI:https://doi.org/10.1021/ja00071a049· OSTI ID:5067343
;  [1];  [2]
  1. Marquette Univ., Milwaukee, WI (United States)
  2. Idaho State Univ., Pocatello, ID (United States)
Several homoleptic and bis-heteroleptic tris-ligated polypyridine complexes of Ru(II) have been prepared in the zeolite Y supercages. Ru(L)[sub n](L[prime])[sub 3[minus]n]-Y (where n = 0, 1, 2, 3 and L, L[prime] = bpy, dmb, mmb, and bpz) complexes have been investigated by electronic absorption, electronic emission, resonance Raman, and time-resolved resonance Raman spectroscopies. Excited-state lifetimes of the entrapped complexes have been measured and their temperature dependence established. While entrapment of the complexes in the zeolite matrix introduces no major modifications in structure or electron distribution, it does induce changes in the efficiency of various excited state energy dissipation pathways, the major effect being an increase in the energy of the metal-centered dd excited states which leads to elimination of one of the major decay and decomposition pathways. 33 refs., 6 figs., 3 tabs.
OSTI ID:
5067343
Journal Information:
Journal of the American Chemical Society; (United States), Journal Name: Journal of the American Chemical Society; (United States) Vol. 115:18; ISSN JACSAT; ISSN 0002-7863
Country of Publication:
United States
Language:
English