TY - JOUR
T1 - Rhenium-based molecular rectangles as frameworks for ligand-centered mixed valency and optical electron transfer
AU - Dinolfo, Peter H.
AU - Williams, Mary Elizabeth
AU - Stern, Charlotte L.
AU - Hupp, Joseph T.
PY - 2004/10/13
Y1 - 2004/10/13
N2 - A series of six neutral, tetrametallic, molecular rectangles has been synthesized that have the form ([Re(CO)3]2BiBzlm) 2-μ,μ′(LL)2, where BiBzlm is 2,2′-bisbenzimidazolate and LL is a reducible, dipyridyl or diazine ligand. X-ray crystallographic studies of the six show that the rectangle frameworks, as defined by the metal atoms, range in size from 5.7 Å × 7.2 Å to 5.7 Å × 19.8 Å. The singly reduced rectangles are members of an unusual category of mixed-valence compounds in which the ligands themselves are the redox centers and interligand electronic communication is controlled by direct ligand orbital overlap rather than by superexchange through the metal ions. Despite nominally identical coordination-defined ligand positioning, the spectrally determined electronic strengths, Hab2, vary by roughly 100-fold. As shown by X-ray crystallography and computational modeling, the observed differences largely reflect detailed geometric configurational differences that can either facilitate or frustrate productive direct orbital overlap.
AB - A series of six neutral, tetrametallic, molecular rectangles has been synthesized that have the form ([Re(CO)3]2BiBzlm) 2-μ,μ′(LL)2, where BiBzlm is 2,2′-bisbenzimidazolate and LL is a reducible, dipyridyl or diazine ligand. X-ray crystallographic studies of the six show that the rectangle frameworks, as defined by the metal atoms, range in size from 5.7 Å × 7.2 Å to 5.7 Å × 19.8 Å. The singly reduced rectangles are members of an unusual category of mixed-valence compounds in which the ligands themselves are the redox centers and interligand electronic communication is controlled by direct ligand orbital overlap rather than by superexchange through the metal ions. Despite nominally identical coordination-defined ligand positioning, the spectrally determined electronic strengths, Hab2, vary by roughly 100-fold. As shown by X-ray crystallography and computational modeling, the observed differences largely reflect detailed geometric configurational differences that can either facilitate or frustrate productive direct orbital overlap.
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U2 - 10.1021/ja0473182
DO - 10.1021/ja0473182
M3 - Article
C2 - 15469297
AN - SCOPUS:5644304207
SN - 0002-7863
VL - 126
SP - 12989
EP - 13001
JO - Journal of the American Chemical Society
JF - Journal of the American Chemical Society
IS - 40
ER -