2000
DOI: 10.1021/ic991225h
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A Bibenzimidazole-Containing Ruthenium(II) Complex Acting as a Cation-Driven Molecular Switch

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Cited by 79 publications
(82 citation statements)
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“…On the basis of previous reports, we concluded that the loss of emission indicates subsequent deprotonation of the amine functions, as deprotonated bibenzimidazole ruthenium complexes are generally nonluminescent. [16,18,20,24,28,33] As the mono-deprotonated and fully deprotonated bibenzimidazole ruthenium complexes are usually well-distinguishable even with the naked eye through a transition from bright red to brown to deep violet, the UV/Vis spectra of K0, K1, and K2 were recorded in acetonitrile upon the addition of either TBAF (for K0, cf. Figure 5, right) or TBAOH (for K0, Figure 6).…”
Section: Resultsmentioning
confidence: 99%
“…On the basis of previous reports, we concluded that the loss of emission indicates subsequent deprotonation of the amine functions, as deprotonated bibenzimidazole ruthenium complexes are generally nonluminescent. [16,18,20,24,28,33] As the mono-deprotonated and fully deprotonated bibenzimidazole ruthenium complexes are usually well-distinguishable even with the naked eye through a transition from bright red to brown to deep violet, the UV/Vis spectra of K0, K1, and K2 were recorded in acetonitrile upon the addition of either TBAF (for K0, cf. Figure 5, right) or TBAOH (for K0, Figure 6).…”
Section: Resultsmentioning
confidence: 99%
“…[11][12][13][14] Owing to their remarkably stable photoredox chemistry, many ruthenium polypyridyl complexes are potent chromophores for lightdriven catalysis, [15,16] dye-sensitized solar cells, [17][18][19] and photocatalytic water splitting. [20,21] Crucial factors for their application herein are (1) high chemical stability, (2) intense absorption of visible light, (3) efficient population of a reactive charge-transfer (CT) excited state, and (4) long excitedstate lifetimes (up to the μs range).…”
Section: Introductionmentioning
confidence: 99%
“…In their fully deprotonated state, these complexes act as metalloligands, that is, the deprotonated biimidazole sphere can bind a second metal center such as zinc(II), nickel(II), or copper(I). [1,2,8,9] The binding of these metal centers results in significant changes to their photophysical properties. This feature, which can be observed for various kinds of bi-(benz)imidazole metal complexes, is of paramount importance for this and further studies, as it can provide a spectroscopic tool for the direct observation of proton release from these molecules.…”
Section: Introductionmentioning
confidence: 99%