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Ruthenium diimines are unique in their emissivity. Optical excitation with light of less than 500 nm leads to a strong emission in the 600-700 nm range. All emissive ruthenium complexes appear to undergo intersystem crossing from the absorptive singlet metal-to-ligand charge-transfer (MLCT) state to an emissive triplet MLCT state localized on the lowest-energy metal-ligand pair. In contrast to this currently accepted model, in which a single emissive state is populated and then equilibrates among other states based on a particular set of conditions, the excitation-wavelength dependence of the [(bpy)2RudppH]3+ emission suggests two emissive pathways. One populates an emissive MLCT state localized on a bpy-Ru pair, and the other populates a lower-energy MLCT state localized on the dpp-Ru pair. 相似文献
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Harry D. Gafney 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(9-11):1187-1202
Highly resolved refractive index patterns or patterns of iron oxide are obtained by photolysis of (CH3)3SnI or Fe(CO)5 absorbed onto Coming's code 7930 porous Vycor glass followed by consolidation to a nonporous glass. The photochemistries of the molecules on the glass surface, as well as the distribution and relative sizes of the photodeposited metal oxides, are described. Rutherford backscattering, small-angle x-ray scattering, and scanning electron microscopy show that the glass consolidates about the iron oxide particle but not about the tin oxide particle. Tin oxide chemically modifies the glass surface so that it does not consolidate at temperatures as high as 1200°C. 相似文献
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Fan J Helmy R Kassis A Grunseich A Mangubat P Hicks C Stevens N Gafney HD 《Inorganic chemistry》2003,42(8):2486-2488
Excitation (410 nm) of the bimetallic [(bpy)(2)Ru(CN)(mu-CN)Rh(NH(3))(4)Br](2+) produces the MLCT state localized on the (bpy)(2)Ru(CN)(2) ligand. Photoinduced cleavage of the bimetallic occurs in the presence of [H(+)], and the dependence yields a K(a) equivalent to that for ground-state cis-(bpy)(2)Ru(CN)(2) implying separation of the bimetallic prior to relaxation. The pH dependence and the emissivity of a bimetallic composed of components that individually quench at a diffusion controlled rate suggest that rupture of the RuCN-Rh bond is due to the reduction in electron density at the cyano ligand that occurs on population of the MLCT state. Unlike known photoinduced metal ligand dissociations, where the excitation energy is consumed in the dissociation, the dissociated "(bpy)(2)Ru(CN)(2) ligand" remains excited. 相似文献
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Aebisher D Azar NS Zamadar M Gandra N Gafney HD Gao R Greer A 《The journal of physical chemistry. B》2008,112(7):1913-1917
Singlet molecular oxygen [1O2 (1Deltag)] is generated cleanly in aqueous solution upon irradiation of a heterogeneous complex, meso-tetra(N-methyl-4-pyridyl)porphine (1) adsorbed onto porous Vycor glass (PVG). The cationic photosensitizer 1 tightly binds onto PVG and gives a stable material, which does not dissociate 1 into the surrounding aqueous phase. The production of 1O2 was measured by monitoring the time-resolved 1O2 (1Deltag) phosphorescence at 1270 nm. Indirect analysis of 1O2 generation was also carried out with the photooxidation of trans-2-methyl-2-pentenoate anion, which afforded the corresponding hydroperoxide. Sensitizer-1-impregnated PVG gives rise to a new singlet oxygen generator but more importantly provides a heterogeneous system for use in water. 相似文献
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