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A meso–meso β‐β β‐β triply linked subporphyrin dimer 6 was synthesized by stepwise reductive elimination of β‐to‐β doubly PtII‐bridged subporphyrin dimer 9 . Dimer 6 was characterized by spectroscopic and electrochemical measurements, theoretical calculations, and picosecond time‐resolved transient absorption spectroscopy. X‐ray diffraction analysis reveals that 6 has a bowl‐shaped structure with a positive Gaussian curvature. Despite the curved structure, 6 exhibits a remarkably red‐shifted absorption band at 942 nm and a small electrochemical HOMO–LUMO gap (1.35 eV), indicating an effectively conjugated π‐electronic network.  相似文献   

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Mössbauer parameters of frozen salt solutions could be correlated with apparent degree of dissociation, γ. KSnCl3 and KSnBr3 were dissolved in 0.5 M H2SO4, whereas NH4 SnCl3 was dissolved in 0.5 M HClO4. Mössbauer studies were made at different concentrations.  相似文献   

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The chemical state of particles of 5wt% Fe in α-Fe2O3 and the subsequently reduced iron particles supported on different particle size (50–200 mesh) of silica (SiO2), alumina (Al2O3), magnesium oxide (MgO) and carbon (C) was examined by Mössbauer spectroscopy at various stages of calcination and reduction. The particle size of the α-Fe2O3 supported on different mesh sizes (50, 100, 140, 200 mesh) of SiO2 has been determined. The strength of metal-support interaction with respect to the kind of support was found to be MgO>SiO2>Al2O3>C.  相似文献   

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The effect of the addition of a second metals such as Zn and Ni on the calcinaton and reduction of alumina, magnesia and silicasupported iron catalysis with total iron loading of 5wt% is investigated by Mössbauer spectroscopy. It is shown that the reducibility of supported α-Fe2O3 is gradually increased by adding the second metal. The values of the magnetic hyperfine field obtained from Mössbauer spectra for the Zn or Ni-added α-Fe2O3 or Fe catalysts decreased with increasing second metal loading.  相似文献   

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