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The axial interaction of chloroindiumtetraphenylporphyrin with pyridine is studied in a mixed binary benzene-pyridine solvent of variable composition. Thermodynamic parameters of the process are determined. It is concluded on the basis of the results that the binding of pyridine to chloroindiumtetraphenylporphyrin is a low-characteristic reaction.  相似文献   
2.
Luminescence and chemical acceptors methods were used to study the photosensitized formation of singlet molecular oxygen (1O2, 1?? g ) by monomer and aggregated forms of copper tetra-4-(morpholine-4-yl)-tetra-5-(2-naphthoxy)phthalocyanine in benzene, benzene-d 6, acetone, DMF, and pyridine. The values of 1O2 quantum yield were determined. The effectiveness of the 1O2 photoproduction was shown to be reduced due mainly to the aggregation of the copper phthalocyanine molecules.  相似文献   
3.
The kinetics of photosensitized oxidation of anthracene with singlet molecular oxygen (1??g) in organic and aqueous-organic media were studied. The bimolecular rate constant of the reaction was determined, and its relation to solvent properties was revealed. On the basis of the obtained data, the empirical reaction rate constant in water was estimated at 2.3 × 106 l mol?1 s?1.  相似文献   
4.
The photogeneration of the singlet molecular oxygen (1O2) by copper tetra(4-tert-butyl) phthalocyanine in organic solvents of different nature was substantiated. The apparent quantum yields of 1O2in benzene and pyridine were determined. The data obtained indicate an influence of the coordinating properties of the solvent on the 1O2yield. However, this factor is not “critical” as in the case of photogeneration of 1O2by copper tetra(5-tert-butylpyrazino)porphyrazine.  相似文献   
5.
It is evident that the solvent effect on tetracene oxidation by singlet molecular oxygen is predominantly conditioned by a specific solvation of the reaction intermediate in aprotic media that is assumed to be a state with a stressed anionic center.  相似文献   
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7.
The kinetics of tetracene oxidation with singlet molecular oxygen in 1,4-dioxane-water and pyridine-water mixed solvents was studied. Water was found to accelerate the reaction. The kinetic effect observed was explained by the solvation properties of water molecules incorporated into the network of H-bonds.  相似文献   
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