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141.
Yoshio Imai N. N. Maldar Masa-Aki Kakimoto 《Journal of polymer science. Part A, Polymer chemistry》1984,22(12):3771-3778
New soluble aromatic polyazomethines with inherent viscosities of 0.4–0.8 dL/g were prepared by the solution polycondensation of 2,5-bis(4-aminophenyl)-3,4-diphenylthiophene, bis(4-aminophenyl) ether, and aromatic dialdehydes in o-chlorophenol at 20°C. The copolyazomethines are generally soluble in chlorinated hydrocarbons, amide-type or phenolic solvents. The thermal stability of the polymers, which showed no weight loss up to 400°C in both air and nitrogen atmospheres. 相似文献
142.
Moriya Y Hasegawa T Hayashi K Maruyama M Nakata S Ogawa N 《Analytical and bioanalytical chemistry》2003,376(3):374-378
Visible reflection spectra of diprotonated meso-tetraphenylporphyrin adsorbates spontaneously formed at a dodecane-aqueous sulfuric acid interface have been measured using a home-made device comprising a prism-cell and variable-angle optics. The tilt angle of the pyrrole ring plane was estimated to be 47 degrees from the interface normal by use of an experimentally evaluated molecular density (1.20x10(-10) mol cm(-2)) of the diprotonated molecule in a monolayer form at the liquid-liquid interface. Positive and negative bands have been observed in the p-polarized partial internal reflection (p-PIR) spectra, whose band locations correspond to those in p-polarized external reflection (p-ER) spectra. Nevertheless, the bands in the p-PIR exhibited reversed sign to those of p-ER spectra. These suggest that the surface selection rule of the p-PIR spectrometry has a reversal rule of p-ER and p-PIR can also be used for the analysis of molecular orientation. 相似文献
143.
The α-haloester having an internal double bond was allowed to react with a catalytic amount of Pd(PPh3)4 to afford a cyclized product in a fairly good yield and the same product was obtained by treatment with Pd(OAc)2 to ketene silyl acetal. 相似文献
144.
Eisaku Nomura Yoshio Otsuji Hisaji Taniguchi 《Journal of inclusion phenomena and macrocyclic chemistry》1995,23(1):53-63
This paper deals with the ability ofp-tert-butylcalix[6]arene derivative1, which has six 3,6,9-trioxadecyl substituents at the phenolic oxygens, to encapsulate CT complexes of alkadienes with iodine. By adding I2 to alkadienes in CH2Cl2 in the presence of1, the absorbance at 363 nm, which was ascribed to I
3
–
ion, increased in the order: 1,5-hexadiene<1,9-decadiene 1,7-octadiene. The reactivity features of the CT complexes in the presence of1 are discussed. 相似文献
145.
146.
Wood TE Dalgleish ND Power ED Thompson A Chen X Okamoto Y 《Journal of the American Chemical Society》2005,127(16):5740-5741
Helical zinc(II) complexes of bis(dipyrromethene)s bearing homochiral amide substituents were synthesized. Analysis of the products by chiral HPLC showed two diastereomeric major products and showed that dipyrromethene double-nuclear helicates are stereochemically stable and do not interconvert. Circular dichroism (CD) studies showed that the complexation reactions had proceeded with modest diastereomeric excesses. Analysis of an analogous symmetric zinc(II) bis(dipyrromethene) lacking homochiral substituents that could act as chromophores discounted induced CD by the chiral auxiliaries. 相似文献
147.
Sensitive, reactive, and hydrophilic fluorogenic reagents for thiols with the benzofurazan skeleton, 4-(N-acetylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole (AcABD-F) and 4-(N-trichloroacetylaminosulfonyl)-7-fluoro-2,1,3-benzoxadiazole (TCAcABD-F) have been developed. These reagents reacted with thiols within 10 min at 60 degrees C. AcABD-F and TCAcABD-F themselves do not fluoresce but are strongly fluorescent after the reaction with thiol compounds. The generated derivatives were highly water-soluble, since they dissociated a proton and ionized in the neutral pH region. The derivatives with four biologically important thiol compounds were separated on a reversed-phase HPLC column and detected fluorometrically at 504 nm with excitation at 388 nm. The detection limit attained for homocysteine with AcABD-F was 25 fmol on column (11 nM) (signal-to-noise ratio = 3), and that for glutathione with TCAcABD-F was 45 fmol on column (20 nM). 相似文献
148.
Yoshio Toda Takashi Ohno Fumikazu Hatayama Hisashi Miyata 《Reaction Kinetics and Catalysis Letters》1998,65(2):213-217
The adsorption of pyridine on V2O5−WO3/ZrO2 has been studied by FTIR. In V2O5/ZrO2 (2 wt.%), the number of both Br?nsted and Lewis acidic sites increased with the addition of WO3, while in V2O5/ZrO2 (5 wt.%), Br?nsted sites increased and Lewis sites did not change. 相似文献
149.
Yoshio Masuda 《Thermochimica Acta》1980,39(3):235-241
The thermal dehydration reactions of two kinds of copper(II) formate dihydrate, which differ in origin and preparation history, have been investigated by means of TG, DTA and DSC. The kinetics of isothermal dehydration were studied by weight loss, and the difference in kinetic behavior between these two samples was related to the difference in origin and preparation history. On the whole, the dehydration mechanisms of these two samples were found to be phase boundary controlled contracting interface reactions. 相似文献
150.
Yoshio Masuda 《Thermochimica Acta》1983,60(2):203-210
The thermal dehydration of some rare earth metal formate dihydrates were studied by means of thermogravimetry, differential thermal analysis and differential scanning calorimetry.The dehydration took place successively as a one step reaction for all of the formate dihydrates examined. The reaction order of dehydration was found to be for all of the salts examined, which indicated that the rate of dehydration was controlled by a chemical process at a phase boundary.The values of the activation energy, frequency factor and the enthalpy change of dehydration for all of the dihydrates were 108–142 kJ mole?1, 1016–1017 min?1 and 109–147 kJ mole?1, respectively.Both the temperature at which the dehydration occurred and the enthalpy change increased as the reciprocal of the radius of the metallic ion increased. 相似文献