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921.
Summary The surface dyeability of the poly(vinyl alcohol) fiber with different degree of formalization was studied by measuring -potential of the fiber in alkaline aqueous solutions (pH 10) of a cationic dye Methylene Blue. With the increase in the dye concentration, the sign of the -potential of the fiber changed from negative to positive and thereafter the positive value approximated to saturated value, and the amount of dye adsorbed (expressed in mol/cm2-fiber) increased also. These results may possibly be attributed to the formation of the electrostatic bond between the fiber and the dye. The linear relations were found between and logC
d
and its slope did not change with rise of temperature. The free energy of dyeing G (negative) calculated from the slope of the -logC
id
curve, etc. increased with increasing the degree of formalization of the fiber. This fact corresponds to the increase in the surface dye adsorption with increasing the degree of formalization. With increasing the degree of formalization, the heat of dyeing H (negative) increased and the entropy of dyeing S (positive) decreased. The positive value of S for each fiber, suggests the formation of hydrophobic bond as a driving force to the dyeing of Methylene blue on the fiber surface in addition to the electrostatic bond.This paper is Part XXVII in a series on Studies on -potentials and Surface Dyeability of Natural and Synthetic Fibers in Dye Solution. Part XXVI: T. Suzawa andK. Kawakami, Nippon Kagaku Kaishi1975, No. 7,1134. 相似文献
922.
The Electron impact mass spectra of (CO)3 MC6H5—X complexes (M = Cr, W; X = OCH3, OC4H9, CO2CH3, CO2C4H9) were recorded. From metastable transitions and by high-resolution measurements complete fragmentation diagrams were obtained; in some cases comparative structure determinations of fragment ions were carried out by collisional activation. The fragmentation of the tungsten complexes considerably differs from that of the chromium compounds. The differences may be attributed to the stronger-electrophilic character as well as to the more pronounced tendency of tungsten to attain higher oxidation states. 相似文献
923.
E.B. Lobkovskii G.L. Soloveichik A.I. Sisov B.M. Bulychev A.I. Gusev N.I. Kirillova 《Journal of organometallic chemistry》1984,265(2):167-173
The structure of a titanium aluminium hydride complex of composition [(C5H5)2TiAlH4]2(CH3)2NC2H4N(CH3)2C6H6 has been determined by X-ray diffraction. The complex forms triclinic crystals with unit cell dimensions a = 8.406(2), b = 10.117(2), c = 11.269(3) Å; α = 112.01(2)°, β = 109.25(2)°, γ = 87.04(2)°, space group P, Z = 2 and density d = 1.21 g/cm3. The structure was refined to give a discrepancy index R = 0.056. The crystals are composed of centrosymmetric molecules of (Cp2TiAlH4)2TMEDA (Cp = η5-cyclopentadienyl) and molecules of crystal benzene. Two moieties of Cp2TiH2AlH2 are linked by a tetramethylethylenediamine molecule (rAlN 2.11 Å). The aluminium atom is bonded to a titanium atom by a double hydride bridge (rAlH b = 1.8, 1.6 Å, rTiH b = 1.6 Å), and has trigonal bipyramidal stereochemistry, [H4N] (rAlH t = 1.6 Å). 相似文献
924.
Synthesis and characterization of a series of Polysulfone (PSF)-Polyester (PEs) block copolymers were studied.The degree of randomness (B) of these block eopolymers was calculated from the intensities of their proton signals in ~1H NMR spectra and lies in the region of 0相似文献
925.
926.
Summary A method for the separation of substituted tetraphenylporphyrins by preparative liquid chromatography is reported. The quality of the columns formed by axial compression of various stationary phases is tested. 相似文献
927.
Selective laser-induced phototautomerism of free-base porphin in different n-alkanes (n-hexane, n-heptane, n-octane, nnonane, n-decane, n-undecane and n-dodecane) has been used to identify tautomer splittings in a number of sites in polycrystalline samples at 2 K. Pairs or lines arising from the two molecular orientations in each site can be reversibly transformed into each other. In the odd n-alkanes the occupation of different sites was not dependent on the rate at which the samples were frozen, but in the even n-alkanes metastable sites were only occupied following rapid quenching. 相似文献
928.
Imines of (1S,9S)-t-butyl-9-amino-octahydro-6,10-dioxo-6H-pyridazino[1,2-a][1,2]diazepine-1-carboxylate undergo thermal (toluene, 110°C) or LiBr-DBU catalysed (MeCN, room temperature) regio- and stereo-specific cycloaddition to a range of chiral dipolarophiles giving enantiopure spiro-cycloadducts in excellent yield. The reactions proceed via intermediate NH azomethine ylides and litho azomethine ylides, respectively and results in the multiplication of chiral centres from 2 (one of which is lost in the process) to 5. 相似文献
929.
Summary A possibility of obtaining insoluble gels with the help of freezing-thawing procedures was demonstrated on an example of aqueous solutions of a thiol-containing poly(acryl amide) derivative. The gel formation was proved to occur as a result of oxidation of free SH groups of polymer chains by water-dissolved air oxygen. 相似文献
930.
Fereidoon Shahidi 《Journal of solution chemistry》1983,12(4):295-301
The partial molar volumes at infinite dilution for a number of hydrochlorides and sodium salts of N-methyl derivatives of , -aminocarboxylic acids in water at 25°C are measured and related to their van der Waals volumes. Results indicate that 4.96±0.48 water molecules hydrate a betaine hydrochloride. Volumes of proton ionization and interaction terms are evaluated. Group contributions to the partial molar volumes are also reported. 相似文献