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71.
Summary The halogen oxidation and nitrosylation of cis-[(SB)M-(CO)4] [M = Cr or Mo, SB = N,N-ethylenebis(p-tolualideneimine), N,N-ethylenebis(p-N,N-dimethylaminobenzalideneimine) or N,N-ethylenebis(methyl-p-methoxyphenylketimine); M = Mo, SB = N,N-ethylenebis-(cinnamylideneimine) or N,N-ethylenebis(methyl-p-methylphenylketimine)] have been studied. Halogenation of [(SB)Cr(CO)4] yielded [(SB)CrX2] (X = Cl, Br or I) where-as [(SB)Mo(CO)4] gave [(SB)Mo(CO)3X2] (X = Br or I) and [(SB)MoX
x
] (X = I, n = 2; X = Cl or Br, n = 4). NOCl produced [(SB)Cr(NO)2Cl2] and [(SB)Mo(CO)2(NO)Cl] when reacted with the corresponding [(SB)M(CO)4]. The complexes were characterized by physico-chemical and spectroscopic measurements. 相似文献
72.
Summary Nitrosochromotropic acid gives a violet coloured soluble complex with CuII in ammonium chloride-ammonium hydroxide buffer solution, which is less stable than CuII-EDTA complex. When microquantities of CuII solution containing 1 or 2 drops of nitrosochromotropic acid in the ph range 7.25 to 8.00, are titrated with EDTA, a sharp colour change from violet to orange occurs at the end point. The method of titration can be carried out from 20° to 40° C, but the copper complex dissociates at higher temperature and gives low results. The separation of Zn2+, Cd2+, Co2+, Ni2+, Pb2+ and alkaline earths, is necessary as they interfere in the titrations with EDTA.
Zusammenfassung Nitrosochromotropsäure bildet mit Kupfer(II) in Ammoniumchlorid-Ammoniak-Pufferlösung einen violett gefärbten löslichen Komplex, der weniger stabil ist als der Kupfer(II)-ÄDTA-Komplex. Mikromengen Kupfer(II) können imph-Bereich von 7,25–8,00 unter Zusatz von 1–2 Tropfen Nitrosochromotropsäurelösung als Indicator mit ÄDTA-Lösung titriert werden, wobei am Endpunkt ein scharfer Umschlag von Violett nach Orange erfolgt. Die Temperatur der Lösung soll 20–40° C betragen; bei höherer Temperatur erhält man zu niedrige Werte, da der Kupferkomplex dann dissoziiert. Zn2+, Cd2+, Co2+, Ni2+, Pb2+ und Erdalkalien müssen vor der Titration abgetrennt werden.相似文献
73.
R. S. Tewari A. Awasthi A. K. Srivastava M. Kumar 《Journal of polymer science. Part A, Polymer chemistry》1984,22(8):1875-1882
The ylide 4-picolinium, p-chloro phenacylide-initiated thermal polymerization of ethyl methacrylate (EMA) was studied. 4-Picolinium p-chloro phenacylide induces the thermal polymerization of ethyl methacrylate at 65°C. The rate of polymerization (Rp) rose as the initiator concentration increased from 2 × 10?3 to 4 × 10?3 M and the initiating exponent was computed as 1.9. The Rp decreased as the concentration of ylide increased from 6 × 10?2 to 1M. The greater initiator concentration also affected the molecular weight inversely. The polymerization was carried out at different temperatures and the overall activation energy was computed as 4.08 Kcal/mol. Polymerization was inhibited in the presence of hydroquinone as a radical scavenger. Kinetic studies and other data show that the overall polymerization takes place in a radical mechanism. The various kinetic parameters, such as the rate and average degree of polymerization, molecular weight, and energy of activation of the present system, were evaluated. 相似文献
74.
Aquo, ammonia and pyridine complexes of copper(II) with 5,5-thiodisalicylic acid have been investigated by TG and DTG. All these complexes decompose in three distinct steps, viz. dehydration, loss of axial bases and decarboxylation of the aromatic ligand. The thermal curves of the aquo and pyridine complexes show water loss in two distinct steps. The decreasing order of thermal stability of the complexes is py > NH3 > H2O.
Zusammenfassung Aquo-, Ammoniak- und Pyridinkomplexe von Kupfer(II) mit 5,5-Thiodisalicylsäure wurden durch TG und DTG untersucht. Diese Komplexe werden in den drei Stufen, Dehydratisierung, Verlust axialer Basen und Decarboxylierung des aromatischen Liganden zersetzt. Die Abbaukurven der Aquo- und Pyridinkomplexe zeigen einen Wasserverlust in zwei Stufen. Die abnehmende Reihenfolge der Thermostabilität der Komplexe ist py > NH3 > H2O.
, (II) 5,5- . , : , . - , . : > NH3 > 2.相似文献
75.
Gupta Madan Mohan Srivastava Alpana Tripathi Arvind Kumar Misra Himanshu Verma Ram Kishore 《平面色谱法杂志一现代薄层色谱法》2006,19(4):282-287
JPC – Journal of Planar Chromatography – Modern TLC - High-performance thin-layer chromatography (HPTLC) has been used for normal-phase separation of the components of hexane,... 相似文献
76.
The force constants, Coriolis coupling constants and mean amplitudes of vibration at 0, 298.16 and 500 K for GaF63?FeF63? have been reported for the first time employing recent vibrational data. The results are discussed in the light of available information. 相似文献
77.
Semi theoretical models have been proposed to account for the mechanism of membrane oscillations involving, electrokinetic phenomena in systems where (i) concentration difference deltaC is finite and deltaP is varying but the current is fixed, and (ii) deltaC=0, pressure difference deltaP is fixed across the membrane and imposed current is fixed. The formalism leads to the van der Pol equation in both cases. Computer simulation has also been attempted, which indicates oscillations in the former case. 相似文献
78.
A model iodophenyl imidazole ribonucleoside has been synthesized to study biodistribution properties in laboratory animals. The key intermediate 5-amino-1-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)imidazole-4-[N-(p-iodophenyl)carboxamide] ( 5 ) was synthesized by coupling N-succinimidyl-5-amino-1-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)imidazole-4-carboxylate ( 4 ) and p-iodoaniline. Deacetylation of the intermediate compound gave 5-amino-1-β-D-ribofuranosylimidazole-4-[N-(p-iodophenyl)]carboxamide ( 6 ). Ring annulation via diazotization of 5 gave 7-(2,3,5-tri-O-acetyl-β-D-ribofuranosyl)imidazo[4,5-d]-v-triazin-[3-N-(p-iodophenyl)]-4-one ( 7 ). Subsequent deacetylation of 7 afforded 7-β-D-ribofuranosylimidazo[4,5-d]-v-triazin-[3-N-(p-iodophenyl)]-4-one ( 8 ). The radiolabeled compounds, [125I] 5 and [125I] 6 were prepared in a manner similar to the corresponding unlabeled compounds except that p-[125I]iodoaniline was used for coupling with 4 . Biodistribution studies of iodine-125-labeled 5 and 6 were performed in female Fischer rats and tumor bearing nude mice. Compound 6 showed uptake in the brain and proliferating tissues such as tumor and bone-marrow. 相似文献
79.
The authors present six general integral formulas (four definite integrals and two contour inegrals) for theH-function of several complex variables, which was introduced and studied in a series of earlier papers by H. M. Srivastava and R. Panda (cf., e.g., [25] through [29]; see also [14] through [18], [20], [24], [32], [34], [35], [37], and [38]). Each of these integral formulas involves a product of the multivariableH-function and a general class of polynomials with essentially arbitrary coefficients which were considered elsewhere by H. M. Srivastava [21]. By assigning suiatble special values to these coefficients, the main results (contained in Theorems 1, 2 and 3 below) can be reduced to integrals involving the classical orthogonal polynomials including, for example, Hermite, Jacobi [and, of course, Gegenbauer (or ultraspherical), Legendre, and Tchebycheff], and Laguerre polynomials, the Bessel polynomials considered by H. L. Krall and O. Frink [9], and such other classes of generalized hypergeometric polynomials as those studied earlier by F. Brafman [3] and by H. W. Gould and A. T. Hopper [8]. On the other hand, the multivariableH-functions occurring in each of our main results can be reduced, under various special cases, to such simpler functions as the generalized Lauricella hypergeometric functions of several complex variables [due to H. M. Srivastava and M. C. Daoust (cf. [22] and [23])] which indeed include a great many of the useful functions (or the products of several such functions) of hypergeometric type (in one and more variables) as their particular cases (see,e. g., [1], [10] and [39]). Many of the aforementioned applications of our integral formulas (contained in Theorems 1, 2 and 3 below) are considered briefly. Further usefulness of some of these consequences of Theorems 1 and 2 in terms of the classical orthogonal polynomials is illustrated by considering a simple problem involving the orthogonal expansion of the multivariableH-function in series of Jacobi polynomials. It is also shown how these general integrals are related to a number of results scattered in the literature. 0261 0262 V 相似文献
80.
IR relative integrated intensities and half-widths of rocking (R) and wagging (W) bands of water in MnCl2 · 2H2O and CoCl2 · 2H2O are presented at 300 K and 120 K. Departure of observed intensity into DW/DR from those predicted by the fixed dipole model is attributed to anisotropic dynamic changes in dipole during these oscillations. A quantity representing the variation of this anisotropy between W and R oscillations is computed and its origin is discussed. An increase by 20% to 50% in both DW and DR on lowering the temperature has also been discussed. 相似文献