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11.
Titanosilicates with complete or partial substitution of Ge or Nb in the framework and having the mineral pharmacosiderite topology were hydrothermally prepared and their ion-exchange properties towards Cs were studied for Ti/Ge/Si, Ti/Si, Nb/Ti/Si and pure Ge phases. The basis for the differences in the ion exchange properties measured as distribution coefficients (Kd) for these materials are detailed via structural characterization using the Rietveld refinement technique on the X-ray powder diffraction data. The differences in affinity towards Cs+ result either from the degree of hydration of the exchanger resulting in different coordination environments or the position of cesium ion in the eight-ring channel. 相似文献
12.
Tripathi SK Patel U Roy D Sunoj RB Singh HB Wolmershäuser G Butcher RJ 《The Journal of organic chemistry》2005,70(23):9237-9247
[Structure: see text]. The synthesis and characterization of a series of organochalcogen (Se, Te) compounds derived from benzyl alcohol 13 are described. The synthesis of the key precursor dichalcogenides 15, 22, and 29 was achieved by the ortho-lithiation route. Selenide 18 was obtained by the reaction of the dilithiated derivative 14 with Se(dtc)2. Oxidation of 15 and 22 with H2O2 afforded the corresponding cyclic ester derivatives 17 and 24, respectively. Oxidation of selenide 18 with H2O2 affords the spirocyclic compound 19. The presence of intramolecular interactions in dichalcogenides 15 and 22 has been proven by single-crystal X-ray studies. The cyclic compounds 17 and 19 have also been characterized by single-crystal X-ray studies. GP(X)-like antioxidant activity of selenium compounds has been evaluated by the coupled bioassay method. Density functional theory calculations at the mPW1PW91 level on ditelluride 22 have identified a fairly strong nonbonding interaction between the hydroxy oxygen and tellurium atom. The second-order perturbation energy obtained through NBO analysis conveys the involvement of n(O) --> sigma(Te-Te) orbital overlap in nonbonding interaction. Post wave function analysis with the Atoms in Molecules (AIM) method identified distinct bond critical point in 15 and 22 and also indicated that the nonbonding interaction is predominantly covalent. Comparison between diselenide 15 and ditelluride 22 using the extent of orbital interaction as well as the value of electron density at the bond critical points unequivocally established that a ditelluride could be a better acceptor in nonbonding interaction, when the hydroxy group acts as the donor. 相似文献
13.
Vinod K. Tiwari Archana Singh Hakkim A. Hussain Bhuwan B. Mishra Vyasji Tripathi 《Monatshefte für Chemie / Chemical Monthly》2007,138(7):653-658
Summary. A convenient and high yielding method for the synthesis of diverse dithiocarbamates having various substituents including
alkyl, aryl, heteroaryl, and alkylaryl at the thiol chain or at the amine chain or at both thiol and amine chains were developed
by the one-pot reaction of mercaptans, amines, and bis(benzotriazolyl)methanethione in presence of amidine base under mild
reaction conditions. 相似文献
14.
Singha K Roy A Dutta PK Tripathi S Sahabuddin S Achari B Mandal SB 《The Journal of organic chemistry》2004,69(19):6507-6510
A simple synthesis of chiral spironucleosides and spirobisnucleosides is described. Intramolecular 1,3-dipolar nitrone cycloaddition reaction of d-glucose-derived precursors having olefin at C-3 and nitrone at C-5, C-1, or C-2 (in nor-series) furnished bisisoxazolidinospirocycles 4-7, 11, and 12 in good yields. Reductive ring opening of the isoxazolidine moieties in 4-6 followed by construction of a nucleoside base upon the generated amino groups smoothly yielded spirobisnucleosides 17 and 18 and spironucleosides 20 and 21. 相似文献
15.
Medha Rele Sudhir Kapoor Shweta Hedge Sergej Naumov Tulsi Mukherjee 《Research on Chemical Intermediates》2006,32(7):637-645
Many photo-physical studies have been reported for the detection of Hg2+ ions. Here we present the effect of Hg
2
2+
ions on the absorption and fluorescence of indole-2-carboxylic acid (I2C). Experimental evidence, supported by density functional
theory B3LYP/LANL2DZ/PCM, for the formation of a I2C-Hg
2
2+
complex, is reported for the first time. It was observed that I2C forms a ground-state complex with Hg
2
2+
ions in a ratio of 3:1. The possibility of I2C to be used as a selective novel chemical sensor for the spectrophotometric
detection of mercurous ions is described. 相似文献
16.
Background
Use of enzymes in low water media is now widely used for synthesis and kinetic resolution of organic compounds. The frequently used enzyme form is the freeze-dried powders. It has been shown earlier that removal of water molecules from enzyme by rinsing with n-propanol gives preparation (PREP) which show higher activity in low water media. The present work evaluates PREP of the lipase (from Rhizomucor miehei) for kinetic resolution of (R,S)-β-citronellol. The acylating agent was vinyl acetate and the reaction was carried out in solvent free media. 相似文献17.
Summary Uranium (VI) has been found to give a yellow colour with nicotinamidoxime in alkaline medium which is highly satisfactory for the spectrophotometric estimation of the metal. The optimumph for development of the colour is 10.9–11.5 in presence of a large excess of the reagent, at 10–40C. The colour intensity is measured at 400 m. Sensitivity is 0.045 g uranium per cm2, with a visual identification limit of 5 g uranium per ml. Beer's law is obeyed in the range of 5–40 ppm of the metal with an optimum range of 8–40 ppm. The colour is stable for at least one hour. All the common anions are without effect, excepting however, phosphate, carbonate, and cyanide which are tolerated only in traces. Use of tartrate or EDTA helps to mask effectively all the interfering cations excepting copper, iron and vanadium. 相似文献
18.
Ajit J. Thakkar A. N. Tripathi Vedene H. Smith 《International journal of quantum chemistry》1984,26(2):157-166
The electronic intracule density, a three-dimensional contraction of the spinless electron pair density, is the probability density function for an interelectronic vector. A computationally efficient algorithm for the evaluation of the basic two-electron intracule integral for GTO s is presented. In order to provide an initial understanding of the topography of intracule distributions, anisotropic intracule densities for the X1Σ ground states of the H2 and N2 molecules are reported and analyzed. 相似文献
19.
Summary A study of the Cd(CN)2 +x X– [Cd(CN)2X
x
]
x–
equilibrium (where X = Cl, Br or CNS) has been carried out at 18° and 38° by measuring the solubility of cadmium cyanide in potassium chloride, bromide and thiocyanate at various concentrations, and at a high ionic strength (6 M) maintained with sodium perchlorate to minimise the effect of activity coefficients. Equilibrium constants forx = 1 and 2 have been calculated and clearly favour the situation wherex = 1. H values for the dissociation of [Cd(CN)2X]– have also been calculated. 相似文献
20.
The interactions between oppositely charged surfactant/polymer mixtures have been studied using conductivity and turbidity measurements. The dependence of aggregation phenomenon on the chain length and head group modifications of conventional cationic surfactants, i.e., hexadecyl- (HTAB), tetradecyl- (TTAB), and dodecyltrimethylammonium bromides (DTAB) and dimeric cationic surfactants, i.e., decyl- (DeDGB) and dodecyldimethylgemini bromides (DDGB), is investigated. It was observed that cationic surfactants induce cooperative binding with anionic polyelectrolytes at critical aggregation concentration (cac). The cac values are considerably lower than the critical micelle concentration (cmc) values for the same surfactant. After the complete complexation, free micelles are formed at the apparent critical micelle concentration (acmc), which is slightly higher in aqueous polyelectrolyte than in pure water. Among the conventional and dimeric cationic surfactants, DTAB and DeDGB, respectively, have been found to have least interactions with oppositely charged polyelectrolytes. 相似文献