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81.
82.
Kapil Upadhyaya Arya Ajay Rohit Mahar Renu Pandey Brijesh Kumar Sanjeev K. Shukla Rama Pati Tripathi 《Tetrahedron》2013
Fused triazoloquinolines have been prepared starting from (E)-3-(2-nitrophenyl)-1-aryl-prop-2-en-1-ones and sugar or benzyl azides in a sequential [3+2] cycloaddition reaction, followed by one pot Pd–C assisted reduction, cyclization and aromatization. The triazolyl fused quinolines with N1-glycosyl substituents as unnatural nucleosides have inherent potential to generate a library of compounds for bioevaluations. 相似文献
83.
Vivek Parashar Pandey Natasha Jaiswal A. K. Srivastava Sanjeev K. Shukla Rama Pati Tripathi 《Journal of carbohydrate chemistry》2013,32(3):132-146
Several pyridylmethyl-C-β-D-glycosides (3a–3l, 6a, and 6h) were synthesized by refluxing 3-(β-D-glucopyranosyl)/(β-D-cellobiosyl)-propanones and dicyanobenzylidenes with ammonium acetate in anhydrous toluene in moderate to good yields. The reaction involves a C?C Michael addition of enamine, formed from glycosyl ketone and ammonium acetate, to the dicayanobenzylidene derivative; subsequent dehydrative cyclization; and oxidative aromatization. Two of these prototypes, compounds 3e and 3k, were deacetylated to the respective glucopyranosyl methyl pyridines 4e and 4k with NaOMe/MeOH. The synthesized compounds were screened for their in vitro α-glucosidase inhibitory activities and one of the compounds showed 20% inhibition as compared to standard drug acarbose displaying 39% inhibition. 相似文献
84.
Sudhansu Bhusan Dash Nilamber Baral Nrusingha C. Pati Padma L. Nayak 《高分子科学杂志,A辑:纯化学与应用化学》2013,50(7-8):1123-1134
Abstract The kinetics of the aqueous polymerization of acrylonitrile initiated by the peroxydiphosphate-thioacetamide redox system was investigated at 35, 40, and 50°C. The rates of polymerization were measured at different concentrations of oxidant, activator, and monomer. Peroxydiphosphate alone did not initiate polymerization under deaerated and undeaerated conditions. Addition of certain water-miscible organic solvents and neutral salts depress the rate and conversion. On the basis of experimental observations of the dependence of the rate of polymerization on various variables, a suitable kinetic scheme has been proposed. 相似文献
85.
The polymerization of methyl methacrylate initiated by the vanadium acetylacetonate complex was investigated under a nitrogen atmosphere at 50°C. The effect of concentration of monomer, complex, acid, dioxane, inhibitor, and the effect of temperature on the rate of polymerization were studied. The rate of polymerization was found to increase upon increasing the concentrations of the monomer, the initiator, and the acid. The overall activation energy has been computed from the Arrhenius plot and a suitable kinetic scheme has been proposed. 相似文献
86.
New trapezoidal, non-linear optical crystals of glycine potassium nitrate (GPN) have been grown by slow cooling from solutions with an initial pH of 4.3. Chemical composition, phase formation and functional groups have been verified by CHN, EDAX, XRF, NMR, XRD, FTIR and Raman studies. UV studies show a much lower cut off wavelength (195 nm) compared to the much investigated glycine sodium nitrate (GSN). The powder SHG efficiency of GPN is found to be 0.6 times compared to that of potassium dihydrogen phosphate (KDP). Cut and polished crystals exposed to light indicate positive photoconductivity. Electrical conductivity studies show an activation energy of 0.16 eV and the dielectric loss is found to decay drastically at higher frequencies (1 MHz) which is desirable in electronic applications. Vickers microhardness studies indicate a Mayer's index value of 2.78. Well resolved, elongated and oriented etch pits have been observed on the side habit face (220) treated in glacial acetic acid for 5 s. Typical circular features resisting the formation of etch pits representing impurity elements have been observed on the cleavage faces. Moisture has been traced on the surface of the crystals subjected to heat treatment. 相似文献
87.
O'Reilly ME Del Castillo TJ Falkowski JM Ramachandran V Pati M Correia MC Abboud KA Dalal NS Richardson DE Veige AS 《Journal of the American Chemical Society》2011,133(34):13661-13673
Synthetic and kinetic experiments designed to probe the mechanism of O(2) activation by the trianionic pincer chromium(III) complex [(t)BuOCO]Cr(III)(THF)(3) (1) (where (t)BuOCO = [2,6-((t)BuC(6)H(3)O)(2)C(6)H(3)](3-), THF = tetrahydrofuran) are described. Whereas analogous porphyrin and corrole oxidation catalysts can become inactive toward O(2) activation upon dimerization (forming a μ-oxo species) or product inhibition, complex 1 becomes more active toward O(2) activation when dimerized. The product from O(2) activation, [(t)BuOCO]Cr(V)(O)(THF) (2), catalyzes the oxidation of 1 via formation of the μ-O dimer {[(t)BuOCO]Cr(IV)(THF)}(2)(μ-O) (3). Complex 3 exists in equilibrium with 1 and 2 and thus could not be isolated in pure form. However, single crystals of 3 and 1 co-deposit, and the molecular stucture of 3 was determined using single-crystal X-ray crystallography methods. Variable (9.5, 35, and 240 GHz) frequency electron paramagnetic resonance spectroscopy supports the assignment of complex 3 as a Cr(IV)-O-Cr(IV) dimer, with a high (S = 2) spin ground state, based on detailed computer simulations. Complex 3 is the first conclusively assigned example of a complex containing a Cr(IV) dimer; its spin Hamiltonian parameters are g(iso) = 1.976, D = 2400 G, and E = 750 G. The reaction of 1 with O(2) was monitored by UV-visible spectrophotometry, and the kinetic orders of the reagents were determined. The reaction does not exhibit first-order behavior with respect to the concentrations of complex 1 and O(2). Altering the THF concentration reveals an inverse order behavior in THF. A proposed autocatalytic mechanism, with 3 as the key intermediate, was employed in numerical simulations of concentration versus time decay plots, and the individual rate constants were calculated. The simulations agree well with the experimental observations. The acceleration is not unique to 2; for example, the presence of OPPh(3) accelerates O(2) activation by forming the five-coordinate complex trans-[(t)BuOCO]Cr(III)(OPPh(3))(2) (4). 相似文献
88.
Palas Baran Pati Eunji Jin Yohan Kim Yongchul Kim Jinhong Mun So Jung Kim Seok Ju Kang Wonyoung Choe Geunsik Lee Hyung‐Joon Shin Young S. Park 《Angewandte Chemie (International ed. in English)》2020,59(35):14891-14895
Polycyclic aromatic hydrocarbons (PAHs) are key components of organic electronics. The electronic properties of these carbon‐rich materials can be controlled through doping with heteroatoms such as B and N, however, few convenient syntheses of BN‐doped PAHs have been reported. Described herein is the rationally designed, two‐step syntheses of previously unknown ixene and BN‐doped ixene (B2N2‐ixene), and their characterizations. Compared to ixene, B2N2‐ixene absorbs longer‐wavelength light and has a smaller electrochemical energy gap. In addition to its single‐crystal structure, scanning tunneling microscopy revealed that B2N2‐ixene adopts a nonplanar geometry on a Au(111) surface. The experimentally obtained electronic structure of B2N2‐ixene and the effect of BN‐doping were confirmed by DFT calculations. This synthesis enables the efficient and convenient construction of BN‐doped systems with extended π‐conjugation that can be used in versatile organic electronics applications. 相似文献
89.
We show that minimization of the Higgs potential within the unifying symmetry [SU(4)]4 together with the requirement that the GIM mechanism should emerge as a consequence of spontaneous breakdown of the symmetry on the flavor side leaves us with onechoice regarding the nature of parity violation: charged current as well as neutral current parity violations must have one and the same origin; if the former is à la SU(2)L×U(1), so must be the latter. Furthermore, there appear to be only two possible alternative forms for the low-energy electroweak symmetry: (i) the familiar SU(2)L×U(1), and (ii) and extended symmetry SU(2)L×U(1)L×?(1)R differing from the former only in the parity-conserving neutral current sector. 相似文献
90.