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1.
2.
Shaginian A Patel M Li MH Flickinger ST Kim C Cerrina F Belshaw PJ 《Journal of the American Chemical Society》2004,126(51):16704-16705
We describe the development of photolabile protecting groups based on the 3,4,5-trimethoxyphenacyl group (TMP). Orthogonal safety-catches were created by introducing an acid-activatible dimethyl ketal (AA-TMP) and an oxidatively activatible 1,3-dithiane (OA-TMP) into the photolabile TMP group. We demonstrate the application of these protecting groups in light-directed synthesis of small molecule microarrays with diversity elements radially attached to a hydroxyproline scaffold. 相似文献
3.
The role of “trapped electron,” photon, and vibronic state coupling has been worked out in relation to an aspect of cancer, namely, to the activity of an anticancer drug. The main emphasis for such study comes from the fact that in cancerous systems the participation of usual electronic states of the molecule may not be sufficient. Because of disorder in the cancer tumour, additional states, viz. trapped electron states, could be formed in the manner of localised states in solids. The drug activity of mitomycin C obtained in this way agrees with the experimental values. An additional feature of the study is that it shows that it will be effective mainly in the initial phases of cancer. 相似文献
4.
Mukul Biswas Madhusudan Banerjee Mrinal M. Maiti 《Journal of polymer science. Part A, Polymer chemistry》1984,22(9):1997-2004
Copper(II)-exchanged-13X molecular sieves, prepared from four copper(II) salts, namely, sulfate, nitrate, chloride, and acetate, and their activities in the polymerization of N-vinylcarbazole at a fixed copper ion exchange level were studied. From the kinetic characteristics of polymerization it was established that the variation in activities of the Cu-exchanged sieves is due primarily to the difference in the pH of the original salt solution, which is responsible for the varying degree of proton exchange with the zeolite during copper ion exchange. A first-order dependence of the rate of polymerization was observed with respect to H+ ion concentration of the original copper-salt solution. It was further established that the rate of polymerization of exchanged copper ion, at a hypothetical zero proton concentration, is low. A mechanism of polymerization of NVC on copper-exchanged-13X zeolite was suggested on the basis of the results obtained. 相似文献
5.
Powder X-ray diffraction (XRD) and Raman spectroscopic study of order-disorder-phase transition with increase in the content of Gd in Nd2−yGdyZr2O7 solid solution is being reported. It has been observed from Rietveld analysis that with increase in concentration of Gd in Nd2−yGdyZr2O7, the value of the x parameter of the 48f oxygen changes from 0.332(1) to 0.343(1) with a sudden change in the slope for y=1.8, which indicates that the structure is transforming from ordered pyrochlore to disordered pyrochlore. In addition to that a sudden and drastic change in the Raman spectra including changes in the position and width of several Raman modes beyond y?1.8 has also been observed which has been correlated with increasing disorder. Based on these studies, it is suggested that there is a discontinuous order-disorder transition from ‘perfect pyrochlore’ to ‘defect pyrochlore’ phase in Nd2−yGdyZr2O7 solid solution. 相似文献
6.
Mukul Biswas Madhusudan Banerjee Mrinal M. Maiti 《Journal of polymer science. Part A, Polymer chemistry》1985,23(10):2631-2646
Kinetics of polymerization of N-vinylcarbazole over Co(II)-13X molecular sieves in toluene have been studied. The rate of polymerization (Rp) has been found to be second order with respect to percent exchange level of Co(II) and also to the NVC concentration at all the reaction temperatures of 40, 50 and 60°C. The rate increases with decreasing pH of the original exchanging salt solution up to a pH of about 3.5, beyond which it falls. The overall activation energy of polymerization has been found to decrease with increase in monomer concentration, exchange level of Co(II), and the hydrogen ion concentration of the original exchange solution. Average degree of polymerization also follows a similar trend. A mechanism of polymerization involving simultaneous propagation on both metal ion Co(II) and proton on a zeolite surface has been suggested. The two propagation routes are characterized by an average activation energy of 10.36 kcal/mol and 5.40 kcal/mol on the metal ion and proton centers, respectively. 相似文献
7.
A novel series of complexes of the type [M(TML)X2]; where TML is a tetradentate macrocyclic ligand; M = Co(II), Ni(II), Cu(II) or Zn(II); X = Cl−, CH3COO− or NO
3
−
have been synthesized by template condensation of benzil and thiocarbohydrazide in the presence of divalent metal salts in
methanolic medium. The complexes have been characterized with the help of elemental analyses, conductance measurements, molecular
weight determination, magnetic measurements, electronic, NMR, infrared and far infrared spectral studies. Electronic spectra
along with magnetic moments suggest the six coordinate octahedral geometry for these complexes. The low value of molar conductance
indicates them to be non-electrolytes. The biological activities of metal complexes have been tested in vitro against a number of pathogenic bacteria to assess their inhibiting potential. 相似文献
8.
S. N. Achary B. R. Ambekar M. D. Mathews A. K. Tyagi P. N. Moorthy 《Thermochimica Acta》1998,320(1-2):239-243
Volume thermal expansion behaviour of a number of rare-earth oxyfluorides (REOF) have been studied using high-temperature X-Ray diffractometry (HT-XRD) in the 298–1075 K range in air. The studies revealed an anomalous expansion for each compound associated with phase transition. The phase transition temperature and the coefficient of volume thermal expansion of five compounds in REOF series determined by this method are reported and compared with our earlier results obtained by dilatometry. 相似文献
9.
Chelates formation of Fe(III) with 7–hydroxy–4–methyl coumarin–6–carboxylic acid (HMCCH)2 and 8–amino–7–hydroxy–4–methyl coumarin (AHMCH) have been studied. It has been observed that Fe(III) forms 1:2 (metal:ligand) chelates with HMCCH2 and AHMCH. The stability constants of these chelates at different ionic strengths and the effect of temperature on the stability constants of these chelates have been studied. The thermodynamic parameters such as entropy change (ΔS), free energy of formation (ΔG) and enthalpy change (ΔH) have also been calculated. The effect of dielectric constant oh the stability constants of these chelates have been studied. Estimation of nanogram quantities of Fe(III) with these ligands and the effect of diverse ions have also been studied and the results have been compared with other methods used for estimation of Fe(III). 相似文献
10.
Saroha Rakesh Panwar Amrish K. Gaur Anurag Sharma Yogesh Kumar Vinay Tyagi Pawan K. 《Journal of Solid State Electrochemistry》2018,22(8):2507-2513
Journal of Solid State Electrochemistry - In the present work, olivine-layered composites, i.e., LiFePO4-Li2MnO3, are successfully synthesized in the form of a single monolithic electrode and layer... 相似文献