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71.
Pradeep Mathur Raj Kumar Joshi Amrendra K. Singh 《Journal of organometallic chemistry》2010,695(24):2687-2694
A facile, one pot, high yield synthesis of α,β-vinylester (1-14) and alkoxy substituted γ-lactones (15-28) has been achieved by the photochemical reaction of terminal acetylene (ferrocenyl phenyl trimethylsillyl, hexyl and cyclohexyl) with alcohol (methanol, ethanol and isopropanol) and carbon monoxide in presence of iron pentacarbonyl as a catalyst. The selectivity of the compounds depends on the time of photolysis of the reaction as well as the solvent used. A stable reaction intermediate ferrole was isolated, and further photolysis with alcohols, resulted in the formation of α,β-vinylester. All the compounds were fully characterised by spectroscopic methods and the molecular structures of compounds 1, 16, 17 and 20 were established crystallographically. 相似文献
72.
73.
We present an analytical proof of the existence of unidirectional optical Bloch oscillations in a waveguide array system. It is shown that the presence of nonreciprocity in the system allows for a complete normal-mode dephasing in one of the propagation directions, resulting in a unidirectional breakdown in Bloch oscillations. A model system consisting of an array of transversely magnetized asymmetric Si/SiO2 waveguides with a magneto-optic cover layer is presented. Large index contrasts between film and cover are critical for practical realizations. 相似文献
74.
75.
Muthiah Manoharan Akin Akinc Rajendra K. Pandey June Qin Philipp Hadwiger Matthias John Kathy Mills Klaus Charisse Martin A. Maier Lubomir Nechev Emily M. Greene Pradeep S. Pallan Eriks Rozners Kallanthottathil G. Rajeev Martin Egli 《Angewandte Chemie (Weinheim an der Bergstrasse, Germany)》2011,123(10):2332-2336
76.
Pradeep Mathur Amrendra K. Singh Vinay K. Singh Shaikh M. Mobin 《Journal of organometallic chemistry》2010,695(7):950-141
Photolysis of a hexane solution of ferrocenylacetylene and sulfur powder in presence of Cr(CO)6 resulted in the formation of 2,6-diferrocenyldithiine and 2,5-diferrocenylthiophene. Similar reactions with Mo(CO)6 or W(CO)6 gave only the thiophene derivative. Formation of ferrocenyl-substituted thioketone complexes was observed in the reaction of ferrocenylacetylene with water and sulfur, in presence of W(CO)6. Use of D2O confirmed water as source of protons for the conversion of acetylenic CH to CH3. 相似文献
77.
Synthesis of Modular “Inorganic–Organic–Inorganic” Polyoxometalates and Their Assembly into Vesicles
78.
Philip Dimitrov Pradeep Iyer Marcel Van Beylen Thieo E. Hogen‐Esch 《Journal of polymer science. Part A, Polymer chemistry》2009,47(8):2198-2206
The anionic polymerization of butadiene initiated with 1,4‐dilithio‐1,1,4,4‐tetraphenylbutane (LiTPB) in diethyl ether (DEE) gives polybutadiene (PBD) with high 1,2 content (>70%), narrow polydispersities (1.04 < Mw/Mn < 1.20), and predicted molecular weights. In THF, this polymerization does not work very well. After removal of DEE and addition of THF, the PBD dianion is end capped quantitatively by addition of 1,1‐diphenylethylene (DPE) to give the diphenylalkyl end capped PBD dianion. Subsequent addition of methyl methacrylate at low temperatures results in the formation of well‐defined PMMA‐b‐PBD‐b‐PMMA triblock copolymers. The results are accounted for by taking into account the effects of Li ion solvation on the BD initiation and end capping of the PBD anion by DPE. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 2198–2206, 2009 相似文献
79.
The oxidation of 34 organic sulphides hy 2,2′-hipyridinium chlorochromate (BPCC) resulted in the formation of the corresponding
sulphoxides. The reaction is first order with respect to both BPCC and the sulphide, and is catalysed by hydrogen ions. The
hydrogen-ion dependence has the form:k
obs = a+b[H+]. The oxidation was studied in 19 different organic solvents. An analysis of the solvent effect by Swain’s equation showed
that the both cation-and anion-solvating powers of the solvents play important roles. The rates of oxidation meta- andp-substituted phenyl methyl sulphides were correlated with Charton’s LDR equation. The rates of theo-compounds showed excellent correlation with the LDRS equation. Oxidation of thep-compounds is more susceptible to the delocalizationeffect. Oxidation of themcompounds exhibited a greater dependence on the field effect. In the oxidation of theo-compounds, the contribution of delocalized effect is slightly more than that of the field effect. The oxidation of alkyl
phenyl sulphides is subject to both polar and steric effects of the alkyl groups. Polar reaction constants are negative, indicating
an electron-deficient sulphur centre in the rate-determining step. A mechanism involving formation of a sulphurane intermediate
in the slow step has been proposed. 相似文献
80.
Sivaiah Areti Jayshree K. Khedkar Sateesh Bandaru Rohit Teotia Jayesh Bellare Chebrolu Pulla Rao 《Analytica chimica acta》2015
A coumarine–imino–C2-glucosyl conjugate (L) was synthesized and characterized. The conjugate L is found to recognize Cu2+ in aqueous HEPES buffer by exhibiting a 95% fluorescence quenching in pH range 7–10 even in the presence of several biologically and ecologically relevant metal ions. Fluorescence on–off behavior has been clearly demonstrated on the basis of the binding variability of Cu2+ to L. The binding has been elicited through the changes observed in fluorescence, absorption, ESI-MS and 1H NMR titrations. All the other thirteen metal ions studied did not show any change in the fluorescence emission. These ions do not interfere with the recognition of Cu2+ by L. The structural features of [CuL]2 complex in both the isomeric forms were established by DFT computational calculations. The utility of L has been demonstrated by showing its sensitivity toward Cu2+ on a thin layer of silica gel. The L gives sensitive fluorescence signals for Cu2+ even in blood serum and exhibits appropriate fluorescence responses in living cells. 相似文献