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Carbon Double Bond (carbon + double_bond)
Selected AbstractsA Nearly Planar Stannene with a Reactive Tin,Carbon Double BondEUROPEAN JOURNAL OF INORGANIC CHEMISTRY, Issue 12 2008Abdoul Fatah Abstract Bis(2,4,6-triisopropylphenyl)-2,7-di- tert -butylfluorenylidenestannane, Tip2Sn=CR2, an isolable stannene that displays a deep-purple colour, was synthesized by dehydrofluorination of the corresponding fluorostannane by tert -butyllithium. It exhibits the shortest Sn=C distance [2.003(5) Å] and the slightest twisting around this unsaturation (10°) among the known stannenes. Its reaction with benzaldehyde according to a [2+2] cycloaddition and that with ,-ethylenic aldehydes and ketones such as crotonaldehyde and methyl vinyl ketone by a [2+4] cycloaddition proceeded in near-quantitative yield. With acetone, an ene reaction occurred. The four-membered ring 1,2-oxastannacyclobutane obtained with benzaldehyde underwent a ring expansion with a second molecule of benzaldehyde to afford the six-membered ring dioxastannacyclohexane.(© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2008) [source] Copper-Catalyzed Oxidative Cleavage of Carbon,Carbon Double Bond of Enol Ethers with Molecular Oxygen.CHEMINFORM, Issue 11 2006Makoto Tokunaga Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF. [source] ChemInform Abstract: Stereocontrolled Synthesis of Carbon,Carbon Double Bond Locked Analogues of Strobilurins Which Are Characterized by a trans-1,2-Disubstituted Cyclopropane Ring.CHEMINFORM, Issue 31 2001Renzo Rossi Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 100 leading journals. To access a ChemInform Abstract of an article which was published elsewhere, please select a "Full Text" option. The original article is trackable via the "References" option. [source] Purification and structure of the major product obtained by reaction of NADPH and NMNH with the myeloperoxidase/hydrogen peroxide/chloride systemFEBS JOURNAL, Issue 10 2001Françoise Auchère The first spectrophotometric study of the reaction of the myeloperoxidase/H2O2/Cl, system with NADPH and NMNH showed that the reaction products were not the corresponding oxidized nucleotides and that modifications would take place on the nicotinamide part of the molecule [Auchère, F. & Capeillère-Blandin, C. (1999) Biochem. J. 343, 603,613]. In this report, in order to obtain more precise information on the structural modifications and mechanism of the reaction, we focus on the purification and isolation of products derived from NADPH and NMNH by RP-HPLC. Electrospray ionization mass spectra indicated that the relative height of the peaks reflected that of the natural isotopic abundance of 35Cl and 37Cl, providing evidence that the products derived from NADPH and NMNH were monochlorinated. Moreover, calculated masses revealed the 1 : 1 addition of HOCl to the molecule. Various 1D and 2D NMR experiments provided data for the assignments of the chemical shifts of protons and carbons and the coupling constants of the protons of the chlorinated nucleotides. Further NOESY experiments allowed the characterization of the spatial structure of the chlorinated product and showed that trans HOCl addition occurred at the C5=C6 carbon double bond of the nicotinamide ring, leading to a chlorohydrin. [source] UV-Light-Driven Immobilization of Surface-Functionalized Oxide Nanocrystals onto Silicon,ADVANCED FUNCTIONAL MATERIALS, Issue 2 2007E. Fanizza Abstract TiO2 nanorods (NRs) and ,-Fe2O3 nanocrystals (NCs) passivated with unsaturated long-chain carboxylic acids, namely 10-undecylenic acid (10UDA) and oleic acid (OLEA), are covalently anchored to Si(100) at room temperature by UV-light-driven reaction of hydrogenated silicon with the carbon,carbon double bond (,CC,) moieties of the capping surfactants. The high reactivity of vinyl groups towards Si provides a general tool for attaching particles of both materials via Si,C bonds. Interestingly, TiO2 NRs were efficiently attached to silicon even when capped by OLEA. This latter finding has been explained by a photocatalytic mechanism involving the primary role of hydroxyl radicals that can be generated upon bandgap TiO2 photoexcitation with UV light. The increased oxide coverage achievable on Si opens access to further surface manipulation, as demonstrated by the possibility of depositing an additional film of Au nanoparticles onto TiO2 via TiO2 -catalyzed visible-light-driven reduction of aqueous AuCl4, ions. Extensive morphological and chemical characterization of the obtained NC-functionalized Si substrates is provided to support the effectiveness of proposed photochemical approaches. [source] Selective extraction of polyunsaturated triacylglycerols using a novel ionic liquid precursor immobilized on a mesoporous complexing adsorbentBIOTECHNOLOGY PROGRESS, Issue 5 2009Patrisha J. Pham Abstract Mesoporous silica (SBA-15) synthesized by using Pluronic123 as the structure-directing template was functionalized by imidazolium-based ionic liquid precursors. Silver salts were then immobilized onto the supported ionic liquids using the incipient wetness impregnation technique. The separation of unsaturated species was achieved through the reversible and specific interaction between silver ions and carbon,carbon double bonds. This adsorbent was examined for the selective separation of polyunsaturated triacylglycerols (PUTAG) using High Pressure Liquid Chromatography (HPLC) with Evaporative Light Scattering Detection (ELSD) as the quantification methodology. AgBF4/SBA15·HPSiOEtIM·PF6 showed an adsorption capacity for linolenin of about 217 mg adsorbed/gram of sorbent. This adsorbent had good selectivity and a high capacity for the most highly unsaturated triacylglycerol when applied to a mixture of triacylglycerols with varying degrees of unsaturation. Consequently, a stepwise methodology was also developed to increase the recovery of the adsorbed components. This adsorbent retained its selectivity and capacity when recycled up to five times. © 2009 American Institute of Chemical Engineers Biotechnol. Prog., 2009 [source] | ||||||||||