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Metal Alkoxides (metal + alkoxide)
Selected AbstractsHyperbranched cyclic and multicyclic polymers by "a2+b4" polycondensationsJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 8 2009Hans R. Kricheldorf Abstract At first, theoretical aspects of "a2+b4" polycondensations (meaning polycondensations of difunctional and tetrafunctional monomers) are discussed and compared with what is known about "a2+b3" polycondensations. The following review of experimental results is subdivided into three sections. First, syntheses of hyperbranched polyethers and polyesters by polycondensations based on equimolar feed ratios will be reported. Second, kinetically controlled (i.e., irreversible) syntheses of multicyclic polymers using equifunctional feed ratios (i.e., a2/b4 ratios of 2:1) will be described. In the third section, syntheses of multicyclic polymers via thermodynamically controlled (reversible) "a2+b4" polycondensations will be discussed. Characteristic for these polycondensations are again equifunctional feed ratios and metal alkoxides as "a2" or "b4" monomers, which catalyze rapid equilibration reactions. Finally, potential applications of the new polymers will shortly be mentioned. © 2009 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 47: 1971,1987, 2009 [source] Biodegradable polymers with variable architectures via ring-expansion polymerizationJOURNAL OF POLYMER SCIENCE (IN TWO SECTIONS), Issue 19 2004Hans R. Kricheldorf Abstract Kinetically controlled ring-expansion polymerizations (REPs) are defined syntheses generating cyclic oligomers and polymers without linear intermediates and without equilibration reactions. This review reports syntheses of cyclic metal alkoxides and their use as initiators for REPs of lactones, cyclic diesters, and cyclocarbonates. In addition to homopolyesters, telechelic oligoesters or polyesters, random copolyesters, and A,B,A triblock copolymers can be prepared by these REPs. The in situ combination of REPs with condensation (mostly acylation) reactions allows a broad variation of end groups. The in situ combination of REPs with polycondensation enables various chain-extension reactions, including the syntheses of multiblock copolymers. With spirocyclic initiators, four-armed stars with functional end groups may be prepared. The in situ combination of REPs with condensation reactions of trifunctional or multifunctional reagents makes a broad variety of networks accessible. The average segment lengths may be controlled via the monomer/initiator ratios of the REP. All materials produced via the aforementioned REP processes are biodegradable and nontoxic, and this allows for biomedical and pharmaceutical applications. © 2004 Wiley Periodicals, Inc. J Polym Sci Part A: Polym Chem 42: 4723,4742, 2004 [source] Chromium-Free Corrosion Resistance of Metals by Ceramic CoatingJOURNAL OF THE AMERICAN CERAMIC SOCIETY, Issue 12 2001Satomi Ono Metal surfaces can be improved in terms of thermal, mechanical, and chemical properties by a ceramic coating. The chromium-free corrosion resistance of stainless steel was achieved using a chemical solution method. Precursor solutions were prepared from metal alkoxides and were deposited on stainless-steel surfaces by dip coating and heat-treating at temperatures <500°C. The stainless steel was coated by silica, zirconia, and titania single-layer coating films, and/or coated by silica/zirconia and silica/titania double-layer coating films. The corrosion resistance was improved remarkably by a submicrometer silica-based coating on the stainless steel. [source] Novel repair method for technical enamels based on sol,gel and sol-dispersion coatings,MATERIALS AND CORROSION/WERKSTOFFE UND KORROSION, Issue 2 2008S. Benfer The aim of the work presented here is the development of a novel repair method for technical enamels by using chemical nanotechnology. Good adhesion of coatings requires good wettability of the substrate by the repair solution. This was achieved by different pre-treatments of the steel substrates. Low sintering temperatures of the coatings can be ensured by the use of nanoparticle-based systems. Based on liquid metal alkoxides, a colloidal alumina sol and metal salts homogeneous sols with up to seven enamel compounds were prepared. The sols were brush coated onto plain and partly enamelled steel substrates and sintered in a furnace, by inductive heating or an IR emitter. Thin (single layer,,,1µm) crack-free layers were obtained on nearly all substrates independent of the sintering conditions investigated. The local sintering methods (IR emitter, inductive heating) allow to produce multiple coating systems in short times. Electrochemical impedance spectroscopy (EIS) provides evidence of the protective effect of these layers compared to the bare substrate, but as a result of their chemical composition the layers are not stable in the electrolytic environment for longer times. The thickness of such multiple coatings (20 layers, ,,8 µm) is still small compared to that of a technical enamel. Therefore, sol dispersion systems containing powder particles and sol components are applied on top of the sol,gel layers to increase the thickness of the sintered layers. [source] The Zirconium Alkoxide-Catalyzed Aldol-Tishchenko Reaction of Ketone AldolsCHEMISTRY - A EUROPEAN JOURNAL, Issue 10 2005Christoph Schneider Prof. Dr. Abstract The aldol-Tishchenko reaction of ketone aldols as enol equivalents has been developed as an efficient strategy to furnish differentiated 1,3- anti -diol monoesters in one step. The thermodynamically unstable ketone aldols undergo a facile retro-aldolization to yield a presumed zirconium enolate in situ, which then undergoes the aldol-Tishchenko reaction in typically high yields and with complete 1,3- anti diastereocontrol. Evaluation of a broad range of metal alkoxides as catalysts and optimization of the reaction protocol led to a modified zirconium alkoxide catalyst with attenuated Lewis acidity and dichloromethane as solvent, which resulted in suppression of the undesired acyl migration to a large extent. Various ketone aldols have been prepared and subjected to the general process, giving rise to a broad range of differently substituted 1,3- anti -diol monoesters, which may be hydrolyzed to the corresponding 1,3- anti -diols. [source] | ||||||||||