Search results for "Organic carbonate"

showing 4 items of 4 documents

Undecylenic acid: A tunable bio-based synthon for materials applications

2016

International audience; An undecylenic acid-based monoglyceride prepared from glycidol and undecylenic acid is used as suitable and tunable synthon for polymerization applications. Epoxidation and acrylation reactions lead to photopolymerizable monomers while transesterification with dimethyl carbonate, metathesis and aminolysis reactions provide access to polyhydroxyurethane-based materials. The successive intermediates were synthesized according to a green chemistry approach implicating solvent-less and catalyzed reactions, and were at each step fully characterized by infrared, 1H and 13C{1H} NMR spectroscopy, elemental analysis and mass spectrometry. Analyses of the resulting polymer mat…

Green chemistryThermogravimetric analysisRenewable resourcesMaterials sciencePolymers and PlasticsOrganic carbonatepolyhydroxyurethanespolyurethanesGeneral Physics and Astronomy02 engineering and technologycyclic carbonates010402 general chemistry01 natural sciences[ CHIM ] Chemical Scienceschemistry.chemical_compoundPolyhydroxyurethanes (PHUs)Aminolysisrenewable building-blockPolymer chemistryMaterials ChemistrymedicineOrganic chemistry[CHIM]Chemical Sciencessolvent-free conditionscastor-oilglycerol carbonatePhotopolymerizationOrganic ChemistrySynthonGlycidolTransesterification021001 nanoscience & nanotechnologyFatty acid0104 chemical scienceschemistryPolymerizationGlycidolpolycarbonatespolymerizationUndecylenic acidderivatives0210 nano-technologymedicine.drug
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Di-n-butyltin(IV)-catalyzed dimethyl carbonate synthesis from carbon dioxide and methanol: An in situ high pressure 119Sn{1H} NMR spectroscopic study

2011

The reactivity of five di-n-butyltin(IV) complexes, n-Bu2Sn(OR)(2) (1), n-Bu2SnO (3), [n-Bu2Sn(OR)](2)O (4), (n-Bu2SnO)(2)(CO2) (6) and (n-Bu2SnO)(6)[(n-Bu2SnOR)(2)(CO3)](2) (7) (R = CH3), with CO2, suggested as possible catalyst precursors and key-intermediates for the direct synthesis of dimethyl carbonate from carbon dioxide and methanol, has been investigated using high-pressure Sn-119{H-1} NMR (HP-NMR) spectroscopy. Four of the five precursors studied, i.e. 3, 4, 6 and 7 give rise to an identical Sn-119{H-1} NMR pattern which can be explicitly attributed to the fingerprint of the dimeric form of the 1-methoxy-3-methylcarbonatotetrabutyldistannoxane {5}(2). However, with 1, a new pair o…

Inorganic chemistryOxideAlkoxidesBiochemistryMedicinal chemistryCatalysisCatalysisInorganic Chemistrychemistry.chemical_compoundMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistrySpectroscopyOrganic carbonatesReactivityOrganic ChemistryOxideChemistryCarbon dioxidechemistryCarbon dioxideProton NMRMethanolDimethyl carbonateOrganooxotin ClusterCarbon dioxide utilizationHigh-pressure NMR spectroscopyRelevantDiorganotin(IV)Journal of Organometallic Chemistry
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High-pressure NMR spectroscopy: An in situ tool to study tin-catalyzed synthesis of organic carbonates from carbon dioxide and alcohols. Part 2 [1]

2015

Dialkoxide diorganotin(IV) complexes are known to readily react with carbon dioxide under pressure and they are considered as suitable catalyst precursor models for the direct synthesis of organic carbonates. To gain a better understanding of CO2 insertion processes with Sn-OR bonds, the reactivity of n-Bu2Sn(OCH(CH3)(2))(2) (2) was investigated using high-pressure NMR (HP-NMR) spectroscopy. In deuterated solvents (isopropanol-d(8) and toluene-d(8)) under 50 bar of CO2 pressure at 80 degrees C, Sn-119{H-1} NMR experiments revealed the exclusive formation of an unprecedented tetraorganodistannoxane species, characterized as the bis[diisopropycarbonatotetrabutyldistannoxane] complex, {[n-Bu2S…

Organic carbonatesOrganic ChemistryInorganic chemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopyBiochemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryDeuteriumTetraorganodistannoxaneCarbon dioxidePolymer chemistrySn-119 NMR spectraMaterials ChemistryHigh pressure NMR spectroscopyReactivity (chemistry)Physical and Theoretical ChemistryTinSpectroscopyCarbon dioxide utilizationDiorganotin(IV)Bar (unit)Journal of Organometallic Chemistry
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Direct electrochemical generation of organic carbonates by dehydrogenative coupling.

2018

Organic carbonates are an important source for polycarbonate synthesis. However, their synthesis generally requires phosgene, sophisticated catalysts, harsh reaction conditions, or other highly reactive chemicals. We present the first direct electrochemical generation of mesityl methyl carbonate by C–H activation. Although this reaction pathway is still challenging concerning scope and efficiency, it outlines a new strategy for carbonate generation.

boron-doped diamondanodeorganic carbonates010402 general chemistryElectrochemistry01 natural sciencesFull Research PaperCatalysislcsh:QD241-441chemistry.chemical_compoundlcsh:Organic chemistryPolycarbonatedehydrogenative couplinglcsh:ScienceMethyl carbonateReaction conditions010405 organic chemistryOrganic ChemistryCombinatorial chemistry0104 chemical sciencesCoupling (electronics)Chemistrychemistryelectrochemistryvisual_artvisual_art.visual_art_mediumCarbonatelcsh:QPhosgeneBeilstein journal of organic chemistry
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