Search results for "Organic carbonates"

showing 3 items of 3 documents

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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