Advanced Synthesis & Catalysis, ISSN 1615-4150, 01/2019, Volume 361, Issue 2, pp. 265 - 282
Among the attempts to consolidate the so‐called circular economy, the conversion of carbon dioxide (CO2) into added‐value products has gained more and more...
iron | epoxides | homogeneous catalysis | carbonates | carbon dioxide fixation | CYCLOHEXENE OXIDE | DOUBLE METAL CYANIDES | CHEMISTRY, ORGANIC | ORGANIC CARBONATES | BIMETALLIC IRON(III) COMPLEXES | MEDIATED FORMATION | HIGHLY EFFICIENT | ALTERNATING COPOLYMERIZATION | COUPLING REACTION | POLY(PROPYLENE CARBONATE) | CYCLIC CARBONATES | CHEMISTRY, APPLIED | Catalysts | Toxicity | Aluminum | Polycarbonates | Carbon dioxide | Chromium | Iron | Magnesium | Catalysis | Carbonates | Aliphatic compounds
iron | epoxides | homogeneous catalysis | carbonates | carbon dioxide fixation | CYCLOHEXENE OXIDE | DOUBLE METAL CYANIDES | CHEMISTRY, ORGANIC | ORGANIC CARBONATES | BIMETALLIC IRON(III) COMPLEXES | MEDIATED FORMATION | HIGHLY EFFICIENT | ALTERNATING COPOLYMERIZATION | COUPLING REACTION | POLY(PROPYLENE CARBONATE) | CYCLIC CARBONATES | CHEMISTRY, APPLIED | Catalysts | Toxicity | Aluminum | Polycarbonates | Carbon dioxide | Chromium | Iron | Magnesium | Catalysis | Carbonates | Aliphatic compounds
Journal Article
Journal of Catalysis, ISSN 0021-9517, 08/2016, Volume 340, pp. 30 - 40
Gold nanoparticles supported onto a nanoporous semicrystalline polymorphic polymer matrix consisting of syndiotactic polystyrene- -1,4-polybutadiene multiblock...
Porous polymers | Azocompounds | Heterogeneous catalysis | Nitroarene reduction | Gold nanoparticles | Mechanism | NITROAROMATIC COMPOUNDS | ROOM-TEMPERATURE | ALCOHOL OXIDATION | AROMATIC AZO-COMPOUNDS | MODEL REACTION | CHEMISTRY, PHYSICAL | LIQUID-PHASE | NANOCLUSTERS | ENGINEERING, CHEMICAL | NITRO-COMPOUNDS | SYNDIOTACTIC POLYSTYRENE | AEROBIC OXIDATION | Polymers | Polymer industry | Prisoners | Nanoparticles | Nitrobenzenes | Chemical tests and reagents | Aniline | Elastomers | Azo compounds
Porous polymers | Azocompounds | Heterogeneous catalysis | Nitroarene reduction | Gold nanoparticles | Mechanism | NITROAROMATIC COMPOUNDS | ROOM-TEMPERATURE | ALCOHOL OXIDATION | AROMATIC AZO-COMPOUNDS | MODEL REACTION | CHEMISTRY, PHYSICAL | LIQUID-PHASE | NANOCLUSTERS | ENGINEERING, CHEMICAL | NITRO-COMPOUNDS | SYNDIOTACTIC POLYSTYRENE | AEROBIC OXIDATION | Polymers | Polymer industry | Prisoners | Nanoparticles | Nitrobenzenes | Chemical tests and reagents | Aniline | Elastomers | Azo compounds
Journal Article
ChemSusChem, ISSN 1864-5631, 08/2019, Volume 12, Issue 15, pp. 3448 - 3452
A FeIII‐triflate complex, bearing a bis‐thioether‐di‐phenolate [OSSO]‐type ligand, was discovered to promote the ring‐opening of glycidol with alcohols under...
ring-opening | iron | glyceryl ethers | homogeneous catalysis | glycidol | Glycerin | Glycerol | Catalysis | Regioselectivity | Earth crust | Catalysts | Selectivity | Ethers | Alcohols
ring-opening | iron | glyceryl ethers | homogeneous catalysis | glycidol | Glycerin | Glycerol | Catalysis | Regioselectivity | Earth crust | Catalysts | Selectivity | Ethers | Alcohols
Journal Article
Polymer International, ISSN 0959-8103, 01/2017, Volume 66, Issue 1, pp. 144 - 150
Binary copolymerization of 4‐methyl‐1,3‐pentadiene (4MPD) with styrene, butadiene and isoprene promoted by the titanium complex...
copolymers | butadiene | NMR | 4‐methyl‐1,3‐pentadiene | isoprene | styrene | 4-methyl-1,3-pentadiene | POLYOLEFINS | POLYMER SCIENCE | METHYL-SUBSTITUTED 1,4-TRANS-POLYBUTADIENES | C-13 NMR-SPECTRA | COMPLEXES | POLYMERIZATION | 3-pentadiene | TETRADENTATE | 4-methyl-1 | FUNCTIONALIZATION | BIS(PHENOLATO) LIGAND | ETHYLENE | POLY-1,2-(4-METHYL-1,3-PENTADIENE) | Chemical industry | Herbicides | Pesticides industry | Nuclear magnetic resonance spectroscopy | Analysis | Butadiene | Stereoselectivity | Copolymers | Catalysts | Styrenes | Titanium | Copolymerization | Isoprene
copolymers | butadiene | NMR | 4‐methyl‐1,3‐pentadiene | isoprene | styrene | 4-methyl-1,3-pentadiene | POLYOLEFINS | POLYMER SCIENCE | METHYL-SUBSTITUTED 1,4-TRANS-POLYBUTADIENES | C-13 NMR-SPECTRA | COMPLEXES | POLYMERIZATION | 3-pentadiene | TETRADENTATE | 4-methyl-1 | FUNCTIONALIZATION | BIS(PHENOLATO) LIGAND | ETHYLENE | POLY-1,2-(4-METHYL-1,3-PENTADIENE) | Chemical industry | Herbicides | Pesticides industry | Nuclear magnetic resonance spectroscopy | Analysis | Butadiene | Stereoselectivity | Copolymers | Catalysts | Styrenes | Titanium | Copolymerization | Isoprene
Journal Article
ChemSusChem, ISSN 1864-5631, 12/2016, Volume 9, Issue 24, pp. 3457 - 3464
Glycidol is converted into glycerol carbonate (GC) by coupling with CO2 in the presence of tetrabutylammonium bromide (TBAB) under mild reaction conditions...
carbon dioxide | cycloaddition | epoxide | density functional theory | hydrogen bond | FUNCTIONALIZED IONIC LIQUID | GRAPHENE OXIDE | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | GLYCEROL CARBONATE | ORGANIC CARBONATES | BIMETALLIC IRON(III) COMPLEXES | CHEMISTRY, MULTIDISCIPLINARY | MILD CONDITIONS | CHEMICAL FIXATION | CYCLIC CARBONATES | CARBON-DIOXIDE | EFFICIENT | Glycerin | Hydroxides | Specific gravity | Hydrogen | Glycerol | Density functionals | Ethylene oxide | Carbonates
carbon dioxide | cycloaddition | epoxide | density functional theory | hydrogen bond | FUNCTIONALIZED IONIC LIQUID | GRAPHENE OXIDE | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | GLYCEROL CARBONATE | ORGANIC CARBONATES | BIMETALLIC IRON(III) COMPLEXES | CHEMISTRY, MULTIDISCIPLINARY | MILD CONDITIONS | CHEMICAL FIXATION | CYCLIC CARBONATES | CARBON-DIOXIDE | EFFICIENT | Glycerin | Hydroxides | Specific gravity | Hydrogen | Glycerol | Density functionals | Ethylene oxide | Carbonates
Journal Article
ChemSusChem, ISSN 1864-5631, 12/2016, Volume 9, Issue 23, pp. 3272 - 3275
The present work deals with the production of monoalkyl glyceryl ethers (MAGEs) through a new reaction pathway based on the reaction of glycidol and alcohols...
Lewis acids | ethers | waste valorization | green chemistry | glycerol | SOLID CATALYSTS | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | DESIGN | CHEMICALS | CATALYZED ETHERIFICATION | SELECTIVE CONVERSION | CHEMISTRY, MULTIDISCIPLINARY | Lewis Acids - chemistry | Alcohols - chemistry | Green Chemistry Technology | Propanols - chemistry | Epoxy Compounds - chemistry | Glyceryl Ethers - chemical synthesis | Catalysis | Glycerin | Glycerol | Green chemistry | Lewis acid | Pathways | Catalysts | Byproducts | Chemical reactions | Ethers | Alcohols
Lewis acids | ethers | waste valorization | green chemistry | glycerol | SOLID CATALYSTS | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | DESIGN | CHEMICALS | CATALYZED ETHERIFICATION | SELECTIVE CONVERSION | CHEMISTRY, MULTIDISCIPLINARY | Lewis Acids - chemistry | Alcohols - chemistry | Green Chemistry Technology | Propanols - chemistry | Epoxy Compounds - chemistry | Glyceryl Ethers - chemical synthesis | Catalysis | Glycerin | Glycerol | Green chemistry | Lewis acid | Pathways | Catalysts | Byproducts | Chemical reactions | Ethers | Alcohols
Journal Article
Polymer International, ISSN 0959-8103, 01/2017, Volume 66, Issue 1, pp. 144 - 150
Journal Article
Polymer International, ISSN 0959-8103, 10/2019, Volume 68, Issue 10, pp. 1681 - 1687
The thin‐film morphology of stereoregular syndiotactic poly(p‐methylstyrene)–(cis‐1,4‐polybutadiene) (sP(pMS–B)) multiblock copolymers has been investigated...
multiblock copolymer | nanostructure | thin film | microstructure | atomic force microscopy | BUTADIENE BLOCK-COPOLYMERS | ISOPRENE | POLYMER SCIENCE | STRATEGY | STYRENE | INSIGHT | POLYSTYRENE | SULFONATION | SEQUENCE | EFFICIENT | CATALYSTS | Syndiotacticity | Atomic force microscopy | Chemical industry | Architecture | Lamellae | Segments | Inclusions | Polymeric films | Thin films | Domains | Organic chemistry | Copolymers | Morphology | Polybutadiene | Polymers
multiblock copolymer | nanostructure | thin film | microstructure | atomic force microscopy | BUTADIENE BLOCK-COPOLYMERS | ISOPRENE | POLYMER SCIENCE | STRATEGY | STYRENE | INSIGHT | POLYSTYRENE | SULFONATION | SEQUENCE | EFFICIENT | CATALYSTS | Syndiotacticity | Atomic force microscopy | Chemical industry | Architecture | Lamellae | Segments | Inclusions | Polymeric films | Thin films | Domains | Organic chemistry | Copolymers | Morphology | Polybutadiene | Polymers
Journal Article
Advanced Synthesis & Catalysis, ISSN 1615-4150, 01/2019, Volume 361, Issue 2, pp. 283 - 288
A new [OSSO]‐Fe(III) metallate complex was prepared and characterized. We demonstrated that such metallate is the real catalytic active species for the...
iron | cycloaddition | homogeneous catalysis | carbon dioxide fixation | CYCLIC CARBONATE SYNTHESIS | MECHANISM | DIOXIDE | CHEMISTRY, ORGANIC | PRESSURE | SOLVENTS | CHEMISTRY, APPLIED | CAPTURE | EFFICIENT | IRON(III) COMPLEXES | Cycloaddition | Catalysis | Carbonates | Catalysts | Tetrabutylammonium bromide | Carbon dioxide
iron | cycloaddition | homogeneous catalysis | carbon dioxide fixation | CYCLIC CARBONATE SYNTHESIS | MECHANISM | DIOXIDE | CHEMISTRY, ORGANIC | PRESSURE | SOLVENTS | CHEMISTRY, APPLIED | CAPTURE | EFFICIENT | IRON(III) COMPLEXES | Cycloaddition | Catalysis | Carbonates | Catalysts | Tetrabutylammonium bromide | Carbon dioxide
Journal Article
ChemSusChem, ISSN 1864-5631, 09/2018, Volume 11, Issue 18, pp. 3139 - 3149
The aerobic oxidation and oxidative esterification of 5‐hydroxymethylfurfural (HMF) catalyzed by gold nanoparticles (AuNPs) supported on a semicrystalline...
gold | oxidation | nanoparticles | polymers | supported catalysts | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | SELECTIVE OXIDATION | CATALYZED OXIDATION | ONE-POT | 2,5-FURANDICARBOXYLIC ACID | PD ALLOY NANOPARTICLES | CHEMISTRY, MULTIDISCIPLINARY | BIOMASS | 2,5-DIFORMYLFURAN | SYNDIOTACTIC POLYSTYRENE | EFFICIENT | Nanoparticles | Oxidation-reduction reaction | Furans | Polymer industry | Conveying machinery | Butadiene | Syndiotacticity | Gold | Polystyrene resins | Concentrators | Hydroxymethylfurfural | Conveyors | Oxidation | Catalysis | Esterification
gold | oxidation | nanoparticles | polymers | supported catalysts | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | SELECTIVE OXIDATION | CATALYZED OXIDATION | ONE-POT | 2,5-FURANDICARBOXYLIC ACID | PD ALLOY NANOPARTICLES | CHEMISTRY, MULTIDISCIPLINARY | BIOMASS | 2,5-DIFORMYLFURAN | SYNDIOTACTIC POLYSTYRENE | EFFICIENT | Nanoparticles | Oxidation-reduction reaction | Furans | Polymer industry | Conveying machinery | Butadiene | Syndiotacticity | Gold | Polystyrene resins | Concentrators | Hydroxymethylfurfural | Conveyors | Oxidation | Catalysis | Esterification
Journal Article
ChemSusChem, ISSN 1864-5631, 05/2017, Volume 10, Issue 10, pp. 2291 - 2300
The disposal of any waste by recovering it within the production plant represents the ultimate goal of every biorefinery. In this scenario, the selective...
lewis acids | green chemistry | life cycle assessment | biobased industry | glycidol | CATALYSIS | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | DESIGN | PUBLISHED ALGORITHMS | ETHERIFICATION | CHEMISTRY, MULTIDISCIPLINARY | CHEMICAL-REACTIONS | SUSTAINABILITY ASSESSMENT | BIOMASS | LEWIS-ACIDS | SYNTHESIS PLANS | Propanols - chemistry | Catalysis | Epoxy Compounds - chemistry | Glyceryl Ethers - chemical synthesis | Catalysts | Glycerol
lewis acids | green chemistry | life cycle assessment | biobased industry | glycidol | CATALYSIS | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | DESIGN | PUBLISHED ALGORITHMS | ETHERIFICATION | CHEMISTRY, MULTIDISCIPLINARY | CHEMICAL-REACTIONS | SUSTAINABILITY ASSESSMENT | BIOMASS | LEWIS-ACIDS | SYNTHESIS PLANS | Propanols - chemistry | Catalysis | Epoxy Compounds - chemistry | Glyceryl Ethers - chemical synthesis | Catalysts | Glycerol
Journal Article
European Polymer Journal, ISSN 0014-3057, 02/2018, Volume 99, p. 368
Random copolymers of 2-vinylfuran with styrene (S-co-2VFs) have been thermoreversibly cross-linked via Diels-Alder (DA) reaction with...
Bismaleimides | Differential scanning calorimetry | Atomic force microscopy | Design for recycling | Nuclear magnetic resonance--NMR | Isothermal annealing | Mechanical properties | Crosslinking | Self healing materials | Thermosetting resins | Stability analysis | Polymeric films | Thermal stability | Thin films | Copolymers | Styrenes | Styrene | Infrared radiation | Polymers | Tensile properties
Bismaleimides | Differential scanning calorimetry | Atomic force microscopy | Design for recycling | Nuclear magnetic resonance--NMR | Isothermal annealing | Mechanical properties | Crosslinking | Self healing materials | Thermosetting resins | Stability analysis | Polymeric films | Thermal stability | Thin films | Copolymers | Styrenes | Styrene | Infrared radiation | Polymers | Tensile properties
Journal Article
ChemSusChem, ISSN 1864-5631, 06/2018, Volume 11, Issue 11, pp. 1829 - 1837
The selective preparation of monoalkylglyceryl ethers (MAGEs) is a task for researchers owing to their broad range of applications. In this work, green...
ethers | lewis acids | green chemistry | life cycle assessment | glycidol | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | LIFE-CYCLE ASSESSMENT | ETHERIFICATION | CHEMISTRY, MULTIDISCIPLINARY | ALCOHOLS | HYDROGEN | POLYETHER | SUBSTRATE | VALUE-ADDED PRODUCT | EFFICIENT | ZEOLITE | Glycerin | Heterogeneous catalysis | Analysis | Green technology | Glycerol | Green chemistry | Chemical synthesis | Sustainable development | Externalities | Economic analysis | Catalysts | Green aspects | Catalysis | Economic conditions | Ethers | Conversion | Environmental impact | Impact analysis | Alcohols
ethers | lewis acids | green chemistry | life cycle assessment | glycidol | GREEN & SUSTAINABLE SCIENCE & TECHNOLOGY | LIFE-CYCLE ASSESSMENT | ETHERIFICATION | CHEMISTRY, MULTIDISCIPLINARY | ALCOHOLS | HYDROGEN | POLYETHER | SUBSTRATE | VALUE-ADDED PRODUCT | EFFICIENT | ZEOLITE | Glycerin | Heterogeneous catalysis | Analysis | Green technology | Glycerol | Green chemistry | Chemical synthesis | Sustainable development | Externalities | Economic analysis | Catalysts | Green aspects | Catalysis | Economic conditions | Ethers | Conversion | Environmental impact | Impact analysis | Alcohols
Journal Article
JOURNAL OF POLYMER SCIENCE PART A-POLYMER CHEMISTRY, ISSN 0887-624X, 10/2016, Volume 54, Issue 19, pp. 3132 - 3139
Group 4 complexes 1-3 [1=(t-BuOS)(2)Ti(O-i-Pr)(2); 2=(t-BuOS)(2)Zr(O-t-Bu)(2); 3=(t-BuOS)(2)Hf(O-t-Bu)(2)] supported by two phenolate bidentate ligands...
copolymers | CYCLIC ESTERS | POLYMER SCIENCE | polyhydroxybutyrate | RACEMIC BETA-BUTYROLACTONE | Biopolymers | group 4 metal complexes | ring-opening polymerization | YTTRIUM | STEREOSELECTIVITY | LACTONES | LIGANDS | LACTIDE | INITIATORS | COPOLYMERIZATION | CATALYSTS | Polymerization | Zirconium | Analysis
copolymers | CYCLIC ESTERS | POLYMER SCIENCE | polyhydroxybutyrate | RACEMIC BETA-BUTYROLACTONE | Biopolymers | group 4 metal complexes | ring-opening polymerization | YTTRIUM | STEREOSELECTIVITY | LACTONES | LIGANDS | LACTIDE | INITIATORS | COPOLYMERIZATION | CATALYSTS | Polymerization | Zirconium | Analysis
Journal Article
Journal of Polymer Science Part A: Polymer Chemistry, ISSN 0887-624X, 10/2016, Volume 54, Issue 19, pp. 3132 - 3139
ABSTRACT Group 4 complexes 1–3 [1 = (t‐BuOS)2Ti(O‐i‐Pr)2; 2 = (t‐BuOS)2Zr(O‐t‐Bu)2; 3 = (t‐BuOS)2Hf(O‐t‐Bu)2] supported by two phenolate bidentate ligands...
copolymers | polyhydroxybutyrate | Biopolymers | group 4 metal complexes | ring-opening polymerization | Ring opening polymerization | Catalysts | Copolymerization | Catalysis | Coordination compounds | Monomers | Isopropanol | Block copolymers
copolymers | polyhydroxybutyrate | Biopolymers | group 4 metal complexes | ring-opening polymerization | Ring opening polymerization | Catalysts | Copolymerization | Catalysis | Coordination compounds | Monomers | Isopropanol | Block copolymers
Journal Article