Search results for "catalysis"

showing 10 items of 5944 documents

Lewis Base Catalyzed Intramolecular Reduction of Salicylaldehydes by Pinacol-Derived Chlorohydrosilane

2018

010405 organic chemistryHydrosilylationPinacolOrganic ChemistryHomogeneous catalysis010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisReduction (complexity)chemistry.chemical_compoundchemistryIntramolecular forceLewis acids and basesPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Triorganotin( iv ) cation-promoted dimethyl carbonate synthesis from CO 2 and methanol: solution and solid-state characterization of an unexpected di…

2018

Two novel C,N-chelated organotin(IV) complexes bearing weakly coordinating carborane moieties were prepared by the reaction of the corresponding C,N-chelated organotin(IV) chloride (i.e. LCNR2SnCl, R = n-Bu (1) and Ph (2); LCN = 2-(N,N-dimethylaminomethyl)phenyl)) with monocarba-closo-dodecaborate silver salt (AgCB11H12; Ag·3). Both products of the metathesis, [LCN(n-Bu)2Sn]+[CB11H12]− (4) and [LCNPh2Sn]+ [CB11H12]− (5), respectively, were characterized by both multinuclear NMR spectroscopy and elemental analysis. The instability of 4 and 5 towards water is discussed. The solid-state structure of LCN(n-Bu)2SnOH·B(C6F5)3 (4a) as a model compound with a Sn–O(H)⋯B linkage is also reported. The…

010405 organic chemistryInfrared spectroscopyGeneral ChemistryNuclear magnetic resonance spectroscopy010402 general chemistryMetathesis01 natural sciencesMedicinal chemistryCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryMaterials ChemistryCarborane[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryMethanolDimethyl carbonateStoichiometryComputingMilieux_MISCELLANEOUS
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Subphthalocyanine basicity: reversible protonation at the azomethine bridge

2017

International audience; Subphthalocyanine (SubPc) could be reversibly protonated at the azomethine bridge. This phenomenon was examined by addressing the pKa of the acid (TFA, MSA, TMSA) and the SubPc electron-withdrawing properties of the peripheral isoindolic substituents (F12 vs. H12 and NO2), which tunes the basic character of the azomethine moiety. The protonation of up to three azomethines was suggested and monitored spectrophotometrically with the appearance of new absorption bands at 610, 630 nm and 660 nm, together with marked colour changes from purple to blue to green. Evidence of such a protonation was also shown by significant changes in the 1H-NMR spectrum and new bands in the…

010405 organic chemistryInfraredChemistry[CHIM.ORGA]Chemical Sciences/Organic chemistryInfrared spectroscopyProtonationGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciences[ CHIM ] Chemical SciencesCatalysis0104 chemical sciencesMaterials ChemistryMoiety[CHIM]Chemical SciencesAbsorption (chemistry)
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Reagent- and Metal-Free Anodic C-C Cross-Coupling of Aniline Derivatives.

2017

The dehydrogenative cross-coupling of aniline derivatives to 2,2′-diaminobiaryls is reported. The oxidation is carried out electrochemically, which avoids the use of metals and reagents. A large variety of biphenyldiamines were thus prepared. The best results were obtained when glassy carbon was used as the anode material. The electrosynthetic reaction is easily performed in an undivided cell at slightly elevated temperature. In addition, common amine protecting groups based on carboxylic acids were employed that can be selectively removed under mild conditions after the cross-coupling, which provides quick and efficient access to important building blocks featuring free amine moieties.

010405 organic chemistryInorganic chemistryGeneral ChemistryGlassy carbon010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesAnodechemistry.chemical_compoundAnilinechemistryMetal freeReagentPolymer chemistryCoupling (piping)Amine gas treatingAngewandte Chemie (International ed. in English)
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Gas phase heterogeneous partial oxidation reactions

2018

Abstract Mixed metal oxides are used as catalysts in the gas phase partial oxidation of hydrocarbons. This paper will present the principles of catalyst choice for selective oxidation reactions as well as the structural features of metal oxide catalysts. The nature of active sites in selective oxidation reactions will also be briefly discussed. We will pay special attention to several representative reactions: (1) ODH of short chain alkanes (from C1 to C4), (2) propene partial oxidation/ammoxidation on bismuth molybdate based catalysts, (3) n-butane direct oxidation to maleic anhydride on VPO type catalysts, and (4) propane direct oxidation/ammoxidation on mixed MoVTe(Sb)Nb–O catalysts. Fin…

010405 organic chemistryInorganic chemistryOxideMaleic anhydrideMolybdate010402 general chemistry01 natural sciencesRedox0104 chemical sciencesCatalysisPropenechemistry.chemical_compoundchemistryPartial oxidationAmmoxidation
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A comparative study of methanol carbonation on unsupported SnO2 and ZrO2

2009

International audience; The aim of this work was to explore the catalytic properties of SnO2 in the coupling of methanol with carbon dioxide to afford dimethyl carbonate. SnO2 nanopowders were produced by hydrolysis of tin tetra-tert-butoxide dissolved in n-butanol. The samples were much more active than a commercial one due to their higher surface areas. In addition, they exhibited excellent recyclability. However, comparison with ZrO2, prepared and tested under the same experimental conditions, showed that zirconia-based catalysts were more selective and are, among the heterogeneous catalysts already reported, still the more selective. SnO2 also catalyzed the formation of dimethyl ether l…

010405 organic chemistryInorganic chemistry[ PHYS.COND.CM-MS ] Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]chemistry.chemical_elementGeneral Chemistry[CHIM.CATA]Chemical Sciences/Catalysis010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysis0104 chemical sciencesCatalysischemistry.chemical_compound[ CHIM.CATA ] Chemical Sciences/Catalysischemistry[PHYS.COND.CM-MS]Physics [physics]/Condensed Matter [cond-mat]/Materials Science [cond-mat.mtrl-sci]Dimethyl etherCrystalliteMethanolDimethyl carbonateTinPowder diffraction
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Regio-, Diastereo-, and Enantioselective Organocatalytic Addition of 4-Substituted Pyrazolones to Isatin-Derived Nitroalkenes

2019

"This is the peer reviewed version of the following article: [FULL CITE], which has been published in final form at [Link to final article using the DOI]. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving."

010405 organic chemistryIsatinOrganic ChemistryEnantioselective synthesis010402 general chemistry01 natural sciences0104 chemical scienceschemistry.chemical_compoundchemistryOrganocatalysisNucleophilic substitutionOrganic chemistryPyrazolonesPhysical and Theoretical ChemistryEuropean Journal of Organic Chemistry
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Synthesis and structural characterization of well-defined bis(oxamato)palladate(II) precatalysts for Suzuki and Heck reactions

2018

Abstract A family of tetra-n-butylammonium salts of bis(oxamato)palladate(II) complexes of formula (n-Bu4N)2[Pd(Lm)2]·pH2O [m = 1–9; L1 = N-phenyloxamate (pma) and p = 2 (1), L2 = N-2-methylphenyloxamate (2-Mepma) and p = 4 (2), L3 = N-4-methylphenyloxamate (4-Mepma) and p = 2 (3), L4 = N-2,3-dimethylphenyloxamate (2,3-Me2pma) and p = 3 (4), L5 = N-2,4-dimethylphenyloxamate (Me2pma) and p = 4 (5), L6 = N-2,5-dimethylphenyloxamate (2,5-Me2pma) and p = 7 (6), L7 = N-3,4-dimethylphenyloxamate (3,4-Me2pma) and p = 6 (7), L8 = N-3,5-dimethylphenyloxamate (3,5-Me2pma) and p = 5 (8)] have been prepared and characterized by spectroscopic methods. The crystal structure of 1 that has been solved by s…

010405 organic chemistryLigandArylCrystal structure010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesCatalysisInorganic ChemistryBond lengthchemistry.chemical_compoundDeprotonationchemistrySuzuki reactionHeck reactionMaterials ChemistryPhysical and Theoretical ChemistryInorganica Chimica Acta
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Scalable and Selective Preparation of 3,3′,5,5′-Tetramethyl-2,2′-biphenol

2016

Biphenols are indispensable building blocks in ligand systems for organic catalysis. 3,3′5,5′-Tetramethyl-2,2′-biphenol is a particular versatile motif in different catalytic systems. We developed an easy to perform and scalable process to give access to large quantities of this important building block by the use of selenium dioxide, a common and readily available oxidizer.

010405 organic chemistryLigandChemistryOrganic ChemistryScalabilityOrganic chemistryPhysical and Theoretical Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistry0104 chemical sciencesCatalysisBlock (data storage)Organic Process Research & Development
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Strong Influence of the Ancillary Ligand over the Photodynamic Anticancer Properties of Neutral Biscyclometalated IrIII Complexes Bearing 2-Benzoazol…

2018

In this paper, the synthesis, comprehensive characterization and biological and photocatalytic properties of two series of neutral IrIII biscyclometalated complexes of general formula [Ir(C^N)2(N^O)], where the N^O ligands are 2‐(benzimidazolyl)phenolate‐N,O (L1, series a) and 2‐(benzothiazolyl)phenolate‐N,O (L2, series b), and the C^N ligands are 2‐(phenyl)pyridinate or its derivatives, are described,. Complexes of types a and b exhibit dissimilar photophysical and biological properties. In vitro cytotoxicity tests conclusively prove that derivatives of series a are harmless in the dark against SW480 cancer cells (colon adenocarcinoma), but express enhanced cytotoxicity versus the same cel…

010405 organic chemistryLigandChemistrymedicine.medical_treatmentOrganic ChemistryPhotodynamic therapy2-arylazolesphotodynamictherapyQuímicaGeneral Chemistry010402 general chemistry01 natural sciencesMedicinal chemistryanticancercomplexesCatalysis0104 chemical sciencesChemistryheterolepticneutraliridium(III)complexesmedicinephosphorescent complexesChemistry - A European Journal
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