Search results for "Bifunctional"

showing 10 items of 123 documents

Unraveling the Role of the Rh–ZrO2 Interface in the Water–Gas-Shift Reaction via a First-Principles Microkinetic Study

2018

The industrially important water–gas-shift (WGS) reaction is a complex network of competing elementary reactions in which the catalyst is a multicomponent system consisting of distinct domains. Herein, we have combined density functional theory calculations with microkinetic modeling to explore the active phase, kinetics, and reaction mechanism of the WGS over the Rh–ZrO2 interface. We have explicitly considered the support and metal and their interface and find that the Rh–ZrO2 interface is far more active toward WGS than Rh(111) facets, which are susceptible to CO poisoning. CO2 forming on the zirconia support rapidly transforms into formate. These findings demonstrate the central role of…

Reaction mechanismkaasutMaterials sciencewater-gas shift010402 general chemistryHeterogeneous catalysis01 natural sciencesCatalysisWater-gas shift reactionCatalysischemistry.chemical_compoundElementary reactionFormaterajapintailmiötBifunctionalta116density functional theorykemialliset reaktiot010405 organic chemistrytiheysfunktionaaliteoriamicrokineticsGeneral Chemistry0104 chemical sciencesheterogeneous catalysischemistryChemical physicskatalyysirajapinnat (pinnat)Density functional theoryACS Catalysis
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Metal- and Reagent-Free Electrochemical Synthesis of Alkyl Arylsulfonates in a Multi-Component Reaction.

2020

Abstract This work presents the first electrochemical preparation of alkyl arylsulfonates by direct anodic oxidation of electron‐rich arenes. The reaction mechanism features a multi‐component reaction consisting of electron‐rich arenes, an alcohol of choice and excess SO2 in an acetonitrile‐HFIP reaction mixture. In‐situ formed monoalkyl sulfites are considered as key intermediates with bifunctional purpose. Firstly, this species functions as nucleophile and secondly, excellent conductivity is provided. Several primary and secondary alcohols and electron‐rich arenes are implemented in this reaction to form the alkyl arylsulfonates in yields up to 73 % with exquisite selectivity. Boron‐doped…

Reaction mechanismoxidationAlcohol010402 general chemistry01 natural sciencesCatalysisC−H activationchemistry.chemical_compoundradical ionsNucleophileMulti-component reactionElectrochemistryBifunctionalAlkylchemistry.chemical_classification010405 organic chemistrygreen chemistryCommunicationOrganic ChemistryGeneral ChemistryCombinatorial chemistryCommunications0104 chemical scienceschemistryReagentSelectivityChemistry (Weinheim an der Bergstrasse, Germany)
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The peroxisome proliferator response element (PPRE) present at positions -681/-669 in the rat liver 3-ketoacyl-CoA thiolase B gene functionally inter…

2000

Although previous data showed that the putative thiolase B PPRE located at -681/-669 bind the PPARalpha-RXRalpha heterodimer in vitro (Kliewer et al. (1992) Nature 358, 771-774), there is no evidence about the functional role of this element. By gel mobility-shift assay, we found an interaction of this PPRE with not only PPARalpha but also with HNF-4. By transfection of cells with the putative PPRE-driven luciferase reporter vector and PPARalpha, we found no significant activation of the luciferase gene expression, in contrast to the case with reporter expression driven by the PPRE of the peroxisomal bifunctional enzyme. On the other hand, HNF-4 activated the luciferase gene expression driv…

Response elementBiophysicsReceptors Cytoplasmic and NuclearBiologyTransfectionBiochemistryDNA-binding proteinPeroxisomal Bifunctional EnzymeGenes ReporterGene expressionAnimalsMolecular BiologyGeneDNA PrimersBase SequenceThiolaseCell BiologyTransfectionDNAAcetyl-CoA C-AcyltransferasePhosphoproteinsMolecular biologyRatsDNA-Binding ProteinsHepatocyte nuclear factor 4Hepatocyte Nuclear Factor 4LiverCOS CellsPeroxisome ProliferatorsTranscription FactorsBiochemical and biophysical research communications
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Epigenetic agents as an adjunct to active chemotherapy in hematological tumor cell lines

2012

Epigenetic therapy is a new promising area in cancer research that is based on the use of a series of molecules capable of affecting tumor cell growth, differentiation and death by modifying the cellular mechanisms underlying the control of gene expression. Significant enhancement of traditional anticancer drug effects has been also reported by several authors. Our recent research focused on the identification of new epigenetic agent-containing drug combinations to be employed in the therapy of leukemia. The results showed that the new combination of an histone deacetylase (HDAC) inhibitor and the ribonucleotide reductase (RR) inhibitor 3’-methyl-adenosine (3’-Me-Ado) is endowed with a sign…

Settore BIO/14 - Farmacologiaepigenetics leukemia histone deacetylase inhibitors ribonucleotide reductase inhibitors bifunctional agents
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New potentially cytotoxic thiolatogold(I) complexes of 1,1′-bis(diphenylphosphino)ferrocene

1996

Abstract 1,1′-Bis[chlorogold(I) diphenylphosphino] ferrocene (1) was chosen as the starting material to synthesize new thiolato gold(I) complexes. This has been achieved by substituting the chlorine atoms by monofunctional and bifunctional thiolates affording ‘open’ thiolatogold complexes and trimetallic ferrocenophane-type structures, respectively. The new 1,1′-bis(2,6-dithia-1-phosphanyl)ferrocene (7) containing directly linked P and S atoms was also prepared but no gold complex was obtained. Compound 2 crystallizes in the monoclinic space group P21/n with a=10.2632), b=21.064(4), c=16.259(3) A , β=97.06(2)° and V=3.488(1) A 3 . The distance between the two gold atoms (3.06 A) indicates a…

StereochemistryHuman bladderChlorine atomMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundFerrocenechemistryColon carcinomaMaterials Chemistry11'-Bis(diphenylphosphino)ferrocenePhysical and Theoretical ChemistryBifunctionalMonoclinic crystal systemInorganica Chimica Acta
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Isomerization and rearrangement of (E)- and (Z)-phenylhydrazones of 3-benzoyl-5-phenyl-1,2,4-oxadiazole: evidence for a “new” type of acid-catalysis …

2008

A kinetic investigation in methanol of the title reaction has evidenced the occurrence of two processes: the 1-E1-Z isomerization and the rearrangement of the (Z)-isomer into the relevant 4-benzoylamino-2,5-diphenyl-1,2,3-triazole (1-Z  T). The latter reaction is in line with the ability of the (Z)-phenylhydrazones of 3-benzoyl-1,2,4-oxadiazoles to undergo the so called mononuclear rearrangement of heterocycles (MRH). The occurrence of both the examined reactions is dependent on a Lewis-acid-catalysis. The obtained results have shown the possibility of a ‘new’ type of acid-catalysis (bifunctional catalysis by Lewis salts) in the MRH. This catalysis operates through a completely different me…

StereochemistryOrganic ChemistryIsomerization reaction MHR reaction copper(II) catalysisOxadiazoleProtonationSettore CHIM/06 - Chimica OrganicaMedicinal chemistryAdductCatalysischemistry.chemical_compoundAcid catalysischemistryMoietyPhysical and Theoretical ChemistryBifunctionalIsomerization
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Synthesis, structural characterisation and biological studies of new mononuclear platinum(II) complexes with sterically hindered heterocyclic ligands

2011

Abstract Three novel cisplatin analogues were synthesized, designed according to an approach which violates the “classical” structure–activity relationship, by replacing the diamine ligands with a planar N donor heterocycle giving a sterically hindered complex. Moreover, the sterical hindrance of antitumor drug candidates potentially makes them less susceptible to deactivation by sulphur-containing proteins and helping to overcome resistance mechanisms. The resulting mononuclear complexes of sterically hindered polidentate heterocyclic N ligands [PtCl(bbp)]Cl ( 1 ) [bbp = 2,6-bis(2-benzimidazolyl)pyridine], [PtCl 2 (dptdn)](H 2 O) ( 2 ) [dptdn = sodium 5,6-diphenyl-3-(2′-pyridyl)-1,2,4-tria…

Steric effectsCisplatinStereochemistryCytotoxicitychemistry.chemical_elementBiological activityPolydentate nitrogen ligandInorganic Chemistrychemistry.chemical_compoundchemistryPolynuclear platinum complexeSettore CHIM/03 - Chimica Generale E InorganicaDiaminePyridineMaterials ChemistrymedicinePhysical and Theoretical ChemistryBifunctionalCytotoxicityPlatinummedicine.drugPolydentate nitrogen ligands; Polynuclear platinum complexes; Cytotoxicity
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Specific interaction of desthiobiotin lipids and water-soluble biotin compounds with streptavidin

1991

As shown for biotin lipids (Ref. 1), the formation of perfect 2-D crystalline streptavidin domains can also be observed in the plane of desthiobiotin lipid monolayers. The binding constant of streptavidin with desthiobiotin (Ka = 5·1013 mol−1) is lower than that with biotin (Ka = 1015 mol−1) (Ref. 2). By adding free biotin into the subphase a competitive replacement and a detaching of the streptavidin domains from the desthiobiotin lipid monolayer takes place. Streptavidin domains built at receptor lipid monolayers are still functional. As could be shown, there are two biotin binding sites at each protein molecule that are fully accessible to biotin (Ref. 1). This can be proven by the inter…

StreptavidinBiotin bindingPolymers and PlasticsOrganic Chemistryfood and beveragesCondensed Matter PhysicsBinding constantchemistry.chemical_compoundBiochemistryBiotinchemistryBiotinylationMonolayerMaterials ChemistryBiophysicsBifunctionalLinkerMakromolekulare Chemie. Macromolecular Symposia
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Influence of preparation conditions on the catalytic performance of mo/h-zsm-5 for methane dehydroaromatization

2021

[EN] Methane, the main component of natural gas, is an interesting source of chemicals and clean liquid fuels, and a promising alternative raw material to oil. Among the possible direct routes for methane conversion, its aromatization under non-oxidative conditions has received increasing attention, despite the low conversions obtained due to thermodynamic limitations, because of its high selectivity to benzene. Mo/H-ZSM-5, the first bifunctional zeolite-catalyst proposed for this reaction, is still considered as one of the most adequate and has been widely studied. Although the mono- or bifunctional nature of the MDA mechanism is still under debate, it is generally accepted that the Mo spe…

TechnologyQH301-705.5QC1-999Inorganic chemistryCatalysts preparation010402 general chemistry01 natural sciencesMethaneCatalysischemistry.chemical_compoundMo/ZSM-5General Materials ScienceBiology (General)Methane aromatizationZeoliteBifunctionalBenzeneQD1-999InstrumentationFluid Flow and Transfer Processes010405 organic chemistryTPhysicsProcess Chemistry and TechnologyGeneral EngineeringAromatizationCatalyst activationEngineering (General). Civil engineering (General)0104 chemical sciencesComputer Science ApplicationsChemistrychemistryZeolitesTA1-2040ZSM-5Selectivity
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Enantioselective Synthesis of 5-Trifluoromethyl-2-oxazolines under Dual Silver/Organocatalysis.

2019

[EN] The first enantioselective formal [3 + 2] cycloaddition between ¿-isocyanoesters and trifluoromethylketones to give 5-trifluoromethyl-2-oxazolines bearing two contiguous stereogenic centers, one of them being a quaternary stereocenter substituted with a CF3 group, has been developed. The reaction is based upon a multicatalytic approach that combines a bifunctional Brønsted base-squaramide organocatalyst and Ag+ as Lewis acid. The reaction could be achieved with a range of aryl and heteroaryl trifluoromethyl ketones, and the resulting oxazolines were obtained with good to excellent diastereo- and enantioselectivity.

Trifluoromethyl010405 organic chemistryArylOrganic ChemistryEnantioselective synthesis010402 general chemistry01 natural sciencesCombinatorial chemistryCycloaddition0104 chemical sciencesStereocenterchemistry.chemical_compoundchemistryCatàlisiOrganocatalysisFISICA APLICADALewis acids and basesBifunctionalQuímica orgànicaThe Journal of organic chemistry
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