Search results for "Catalysis"

showing 10 items of 5944 documents

Spin Switching with Triazolate-Strapped Ferrous Porphyrins

2019

Fe(III) porphyrins bridged with 1,2,3-triazole ligands were synthesized. Upon deprotonation, the triazolate ion coordinates to the Fe(III) ion, forming an overall neutral high-spin Fe(III) porphyrin in which the triazolate serves both as an axial ligand and as the counterion. The second axial coordination site is activated for coordination and binds p-methoxypyridine, forming a six-coordinate low-spin complex. Upon addition of a phenylazopyridine as a photodissociable ligand, the spin state of the complex can be reversibly switched with ultraviolet and visible light. The system provides the basis for the development of switchable catalase- and peroxidase-type catalysts and molecular spin sw…

chemistry.chemical_classificationkemiallinen synteesiSpin states010405 organic chemistryLigandkompleksiyhdisteet010402 general chemistry01 natural sciencesPorphyrin0104 chemical sciencesIonCatalysisInorganic Chemistrychemistry.chemical_compoundCrystallographyDeprotonationchemistrycoordination complexesPhysical and Theoretical ChemistryCounterionta116chemical synthesisVisible spectrumInorganic Chemistry
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The Influence of the Amide Linkage in the FeIII-Binding Properties of Catechol-Modified Rosamine Derivatives

2015

The two new fluorescent ligands RosCat1 and RosCat2 contain catechol receptors connected to rosamine platforms through an amide linkage and were synthesized by using microwave-assisted coupling reactions of carboxyl- or amine-substituted rosamines with the corresponding catechol units and subsequent deprotection. RosCat1 possesses a reverse amide, whereas RosCat2 has the usual oriented amide bond (HNCO vs. CONH, respectively). The ligands were characterized by means of NMR spectroscopy, mass-spectrometry, and DFT calculations and X-ray crystallography studies for RosCat1. The influence of the amide linkage on the photophysical properties of the fluorescent ligands was assessed in different …

chemistry.chemical_classificationligand designCatecholChemistryStereochemistryOrganic ChemistryChemistry (all)Quantum yieldGeneral ChemistryNuclear magnetic resonance spectroscopyamideCatalysisCoupling reactionCoordination complexCrystallographychemistry.chemical_compoundironSettore CHIM/03 - Chimica Generale E InorganicaAmidePeptide bondChelationcoordination modemass spectrometry
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Electrical Behaviour of Heterobimetallic [MM′(EtCS2)4] (MM′=NiPd, NiPt, PdPt) and MM′X-Chain Polymers [PtM(EtCS2)4I] (M=Ni, Pd)

2012

Herein, we report the isolation of new heterobimetallic complexes [Ni0.6Pd1.4ACHTUNGTRENUNG(EtCS2)4] (1), [NiPtACHTUNGTRENUNG(EtCS2)4] (2) and [Pd0.4Pt1.6ACHTUNGTRENUNG(EtCS2)4] (3), which were constructed by using transmetallation procedures. Subsequent oxidation with iodine furnished the MM'X monodimensional chains [Ni0.6Pt1.4ACHTUNGTRENUNG(EtCS2)4I] (4) and [Ni0.1Pd0.3Pt1.6ACHTUNGTRENUNG(EtCS2)4I] (5). The physical properties of these systems were investigated and the chain structures 4 and 5 were found to be reminiscent of the parent [Pt2ACHTUNGTRENUNG(EtCS2)4I] species. However, they were more sensitively dependent on the localised nature of the charge on the Ni ion, which caused spont…

chemistry.chemical_classificationmolecular electronicsOrganic ChemistryNanotechnologyGeneral ChemistryPolymerDFTinorganic polymerCatalysisIonCrystallographyTransmetalationchemistryConduction bandChemistry - A European Journal
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Multicomponent Synthesis of Benzothiophen-2-acetic Esters by a Palladium Iodide Catalyzed S-cyclization – Alkoxycarbonylation Sequence

2021

A catalytic carbonylative approach to the multicomponent synthesis of benzothiophene derivatives from simple building blocks [1-(2-(methylthio)phenyl)prop-2-yn-1-ols, carbon monoxide, and an alcohol)] is presented. It is based on an S-cyclization-demethylation-alkoxycarbonylation-reduction sequence promoted by the PdI2/KI catalytic system, occurring under relatively mild conditions (40 atm, 80 °C, 15 h). Benzothiophene-2-acetic esters are obtained in moderate to good yields (35–70%) starting from variously substituted substrates in combination with different alcohols as external nucleophiles (17 examples). (Figure presented.).

chemistry.chemical_classificationmulticomponent reactionIodidechemistry.chemical_elementGeneral ChemistrycarbonylationSettore CHIM/06 - Chimica OrganicapalladiumCombinatorial chemistryCatalysischemistrybenzothiophenesS-cyclizationCarbonylationPalladiumSequence (medicine)
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Traceless chirality transfer from a norbornene β-amino acid to pyrimido[2,1-a]isoindole enantiomers

2017

Abstract The synthesis of two enantiomeric pairs of pyrimidoisoindoles 9a, 9b and 10a, 10b is reported. During a domino ring-closure reaction, followed by cycloreversion, the chirality of diendo-(−)-(1R,2S,3R,4S)-3-aminobicyclo[2.2.1]hept-5-ene-2-carboxamide [(−)-1] was successfully transfered to heterocycles (+)-9a, (+)-10a, (−)-9b, (−)-10b and (−)-10c.

chemistry.chemical_classificationpharmacyamino acidsheterocycles010405 organic chemistryStereochemistrybiologyOrganic Chemistry010402 general chemistrychemistry01 natural sciencesCatalysis0104 chemical sciencesAmino acidInorganic Chemistrychemistry.chemical_compoundchemistryPhysical and Theoretical ChemistryEnantiomerIsoindoleChirality (chemistry)ta116NorborneneTetrahedron: Asymmetry
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Synthesis, characterization and catalytic properties for olefin polymerization of two new dimeric zirconium(IV) complexes having diamine-bis(phenolat…

2015

Abstract Reaction of the zirconium tetrachloride with one equivalent of the sodium salt of the diamine bis (phenolate) ligand, L1H2 (Me2NCH2CH2N-(CH2-2-OH-3,5-tBu-C6H2)2) or L2H2 (Me2NCH2CH2N-(CH2-2-OH-3,5-tBu-C6H2)(CH2-2-OH-C6H4)) in the presence of air led to formation of [Lig1ZrCl]2(μ-O) and [Lig2ZrCl]2(μ-O), respectively. These novel oxo-bridged dinuclear zirconium complexes were characterized by elemental analysis, 1H NMR spectroscopy and by single-crystal X-ray diffraction. Their reactivities in polymerization of ethylene and 1-octene, upon activation with Al(iBu)3/Ph3CB(C6F5)4 and MAO, were examined. It was found that lack of t-Bu substituents on one phenolate ring cause a significan…

chemistry.chemical_classificationpolyethyleneZirconiumEthyleneLigandProcess Chemistry and Technologychemistry.chemical_elementPolymerCatalysisCatalysispoly(1-octene)chemistry.chemical_compoundPolymerizationchemistryDiaminezirconium catalystPolymer chemistryTetrachloridediamine-bis(phenolate) ligandOrganic chemistryZiegler–Natta polymerizationApplied Catalysis A : General : an International Journal Devoted to Catalytic Science and its Applications
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(Co)polymerization behavior of supported metallocene catalysts. I. Ligand and substituent effect

2005

Ethylene polymerization and its copolymerization with 1-hexene with a set of supported metallocene catalysts were studied. As a carrier, the complex of mag- nesium chloride with tetrahydrofuran, which was previously pretreated with a triiso- butylaluminium (TIBA), was used. The investigated metallocene compound differs in the metal type (Zr or Ti), the nature of the alkyl substituent in the cyclopentadienyl ring, and the type of ligand (Cp or Ind). The effect of catalyst composition on the anchored metal content, catalyst activity, comonomer reactivity, and polymer proper- ties was investigated. The results obtained with supported catalysts were compared with those obtained with their homog…

chemistry.chemical_classificationsupportPolymers and PlasticsComonomermetallocene catalystsOrganic ChemistrySubstituentHomogeneous catalysiscopolymerizationchemistry.chemical_compoundchemistryCyclopentadienyl complexPolymerizationPolymer chemistryMaterials ChemistrystructureMetalloceneTetrahydrofuranAlkylJournal of Polymer Science Part A: Polymer Chemistry
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(Co)polymerisation Behaviour of Supported Metallocene Catalysts: Carrier Effect

2006

The polymerisation and copolymerisation of ethylene with 1-hexene over metallocene catalysts L 2 ZrCl 2 / MAO (L = Cp, n-BuCp, t-BuCp, i-PrCp, Me 5 Cp) supported on different types of carriers (MgCl 2 (MeOH) 6 or silica with CH 3 surface groups obtained in the sol-gel process) were studied. It was demonstrated that both the metallocene structure and the type of inorganic support affected catalyst activity and polymer properties such as melting point, molecular weight and molecular weight distribution. The metallocene structure also determined comonomer incorporation, both for homogeneous and supported catalytic systems. When a catalyst is anchored on a support, it becomes less effective at …

chemistry.chemical_classificationsupportsPolymers and PlasticsComonomermetallocene catalystsOrganic ChemistryPolymerPolyethyleneCondensed Matter PhysicsCatalysischemistry.chemical_compoundchemistryPolymerizationPolymer chemistryopolymerizationMaterials ChemistryCopolymerMolar mass distributionstructurePhysical and Theoretical ChemistryCrystafSSAMetalloceneMacromolecular Chemistry and Physics
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An insight into the synthesis of novel aryl-substituted alicyclic β-amino acid derivatives through substrate-directed palladium-catalysed regio- and …

2015

Novel aryl-substituted alicyclic β-amino acid derivatives were synthesized through substrate-determined palladium-catalysed cross-coupling of aryl iodides with five- or six-membered cycloalkene β-amino esters. The arylations were investigated with different catalysts, solvents, bases and aryl halides, and with some cyclohexene 2-aminocarboxylate isomers. The stereochemistry and the position of the ring olefinic bond of the starting 2-aminocycloalkanecarboxylate influenced the coupling reaction, and predetermined the structure of the arylated product.

chemistry.chemical_classificationsynthesisGeneral Chemical EngineeringArylCyclohexenechemistry.chemical_elementGeneral ChemistryRing (chemistry)Medicinal chemistryCoupling reactionCatalysischemistry.chemical_compoundAlicyclic compoundchemistrycross-couplingOrganic chemistryta116CycloalkenePalladiumRSC Advances
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Iron(III) Chloride as a Mild Catalyst for the Dearomatizing Cyclization of N-Acylindoles

2020

A catalytic approach for the preparation of indolines by dearomatizing cyclization is presented. FeCl3 acts as a catalyst to afford tetracyclic 5a,6-dihydro-12H-indolo[2,1-b][1,3]benzoxazin-12-ones in good yields. The cyclization also proceeds with tosylamides forming C-N bonds in 53% yield.

chemistry.chemical_compound010405 organic chemistryChemistryYield (chemistry)Organic Chemistry010402 general chemistry01 natural sciencesMedicinal chemistryIron(III) chloride0104 chemical sciencesCatalysisThe Journal of Organic Chemistry
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