Search results for " LIGANDS"

showing 10 items of 196 documents

Investigation into the reactivity of oxoniobocene complexes [Cp*2Nb(O)R] (Cp*=η5-C5Me5; R=H, OH, OMe) towards heterocumulenes: formation of carbamat…

2001

Abstract The reaction of [Cp*2NbCl2] (Cp*=η5-C5Me5) with KOH or Ba(OH)2·8H2O in THF was investigated under slightly modified conditions. In addition to the known complex [Cp*2Nb(O)H] (1), the new compound [Cp*2Nb(O)OH] (2) was formed. The reaction of 2 with PhNCS gave yellow [Cp*2Nb(O){SC(O)NHPh}] (3), while PhNCO formed yellow [Cp*2Nb(O){OC(O)NHPh}] (4). Complexes 3 and 4 were analytically and spectroscopically characterized. X-ray diffraction analyses of both compounds show that they contain either η1-S-thiocarbamato (3) or η1-O-carbamato ligand (4) along with a terminal NbO group. The reaction of 1 with one equivalent of PhNCO mainly gave orange [Cp*2NbH{OC(O)NPh}] (5) along with so…

Coordination sphereChemistryStereochemistryOrganic ChemistryHydride ligandsBiochemistryMedicinal chemistryCycloadditionCatalysisInorganic ChemistryHeterocumuleneMaterials ChemistryMoleculeChelationPhysical and Theoretical ChemistryJournal of Organometallic Chemistry
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Ammonia Activation by a Nickel NCN-Pincer Complex featuring a Non-Innocent N-Heterocyclic Carbene: Ammine and Amido Complexes in Equilibrium

2015

A Ni0-NCN pincer complex featuring a six-membered N-heterocyclic carbene (NHC) central platform and amidine pendant arms was synthesized by deprotonation of its NiII precursor. It retained chloride in the square-planar coordination sphere of nickel and was expected to be highly susceptible to oxidative addition reactions. The Ni0 complex rapidly activated ammonia at room temperature, in a ligand-assisted process where the carbene carbon atom played the unprecedented role of proton acceptor. For the first time, the coordinated (ammine) and activated (amido) species were observed together in solution, in a solvent-dependent equilibrium. A structural analysis of the Ni complexes provided insig…

Coordination spheretyppiliganditN-heterosykliset karbeenitammoniakkiPhotochemistryammoniaCatalysisAmidinenikkelikomopleksichemistry.chemical_compoundDeprotonationPolymer chemistrypincer ligandsN-heterocyclic carbenesta116bond activationChemistryLigandTransition metal carbene complexnickel complexGeneral ChemistryGeneral Medicinesidoksen aktivointiOxidative additionPincer movementCarbeneAngewandte Chemie
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Spin Cross-Over (SCO) Complex Based on Unsymmetrical Functionalized Triazacyclononane Ligand: Structural Characterization and Magnetic Properties

2019

International audience; The unsymmetrical ligand 1-(2-aminophenyl)-4,7-bis(pyridin-2-ylmethyl)-1,4,7-triazacyclononane (L6) has been prepared and characterized by NMR spectroscopy. The L6 ligand is based on the triazamacrocycle (tacn) ring that is functionalized by two flexible 2-pyridylmethyl and one rigid 2-aminophenyl groups. Reaction of this ligand with Fe(ClO4)2·xH2O led to the complex [Fe(L6)](ClO4)2 (1), which was characterized as the first Fe(II) complex based on the unsymmetrical N-functionalized tacn ligand. The crystal structure revealed a discrete monomeric [FeL6]2+ entity in which the unsymmetrical N-functionalized triazacyclononane molecule (L6) acts as hexadentate ligand. As …

Crystal structure010402 general chemistryRing (chemistry)01 natural scienceslcsh:Chemistrychemistry.chemical_compoundSpin crossoverPyridineMagnetic propertiesMacrocycle ligands; Iron complex; High spin and Low spin; Spin Cross-Over; Magnetic propertiesMaterials ChemistryMolecule[CHIM.COOR]Chemical Sciences/Coordination chemistryIron complex010405 organic chemistryLigand[CHIM.MATE]Chemical Sciences/Material chemistryNuclear magnetic resonance spectroscopy0104 chemical sciencesElectronic Optical and Magnetic MaterialsCrystallographyMonomerchemistrylcsh:QD1-999Chemistry (miscellaneous)Macrocycle ligandsHigh spin and Low spinSpin Cross-OverMagnetochemistry
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Complexation behaviour of hexadentate ligands possessing N2O4and N2O2S2cores: differential reactivity towards Co(ii), Ni(ii) and Zn(ii) salts and str…

2004

Reactions of divalent metal salts of Co, Ni and Zn with 1,2-di(salicylaldimino-o-phenylthio) ethane (H2L1) and 1,2-di(naphthaldimino-o-phenylthio) ethane (H2L2), having N2O2S2 cores, and 1,2-di(O-salicylaldimino-o-hydroxyphenyl) ethane (H2L3), having a N2O4 core, have been explored. Out of the three ligands and the nine products obtained from the corresponding reactions, two ligands and seven products were crystallographically characterized. However, all the ligands and the products were characterized by analytical and spectral methods. Reaction of H2L1 and H2L2 with Co(II) salts results in oxidative cleavage of the C-S bond to produce a Co(III) product bound to two dissimilar tridentate li…

Crystal-StructureC-SChemistryInorganic chemistrySize-Specific TransformationsNso-Donor LigandsNickel(Ii) ComplexesCobaltGeneral ChemistryCrystal structureBaseS Bond-CleavageThioethersChemical reactionCatalysisBond lengthCrystallographyOctahedronChemical bondMaterials ChemistryChelationReactivity (chemistry)Metal-ComplexesBond cleavageNew J. Chem.
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[Ag67(SPhMe2)32(PPh3)8]3+: Synthesis, Total Structure, and Optical Properties of a Large Box-Shaped Silver Nanocluster

2016

Engineering the surface ligands of metal nanoparticles is critical in designing unique arrangements of metal atoms. Here, we report the synthesis and total structure determination of a large box-shaped Ag67 nanocluster (NC) protected by a mixed shell of thiolate (2,4-dimethylbenzenethiolate, SPhMe2) and phosphine (triphenylphosphine, PPh3) ligands. Single crystal X-ray diffraction (SCXRD) and electrospray ionization mass spectrometry (ESI-MS) revealed the cluster formula to be [Ag67(SPhMe2)32(PPh3)8]3+. The crystal structure shows an Ag23 metal core covered by a layer of Ag44S32P8 arranged in the shape of a box. The Ag23 core was formed through an unprecedented centered cuboctahedron, i.e.,…

CuboctahedronElectrospray ionizationnanoclusters02 engineering and technologyElectronic structureCrystal structure010402 general chemistry01 natural sciencesBiochemistryCatalysisMetalchemistry.chemical_compoundColloid and Surface ChemistryTriphenylphosphinemetal nanoparticlesta116ta114ChemistryLigandGeneral Chemistry021001 nanoscience & nanotechnology0104 chemical sciencesCrystallographysurface ligandsvisual_artvisual_art.visual_art_medium0210 nano-technologySingle crystalJournal of the American Chemical Society
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Photoinduced HS state in the first spin-crossover chain containing a cyanocarbanion as bridging ligand

2009

A new polymeric approach, based on cyanocarbanion ligands, for the design of spin crossover (SCO) compounds led us to the compound [Fe(abpt)2(tcpd)] (1) (tcpd^2 = (C[C(CN)2|3)^2 , abpt = 4-amino-3,5-bis(pyridin-2-yl)-1,2,4-triazole) which has been characterised as the first SCO molecular chain involving a cyanocarbanion as bridging ligand. Gomez Garcia, Carlos Jose, Carlos.Gomez@uv.es

Cyanocarbanion ligandsChemistryStereochemistryUNESCO::QUÍMICAPolimeryc approachMetals and AlloysBridging ligandBridging ligandGeneral ChemistryState (functional analysis)UNESCO::QUÍMICA::Química macromolecular:QUÍMICA [UNESCO]CatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsChain (algebraic topology)Polimeryc approach ; Cyanocarbanion ligands ; Photoinduction ; Bridging ligandSpin crossoverPhotoinductionMaterials ChemistryCeramics and Composites:QUÍMICA::Química macromolecular [UNESCO]
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Enantiocontrol in the intermolecular cyclopropanation reaction catalyzed by dirhodium(II) complexes with ortho-metalated aryl phosphine ligands

2001

(P) and (M) dirhodium(II) complexes with ortho-metalated aryl phosphines are assessed as chiral catalysts in the enantioselective cyclopropanation of styrenes by ethyl diazoacetate; enantioselectivities up to 91% and up to 87%, respectively, for cis- and trans-2-arylcyclopropanecarboxylates are observed. Barberis, Mario, Mario.Barberis@uv.es ; Lahuerta Peña, Pascual, Pascual.lahuerta@uv.es ; Perez Prieto, Julia, Julia.Perez@uv.es ; Sanau Torrecilla, Mercedes, Mercedes.Sanau@uv.es

CyclopropanationUNESCO::QUÍMICAMedicinal chemistry:QUÍMICA [UNESCO]CatalysisCatalysischemistry.chemical_compoundEthyl diazoacetateMaterials ChemistryOrganic chemistryPhosphine ligandsEnantiocontrol ; Intermolecular cyclopropanation ; Catalyst ; Phosphine ligandsArylIntermolecular forceMetals and AlloysEnantioselective synthesisGeneral ChemistryUNESCO::QUÍMICA::Química macromolecularSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsEnantiocontrolchemistryCeramics and Composites:QUÍMICA::Química macromolecular [UNESCO]CatalystIntermolecular cyclopropanationPhosphine
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γδ T cells as a potential tool in colon cancer immunotherapy

2014

γδ T cells are capable of recognizing tumor cells and exert potent cellular cytotoxicity against a large range of tumors, including colon cancer. However, tumors utilize numerous strategies to escape recognition or killing by patrolling γδ T cells, such a downregulation of NKG2D ligands, MICA/B and ULBPs. Therefore, the combined upregulation of T-cell receptorand NKG2D ligands on tumor cells and induction of NKG2D expression on γδ T cells may greatly enhance tumor killing and unlock the functions of γδ T cells. Here, we briefly review current data on the mechanisms of γδ T-cell recognition and killing of colon cancer cells and propose that γδ T cells may represent a promising target for the…

Cytotoxicity ImmunologicColorectal cancermedicine.medical_treatmentImmunologyNkg2d ligandsLarge rangeLigandsDownregulation and upregulationT-Lymphocyte SubsetsmedicineHumansImmunology and AllergyIn patientCell-mediated cytotoxicitybusiness.industryReceptors Antigen T-Cell gamma-deltaImmunotherapymedicine.diseaseNKG2Dgamma delta cellcolon cancerOncologyColonic NeoplasmsImmunologyNeoplastic Stem CellsImmunotherapybusinessImmunotherapy
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RNA Transfer by Electroporation into Mature Dendritic Cells Leading to Reactivation of Effector-Memory Cytotoxic T Lymphocytes: A Quantitative Analys…

2005

Previous studies have analyzed transfer of RNA-encoded tumor-associated antigens (TAAs) into immature dendritic cells (DCs) because of their exceptional ability to internalize antigens. Concerns have been raised regarding the use of immature DCs in clinical studies because of their capacity to tolerize T cells. Therefore, we focused on optimizing RNA transfer into mature DCs using the method of electroporation and obtained high protein expression in 90% of mature DCs. Particular emphasis was placed on quantifying RNA transfer. Reconstitution of peptide-MHC (pMHC) ligands on RNA-pulsed DCs was measured with the help of effector-memory cytotoxic T lymphocytes (CTLs) specific for the melanoma-…

Cytotoxicity Immunologicchemical and pharmacologic phenomenaBiologyLymphocyte ActivationTransfectionEpitopeAntigenCell Line TumorDrug DiscoveryGeneticsHumansCytotoxic T cellMelanomaMolecular BiologyPharmacologyEffectorElectroporationRNAhemic and immune systemsDendritic CellsTransfectionMolecular biologyElectroporationPhenotypedendritic cells; RNA transfection; electroporation; effector-memory cytotoxic T lymphocytes; peptide-MHC ligands; tumor immunotherapy; melanoma; tyrosinase; CDK4; EGFPRNAMolecular MedicineImmunotherapyRNA transfectionT-Lymphocytes CytotoxicMolecular Therapy
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Cascade complex formation by phosphate in the cobalt(II)/[30]aneN10 anaerobic system

1993

Abstract The interaction of phosphate with the mono- and binuclear cobalt(II) complexes of [30]aneN 10 (1,4,7,10,13,16,19,22,25,28-decaazacyclotriacontane) has been studied by potentiometry in 0.15 mol dm −3 NaClO 4 solution at 298.15 K under anaerobic conditions. The stable species [CoH 2 ([30]aneN 10 )PO 4 ] + , [CoH 4 ([30]aneN 10 )PO 4 ] 3+ , [Co 2 H([30]aneN 10 )PO 4 ] 2+ , [Co 2 H 2 ([30]aneN 10 )PO 4 ] 3+ and [Co 2 H 3 ([30]aneN 10 )PO 4 ] 4+ , where the phosphate anion is directly bound to the metal ions or acts as a second sphere ligand, are formed and their stability constants have been determined. The results obtained allowed for the selection of suitable conditions for the study…

DIOXYGEN CARRIERS; DIOXYGEN BINDING; Co(II) COMPLEXES; POLYAMINE LIGANDS; DITOPIC POLYAMINES; OPEN-CHAIN POLYAZAALKANES; THERMODYNAMICS; ANION COORDINATION CHEMISTRY; INCLUSION COMPLEXESINCLUSION COMPLEXESMetal ions in aqueous solutionComplex formationInorganic chemistryDIOXYGEN BINDINGchemistry.chemical_elementMedicinal chemistryCo(II) COMPLEXESInorganic Chemistrychemistry.chemical_compoundOPEN-CHAIN POLYAZAALKANESANION COORDINATION CHEMISTRYTHERMODYNAMICSMaterials ChemistryDIOXYGEN CARRIERSPhysical and Theoretical ChemistryLigandPhosphatePhosphate anionchemistryDITOPIC POLYAMINESChemical equilibriumAnaerobic exerciseCobaltPOLYAMINE LIGANDS
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