Search results for " LIGANDS"

showing 10 items of 196 documents

The selection of aptamers specific for membrane molecular targets

2010

AbstractA growing number of RNA aptamers have been selected experimentally using the SELEX combinatorial approach, and these aptamers have several advantages over monoclonal protein antibodies or peptides with respect to their applications in medicine and nanobiotechnology. Relatively few successful selections have been reported for membrane molecular targets, in contrast to the situation with non-membrane molecular targets. This review compares the procedures and techniques used in selections against membrane proteins and membrane lipids. In the case of membrane proteins, the selections were performed against soluble protein fragments, detergent-membrane protein mixed micelles, whole cells…

AptamerMembrane lipidsReviewBiologyAptamersBiochemistryCell membraneMembrane LipidsRaftsMembrane transportersmedicineMolecular BiologyMembranesSELEXVesicleCell MembraneSELEX Aptamer TechniqueMembrane ProteinsCell BiologyAptamers NucleotideLipidsmedicine.anatomical_structureMembraneMembrane proteinBiochemistryLiposomesVirusesSELEX Aptamer TechniqueRNASystematic evolution of ligands by exponential enrichmentCellular and Molecular Biology Letters
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Sequestration of alkyltin(IV) cations by complexation with amino-polycarboxylic chelating agents

2013

Abstract The binding capacity of four amino-polycarboxylic ligands (APCs) [nitrilotriacetate (NTA), ethylenediamine- N , N , N′ , N′ -tetraacetate (EDTA), (S,S)-ethylenediamine- N , N ′-disuccinic acid (S,S-EDDS) and diethylenetriamine- N , N , N′ , N″ , N″ -pentaacetate (DTPA)] towards mono-, di- and tri-alkyltin(IV) cations [(CH 3 )Sn 3 + , (CH 3 ) 2 Sn 2 + , (C 2 H 5 ) 2 Sn 2 + , (CH 3 ) 3 Sn + or (C 2 H 5 ) 3 Sn + ] was studied, in aqueous solutions, by ISE-H + potentiometry, at I  = 0.1 mol L − 1 (NaCl) and at T  = 298.15 K. In all the systems R x Sn (4 − x)+  − APC (R = CH 3 or C 2 H 5 ) a strong 1:1 species is formed together with protonated, hydroxo and dinuclear complexes. The valu…

Aqueous solutionComplexation in aqueous solutionStereochemistryLigandEthylenediamineProtonationAlkyltin(IV) cations; Amino-polycarboxylic ligands; Complexation in aqueous solution; Sequestration ability of complexones;Condensed Matter PhysicsMedicinal chemistryAtomic and Molecular Physics and OpticsAlkyltin(IV) cationElectronic Optical and Magnetic MaterialsIonAmino-polycarboxylic ligandchemistry.chemical_compoundSequestration ability of complexoneschemistryDiethylenetriamineMaterials ChemistryChelationSettore CHIM/01 - Chimica AnaliticaPhysical and Theoretical ChemistrySimple correlationSpectroscopy
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Ti(iv)-amino triphenolate complexes as effective catalysts for sulfoxidation

2010

C 3 -symmetric Ti (IV) amino triphenolate complexes efficiently catalyze, without previous activation and in excellent yields, the oxidation of sulfides at room temperature, using both CHP and the more environment friendly aqueous hydrogen peroxide as terminal oxidants, with catalyst loadings down to 0.01%. The Ti(IV) catalysts and the intermediate Ti(IV)-peroxo complexes have been characterized in solution by 1H NMR and ESI-MS techniques and via density functional studies.

Aqueous solutionoxidationChemistryhydrogen peroxideEnvironmentally friendlysulfoxidationCatalysisInorganic Chemistrychemistry.chemical_compoundtitanium complexes; sulfoxidation; hydrogen peroxide; tripodal ligands; c3 symmetry; oxidationProton NMROrganic chemistryFunctional studiestitanium complexesc3 symmetryHydrogen peroxidetripodal ligands
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Highly Robust but Surface-Active : An N-Heterocyclic Carbene-Stabilized Au25 Nanocluster

2019

Surface organic ligands play a critical role in stabilizing atomically precise metal nanoclusters in solutions. However, it is still challenging to prepare highly robust ligated metal nanoclusters that are surface-active for liquid-phase catalysis without any pre-treatment. Now, an N-heterocyclic carbene-stabilized Au25 nanocluster with high thermal and air stabilities is presented as a homogenous catalyst for cycloisomerization of alkynyl amines to indoles. The nanocluster, characterized as [Au25(iPr2-bimy)10Br7]2+ (iPr2-bimy=1,3-diisopropylbenzimidazolin-2-ylidene) (1), was synthesized by direct reduction of AuSMe2Cl and iPr2-bimyAuBr with NaBH4 in one pot. X-ray crystallization analysis …

Au25katalyytitkatalyysicarbene ligandsnanohiukkasetgold nanoclustershomogeneous catalysisgold catalysiskulta
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β-Catenin Activation Regulates Tissue Growth Non–Cell Autonomously in the Hair Stem Cell Niche

2014

Coordinated Hair Growth Wnt/β-catenin signaling is a key pathway that plays a conserved role in regulating stem cell function during adult tissue regeneration. Using time-lapse imaging of live mice, Deschene et al. (p. 1353 ) show that genetic activation of β-catenin within hair follicle stem cells generates axes of hair growth by coordinated cell divisions and cell movements, even when the normal niches—the dermal papillae—are laser-ablated. Activated β-catenin enhances Wnt ligand secretion, and these ligands can then activate Wnt signaling in adjacent cells that do not have activated β-catenin, indicating how activated stem cells could influence neighboring cells during normal growth and …

Beta-cateninWnt ProteinCellular differentiationLigandBiologyLigandsModels BiologicalArticleMiceStem CellmedicineAnimalsStem Cell NicheAnimals; Cell Differentiation; Cell Division; Hair; Hair Follicle; Ligands; Mice; Models Biological; Mutation; Stem Cell Niche; Stem Cells; Tamoxifen; Up-Regulation; Wnt Proteins; beta Catenin; Wnt Signaling Pathway; Medicine (all); MultidisciplinaryWnt Signaling Pathwaybeta CateninMultidisciplinaryintegumentary systemAnimalStem CellsMedicine (all)Regeneration (biology)Mesenchymal stem cellWnt signaling pathwayCell DifferentiationHair follicleUp-RegulationCell biologyWnt ProteinsTamoxifenmedicine.anatomical_structureCateninMutationbiology.proteinStem cellHair FollicleCell DivisionHairScience
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Hybrid ferrocene ligands (P, N) : synthesis, coordination to metals and applications in arylation coupling catalysis

2017

The research theme developed during this thesis concerns the development of new hybrid ferrocene hybrid (P, N) ligands with controlled conformation, robust and stable to air. These hybrid tetradent ligands comprise two types of coordinating functions with distinct steric and electronic properties. Their coordination chemistry with metals such as gold or palladium has been studied and some isolated Au (I) complexes have been used in the arylation coupling catalysis of aryl iodides.

Bis(aminométhyl)-ferrocèneN) à conformation contrôléeNitrogenCouplage C-CRMN 15NBis (aminomethyl)-ferroceneAzoteFunctionalization of ferrocenePhosphorusOrHybrid ligandsHybrid ligands (PFonctionnalisation de ferrocène[CHIM.OTHE] Chemical Sciences/OtherLigands hybridesPhosphoreLigands hybrides-(PGoldFerrocene15N NMRLigands multidentes[CHIM.OTHE]Chemical Sciences/OtherN) with controlled conformationPalladiumC-C cross Coupling
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Orbital Decomposition of the Carbon Chemical Shielding Tensor in Gold(I) N-Heterocyclic Carbene Complexes.

2020

The good performance of N‐heterocyclic carbenes (NHCs), in terms of versatility and selectivity, has called the attention of experimentalists and theoreticians attempting to understand their electronic properties. Analyses of the Au(I)–C bond in [(NHC)AuL]+/0 (L stands for a neutral or negatively charged ligand), through the Dewar–Chatt–Duncanson model and the charge displacement function, have revealed that NHC is not purely a σ‐donor but may have a significant π‐acceptor character. It turns out, however, that only the σ‐donation bonding component strongly correlates with one specific component of the chemical shielding tensor. Here, in extension to earlier works, a current density analysi…

C-13 NMR-SPECTROSCOPYElectronic structureRING CURRENTS010402 general chemistry01 natural sciencesInorganic Chemistrychemistry.chemical_compoundDONATION Author InformationGROUP-11MAGNETIC-PROPERTIESTensorGold(I) NHC ComplexesFull Paper010405 organic chemistryChemistryLigandElectron donationCAPTIVE INTERMEDIATEFull PapersSymmetry (physics)0104 chemical sciencesChemical shielding tensorChemistryChemical physicsElectron back‐donationElectromagnetic shieldingElectron back-donationPATTERNSDiamagnetismDONATIONGoldCarbeneCurrent densityCarbene ligandsCONTINUOUS TRANSFORMATIONBONDAPPROXIMATIONEuropean journal of inorganic chemistry
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Photochemical ligand rearrangement in dirhodium(II) compounds. Structure of Rh2(O2CCH3)2(η2-O2CCH3)[(C6H4)PPh2] (η2-PCCl)(PCClP-ClC6H4)Ph2

1995

Abstract The photochemical reaction of the adducts Rh2(O2CCH3)3[(C6H4)P(o-ClC6H4)Ph]· (P(p-XC6H4)3) (X=H, Me, Cl), yield the compounds Rh2(O2CCH3)2(η2-O2CCH3)[(p-XC6H3)P (p-XC6H4)2](η2-PCCl), (PCCl=P(o-ClC6H4)Ph2) in a ligand rearrangement reaction that involves activation of CH and RhC bonds. The factors that favour this process are studied by carrying out photochemical reactions with different phosphines. The structures of Rh2(O2CCH3)2(η2-O2CCH3) [(C6H4)PPh2](η2-PCCl) has been determined by X-ray diffraction. Mr=1321.1, orthorhombic, space group Pbcn, a=20.339(8), b=20.07(6), c=23.07(3) A , V=9413(3) A 3 , Z=8, D x =1.86 g cm −3 . Mo Kα radiation (graphite crystal monochromator, λ=0.071…

Chelating ligandsChemistryLigandCrystal structurePhotochemistryAdductInorganic ChemistryBond lengthchemistry.chemical_compoundMaterials ChemistryRearrangement reactionOrthorhombic crystal systemPhysical and Theoretical ChemistryTriphenylphosphineInorganica Chimica Acta
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Malonato complexes of oxidovanadium(IV): Synthesis, structural characterization and exploration of their insulin mimetic properties

2011

Abstract Several bis-malonatooxidovanadium(IV) complexes of the general type [M2(H2O)n][VO(mal)2(H2O)] (where M = Li(1), Na(2), K(3), Cs(4) and NH4(5); n = 3.5, 1, 3, 1 and 1, respectively) were isolated in good yield and high purity. These complexes were fully characterized by various physicochemical techniques (elemental analysis, UV–Vis, IR, EPR, CV, etc.) complexes 1, 2 and 3 were structurally characterized by single crystal X-ray diffraction technique. In vivo antidiabetic properties of bis-malonato complexes 1, 2, 3 and 5 have been studied using Streptozotocin induced diabetic rats. Significant lowering of blood sugar level has been noticed. At the same time these complexes were found…

Chelating ligandsStereochemistryChemistryStreptozotocinMedicinal chemistrylaw.inventionInorganic ChemistryIn vivolawYield (chemistry)X-ray crystallographyMaterials ChemistrymedicinePhysical and Theoretical ChemistryInsulin mimeticElectron paramagnetic resonanceSingle crystalmedicine.drugInorganica Chimica Acta
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Dinuclear Palladium(II) and -(III) Compounds with O,O-Chelating Ligands. Room-Temperature Direct 2-Phenylation of 1-Methylindole

2012

New dinuclear palladium(III) compounds of general formula Pd2[(C6H4)PPh2]2[O–O]2Cl2, O–O being chelating phenolates C6H4OC(O)R (R = CH3, 3a; R = C2H5, 3b; R = OPh, 3c) or acetylacetonates RC(O)CHC(O)R (R = CH3, 4a; R = CF3, 4b; R = C(CH3)3, 4c), have been obtained by oxidation with PhICl2 of the corresponding palladium(II) compounds. The stability of the new compounds has been studied by 31P NMR spectroscopy from 200 to 298 K. DFT calculations of the stability of the complexes have also been performed. In agreement with these calculations, only compound Pd2[(C6H4)PPh2]2[(CF3C(O)CHC(O)CF3]2Cl2, 6b, showed the highest thermal stability. 6b was characterized by X-ray diffraction methods, prese…

Chelating ligandsStereochemistryOrganic Chemistrychemistry.chemical_elementMedicinal chemistryCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryThermal stabilityChelation1-Methylindole31p nmr spectroscopyPhysical and Theoretical ChemistryPalladiumOrganometallics
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