Search results for "Chelation"

showing 10 items of 286 documents

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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Fluorescent Type II Materials from Naphthylmethyl Polyamine Precursors

2004

Speciation studies in aqueous solution on the interaction of Cu2+ and Zn2+ with a series of polyaminic ligands N-naphthalen-1-ylmethyl-N′-{2-[(naphthalen-1-ylmethyl)-amino]-ethyl}-ethane-1,2-diamine (Ll), N-naphthalen-1-ylmethyl-N′-(2-{2-[(naphthalen-1-ylmethyl)-amino]-ethylamino}-ethyl)-ethane-1,2-diamine (L2) and N-naphthalen-1-ylmethyl-N′-[2-(2-{2-[(naphthalen-1-ylmethyl)-amino]-ethylamino}-ethylamino)-ethyl]-ethane-1,2-diamine (L3) containing two naphthylmethyl groups at their termini and N 1-(2-{2-[(naphthalen-1-ylmethyl)-amino]-ethylamino}-ethyl)-ethane-1,2-diamine (L4) containing just one naphthylmethyl group have been carried out at 298.1 K in 0.15 mol dm−3 NaCl. In the case of the …

chemistry.chemical_compoundAqueous solutionchemistryMetal ions in aqueous solutionInorganic chemistryChelationGeneral ChemistryPolyamineMedicinal chemistryFluorescenceSupramolecular Chemistry
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Efficient Synthesis of 1,4,7-Triazacyclononane and 1,4,7-Triazacyclononane-Based Bifunctional Chelators for Bioconjugation (Eur. J. Org. Chem. 35/201…

2014

chemistry.chemical_compoundBioconjugationChemistryOrganic ChemistryOrganic chemistryChelationPhysical and Theoretical ChemistryBifunctionalEuropean Journal of Organic Chemistry
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Efficient Synthesis of 1,4,7-Triazacyclononane and 1,4,7-Triazacyclononane-Based Bifunctional Chelators for Bioconjugation

2014

The reaction of diethylenetriamine with chloroacetaldehyde yielded a bicyclic aminal intermediate for the synthesis of 1,4,7-triazacyclononane (TACN), a macrocyclic polyamine the derivatives of which find applications as catalysts, bleaching agents, and chelators for medical imaging. This new synthetic protocol outperforms the synthetic methods described so far because it does not involve any cyclization step. Moreover, this aminal intermediate allowed access to a new family of TACN derivatives functionalized on the carbon skeleton, for example, C-aminomethyl-TACN. This novel compound is a precursor of valuable bifunctional chelating agents for nuclear medicine, in particular, for the prepa…

chemistry.chemical_compoundBioconjugationchemistryBicyclic moleculeOrganic ChemistryDiethylenetriamineAminalOrganic chemistryChloroacetaldehydeChelationPhysical and Theoretical ChemistryBifunctionalCatalysisEuropean Journal of Organic Chemistry
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Selectively Functionalized Constrained Polyazamacrocycles: Building Blocks for Multifunctional Chelating Agents

2013

A new class of cross-bridged and side-bridged 1,4,7,10-tetraazacyclotridecanes (homocyclens) bearing an aminomethyl pendant arm on the carbon skeleton has been prepared. The regioselectivity of the quaternization of the bis-aminal intermediates is discussed on the basis of X-ray diffraction and NMR experiments. These new polyazamacrocycles are valuable precursors of bifunctional chelating agents for applications in nuclear medicine.

chemistry.chemical_compoundChemistryOrganic ChemistryCarbon skeletonRegioselectivityOrganic chemistryChelationPhysical and Theoretical ChemistryBifunctionalCombinatorial chemistryEuropean Journal of Organic Chemistry
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{1,1′-Bis[bis(5-methyl-2-furyl)phosphino]ferrocene-κ2P,P′}dichloroplatinum(II) dichloromethane hemisolvate

2005

The synthesis of the title compound, [FePtCl2(C15H14O2P)2]·0.5CH2Cl2, has been achieved by reacting PtCl2(PhCN)2 with the 1,1′-bis­[bis­(5-methyl-2-furyl)phosphino]ferrocene chelating ligand. The environment at the Pt atom can be described as distorted square-planar, with two cis-Cl atoms and two cis-P atoms.

chemistry.chemical_compoundchemistryFerroceneStereochemistryAtomchemistry.chemical_elementGeneral Materials ScienceChelationGeneral ChemistryCondensed Matter PhysicsPlatinumMedicinal chemistryMethaneActa Crystallographica Section E Structure Reports Online
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Nickel as a Lewis Base in a T‐Shaped Nickel(0) Germylene Complex Incorporating a Flexible Bis(NHC) Ligand

2018

Flexible, chelating bis(NHC) ligand 2, able to accommodate both cis- and trans-coordination modes, was used to synthesize (2)Ni(η 2 -cod), 3. In reaction with GeCl2, this produced (2)NiGeCl2, 4, featuring a T-shaped Ni(0) and a pyramidal Ge center. Complex 4 could also be prepared from [(2)GeCl]Cl, 5, and Ni(cod)2, in a reaction that formally involved Ni-Ge transmetalation, followed by coordination of the extruded GeCl2 moiety to Ni. A computational analysis showed that 4 possesses considerable multiconfigurational character and the Ni→Ge bond is formed through σ-donation from the Ni 4s, 4p, and 3d orbitals to Ge. (NHC)2Ni(cod) complexes 9 and 10, as well as (NHC)2GeCl2 derivative 11, incor…

chemistry.chemical_elementBite angleorganometalliyhdisteet010402 general chemistry01 natural sciencesCatalysisTransmetalationchemistry.chemical_compoundnickelPolymer chemistryMoietyChelationLewis acids and basesN-heterocyclic carbenesta116010405 organic chemistryLigandGeneral MedicineGeneral Chemistrykompleksiyhdisteet0104 chemical sciencesT-geometryNickelgermaniummetal-only Lewis pairschemistrynikkeliDerivative (chemistry)Angewandte Chemie International Edition
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Imidotungsten(VI) complexes with chelating phenols as ROMP catalysts

2011

Abstract Tungsten(VI) complexes of the type [W(NPh)Cl3(L)] (L = chelating phenolate) were studied as catalyst precursors for ROMP of 2-norbornene, dicyclopentadiene and 5-vinyl-2-norbornene. These compounds form active catalysts when treated by ethyl magnesium bromide. Moreover, polymerisations can be run under ambient atmosphere without complicated inert atmosphere techniques. Synthesis and crystal structure of a new precursor complex [W(NPh)Cl3(LS)] (LS = 2,4-di-tert-butyl-6-(phenylthiomethyl)phenolate) are also described.

chemistry.chemical_elementROMPCrystal structureTungstenCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryDicyclopentadienePolymer chemistryMaterials ChemistryOrganic chemistryChelationPhenolsPhysical and Theoretical ChemistryInert gasta116Inorganic Chemistry Communications
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Dibromido[N-(1-diethylamino-1-oxo-3-phenylpropan-2-yl)-N′-(pyridin-2-yl)imidazol-2-ylidene]palladium(II) dichloromethane monosolvate

2019

In the molecule of the title N,N′-disubstituted imidazol-2-ylidene palladium(II) complex, [PdBr2(C21H24N4O)]·CH2Cl2, the palladium(II) atom adopts a slightly distorted square-planar coordination (r.m.s. deviation = 0.0145 Å), and the five-membered chelate ring is almost planar [maximum displacement = 0.015 (8) Å]. The molecular conformation is enforced by intramolecular C—H...Br hydrogen bonds. In the crystal, complex molecules and dichloromethane molecules are linked into a three-dimensional network by C—H...O and C—H...Br hydrogen bonds.

crystal structureHydrogen bondchemistry.chemical_element02 engineering and technologyGeneral MedicineCrystal structure010402 general chemistry021001 nanoscience & nanotechnologyRing (chemistry)palladium01 natural sciencesMedicinal chemistryMethane0104 chemical scienceschemistry.chemical_compoundchemistrylcsh:QD901-999Chelationlcsh:Crystallography0210 nano-technologyMaximum displacementimidazol-2-ylidenePalladiumIUCrData
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Crystal structure of bis­(2-methyl-1H-imidazol-3-ium) di­hydroxidobis(oxalato-κ2 O 1,O 2)stannate(IV) monohydrate

2016

The SnIV atom in the anion of the title compound is six-coordinated by two OH groups and four O atoms from two chelating oxalate ligands. Several N—H⋯O and O—H⋯O hydrogen bonds involving the stannate dianions, the cations and the water mol­ecules result into a three-dimensional network structure.

crystal structureStannateorganotin(IV) complexInorganic chemistrySalt (chemistry)Crystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciences[ CHIM ] Chemical SciencesOxalateResearch Communicationschemistry.chemical_compound[CHIM]Chemical SciencesGeneral Materials ScienceChelationchemistry.chemical_classificationCrystallographyHydrogen bondGeneral ChemistryCondensed Matter PhysicsAcceptor3. Good health0104 chemical sciencesCrystallographychemistryQD901-999hydrogen bondsHydroxideActa Crystallographica Section E: Crystallographic Communications
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