Search results for "Metal complex"

showing 10 items of 67 documents

Speciation of tin(II) in aqueous solution: thermodynamic and spectroscopic study of simple and mixed hydroxocarboxylate complexes

2013

This contribution reports the results of potentiometric and Mossbauer investigations on the formation, stability, and structure of binary and ternary mono- and binuclear complexes of Sn2+ with three hydroxocarboxylic ligands (namely L = tartrate, malate, and citrate) and chloride at T = 298.15 K in different ionic media and ionic strengths (0.15 and 1.00 mol dm−3 in NaCl(aq) and 1.00 mol dm−3 in NaNO3(aq)). The stability constants of various simple Sn i H j L (2+−) and mixed Sn i H j L k Cl (2+−−) species obtained in the different experimental conditions are reported, and various speciation diagrams of the simple and mixed systems are shown in different conditions. The sequestering ability …

chemistry.chemical_classificationAqueous solutionMössbauer spectroscopyPotentiometric titrationEnthalpyInorganic chemistrySequestrationIonic bondingComputer programGeneral ChemistryChlorideCoordination chemistryCoordination complexTrigonal bipyramidal molecular geometrychemistrySettore CHIM/03 - Chimica Generale E InorganicamedicineMetal complexeSettore CHIM/01 - Chimica AnaliticaStability constantsTernary operationmedicine.drugMonatshefte für Chemie - Chemical Monthly
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2,2′:6′,2″-Terpyridine Trimethylplatinum(IV) Iodide Complexes as Bifunctional Halogen Bond Acceptors

2016

Three new organometallic trimethylplatinum(IV) iodide complexes of 2,2′:6′,2″-terpyridines have been synthesized and characterized by 1H NMR spectroscopy, mass spectrometry, elemental analysis, and single crystal X-ray diffraction analysis. The X-ray crystal structures of PtMe3I(L) complexes 1–3 {L for 1 = 4′-chloro-2,2′:6′,2″-terpyridine, 2 = 4′-(4-cyanophenyl)-2,2′:6′,2″-terpyridine, and 3 = 4′-(4-tolyl)-2,2′:6′,2″-terpyridine} reveal distorted octahedral coordination geometry of the platinum(IV) metal centers with bidentate coordination of the terpyridine ligands. Complexation of 1–3 with iodopentafluorobenzene (IPFB) afforded single-crystal structures of halogen bond (XB) complexes 1a–3…

chemistry.chemical_classificationDenticityHalogen bond010405 organic chemistryhalogen bondsIodideGeneral ChemistryCrystal structurehalogen bond acceptors010402 general chemistryCondensed Matter PhysicsPhotochemistry01 natural sciencestransition metal complexes0104 chemical scienceschemistry.chemical_compoundCrystallographychemistryPyridineGeneral Materials ScienceTerpyridineBifunctionalta116Coordination geometryCrystal Growth & Design
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1‑Phenyl-3-(pyrid-2-yl)benzo[e][1,2,4]triazinyl: The First "Blatter Radical" for Coordination Chemistry

2014

A neutral air- and moisture-stable N,N′-chelating radical ligand, 1-phenyl-3-(pyrid-2-yl)benzo[e][1,2,4]triazinyl (1) was synthesized and characterized by electron paramagnetic resonance spectroscopy, X-ray crystallography, and magnetic measurements. Subsequent reaction of 1 with Cu(hfac)2·2H2O (hfac = hexafluoroacetylacetonate) under ambient conditions afforded the coordination complex Cu(1)(hfac)2 in which the radical binds to the metal in a bidentate fashion. Magnetic susceptibility data collected from 1.8 to 300 K indicate a strong ferromagnetic metal-radical interaction in the complex and weak antiferromagnetic radical···radical interactions between the Cu(1)(hfac)2 units. Detailed com…

chemistry.chemical_classificationDenticityStereochemistryLigandpysyvät radikaalitRadicalmetal complexes[CHIM.INOR]Chemical Sciences/Inorganic chemistryMedicinal chemistryMagnetic susceptibilityCoordination complexInorganic ChemistryMetalParamagnetismCoordination Chemistrystable radicalschemistryBlatter radikaalivisual_artvisual_art.visual_art_mediumAntiferromagnetismBlatter radicalPhysical and Theoretical Chemistryta116metallikompleksit
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Base-assisted synthesis of 4-pyridinate gold(I) metallaligands: a study of their use in self-assembly reactions

2021

Made available in DSpace on 2021-06-25T12:16:58Z (GMT). No. of bitstreams: 0 Previous issue date: 2021-05-06 Ministerio de Economia y Competitividad (MINECO/FEDER) of Spain Conselho Nacional de Desenvolvimento Científico e Tecnológico (CNPq) Coordenação de Aperfeiçoamento de Pessoal de Nível Superior (CAPES) The synthesis of di- and tritopic gold(I) metallaligands of the type [(Au4-py)(2)(mu(2)-diphosphane)] (diphosphane = bis(diphenylphosphanyl)isopropane or dppip (1), 1,2-bis(diphenylphosphanyl)ethane or dppe (2), 1,3-bis(diphenylphosphanyl)propane or dppp (3) and 1,4-bis(diphenylphosphanyl)butane or dppb (4)) and [(Au4-py)(3)(mu(3)-triphosphane)] (triphosphane = 1,1,1-tris(diphenylphosph…

chemistry.chemical_elementOrNuclear magnetic resonance spectroscopyLigandsMedicinal chemistryAcceptorComplexos metàl·licsTriphosInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundTriphosphaneLligandschemistryMetal complexesDiphosphaneGoldPlatinumPalladium
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A Gadolinium(III) Complex Based on the Thymine Nucleobase with Properties Suitable for Magnetic Resonance Imaging

2021

The paramagnetic gadolinium(III) ion is used as contrast agent in magnetic resonance (MR) imaging to improve the lesion detection and characterization. It generates a signal by changing the relaxivity of protons from associated water molecules and creates a clearer physical distinction between the molecule and the surrounding tissues. New gadolinium-based contrast agents displaying larger relaxivity values and specifically targeted might provide higher resolution and better functional images. We have synthesized the gadolinium(III) complex of formula [Gd(thy)2(H2O)6](ClO4)3·2H2O (1) [thy = 5-methyl-1H-pyrimidine-2,4-dione or thymine], which is the first reported compound based on gadolinium…

crystal structureMaterials scienceMagnetometerQH301-705.5GadoliniumContrast Mediachemistry.chemical_elementmetal complexesCrystallography X-Ray010402 general chemistry01 natural sciencesArticleCatalysisIonNucleobaselaw.inventionInorganic Chemistrymagnetic resonanceMagneticsParamagnetismchemistry.chemical_compoundNuclear magnetic resonanceHeterocyclic CompoundslawthyminemedicineMoleculePhysical and Theoretical ChemistryBiology (General)Molecular BiologyQD1-999SpectroscopyMolecular Structuremedicine.diagnostic_test010405 organic chemistryOrganic ChemistryWaterMagnetic resonance imagingGeneral Medicinecontrast agentMagnetic Resonance Imaging0104 chemical sciencesComputer Science ApplicationsThymineChemistrychemistryrelaxivityProtonsgadolinium
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Synthesis of a labile sulfur-centred ligand, [S(H)C(PPh2S)2]-: structural diversity in lithium(i), zinc(ii) and nickel(ii) complexes

2016

A high-yield synthesis of [Li{S(H)C(PPh2S)2}]2 [Li2·(3)2] was developed and this reagent was used in metathesis with ZnCl2 and NiCl2 to produce homoleptic complexes 4 and 5b in 85 and 93% yields, respectively. The solid-state structure of the octahedral complex [Zn{S(H)C(PPh2S)2}2] (4) reveals notable inequivalence between the Zn–S(C) and Zn–S(P) contacts (2.274(1) Å vs. 2.842(1) and 2.884(1) Å, respectively). Two structural isomers of the homoleptic complex [Ni{S(H)C(PPh2S)2}2] were isolated after prolonged crystallization processes. The octahedral green Ni(II) isomer 5a exhibits the two monoprotonated ligands bonded in a tridentate (S,S′,S′′) mode to the Ni(II) centre with three distinctl…

elektronirakenteetrikkipohjaiset liganditmetal complexesisomerisaatiosulphur-centered ligandsmetallikompleksitisomerizationelectronic structures
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Synthesis, structure and photophysical properties of a highly luminescent terpyridine-diphenylacetylene hybrid fluorophore and its metal complexes

2014

A new fluorescent terpyridyl-diphenylacetylene hybrid fluorophore 4'-[4-{(4-methoxyphenyl)ethynyl}phenyl]-2,2':6',2''-terpyridine, L, was synthesized via Sonogashira cross-coupling of 4'-(4-bromophenyl)-2,2':6',2''-terpyridine and 4-ethynylanisole in the presence of Pd(PPh3)4/CuI as a catalyst. The solid state structure of L shows a trans arrangement of pyridine nitrogen atoms along the interannular bond in the terpyridine domain. Five transition metal complexes of L, {[FeL2](CF3SO3)2 (1), [ZnL2](ClO4)2 (2), [CdL2](ClO4)2 (3), [RuL2](PF6)2 (4), and PtMe3IL (5)}, have also been synthesized and characterized by spectroscopic methods and single crystal X-ray analysis. The X-ray crystal structu…

fluorophoreDenticityterpyridiinisynthesisQuantum yieldmetal complexesCrystal structure010402 general chemistryPhotochemistry01 natural sciencesInorganic Chemistrycrystal structureschemistry.chemical_compoundPyridineta116Diphenylacetylenephotophysical properties010405 organic chemistryLigandterpyridinekiderakenteet0104 chemical sciencesCrystallographyfluoroforitchemistryIntramolecular forcevalofysikaaliset ominaisuudetTerpyridinevalmistusmetallikompleksitDalton Transactions
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Synthesis, structure and photophysical properties of a highly luminescent terpyridine-diphenylacetylene hybrid fluorophore and its metal complexes

2015

A new fluorescent terpyridyl-diphenylacetylene hybrid fluorophore 4′-[4-{(4-methoxyphenyl)ethynyl}phenyl]-2,2′:6′,2′′-terpyridine, L, was synthesized via Sonogashira cross-coupling of 4′-(4-bromophenyl)-2,2′:6′,2′′-terpyridine and 4-ethynylanisole in the presence of Pd(PPh3)4/CuI as a catalyst. The solid state structure of L shows a trans arrangement of pyridine nitrogen atoms along the interannular bond in the terpyridine domain. Five transition metal complexes of L, {[FeL2](CF3SO3)2 (1), [ZnL2](ClO4)2 (2), [CdL2](ClO4)2 (3), [RuL2](PF6)2 (4), and PtMe3IL (5)}, have also been synthesized and characterized by spectroscopic methods and single crystal X-ray analysis. The X-ray crystal structu…

fluorophorecrystal structuresfluoroforitterpyridiinivalofysikaaliset ominaisuudetmetal complexessynteesiterpyridinevalmistusmetallikompleksitphotophysical propertieskiderakenteet
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Azonia spiro polyaza macrocycles containing biphenyl subunits as anion and cation receptors

2011

Abstract The reaction of N-Boc triprotected cyclam with bis(chloromethyl)biphenyl followed by the corresponding deprotection of the nitrogen atoms allows the preparation of receptor 3 containing an azonia spiro subunit. This receptor shows slightly increased basicity than cyclam, in particular for the formation of the appropriate triply charged species as a consequence of the reduced capacity of the structure present in 3 to stabilize the species with lower protonation degrees through the formation of intramolecular hydrogen bonds. The properties of 3 as a receptor for Cu2+ and Zn2+ and the anions derived from PO 4 3 − ( Pi ) , P 2 O 7 4 − ( PPi ) , P 3 O 10 5 − ( TPP ) and ATP have been st…

inorganic chemicalsBiphenylAqueous solutionHydrogen bondStereochemistryChemistryOrganic ChemistrySupramolecular chemistryStackingProtonationBiochemistryMedicinal chemistryAnion recognitionchemistry.chemical_compoundMetal complexesIntramolecular forceDrug DiscoveryCyclamPolyaza cyclophanesSupramolecular chemistryMacrocyclesTetrahedron
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Experimental and computational studies of transition metal complexes with polydentate amino- and amidophenolate ligands : synthesis, structure, react…

2013

Chelating polydentate ligands play a key role in several areas of modern coordination chemistry. They can be exploited, for example, in catalysis, bioinorganic chemistry, heavy metal abstraction and molecular magnetism. Furthermore, compounds of this type can be found in natural chemicals, commercial products and industrial applications. In this dissertation, several 3d, 4d and 5d transition metal complexes with polydentate amino- and amidophenolate ligands were prepared and their structure, reactivity and magnetic properties were studied with experimental and computational techniques. In the first part of the dissertation, the solid-state structure, reactivity and magnetic properties of 12…

kemiallinen synteesisynthesisx-ray diffractionmagneetiset ominaisuudetsiirtymämetallitkompleksiyhdisteetstructuremagnetic propertiesepäorgaaninen kemialaskennallinen kemiaröntgenkristallografiatransition metal complexes
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