Search results for "Derivative"

showing 10 items of 1074 documents

S-shaped decanuclear heterometallic [Ni8Ln2] complexes [Ln(iii) = Gd, Tb, Dy and Ho]: theoretical modeling of the magnetic properties of the gadolini…

2014

The reaction of 8-quinolinol-2-carboaldoxime (LH2) with Ni(II) and Ln(III) salts afforded the heterometallic decanuclear compounds [Ni8Dy2(μ3-OH)2(L)8(LH)2(H2O)6](ClO4)2·16H2O (1), [Ni8Gd2(μ3-OH)2(L)8(LH)2(H2O)4(MeOH)2](NO3)2·12H2O (2), [Ni8Ho2(μ3-OH)2(L)8(LH)2(H2O)4(MeOH)2](ClO4)2·2MeOH·12H2O (3) and [Ni8Tb2 (μ3-OH)2(L)8(LH)2(MeOH)4(OMe)2]·2CH2Cl2·8H2O (4). While compounds 1-3 are dicationic, compound 4 is neutral. These compounds possess an S-shaped architecture and comprise a long chain of metal ions bound to each other. In all the complexes, the eight Ni(II) and two Ln(III) ions of the multimetallic ensemble are hold together by two μ3-OH, eight dianionic (L(2-)) and two monoanionic oxi…

StereochemistryGadoliniumMetal ions in aqueous solutionchemistry.chemical_elementOximeIonInorganic Chemistrychemistry.chemical_compoundMolecular wireCrystallographychemistryFerromagnetismAntiferromagnetismDerivative (chemistry)Dalton Trans.
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2-Methyl-1-phenylsulfanyl-1,2-dicarba-closo-dodecaborane(12)

2002

In the title o-carborane derivative, C(9)H(18)B(10)S, the methyl and phenylsulfanyl groups are connected to the C atoms of the carborane cage. The C(cage)-C(cage) distance is 1.708 (4) A.

StereochemistryGeneral MedicineCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesMedicinal chemistryGeneral Biochemistry Genetics and Molecular Biology3. Good health0104 chemical scienceschemistry.chemical_compoundchemistryCarboraneDerivative (chemistry)Acta Crystallographica Section C Crystal Structure Communications
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Straightforward Regio- and Diastereoselective Synthesis, Molecular Structure, Intermolecular Interactions and Mechanistic Study of Spirooxindole-Engr…

2021

Straightforward regio- and diastereoselective synthesis of bi-spirooxindole-engrafted rhodanine analogs 5a–d were achieved by one-pot multicomponent [3 + 2] cycloaddition (32CA) reaction of stabilized azomethine ylide (AYs 3a–d) generated in situ by condensation of L-thioproline and 6-chloro-isatin with (E)-2-(5-(4-chlorobenzylidene)-2,4-dioxothiazolidin-3-yl)-N-(2-morpholinoethyl)acetamide. The bi-spirooxindole-engrafted rhodanine analogs were constructed with excellent diastereo- and regioselectivity along with high chemical yield. X-ray crystallographic investigations for hybrid 5a revealed the presence of four contiguous stereocenters related to C11, C12, C19 and C22 of the spiro struct…

StereochemistryHirshfeld DFTPharmaceutical ScienceAzomethine ylideOrganic chemistryArticleAnalytical ChemistryStereocenterchemistry.chemical_compoundQD241-441spirooxindole; rhodanine; azomethine ylides; [3 + 2] cycloaddition (32CA) reactions; hydrogen bonding; Hirshfeld DFT; supernucleophilesNucleophileDrug DiscoveryrhodanineReactivity (chemistry)Physical and Theoretical Chemistryheterosykliset yhdisteetsupernucleophilesvetysidoksettiheysfunktionaaliteoriaRegioselectivityazomethine ylidesspirooxindolehydrogen bondingCycloaddition[3 + 2] cycloaddition (32CA) reactionsRhodaninechemistryChemistry (miscellaneous)Molecular MedicineDerivative (chemistry)Molecules; Volume 26; Issue 23; Pages: 7276
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Synthesis and Reactivity of New Complexes of Rhodium and Iridium with Bis(dichloroimidazolylidene) Ligands. Electronic and Catalytic Implications of …

2006

The preparation of a new bis(dichloroimidazolylidene) ligand has provided chelate-N-heterocyclic complexes of Rh(I) and Ir(I), which have been fully characterized. The crystal structures of three of the new complexes are described. The study of the electronic properties of the new ligands was made on the basis of the ν(CO) stretching frequencies of the carbonyl derivatives, showing that the chloroimidazolylidene ligand is significantly less σ-donating than the related nonchlorinated analogue. This electronic modification of the ligand has important implications for the catalytic properties of the compounds obtained, as observed from enhanced activity shown in catalytic hydrosilylation of te…

StereochemistryHydrosilylationLigandOrganic Chemistrychemistry.chemical_elementCrystal structureMedicinal chemistryRhodiumCatalysisInorganic Chemistrychemistry.chemical_compoundchemistryCarbonyl derivativesReactivity (chemistry)IridiumPhysical and Theoretical ChemistryOrganometallics
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Synthesis of a Linear Assembly Consisting of a Central Ru(Phen)32+ Derivative and Two Peripheral Porphyrins

2002

A ruthenium(II) precursor complex containing a bis-phenanthroline ligand, leading to a controlled helical structure around the metal centre, and a third phenanthroline-type ligand has been prepared. The spatial arrangement of the system is such that two chemical groups are disposed trans to one another on an axis running through the Ru centre. By appropriate functional group transformation, these two groups can be attached to monosubstituted zinc(II) porphyrins (PZn) to afford a linear array consisting of a central ruthenium(II) complex and two peripheral PZn motifs. (© Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002)

StereochemistryLigandOrganic Chemistrychemistry.chemical_elementZincLinear arrayRutheniumMetalchemistry.chemical_compoundCrystallographychemistryvisual_artFunctional groupChemical groupsvisual_art.visual_art_mediumPhysical and Theoretical ChemistryDerivative (chemistry)European Journal of Organic Chemistry
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A novel polynitrile ligand with different coordination modes: Synthesis, structure and magnetic properties of the series [M(tcnoprOH)2(H2O)2] (M=Mn, …

2008

International audience; A novel polynitrile ligand (tcnoprOH− = [(NC)2CC(OCH2CH2CH2OH)C(CN)2]−) with up to five potentially coordinating groups has been synthesized in a one-pot reaction from a cyclic acetal and malononitrile. The combination of this novel ligand with different transition metal ions has led to the synthesis of two different structural types with the same formula but with different coordination modes in the ligand. Mn(II) and Cu(II) lead to a μ2-N,O-coordinating mode in the series of compounds formulated as [M(N,O-tcnoprOH)2(H2O)2] (M = MnII (1) and CuII (2)), whereas Co(II) and, most probably Ni(II), lead to a μ2-N,N′-coordinating mode in [Co(N,N′-tcnoprOH)2(H2O)2] (3). Bot…

StereochemistryMetal ions in aqueous solutionZero field splitting[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciencesAnalytical ChemistryInorganic ChemistryPolynitrile ligandschemistry.chemical_compoundParamagnetismGroup (periodic table)Magnetic properties[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistrySpectroscopyMalononitrile010405 organic chemistryLigandOrganic ChemistryAcetalMagnetic chains3. Good health0104 chemical sciencesCrystallographychemistryChain complexesDerivative (chemistry)
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Four-, five- and six-coordinated Zn-II complexes of OH-containing ligands: Syntheses, structure and reactivity

2002

Four-, five- and six-coordinated complexes of Zn-II with OH-rich molecules possessing an ONO binding core were synthesized, characterized and their structures were established by single-crystal X-ray diffraction, The corresponding metal ion geometries were found to be distorted tetrahedral, square pyramidal and octahedral, respectively. The complexes exhibit interesting lattice structures such as layered and corrugated sheets owing to the presence of a number of weak intermolecular interactions. The five-coordinated, water-bound Zn-II complex was studied because of its putative hydrolysis property towards p-nitrophenyl acetate. (C) Wiley-VCH Verlag GmbH, 69451 Weinheim, Germany, 2002.

StereochemistryMetalloenzymesCrystal structureInorganic ChemistryX-Ray DiffractionCrystal-StructuresElectrochemistryMoleculeReactivity (chemistry)IonMonooxovanadium(V)ChemistryHydrogen bondIntermolecular forceCarbonic-AnhydraseNO LigandsHydrogen BondsSquare pyramidal molecular geometryCrystallographyVanadium(V) ComplexesRecognitionZincZinc EnzymesOctahedronX-ray crystallographyDerivativesModelIndraStra Global
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Crystal structures and absolute configurations of dexmedetomidine and its tosyl derivative

1993

Abstract X-ray diffraction data were used to determine the absolute configuration of dexmedetomidine, a new member of a class of drugs with 4-arylalkyl-1H-imidazole structure. When the anomalous effect of the parent compound proved to be too small for determination of the absolute configuration the tosyl derivative, with the same configuration, was synthesised and used as a reference. Stability of the stereogenic center was verified by HPLC technique. The absolute configuration of the compounds is S. Complete crystal structures are reported for both compounds. Co radiation was used for measurements.

StereochemistryOrganic ChemistryAbsolute configurationCrystal structureCatalysisStereocenterInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryTosylX-ray crystallographyMoleculePhysical and Theoretical ChemistryEnantiomerDerivative (chemistry)Tetrahedron: Asymmetry
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Synthesis of a technetium-99m labelledL-tyrosine derivative with thefac-99mTc(I)(CO)3-core using a simple kit-procedure

2004

Summary The synthesis of a novel technetium-99m labelled derivative of l-tyrosine as a potential tumour imaging agent for nuclear medicine diagnosis is reported. The synthesis involved the labelling precursor fac-[ 99m Tc(OH2)(CO)3] + which was synthesized using the commercially available Isolink 1 -labelling kit and the tyrosine derivative O-(N,Nbis(carboxymethyl)aminoethyl)-l-tyrosine trifluoroacetate. The labelled compound O( 99m Tc(I)-tricarbonyl-N,N-bis(carboxymethyl)aminoethyl)-l-tyrosine was obtained in a radiochemical yield of 70–80% within 60 min with a radiochemical purity greater than 98% without any HPLC purification step. Purification was achieved merely by solid phase extracti…

StereochemistryOrganic ChemistryBiochemistryChemical synthesisHigh-performance liquid chromatographyAnalytical ChemistryChiral column chromatographychemistry.chemical_compoundchemistryLabellingYield (chemistry)Drug DiscoveryRadiology Nuclear Medicine and imagingSolid phase extractionCarboxylateSpectroscopyDerivative (chemistry)Nuclear chemistryJournal of Labelled Compounds and Radiopharmaceuticals
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The first example of natural cyclic carbonate in terpenoids

2006

Abstract The first natural occurring cyclic carbonate terpenoid, the guaianolide hololeucin ( 1 ), was isolated from the aerial part of Centaurea hololeuca . Its structure was elucidated on the basis of extensive proton, 13 C and two-dimensional NMR experiments, as well as by transformation in its diacetyl derivative.

StereochemistryOrganic ChemistrySESQUITERPENE LACTONESBiochemistryDiacetylTerpenoidGUAIANOLIDESchemistry.chemical_compoundchemistryDrug DiscoveryOrganic chemistryCarbonateCONSTITUENTSDerivative (chemistry)Tetrahedron Letters
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