Search results for "magnetic resonance spectroscopy"

showing 10 items of 1362 documents

Organometallic complexes with biological molecules

2002

Novel triorganotin(IV) complexes of two beta-lactamic antibiotics, 6-[D-(-)-beta-amino-p-hydroxyphenyl-acetamido]penicillin (=amoxicillin) and 6-[D-(-)-alpha-aminobenzyl]penicillin (=ampicillin), have been synthesized and investigated both in solid and solution states. The complexes corresponded to the general formula R(3)Sn(IV)antib*H(2)O (R=Me, n-Bu, Ph; antib=amox=amoxicillinate or amp=ampicillinate). Structural investigations about configuration in the solid state have been carried out by interpreting experimental IR and 119Sn Mossbauer data. In particular, IR results suggested polymeric structures both for R(3)Sn(IV)amox.H(2)O and R(3)Sn(IV)amp*H(2)O. Moreover, both antibiotics appear …

DenticityChemistryStereochemistryNuclear magnetic resonance spectroscopyBiochemistryMedicinal chemistryInorganic ChemistryTrigonal bipyramidal molecular geometrychemistry.chemical_compoundMoietyMoleculeCarboxylateSolvolysisChromosome breakageJournal of Inorganic Biochemistry
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Interactions of metal ions with a 2,4-diaminopyrimidine derivative (trimethoprim)

2000

The interaction of copper (II), zinc(II) and cadmium(II) with Trimethoprim (2,4-diamino-5-(3',4',5'-trimethoxybenzyl) pyrimidine) has been studied. The crystal structures of [Zn(Trim)2Cl2] (2) and [Cd(Trim)Cl2(CH3OH)]n (4) are reported. Compound (2) exhibits a distorted tetrahedral environment around the metal center and crystallizes in the triclinic space group P1 with a=10.2397(6), b=10.4500(6), c=16.3336(16) A, alpha=96.141(8), beta=106.085(5), gamma=96.551(5) degrees and Z=2. In complex (4), the Cd(II) centers are bridged sequentially by two chlorine ions to form infinite chains and present a six-coordinated environment; the compound crystallizes in the monoclinic P2(1)/C space group wi…

DenticityChemistryStereochemistrychemistry.chemical_elementCrystal structureZincNuclear magnetic resonance spectroscopyTriclinic crystal systemBiochemistryInorganic Chemistrychemistry.chemical_compoundCrystallographyDiaminopyrimidineMoleculeMonoclinic crystal systemJournal of Inorganic Biochemistry
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Organotin(IV) complexes with tetraethyl ethylene- and propylene-diphosphonates

1995

The series of organotin halide complexes with tetraethyl ethylene- and propylene-diphosphonates R n SnX 4-n .L [n=0, X=Cl; n=1, R=Me, X=Cl, Br; n=1, R=Ph, X=Cl; n=2 R=Me, Et, Bu, X=Cl, Br; n=2, R=Ph, X=Cl; L=(EtO) 2 P(O)CH 2 CHR'P(O)(OEt) 2 , R'=H, Me] were synthesized and characterized by means of NMR and Mossbauer spectroscopy. The crystal structure of the complex of diphenyltin dichloride with propylenediphosphonate was determined. The complex consists of polymer chains with bridging bidentate ligands and an octahedral tin environment containing two types of phosphoryl fragments. All of the R 2 SnX 2 adducts have trans-R 2 SnX 4 geometries of tin coordination octahedra according to the q…

DenticityCoordination sphereEthyleneChemistryStereochemistryGeneral ChemistryNuclear magnetic resonance spectroscopyQuadrupole splittingCrystal structureMedicinal chemistryAdductInorganic Chemistrychemistry.chemical_compoundMössbauer spectroscopyApplied Organometallic Chemistry
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Synthesis and spectroscopic characterization of R3SnIV derivatives ofN-acetyldipeptides

1993

Triorganotin(IV) derivatives of N-acetyldipeptides R3SnAcDip; RMe, Et, n-Bu, n-Oct, Cy or Ph (HAcDipN-acetylglycylglycine and N-acetylglycylvaline; RMe, n-Bu, Cy, HAcDipN-acetylglycylalanine) were obtained by neutralization of R3SnOH and HAcDip. The complexes were studied by means of 119Sn Mossbauer, IR and 1H, 13C and 119Sn NMR spectroscopy. The CSnC bond angles have been inferred by rationalization of Mossbauer nuclear quadrupole splittings as well as from NMR coupling constants. Correlations of Mossbauer isomer shifts with partial atomic charges on tin atoms have been determined: Polymeric trigonal bipyramidal structures, with near-planar R3Sn units and axial carboxylate (unidentate) and…

DenticityInorganic chemistrychemistry.chemical_elementGeneral ChemistryNuclear magnetic resonance spectroscopyInorganic ChemistryCrystallographychemistry.chemical_compoundTrigonal bipyramidal molecular geometryMolecular geometrychemistryAmideMössbauer spectroscopyCarboxylateTinApplied Organometallic Chemistry
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Dynamic chemical devices: photoinduced electron transfer and its ion-triggered switching in nanomechanical butterfly-type bis(porphyrin)terpyridines.

2005

A series of butterfly-type molecular constructs has been prepared in good yield by using a double Stille coupling synthetic protocol. They are composed of a terpyridine (terpy) scaffold and two wings composed of appended porphyrins that are capable of switching from an extended W geometry to a compact U geometry upon cation coordination of the terpy unit. The porphyrin moieties exist in the constructs either as free bases or they can be sequentially metallated, thus giving rise to wings of different "colours". Stationary and time-resolved emission studies of the HZn, ZnAu and Zn2Au constructs show that the electronic properties are strongly dependent on the geometry. In the extended W confo…

DenticityMagnetic Resonance SpectroscopyPorphyrinsChemical PhenomenaPhotochemistryPyridinesMolecular ConformationElectronsPhotochemistryCrystallography X-RayLigandsCatalysisPhotoinduced electron transferchemistry.chemical_compoundElectron transferLigandHydrogen bondChemistry PhysicalOrganic ChemistryTemperatureGeneral ChemistryHydrogen-Ion ConcentrationPorphyrinZincSpectrometry FluorescencechemistryExcited stateSpectrometry Mass Matrix-Assisted Laser Desorption-IonizationIndicators and ReagentsSpectrophotometry UltravioletTerpyridineChemistry (Weinheim an der Bergstrasse, Germany)
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Synthetic, structural and biochemical studies of polynuclear platinum(II) complexes with heterocyclic ligands.

2008

"Non-classical" di- and trinuclear Pt(II) complexes with polydentate nitrogen ligands; ionic [(PtCl(2))(2)(tptz)(2)(mu-PtClNCPh)]Cl (1) [tptz =2,4,6-tris(2-pyridyl)-1,3,5-triazine], [(PtCl(2))(2)(bptz)(2)(mu-Pt)]Cl(2) (2) [bptz = 3,6-bis(2-pyridyl)-1,2,4,5-tetrazine] and neutral [(PtCl(2))(2)(tptz)(2)(mu-PtCl(2))](H(2)O)(4) (3), [(PtCl(2))(2)(mu-tppz)](CHCl(3)) (4) [tppz = 2,3,5,6-tetra(2-pyridyl)pyrazine] complexes, have been prepared and structurally characterized. The neutral tptz and tppz complexes present three and two separate PtCl(2) moieties, respectively, in a cis position, presumably acting in a bifunctional mode towards DNA; the cationic tptz and bptz complexes contain monofuncti…

DenticityMagnetic Resonance SpectroscopyPyrazineSpectrophotometry InfraredStereochemistryCell SurvivalCytotoxicitychemistry.chemical_elementPlatinum CompoundsLigandsChemical synthesisPolydentate nitrogen ligandchemistry.chemical_compoundHeterocyclic CompoundsCell Line TumorDrug DiscoveryHumansBifunctionalPharmacologyMolecular StructureLigandOrganic ChemistryCationic polymerizationBiological activityGeneral MedicinechemistryPolynuclear platinum complexeSettore CHIM/03 - Chimica Generale E InorganicaPlatinumEuropean journal of medicinal chemistry
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Organometallic complexes with biological molecules, IV. Di- and tri-organotin(IV) amoxicillin derivatives: Solid-state and solution-phase spectroscop…

1995

Novel di- and tri-organotin(IV) derivatives of amoxicillin (amoxicillin - =Amox - =6-[D(-)-β-amino-p-hydroxyphenylacetamido] penicillinate) have been prepared. The isolated compounds showed stoichiometries of the type R 2 SnClAmox.2H 2 O, R 3 SnClAmoxNa.2H 2 O and R 2 SnAmox 2 .2H 2 O (R=Me, Bu, Ph). The infrared spectra suggest that Amox − , in both R 2 SnClAmox.2H 2 O and R 2 SnAmox 2 .2H 2 O, behaves as a monoanionic bidentate ligand, coordinating the tin(IV) atom through the ester-type carboxylate, as well as through the lactamic carbonyl. In R 3 SnClAmoxNa.2H 2 O, Amox - coordinates the organotin(IV) moieties through the lactamic carbonyl. In all of the compounds, water molecules are n…

DenticityStereochemistryInfrared spectroscopyGeneral ChemistryNuclear magnetic resonance spectroscopyInorganic ChemistryCrystallographyTrigonal bipyramidal molecular geometryBipyramidchemistry.chemical_compoundchemistryCarboxylateCoordination geometryAntibacterial agentApplied Organometallic Chemistry
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Polypyridyl-functionalizated alkynyl gold(i) metallaligands supported by tri- and tetradentate phosphanes

2017

A series of alkynyl gold(I) tri and tetratopic metallaligands of the type [Au3(CuC-R)3(μ3-triphosphane)] (R = 2,2'-bipyridin-5-yl or C10H7N2, 2,2':6',2''-terpyridin-4-yl or C15H10N3; triphosphane = 1,1,1-tris(diphenylphosphanyl) ethane or triphos, 1,3,5-tris(diphenylphosphanyl)benzene or triphosph) and [Au4(CuC-R)4 (μ4-tetraphosphane)] (R = C10H7N2, C15H10N3; tetraphosphane = tetrakis(diphenylphosphanylmethyl)methane or tetraphos, 1,2,3,5-tetrakis(diphenylphosphanyl)benzene or tpbz, tetrakis(diphenylphosphaneylmethyl)-1,2- ethylenediamine or dppeda) were obtained in moderate to good yields. All complexes could be prepared by a Q4 reaction between the alkynyl gold(I) polymeric species [Au(Cu…

DenticityStereochemistryOrCrystal structureLigands010402 general chemistry01 natural sciencesMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundcoordination complexesta116kemiallinen synteesiligands010405 organic chemistryChemistryLigandAromaticitykompleksiyhdisteetliganditNuclear magnetic resonance spectroscopyTriphos0104 chemical sciencesLligandsTriphosphaneCompostos d'orIntramolecular forceGoldGold compoundschemical synthesisDalton Transactions
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Structural characterization of triorganotin(IV) complexes with sodium fusidate and DFT calculations

2010

Abstract Three new complexes of the steroid sodium fusidate (sodium 2-[(1 S ,2 S ,5 R ,6 S ,7 S ,10 S ,11 S ,13 S , 14 Z ,15 R ,17 R )-13-(acetyloxy)-5,17-dihydroxy-2,6,10,11-tetramethyl tetracyclo[8.7.0.0 2,7 .0 11,15 ] heptadecan-14-ylidene]-6-methylhept-5-enoate = (NaFusidate, Na FA )]), with triorganotin(IV) moieties have been prepared and investigated by conventional techniques as FTIR, Mossbauer, ESI-MS and NMR spectroscopy. The isolated compounds showed stoichiometries organotin(IV)/fusidate 1/1, R 3 Sn(IV) FA (R = Me, FA1 ; Bu, FA2 ; Ph, FA3 ). The ligand coordination sites were determined by FTIR spectroscopic measurements. In the complexes, the carboxylate group of the fusidate li…

DenticityTriorganotin(IV)Mössbauer spectroscopyLigandOrganic ChemistryInorganic chemistrychemistry.chemical_elementQuadrupole splittingNuclear magnetic resonance spectroscopyBiochemistrySteroid carboxylate Triorganotin(IV) NMRFTIRMössbauer spectroscopySteroid carboxylateNMRInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerFTIRchemistryMössbauer spectroscopyMaterials ChemistryCarboxylatePhysical and Theoretical ChemistryTin
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Construction of Coordination Polymers from Semirigid Ditopic 2,2′-Biimidazole Derivatives: Synthesis, Crystal Structures, and Characterization

2017

Eight coordination polymers (CPs), {[Ag(L1)]ClO4}n (1), {[Ag(L2)1.5]ClO4·C2H3N}n (2a), {[Ag(L2)]ClO4}n (2b), [Zn(L1)Cl2]n (3), {[Zn(L2)Cl2]·CHCl3}n (4), {[Cu(L1)2Cl]Cl·H2O}n (5), [Cu2(L2)(μ-Cl)2]n (6), and [Cu4(L2)(μ-Cl)4]n (7) were synthesized via self-assembly of corresponding metal ions and biimidazole based ditopic ligands, 1,1′-bis(pyridin-3-ylmethyl)-2,2′-biimidazole L1 and 1,1′-bis(pyridin-4-ylmethyl)-2,2′-biimidazole L2. These ligands possess conformational flexibility and two pairs of coordination sites: pyridine nitrogen (NPy) atoms and imidazole nitrogen (NIm) atoms. Depending on the metal center in CPs, the biimidazole compounds act as tetra- (1, 7), tri- (2a), or bidentate (2a,…

Denticitykemia010405 organic chemistryStereochemistryMetal ions in aqueous solutionCenter (category theory)General ChemistryCrystal structureNuclear magnetic resonance spectroscopy010402 general chemistryCondensed Matter Physics01 natural sciences0104 chemical sciencescoordination polymersCrystallographychemistry.chemical_compoundchemistryPyridineImidazoleGeneral Materials Sciencepolymeeritta116Single crystalpolymersCrystal Growth & Design
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