Search results for " split"

showing 10 items of 264 documents

Interpretation of Mössbauer Parameters of Iron Compounds

1978

The task of this section is to show that for the interpretation of Mossbauer parameters — in the present case of electron densities, field gradients and magnetic hyperfine fields — bonding effects can play an important role, and free-ion or crystal field approaches may be a poor approximation.

CrystalMaterials scienceField (physics)Condensed matter physicsAtomic orbitalMössbauer spectroscopyElectronQuadrupole splittingHyperfine structureElectric field gradient
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Homoleptic iron(II) complexes with the ionogenic ligand 6,6′-Bis(1H-tetrazol-5-yl)-2,2′-bipyridine: spin crossover behavior in a singular 2D spin cro…

2015

Deprotonation of the ionogenic tetradentate ligand 6,6′-bis(1H-tetrazol-5-yl)-2,2′-bipyridine [H2bipy(ttr)2] in the presence of FeII in solution has afforded an anionic mononuclear complex and a neutral two-dimensional coordination polymer formulated as, respectively, NEt3H{Fe[bipy(ttr)2][Hbipy(ttr)2]}·3MeOH (1) and {Fe[bipy(ttr)2]}n (2). The anions [Hbipy(ttr)2]− and [bipy(ttr)2]2– embrace the FeII centers defining discrete molecular units 1 with the FeII ion lying in a distorted bisdisphenoid dodecahedron, a rare example of octacoordination in the coordination environment of this cation. The magnetic behavior of 1 shows that the FeII is high-spin, and its Mössbauer spectrum is characteriz…

DEVICESCoordination polymerStereochemistryPRESSURE010402 general chemistry01 natural sciences22'-BipyridineInorganic ChemistrySINGLE MOLECULESchemistry.chemical_compoundDeprotonationSpin crossoverSYSTEMS[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryHomolepticSYNERGYCRYSTAL010405 organic chemistryLigandCOMPOUNDQuadrupole splittingSTATE3. Good health0104 chemical sciencesCrystallographychemistryOctahedronFISICA APLICADAMOSSBAUERPHASE-TRANSITIONS
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Slow Magnetic Relaxation in a Co (II)–Y (III) Single‐Ion Magnet with Positive Axial Zero‐Field Splitting

2013

This work was supported by the MINECO (Spain) (Project CTQ2011-24478), the Junta de Andalucía (FQM-195 and Project of excellence P08-FQM-03705), and the University of Granada. E.R. and E.Cr. thank MINECO grant No. CTQ2011-23862-C02-01 and Generalitat de Catalunya grant No. 2009SGR-1459, for financial support. We would like to thank Prof. Liviu Chibotaru for providing us the SINGLE_ANISO program and Dr. Andrew Ozarowski for the EPR simulation software. E.K.B. thanks the EPSRC and Leverhulme Trust for financial support. The NHMFL is funded by the NSF, DoE, and the state of Florida. J.C. acknowledges financial support by the Spanish Ministerio de Ciencia e Innovación through projects CTQ2010-1…

DYNAMICSModels Molecularpositive zero-field splittingINSchemistry.chemical_elementZero field splitting010402 general chemistry01 natural sciences7. Clean energyCatalysisO ligandsMOLECULE MAGNETNuclear magnetic resonancesingle ion magnetsYttriumMagnetic relaxationCompartmental ligandAnisotropyHYSTERESISComputingMilieux_MISCELLANEOUSANISOTROPY[PHYS]Physics [physics]IonsMolecular StructureCondensed matter physicsSingle ion010405 organic chemistryChemistryCobaltGeneral ChemistryYttriumNBARRIERcobaltCo(II)FAMILY0104 chemical sciencesyttriumHysteresisPositive axial ZFSDYSPROSIUM(III)TBMagnetic FieldsMagnetMagnetsSingle ion magnetCOMPLEXESCobaltBEHAVIOR
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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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Exchange Coupling Mediated by N–H···Cl Hydrogen Bonds: Experimental and Theoretical Study of the Frustrated Magnetic System in Bis(o-phenylenediamine…

2012

The title compound crystallizes in the monoclinic P2(1)/c space group with a = 11.2470(3) A, b = 5.9034(2) A, c = 12.0886(3) A, β = 115.143(1)°, and V = 726.58(4) A(3) and consists of discrete monomeric NiCl(2)(o-phenylendiamine)(2) molecules. Each o-phen ligand coordinates in a bidentate mode with the chloride ions occupying trans positions in the resulting tetragonally distorted octahedral coordination sphere. Two discrete sets of N-H···Cl hydrogen bonds link the octahedral molecules into a two-dimensional network, with type 1 interactions linking adjacent monomers along the c axis and type 2 interactions linking monomers along the diagonals in the bc plane. Analysis of the magnetic data …

DenticityCoordination sphereHydrogen bondStereochemistryZero field splittingInorganic ChemistryCrystallographychemistry.chemical_compoundOctahedronchemistryMoleculeAntiferromagnetismPhysical and Theoretical ChemistryNickel(II) chlorideInorganic Chemistry
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Characterization of complexes formed between [Me2Sn(IV)]2+ and carboxymethylcelluloses.

2006

Complexes formed between carboxymethylcellulose (CMC) and the [Me(2)Sn(IV)]2+ cation have been prepared in the solid state and characterized by FTIR and Mossbauer spectroscopy. The complexes contained CMC with varying molar weight and degree of carboxylation, and the complexes were isolated both from acidic and from neutral solutions at varying metal-to-ligand ratios. The characteristic vibration bands of the ligands were identified from their pH-dependent FTIR spectra. In the organotin(IV) complexes obtained at pH approximately 2, the -COO- moieties were found to be coordinated in a monodentate manner, and the band characteristic of the protonated (unbound) -COO- group(s) was also identifi…

DenticityMetal ions in aqueous solutionInorganic chemistryInfrared spectroscopyBiochemistryAnalytical ChemistrySpectroscopy MossbauerDeprotonationSpectroscopy Fourier Transform InfraredOrganotin CompoundsCarboxymethylcelluloseValence (chemistry)Sn(IV)Molecular StructureLigandChemistryOrganic ChemistryStructureTin CompoundsGeneral MedicineQuadrupole splittingInfrared spectraTrigonal bipyramidal molecular geometryCrystallographyCarboxymethylcellulose SodiumMössbauer spectraCarbohydrate research
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Syntheses, structural characterisation and magnetic properties of Fe(ii) and Mn(ii) compounds with the pentacyanopropenido ligand; structural charact…

2006

International audience; Reactions between the metal(II) salts [M(CH3CN)n](BF4)2 (M = Fe, n = 6; M = Mn, n = 4) and some organic anionic polynitriles were studied. With the pentacyanopropenide anion pcp− [pcp− = (NC)2CC(CN)C(CN)2−], were obtained, according to the experimental conditions, the new complexes [M(pcp)2(H2O)4] (1, M = Fe; 2, M = Mn) and [M(pcp)2] (3, M = Fe; 4 = Mn). Use of the hexacyano-3,4-diazahexadienediide anion [(NC)2CC(CN)NNC(CN)C(CN)22−] instead of pcp− did not afford polynitrile metal complexes but led to a new organic derivative 5, of formula C10N8H2. Crystallographic studies indicated that the isostructural compounds 1 and 2 involve discrete monomeric units with pcp li…

DenticityStereochemistryZero field splitting[CHIM.INOR]Chemical Sciences/Inorganic chemistry010402 general chemistry01 natural sciences[ CHIM ] Chemical SciencesCatalysisMetalDelocalized electronMaterials Chemistry[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryIsostructuralBicyclic molecule010405 organic chemistryChemistryHydrogen bondLigand[ CHIM.COOR ] Chemical Sciences/Coordination chemistry[ CHIM.INOR ] Chemical Sciences/Inorganic chemistryGeneral Chemistry0104 chemical sciencesCrystallographyvisual_artvisual_art.visual_art_medium
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Organometallic complexes with biological molecules II. Synthesis, solid-state characterization andin vivo Cytotoxicity of Diorganotin(IV)chloro and T…

1994

Several new diorganotin(IV)chloro and triorganotin(IV)chloro penicillin G derivatives have been prepared. The isolated compounds showed 1:1 stoichiometry, with formulae R2SnClpenG and R3SnClpenGNa, respectively (penG− = penicillin G− = 4- thia - 1 - azabicyclo[3.2.0]heptane-2-carboxylate, 3,3-dimethyl-7-oxo-6-(2-phenylacet-amido) anion; R = Me, Bu, Ph). The coordination environment around the the tin(IV) atom, in all of the complexes, was trigonal bipyramidal. Penicillin G behaved as a monoanionic, bismonodentate ligand in R2SnClpenG through the β-lactamic carbonyl and unidentate ester-type carboxylate anion, and as unidentate through the β-lactamic carbonyl in R3SnClpenGNa, as inferred on …

DenticityThiocyanateLigandStereochemistryGeneral ChemistryQuadrupole splittingCyanateMedicinal chemistryInorganic Chemistrychemistry.chemical_compoundTrigonal bipyramidal molecular geometrychemistryLactamCarboxylateApplied Organometallic Chemistry
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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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Experimental Investigation of Fused Biconical Fiber Couplers for Measuring Refractive Index Changes in Aqueous Solutions

2016

A detailed experimental study of a simple and compact fiber optic sensor based on a fused biconical fiber coupler is presented, in which the sensitivity is improved by operating the coupler beyond the first coupling cycle. The sensor is demonstrated to perform high sensitivity measurements of refractive index changes by means of variation of sugar concentration in water. The device is operated to achieve a linear transmission response, allowing a linear relation between the sugar concentration and the output signal. The initial sensitivity was measured as 0.03 units of normalized transmission per unit of sugar concentration (g/100 mL), with a noise detection limit of a sugar concentration o…

Detection limitMaterials sciencebusiness.industryAnalytical chemistryPolarization-maintaining optical fiber02 engineering and technologyGraded-index fiber020210 optoelectronics & photonicsNormalized frequency (fiber optics)OpticsFiber optic sensor0202 electrical engineering electronic engineering information engineeringFiber optic splitterElectrical and Electronic EngineeringbusinessInstrumentationRefractive indexPhotonic-crystal fiberIEEE Sensors Journal
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