Search results for "SB"

showing 10 items of 1841 documents

Tin(IV) and organotin(IV) derivatives of bis(pyrazolyl)acetate: Synthesis, spectroscopic characterization and behaviour in solution.

2005

Abstract Novel heteroscorpionate-containing tin and organotin(IV) complexes, [SnRnX3 − n(L)], R = Me, Bun, Ph, or cy; X = Cl, Br or I, n = 0, 1, 2 or 3; L = bis(pyrazol-1-yl)acetate (bpza) or bis(3,5-dimethylpyrazol-1-yl)acetate (bdmpza), have been synthesized and characterized by spectral (IR, 1H, 13C and 119Sn NMR, 119mSn Mossbauer) and analytical data. In [SnI3(bdmpza)], the ligand is fac-N,N′,O-tridentate, the three iodine atoms thus also fac about the six-coordinate tin(IV) atom. Neutral bpzaH reacts with BunSnCl3, PhSnCl3 and SnCl4 in Et2O in the absence of base, yielding 1:1 adducts [XSnCl3(bpzaH)] (X = R or Cl).

chemistry.chemical_classificationAcetate synthesisBase (chemistry)LigandStereochemistryOrganic ChemistryX-raychemistry.chemical_elementBiochemistryMedicinal chemistryAdductInorganic ChemistrychemistryMössbauer spectroscopyMaterials ChemistryPhysical and Theoretical ChemistryTinSingle crystalJournal of Organometallic Chemistry
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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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Equilibria involved in the diorganotin(IV) and triorganotin(IV) phosphomycin interaction in aqueous solution

2007

Four new diorganotin(IV), (R = Me, Bu), and triorganotin(IV), (R = Me, Ph), derivatives of the phosphomycin disodium salt antibiotic[(1R,2S)-1,2-epoxypropylphosphonate]Na2 have been synthesized and their solid state configuration studied by X-ray crystallography, FT-IR, Mossbauer, UV–Vis spectroscopies. The X-ray diffraction investigation, performed on the bis[trimethyltin(IV)]- phosphomycin, showed that the coordination geometry at all the Sn atoms is trigonal bipyramidal. The structure of the complex forms an unusual polymeric zig-zag planar network. The FT-IR and the 119Sn Mo¨ssbauer studies supported the formation of trigonal bipyramidal (Tbp) molecular structures, both in the diorganot…

chemistry.chemical_classificationAqueous solutionTrimethyltin(IV)LigandChemistryPotentiometric titrationInorganic chemistrySalt (chemistry)ISE-H+ potentiometric studyProtonationGeneral Chemistrydimethyltin(IV)Medicinal chemistryInorganic ChemistryFT-IRMossbauerX-rayOrganotinStability constants of complexesIonic strengthISE-H+ potentiometric study; UV–visible study; dimethyltin(IV); Trimethyltin(IV); phosphomycinUV–visible studyphosphomycinPotentiometric and spectrophotometric titrations
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119Sn Mössbauer spectroscopic studies of the products of the reaction of triorganotin(IV) derivatives with 6-thiopurine

1985

Abstract A structural study of the products of the reaction of R 3 Sn IV derivatives (R = Me, Bu n , Ph) with 6-thiopurine, 6-TPH 2 , and its sodium salt, 6-TPHNa, has been undertaken using Mossbauer spectroscopy and the point-charge model rationalization of the Mossbauer parameter nuclear quadrupole splitting. The synthetic reactions have been carried out at ca . 0 °C, 20 °C and 50 °C. The Mossbauer spectra of the complexes AlK 3 Sn(6-TPH) are consistent with the occurrence of two distinct tin(IV) sites in samples prepared at the lower temperature, while one only site appears by increasing the temperature of the reaction. Two tin sites constantly occur in the products of the reactions invo…

chemistry.chemical_classificationChemistryLigandInorganic chemistrychemistry.chemical_elementQuadrupole splittingInorganic ChemistryCrystallographyTrigonal bipyramidal molecular geometryMössbauer spectroscopyMaterials ChemistryMoietyPhysical and Theoretical ChemistryTinInorganic compoundStoichiometryInorganica Chimica Acta
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Bis(triorganometal) and diorganometal 1,3-dithiolates (R3M)2(C6H3XS2) and R2M(C6H3XS2) (M = Sn, Pb; X= H, Cl)

1984

Abstract Bis(triorganometal) and diorganometal 1,3-dithiolates (R3M)2(C6H3XS2) (C6H5XS2 1,3-dithiobenzene (for X = H) or 1,3-dithio-4-chlorobenzene (for X = Cl); M = Sn, X = Cl, R = CH3, C6H5; M = Pb, X = H, Cl, R = CH3, C2H5) and R2M(C6H3XS2) (R = CH3, C2H5, C6H5; M = Sn, X = Cl; M = Pb, X = H, Cl) have been prepared as the first organometal IVB derivatives of 1,3-dithiols, and investigated by vibrational, 1H NMR, and (in the case of organotin compounds) Mossbauer spectroscopy. The triorganometal derivatives are monomeric and the diorganometal derivatives dimeric in solution (37° C). For the latter a twelve-membered ring structure is proposed for both solution and the solid state.

chemistry.chemical_classificationChemistryStereochemistryOrganic ChemistryDithiolNuclear magnetic resonance spectroscopyRing (chemistry)BiochemistryInorganic Chemistrychemistry.chemical_compoundCrystallographyMonomerMössbauer spectroscopyMaterials ChemistryProton NMRMoleculePhysical and Theoretical ChemistryInorganic compoundJournal of Organometallic Chemistry
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Structural selectivity provided by starburst dendrimers as pseudostationary phase in electrokinetic chromatography

1995

Abstract Starburst dendrimers (SBDs) were used as a pseudostationary phase in electrokinetic chromatography (EKC) of hydrophobic compounds. The selectivity of SBD-mediated EKC (SBD-EKC) was different from those in micellar EKC (MEKC) systems, in spite of the apparent structural resemblance between micelles and SBDs. The SBDs provided similar selectivity as polymer gel packing materials in reversed-phase liquid chromatography (RPLC), showing little selectivity for alkyl groups and clear preference for aromatic compounds, especially for rigid, planar polynuclear aromatic hydrocarbons. The alkylation of SBDs resulted in the increased retention and hydrophobic selectivity while maintaining the …

chemistry.chemical_classificationChromatographyOrganic ChemistryGeneral MedicineSBDSAlkylationBiochemistryMicelleAnalytical ChemistryElectrokinetic phenomenaHydrocarbonchemistryDendrimerOrganic chemistrySelectivityAlkylJournal of Chromatography A
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Cooperative High-Temperature Spin Crossover Accompanied by a Highly Anisotropic Structural Distortion

2016

Spin transitions are a spectacular example of molecular switching that can provoke extreme electronic and structural reorganizations in coordination compounds. A new 3D cyanoheterometallic framework, [Fe(pz)(Au(CN)2)2], has been synthesized in which a highly cooperative spin crossover has been observed at 367 and 349 K in heating and cooling modes, respectively. Mössbauer spectroscopy revealed a complete transition between the diamagnetic and paramagnetic states of the iron centres. The low-spin-to-high-spin transition induced a drastic structural distortion involving a large one-directional expansion (ca. 10.6%) and contraction (ca. 9.6%) of the lattice. Negative thermal expansion along th…

chemistry.chemical_classificationCondensed matter physicsCooperative effects010405 organic chemistryChemistryTransition temperatureIronMetal-organic frameworks010402 general chemistrySpin crossover01 natural sciences0104 chemical sciencesCoordination complexInorganic ChemistryParamagnetismNuclear magnetic resonanceNegative thermal expansionSpin crossoverQD156Mössbauer spectroscopyMagnetic propertiesQD473DiamagnetismAnisotropy
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Reactivity of CuI and CuBr toward Et2S: a reinvestigation on the self-assembly of luminescent copper(I) coordination polymers.

2010

CuI reacts with SEt(2) in hexane to afford the known strongly luminescent 1D coordination polymer [(Et(2)S)(3){Cu(4)(mu(3)-I)(4)}](n) (1). Its X-ray structure has been redetermined at 115, 235, and 275 K in order to address the behavior of the cluster-centered emission and is built upon Cu(4)(mu(3)-I)(4) cubane-like clusters as secondary building units (SBUs), which are interconnected via bridging SEt(2) ligands. However, we could not reproduce the preparation of a coordination polymer with composition [(Et(2)S)(3){Cu(4)(mu(3)-Br)(4)}](n) as reported in Inorg. Chem. 1975, 14, 1667. In contrast, the autoassembly reaction of SEt(2) with CuBr results in the formation of a novel 1D coordination…

chemistry.chemical_classificationCoordination polymerInorganic chemistrychemistry.chemical_elementBridging ligandPolymerCrystal structureCopperInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryDensity functional theorySBusPhysical and Theoretical ChemistryLuminescenceInorganic chemistry
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Bis(3,5-dimethyl-1H-pyrazolyl)selenide--a new bidentate bent connector for preparation of 1D and 2D co-ordination polymers.

2007

The synthesis and description of eight polymeric complexes formed by transition metals with the bifurcated ligand bis(3,5-dimethyl-1H-pyrazolyl)selenide are discussed together with X-ray crystal analysis as well as variable temperature magnetic susceptibility and characterization by Mossbauer spectroscopy. Preferable types of binding patterns of the ligand were determined, which include a variation of the bridging modes (cis- and trans-) and of the separation length, where the latter parameter together with bending of the ligand molecule were found to be dependent on the type of co-ordination geometry of the central atom and the nature of the anion. A strategy for increasing the structure d…

chemistry.chemical_classificationDenticityBent molecular geometryInorganic chemistryPolymerMagnetic susceptibilityIonInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryTransition metalSelenideMössbauer spectroscopyDalton transactions (Cambridge, England : 2003)
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Synthesis, infrared and M�ssbauer characterization and X-ray crystal structure of 1,10-phenanthrolinium tetrachloromethoxy phenylantimonate(V)

1991

The compound has been characterized by X-ray crystal structure determination, Mossbauer and i.r. spectroscopy. It crystallizes in the monoclinic space groupP21/c (No. 14) witha=24.228(4),b=8.335(2),c=23.975(4) A,β=117.83(3)° andZ=8. Least-squares refinement on 3749 observed reflections gave finalR=0.034 (Rw=0.037). The compound is constituted by [(C6H5)SbCl4OMe]− anions andphenH+cations. The coordination polyhedron about Sb is an octahedron (Sb-Cl 2.416(3), Sb-O 1.962(7) and Sb-C 2.138(9) A). The whole structure is characterized by two short contacts (O(1)⋯N(2) 2.76(1) O(2)⋯N(4) 2.75(1) A) involving the methoxy oxygens of the two independent anionic units [(C6H5)SbCl4OMe]− and two nitrogens…

chemistry.chemical_classificationGeneral ChemistryCrystal structureCondensed Matter Physicschemistry.chemical_compoundCrystallographychemistryOctahedronStructural BiologyX-ray crystallographyMössbauer spectroscopySpectroscopyInorganic compoundSpectroscopyOrganometallic chemistryMonoclinic crystal systemJournal of Crystallographic and Spectroscopic Research
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