Search results for "carbamate"

showing 10 items of 219 documents

Copper complexes with dithiocarbamates derived from natural occurring amino acids. Crystal and molecular structure of [Cu(en)(EtOH)(H2O)3][Cu(dtc-pro…

2002

Abstract Reaction of Cu(II) salts with dithiocarbamates derived from the amino acids asparagine, glutamine, serine, threonine and tyrosine leads to reduction of the metallic cation and formation of Cu(I) complexes, whereas reaction with proline dithiocarbamate takes place without reduction, leading to formation of a Cu(II) coordination compound. Simultaneous reaction of proline dithiocarbamate and ethylenediamine with Cu(II) leads to the formation of the mixed complex [Cu(en)(EtOH)(H2O)3][Cu(dtc-pro)2]. In the anion, the Cu(II) centre possesses a D2h local symmetry, coordinated by two bidentate dithiocarbamate ligands, while the Cu(II) centre is in a distorted octahedral coordination in the…

chemistry.chemical_classificationDenticityChemistryStereochemistrychemistry.chemical_elementEthylenediamineCrystal structureMedicinal chemistryCopperCoordination complexAmino acidInorganic ChemistryMetalchemistry.chemical_compoundvisual_artMaterials Chemistryvisual_art.visual_art_mediumPhysical and Theoretical ChemistryDithiocarbamatePolyhedron
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Reactivity of the di-μ-hydroxo-complexes [{Pd(NN)}2(μ-OH)2][ClO4]2 (NN=bis(pyrazol-1-yl)alkanes) towards protic electrophiles. Hydration of coordin…

2000

Abstract The hydroxo-complexes [{Pd(μ-OH)(NN)}2][ClO4]2 (NN=bpzm:bis(pyrazol-1-yl) methane: a-compounds, bpzm*:bis(3,5-dimethylpyrazol-1-yl)methane; b-compounds) react with a wide variety of weak protic electrophiles H(LL) in a 1:2 molar ratio to give the mononuclear cationic palladium(II) derivatives of general formula [Pd(LL)(NN)][ClO4] [LL=2-pyridine-methoxo (OCH2-py) (1a,b); picolinate (pic) (2a,b); 8-hydroxiquinolinate (oxin) (3a,b)] or the dinuclear complexes [{Pd(NN)}2(μ-ox)][ClO4]2 [ox=oxalate: (4a,b)] and [{Pd(μ-LL)(NN)}2][ClO4]2 [LL=pyrazolate (pz) (5a,b); p-thiocresolate (SC6H4Me-p) (6a,b); triazolate (tz) (7b); thiophenolate (SPh) (8b)] when reacting with oxalic acid, azole…

chemistry.chemical_classificationNucleophilic additionStereochemistrychemistry.chemical_elementCrystal structureMedicinal chemistryOxalateInorganic Chemistrychemistry.chemical_compoundDeprotonationchemistryElectrophileMaterials ChemistryReactivity (chemistry)Physical and Theoretical ChemistryDithiocarbamatePalladiumPolyhedron
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Reactivity Towards Acidic Protic Ligands of Cyclopalladated Di‐μ‐hydroxo Complexes

2008

The dinuclear hydroxo complexes [{Pd(μ-OH)(C∧N)}2] [C∧N = 2-(2-pyridyl)phenyl (Phpy) (I), 7,8-benzoquinolyl (Bzq) (II) and 2-(2-oxazolinyl)phenyl (Phox) (III)] react in a 1:2 molar ratio with a wide variety of protic electrophiles H(L∧L) bearing different sets of donor atoms (L∧L = O∧O or O∧N) to give the mononuclear neutral palladium(II) derivatives with the general formula [Pd(L∧L)(C∧N)] [O∧O = salicylaldehydate (sal) (1), acetylacetonate (acac) (2) and benzoylacetonate (bzac) (3); O∧N = N-phenylsalicylaldiminate (N-Phsal) (4), N-p-chlorophenylsalicylaldiminate (N-pClPhsal) (5), 2-pyrrolecarbaldeydate (2-pcal) (6), 8-hydroxyquinolinate (oxin) (7)]. Structural characterisation of complexes…

chemistry.chemical_classificationStereochemistrychemistry.chemical_elementMedicinal chemistryInorganic ChemistryDeprotonationchemistryMolar ratioElectrophileProton NMRAmine gas treatingReactivity (chemistry)DithiocarbamatePalladiumEuropean Journal of Inorganic Chemistry
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Affinity Cleavage of Carbamoyl-Phosphate Synthetase I Localizes Regions of the Enzyme Interacting with the Molecule of ATP that Phosphorylates Carbam…

1995

Two ATP molecules are used in the reaction catalyzed by carbamoyl-phosphate synthetase I. One molecule (ATPA) phosphorylates HCO3- and the other (ATPB) phosphorylates carbamate. Carbamoyl-phosphate synthetase I is a 160-kDa polypeptide consisting of a 40-kDa N-terminal moiety and a 120-kDa C-terminal moiety, the latter being composed of two similar halves of molecular mass 60 kDa. We showed [Alonso, E., Cervera, J., Garcia-Espana, A., Bendala, E. & Rubio, V. (1992) J. Biol. Chem. 267, 4524-4532] that Fe.ATP bound at the site for ATPB catalyzes the oxidative inactivation of carbamoyl-phosphate synthetase I in a model oxidative system consisting of Fe3+, ascorbate, and O2, and we detected ATP…

chemistry.chemical_classificationbiologyChemistryProtein domainCarbamate kinaseCleavage (embryo)BiochemistryCarbamoyl phosphate synthetase IAmino acidBiochemistrybiology.proteinMoietyNucleotideBinding siteEuropean Journal of Biochemistry
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Phase selective synthesis of ZnS nanoparticles from structurally new dithiocarbamate precursor

2015

Abstract A phase selective solvothermal synthesis of ZnS (wurzite) nanoparticles with a flower-like morphology using a dithiocarbamate precursor, [Zn(4-dpmpzdtc)2(dpmpz)] (1) (where, dpmpz=(diphenylmethyl)piperazine), is described. The nanoparticles were identified as ZnS (wurzite) with the particle size of about 3 to 10 nm by scanning and transmission electron microscopy as well as powder X-ray diffraction (XRD). In addition, the precursor complex 1 was characterized using single crystal X-ray diffraction.

chemistry.chemical_classificationcrystal structureMaterials sciencesynthesisMechanical EngineeringSolvothermal synthesisInorganic chemistryNanoparticleCrystal structureCondensed Matter PhysicsPiperazinechemistry.chemical_compoundchemistryMechanics of MaterialsTransmission electron microscopyPhase (matter)solvothermalwurziteGeneral Materials SciencenanoparticlesDithiocarbamateSingle crystalta116Nuclear chemistryMaterials Letters
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Synthesis and thermal decomposition studies of homo- and heteroleptic tin(iv) thiolates and dithiocarbamates: molecular precursors for tin sulfides

2002

The syntheses and X-ray structures of novel heteroleptic thiolate/dithiocarbamate derivatives (Et2NCS2)2(RS)2Sn (R = Cy, CH2CF3) have been examined and their thermal decompositions compared with those of selected tin(II) and tin(IV) dithiocarbamates. The heteroleptic species decompose to SnS by initial elimination of RSSR to afford (Et2NCS2)2Sn and subsequent loss of [Et2NC(S)]2S. In contrast, (Et2NCS2)4Sn decomposes via [(Et2NCS2)2SnS]2, whose structure has been determined, and finally to SnS2 by sequential elimination of [Et2NC(S)]2S. The two families of compounds, (R2NCS2)4Sn and (Et2NCS2)2(RS)2Sn, thus provide single-source materials for bulk SnS2 and SnS, respectively, by virtue of the…

chemistry.chemical_classificationtin thiolatesMössbauer spectroscopyChemistryInorganic chemistryThermal decompositionSolid-statechemistry.chemical_elementGeneral ChemistryCrystal structureChemical vapor depositionMedicinal chemistryDecompositionchemical vapor depositionSettore CHIM/03 - Chimica Generale E InorganicaTinDithiocarbamateX-ray crystallographyJournal of the Chemical Society, Dalton Transactions
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Detecting residues of urea and carbamate pesticides

2004

chemistry.chemical_compoundCarbamate pesticidesChromatographyPesticide residuechemistryEnvironmental chemistryUreaGas chromatographyPesticideContaminationFood contaminant
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Stability in physiological saline of intravenous busulfan in a polyolefin pack

2008

Abstract Introduction Although it has been used orally, the variability in its absorption and the risk of causing vomiting has lead to a push towards the intravenous use of busulfan. This study looks at the stability of 60 mg of busulfan, in fixed volumes of 250 mL (0.24 mg/mL) and 500 mL (0.12 mg/mL) of physiological saline and different conservation conditions, in a new plastic pack made from polyolefin/polyamide laminates. Material and methods High-performance liquid chromatography with ultraviolet detection was used to determine the concentration of busulfan derivate with sodium diethyldithiocarbamate trihydrate. Stability was assessed for both concentrations; refrigerated and at room t…

chemistry.chemical_compoundIntravenous useChromatographyIntravenous busulfanchemistrymedicineAbsorption (skin)Physiological salineBusulfanSodium diethyldithiocarbamatePolyolefinmedicine.drugFarmacia Hospitalaria (English Edition)
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Synthesis and structural studies on Ni(II) dithiocarbamates : Exploring intramolecular Ni···H-C interactions

2017

Five new Ni(II) dithiocarbamates with NiS4, NiS2PN and NiS2PCl coordination spheres, viz. [Ni(bupmbzdtc)2] (1), [Ni(bupmbzdtc)(PPh3)(NCS)] (2), [Ni(bupmbzdtc)(PPh3)Cl] (3), [Ni(4-dpmpzdtc)(PPh3)Cl] (4) and [Ni(pbbzbudtc)(PPh3)(NCS)] (5), where bupmbzdtc = N-butyl(p-methylbenzyl)dithiocarbamato anion, 4-dpmpzdtc = 4-(diphenylmethyl)piperazinecarbodithioato anion, pbbzbudtc = N-(p-bromobenzyl)butyl-dithiocarbamato anion and PPh3 = triphenylphosphine, were synthesized and characterized by UV, IR, NMR and single crystal X-ray diffraction methods. Spectral results suggest a square planar geometry around the Ni(II) metal center for all the synthesized complexes. Single crystal X-ray structural an…

dithiocarbamateC-H···Ni interactionX-ray structural analysisNMR
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Synthesis of Both Ionic Species of Ammonium Dithiocarbamate Derived Cholic Acid Moieties

2011

The reaction of 3-aminopropylamide of cholic acid with CS₂ produced a bile acid derivative of dithiocarbamic acid which further formed an ammonium salt with another molecule of 3-aminopropylamide of cholic acid. The cationic 3-ammonium propylamide of cholic acid did not react further with CS₂ and the formed salt was stable in the reaction mixture, even when excess CS₂ was used. When the reaction was carried out in the presence of aqueous sodium hydroxide, only the bile acid derivative of sodium dithiocarbamate was formed. The dithiocarbamate derivatives were characterized by ¹H- and ¹³C-NMR spectroscopy and ESI-TOF mass spectrometry. peerReviewed

dithiocarbamateNMR spectroscopyaminesteroidpolycyclic compoundscholic acid
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