Search results for "Fosfina"

showing 6 items of 6 documents

The Important Role of the Nuclearity, Rigidity, and Solubility of Phosphane Ligands in the Biological Activity of Gold(I) Complexes

2018

A series of 4-ethynylaniline gold(I) complexes containing monophosphane (1,3,5-triaza-7-phosphaadamantane (pta; 2), 3,7-diacetyl-1,3,7-triaza-5-phosphabicyclo[3.3.1]nonane (3), and PR3 , with R=naphthyl (4), phenyl (5), and ethyl (6)) and diphosphane (bis(diphenylphosphino)acetylene (dppa; 7), trans-1,2-bis(diphenylphosphino)ethene (dppet; 8), 1,2-bis(diphenylphosphino)ethane (dppe; 9), and 1,3-bis(diphenylphosphino)propane (dppp; 10)) ligands have been synthesized and their efficiency against tumor cells evaluated. The cytotoxicity of complexes 2-10 was evaluated in human colorectal (HCT116) and ovarian (A2780) carcinoma as well as in normal human fibroblasts. All the complexes showed a hi…

FosfinaMolecular ConformationOrCrystal structureCrystallography X-RayLigandsMedicinal chemistry01 natural scienceskultachemistry.chemical_compoundCoordination ComplexesDiphosphaneSolubilityCytotoxicityta116bcl-2-Associated X ProteinMembrane Potential Mitochondrialbioaktiiviset yhdisteetBiological activitybiological activity of gold(I) complexesAcetyleneProto-Oncogene Proteins c-bcl-2rigidityCompostos d'ornuclearityPhosphineCell SurvivalPhosphinesAntineoplastic Agentsphosphane ligands010402 general chemistryCatalysisCell LineStructure-Activity RelationshipMoleculeHumans010405 organic chemistrysolubilityOrganic ChemistryGeneral ChemistrykompleksiyhdisteetHCT116 Cells0104 chemical sciencesLligandschemistryQuantum TheoryGoldNonaneReactive Oxygen SpeciesGold compoundsChemistry: A European Journal
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The cyclic [N(PiPr2E)2]+ (E = Se, Te) cations: a new class of inorganic ring system.

2006

The two-electron oxidation of [(tmeda)NaN(PiPr2E)2] with iodine produces the cyclic [N(PiPr2E)2]+ (E = Se, Te) cations, which exhibit long E–E bonds in the iodide salts. peerReviewed

chemistry.chemical_classificationStereochemistryIodideMetals and Alloyschemistry.chemical_elementliganditGeneral ChemistryRing (chemistry)IodineMedicinal chemistryCatalysisSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsdikalkogenoimidodifosfinaatitdichalcogenoimidodiphosphinateschemistryMaterials ChemistryCeramics and CompositesChemical communications (Cambridge, England)
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Synthesis, Spectroscopic, and Structural Investigation of the Cyclic [N(PR2E)2]+ Cations (E = Se, Te; R = iPr, Ph): the Effect of Anion and R-Group E…

2006

Two-electron oxidation of the [N(PiPr2E)2]- anion with iodine produces the cyclic [N(PiPr2E)2]+ (E = Se, Te) cations, which exhibit long E−E bonds in the iodide salts [N(PiPr2Se)2]I (4) and [N(PiPr2Te)2]I (5). The iodide salts 4 and 5 are converted to the ion-separated salts [N(PiPr2Se)2]SbF6 (6) and [N(PiPr2Te)2]SbF6 (7) upon treatment with AgSbF6. Compounds 4−7 were characterized in solution by multinuclear NMR, vibrational, and UV−visible spectroscopy supported by DFT calculations. A structural comparison of salts 4−7 and [N(PiPr2Te)2]Cl (8) confirms that the long E−E bonds in 4, 5, and 8 can be attributed primarily to the donation of electron density from a lone pair of the halide count…

dikalkogenoimidodifosfinaatitdichalcogenoimidodiphosphinatesligandit
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New tellurium-containing ring systems

2007

The recent discovery of a suitable synthesis of the monoanionic ditelluroimidodiphosphinate ligands [TePR2NPR2Te]− (R = Ph, iPr, tBu) has facilitated investigations of the fundamental chemistry of these chelating inorganic ligands. This article is focused on aspects of that chemistry in which the behaviour of this ditelluro PNP ligand differs from that of the well-studied dithio and diseleno congeners. The emphasis is on new tellurium-containing ring systems formed in: (a) redox transformations and (b) the synthesis of metal complexes. peerReviewed

ditelluroimidodiphosphinate ligandchalcogen chemistrykalkogeenikemiaditelluroimidodifosfinaatti ligandit
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New Insights into the Chemistry of Imidodiphosphinates from Investigations of Tellurium-Centered Systems

2010

Dichalcogenido-imidodiphosphinates, [N(PR2E)2]− (R = alkyl, aryl), are chelating ligands that readily form cyclic complexes with main group metals, transition metals, lanthanides, and actinides. Since their discovery in the early 1960s, researchers have studied the structural chemistry of the resulting metal complexes (where E = O, S, Se) extensively and identified a variety of potential applications, including as NMR shift reagents, luminescent complexes in photonic devices, or single-source precursors for metal sulfides or selenides. In 2002, a suitable synthesis of the tellurium analogs [N(PR2Te)2]− was developed. In this Account, we describe comprehensive investigations of the chemistry…

imidodiphosphinatesimidodifosfinaatit
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Experimental and Theoretical Investigations of Structural Isomers of Dichalcogenoimidodiphosphinate Dimers: Dichalcogenides or Spirocyclic Contact Io…

2007

A synthetic protocol for the tert-butyl-substituted dichalcogenoimidodiphosphinates [Na(tmeda){(EPtBu2)2N}] (3 a, E=S; 3 b, E=Se; 3 c, E=Te) has been developed. The one-electron oxidation of the sodium complexes [Na(tmeda){(EPR2)2N}] with iodine produces a series of neutral dimers (EPR2NPR2E[BOND])2 (4 b, E=Se, R=iPr; 4 c, E=Te, R=iPr; 5 a, E=S, R=tBu; 5 b, E=Se, R=tBu; 5 c, E=Te, R=tBu). Attempts to prepare 4 a (E=S, R=iPr) in a similar manner produced a mixture including HN(SPiPr2). Compounds 4 b, 4 c and 5 a–c were characterised by multinuclear NMR spectra and by X-ray crystallography, which revealed two alternative structures for these dimeric molecules. The derivatives 4 b, 4 c, 5 a an…

structural isomerismdikalkogenoimidodifosfinaattirakenteellinen isomeriadichalcogenoimidodiphosphinate
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