Search results for "Diselenide"

showing 9 items of 9 documents

Synthesis, reactivity and structural studies of selenide bridged carboranyl compounds.

2006

Reaction of the lithium salt Li[1-R-1,2-closo-C(2)B(10)H(10)] with selenium under mild conditions, followed by hydrolysis gave the diselenide compound (1-Se-2-R-1,2-closo-C(2)B(10)H(10))(2) in contrast to the well-reported mercapto compounds 1-SH-2-R-1,2-closo-C(2)B(10)H(10) obtained using a similar synthetic procedure. Details for the preparation and X-ray structural characterisation of the new compounds (2-Me-1,2-closo-C(2)B(10)H(10))(2)Se, (1-Se-2-R-1,2-closo-C(2)B(10)H(10))(2) (R = Me, Ph, ) are specified. To further explore the mechanism of the dimerization reaction, the complex [Au(1-Se-2-Me-1,2-closo-C(2)B(10)H(10))(PPh(3))] was synthesized, confirming the existence of the intermedia…

010405 organic chemistryLigandInorganic chemistrychemistry.chemical_elementNuclear magnetic resonance spectroscopy010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic ChemistryDiselenidechemistry.chemical_compoundChalcogenchemistrySelenideReactivity (chemistry)Cyclic voltammetrySeleniumDalton transactions (Cambridge, England : 2003)
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Bond stretching and redox behavior in coinage metal complexes of the dichalcogenide dianions [(SPh2P)2CEEC(PPh2S)2]2- (E=S, Se): diradical character …

2011

The metathetical reactions of a) [Li(tmeda)](2)[(S)C(PPh(2)S)(2)] (Li(2)·3c) with CuCl(2) and b) [Li(tmeda)](2)[(SPh(2)P)(2)CSSC(PPh(2)S)(2)] (Li(2)·4c) with two equivalents of CuCl both afford the binuclear Cu(I) complex {Cu(2)[(SPh(2)P)(2)CSSC(PPh(2)S)(2)]} (5c). The elongated (C)S-S(C) bond (ca. 2.54 and 2.72 A) of the dianionic ligand observed in the solid-state structure of 5c indicate the presence of diradical character as supported by theoretical analyses. The treatment of [Li(tmeda)](2)[(SPh(2)P)(2)CSeSeC(PPh(2)S)(2)] (Li(2)·4b) and Li(2)·4c with AgOSO(2)CF(3) produce the analogous Ag(I) derivatives, {Ag(2)[(SPh(2)P)(2)CEEC(PPh(2)S)(2)]} (6b, E=Se; 6c, E=S), respectively. The disele…

DiradicalChemistryStereochemistryLigandOrganic ChemistryCoinage metalsGeneral ChemistryNuclear magnetic resonance spectroscopyMetathesisCatalysisMetalDiselenideCrystallographyvisual_artvisual_art.visual_art_mediumta116IsomerizationChemistry (Weinheim an der Bergstrasse, Germany)
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A Synthetic Route to 3-(Heteroaryl)-7-hydroxycoumarins Designed for Biosensing Applications

2014

A straightforward method to synthesize 3-(2-benzimidazolyl)-7-hydroxycoumarins, based on the condensation reaction of 7-acetoxy-3-formylcoumarin with various C- and/or N-substituted ortho-phenylenediamine derivatives is presented. This unusual approach proved particularly effective for introducing different hydrophilic groups (carboxylic or sulfonic acids or trimethylalkylammonium moieties) onto the heteroaryl scaffold, leading to cyan-green emitting coumarins that were both water-soluble and strongly fluorescent under physiological conditions. The further extension of this condensation reaction to bis(2-aminophenyl)diselenide enabled the first synthesis of 3-(2-benzoselenazolyl)-7-hydroxyc…

Protease010405 organic chemistryChemistrymedicine.medical_treatmentOrganic Chemistry010402 general chemistryCondensation reaction01 natural sciencesFluorescence0104 chemical sciencesDiselenidemedicineOrganic chemistryPhysical and Theoretical ChemistryBiosensorEuropean Journal of Organic Chemistry
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CCDC 821786: Experimental Crystal Structure Determination

2011

Related Article: M.Risto, T.Chivers, J.Konu|2011|Dalton Trans.|40|8238|doi:10.1039/c1dt10646e

Space GroupCrystallography(mu~2~-bis(bis(diphenylphosphorothioyl)methanido) diselenide)-di-thallium(i) dichloromethane solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 616223: Experimental Crystal Structure Determination

2007

Related Article: A.Laromaine, F.Teixidor, R.Kivekas, R.Sillanpaa, M.Arca, V.Lippolis, E.Crespo, C.Vinas|2006|Dalton Trans.||5240|doi:10.1039/b610944f

Space GroupCrystallography12-bis(2-Methyl-12-dicarba-closo-dodecaboranyl)diselenide toluene solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 616224: Experimental Crystal Structure Determination

2007

Related Article: A.Laromaine, F.Teixidor, R.Kivekas, R.Sillanpaa, M.Arca, V.Lippolis, E.Crespo, C.Vinas|2006|Dalton Trans.||5240|doi:10.1039/b610944f

Space GroupCrystallographyCrystal System12-bis(2-Phenyl-12-dicarba-closo-dodecaboranyl)diselenideCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 616222: Experimental Crystal Structure Determination

2007

Related Article: A.Laromaine, F.Teixidor, R.Kivekas, R.Sillanpaa, M.Arca, V.Lippolis, E.Crespo, C.Vinas|2006|Dalton Trans.||5240|doi:10.1039/b610944f

Space GroupCrystallographyCrystal SystemCrystal StructureCell Parameters12-bis(2-Methyl-12-dicarba-closo-dodecaboranyl)diselenideExperimental 3D Coordinates
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Scanning tunneling microscopy investigation of tricycloquinazoline liquid crystals on gold

2000

Self-assembled monolayers (SAMs) of hexaalkylthioether derivatives of tricycloquinazoline (TCQ) on Au(111) and tungsten diselenide (WSe2) were investigated by scanning tunneling microscopy (STM). The Au(111) surfaces were found to be etched by the thioether containing solutions. Corroded surfaces which are similar to gold surfaces that were coated with SAMs of thiols or disulfides were revealed by STM. Atomic adsorption spectroscopy proved that an amount of gold that corresponds to ca. 30% of a monolayer was dissolved in the assembly solutions. On gold, the aromatic cores of the molecules were found to be in face-on orientation. The alkyl substituents were in most cases folded upwards and s…

chemistry.chemical_classificationChemistryMetals and AlloysSelf-assembled monolayerSurfaces and InterfacesSurfaces Coatings and FilmsElectronic Optical and Magnetic Materialslaw.inventionCrystallographychemistry.chemical_compoundAdsorptionLiquid crystallawMonolayerMaterials ChemistryOrganic chemistryTungsten diselenideSelf-assemblyScanning tunneling microscopeAlkylThin Solid Films
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Mo-Based Oxidizers as Powerful Tools for the Synthesis of Thia- and Selenaheterocycles.

2019

A highly efficient synthetic protocol for the synthesis of thia- and selenaheterocycles has been developed. By employing a MoCl5 -mediated intramolecular dehydrogenative coupling reaction, a broad variety of structural motifs was isolated in yields up to 94 %. The electrophilic key transformation is tolerated by several labile moieties like halides and tertiary alkyl groups. Due to the use of disulfide or diselenide precursors, a high atom efficiency was achieved.

chemistry.chemical_classificationcyclization010405 organic chemistryChemistryoxidationOrganic ChemistryHalideGeneral Chemistry010402 general chemistry01 natural sciencesCombinatorial chemistryCatalysisCoupling reactionC−H activationsulfur heterocycles0104 chemical sciencesDiselenidemolybdenumAtom economyIntramolecular forceElectrophileStructural motifAlkylChemistry (Weinheim an der Bergstrasse, Germany)
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