Search results for "Borane"

showing 10 items of 278 documents

CCDC 1534777: Experimental Crystal Structure Determination

2017

Related Article: Elena Oleshkevich, Clara Viñas, Isabel Romero, Duane Choquesillo-Lazarte, Matti Haukka, Francesc Teixidor|2017|Inorg.Chem.|56|5502|doi:10.1021/acs.inorgchem.7b00610

Space GroupCrystallographycatena-[bis(mu-17-dicarba-closo-dodecaborane(11)-1-phosphinato)-bis(methanol)-manganese(ii) methanol solvate]Crystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 234460: Experimental Crystal Structure Determination

2006

Related Article: R.Nunez, O.Tutusaus, F.Teixidor, C.Vinas, R.Sillanpaa, R.Kivekas|2005|Chem.-Eur.J.|11|5637|doi:10.1002/chem.200500288

Space GroupCrystallographycommo-(33'-Cobalta(iii)bis(8-(dimethylsulfido)-12-dicarbaundecaborane(10))) chloride ethanol solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 175912: Experimental Crystal Structure Determination

2002

Related Article: C.Gimenez-Saiz, A.M.Z.Slawin, J.D.Woollins|2002|CrystEngComm|4|84|doi:10.1039/b111262g

Space GroupCrystallographypentakis(bis(Ethylenedithio)tetrathiafulvalene) decaiodo-decaborane dichloromethane solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1534778: Experimental Crystal Structure Determination

2017

Related Article: Elena Oleshkevich, Clara Viñas, Isabel Romero, Duane Choquesillo-Lazarte, Matti Haukka, Francesc Teixidor|2017|Inorg.Chem.|56|5502|doi:10.1021/acs.inorgchem.7b00610

Space GroupCrystallographytetraaqua-bis(17-dicarba-closo-dodecaborane(11)-1-phosphinato)-manganese(ii) dihydrateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 815318: Experimental Crystal Structure Determination

2011

Related Article: E.Pardo, M.Verdaguer, P.Herson, H.Rousseliere, J.Cano, M.Julve, F.Lloret, R.Lescouezec|2011|Inorg.Chem.|50|6250|doi:10.1021/ic200616p

Space GroupCrystallographytetrakis(mu~2~-cyano)-tetrakis(22'-bipyridine)-bis(11'1''1'''-boranetetrayltetrakis(1H-pyrazole))-dicyano-di-manganese(ii)-di-iron(iii) diperchlorate acetonitrile solvateCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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2-Methyl-1-phenylsulfanyl-1,2-dicarba-closo-dodecaborane(12)

2002

In the title o-carborane derivative, C(9)H(18)B(10)S, the methyl and phenylsulfanyl groups are connected to the C atoms of the carborane cage. The C(cage)-C(cage) distance is 1.708 (4) A.

StereochemistryGeneral MedicineCrystal structure010402 general chemistry010403 inorganic & nuclear chemistry01 natural sciencesMedicinal chemistryGeneral Biochemistry Genetics and Molecular Biology3. Good health0104 chemical scienceschemistry.chemical_compoundchemistryCarboraneDerivative (chemistry)Acta Crystallographica Section C Crystal Structure Communications
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A Discrete P⋅⋅⋅II⋅⋅⋅P Assembly: The Large Influence of Weak Interactions on the31P NMR Spectra of Phosphane–Diiodine Complexes

2006

Thioethers, except derivatives of [7-R-7,8-C2B9H11] , are more weakly coordinating ligands than phosphanes. This difference is evidenced by the I I distances in the spokeshaped charge-transfer (CT) complexes R2S·I2 and R3P·I2 (Figure 1). The I I distance is sensitive to the strength of the interaction between the s* LUMO orbital on I2 and the HOMO orbital of the donor atom: the stronger the donor, the longer the I I distance. In these spoke CT complexes, the I I distance varies from 3.2 0.2 7 in R3P·I2 adducts [5] to 2.80 0.05 7 in R2S·I2 adducts, [6] indicating the weaker donor character of the thioether group. Whereas extended I2 arrays, spoke adducts of I2, polyiodides, and other structu…

StereochemistryInteractionsPhosphanes010402 general chemistry01 natural sciencesCatalysisAdductPolyiodidechemistry.chemical_compoundThioetherMoleculeNon-covalent interactionsCarboranesHOMO/LUMOchemistry.chemical_classificationiodine010405 organic chemistryChemistryLigandStructure elucidationGeneral MedicineGeneral ChemistryNoncovalent0104 chemical sciencesChemistryCarboraneAngewandte Chemie International Edition
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Uncommon coordination behaviour of P(S) and P(Se) units when bonded to carboranyl clusters: experimental and computational studies on the oxidation o…

2010

Oxidation of closo-carboranyl diphosphines 1,2-(PR(2))(2)-1,2-closo-C(2)B(10)H(10) (R=Ph, iPr) and closo-carboranyl monophosphines 1-PR(2)-2-R'-1,2-closo-C(2)B(10)H(10) (R=Ph, iPr, Cy; R'=Me, Ph) with hydrogen peroxide, sulfur and elemental black selenium evidences the unique capacity of the closo-carborane cluster to produce uncommon or unprecedented P/P(E) (E=S, Se) and P=O/P=S chelating ligands. When H(2)O(2) reacts with 1,2-(PR(2))(2)-1,2-closo-C(2)B(10)H(10) (R=Ph, iPr), they are oxidized to 1,2-(OPR(2))(2)-1,2-closo-C(2)B(10)H(10) (R=Ph, iPr). However, when S and Se are used, different reactivity is found for 1,2-(PPh(2))(2)-1,2-closo-C(2)B(10)H(10) and 1,2-(PiPr(2))(2)-1,2-closo-C(2)…

Steric effectsDenticity010405 organic chemistryChemistryStereochemistryOrganic ChemistryGeneral Chemistry010402 general chemistry01 natural sciencesCatalysis0104 chemical sciencesChalcogenchemistry.chemical_compoundDiphosphinesElectronic effectCarboraneReactivity (chemistry)ta116PhosphineChemistry (Weinheim an der Bergstrasse, Germany)
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Icosahedral carboranes as scaffolds for congested regioselective polyaryl compounds: the distinct distance tuning of C–C and its antipodal B–B

2019

Four-fold aryl substituted o-carborane derivatives with defined patterns of substitution at the antipodal region of the cluster carbon atoms have been achieved. It is proven that this region is congested but lacks steric hindrance. Also, the two antipodal sites Cc–Cc and B9–B12 are affected very distinctly by electron donor substituents.

Steric effectsIcosahedral symmetryAntipodal pointElectron donorCrystal structure010402 general chemistry01 natural sciencesCatalysischemistry.chemical_compoundMaterials ChemistryCluster (physics)BoronO-carboranes010405 organic chemistryChemistryArylMetals and AlloysRegioselectivityGeneral Chemistry3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsPharmacophoresCrystallographyCrystal-structureCeramics and CompositesChemical Communications
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Synthesis and Characterization of New Fluorescent Styrene-Containing Carborane Derivatives: The Singular Quenching Role of a Phenyl Substituent

2011

A set of neutral and anionic carborane derivatives in which the styrenyl fragment is introduced as a fluorophore group has been successfully synthesized and characterized. The reaction of the monolithium salts of 1-Ph-1,2-C(2)B(10)H(11), 1-Me-1,2-C(2)B(10)H(11) and 1,2-C(2)B(10)H(12) with one equivalent of 4-vinylbenzyl chloride leads to the formation of compounds 1-3, whereas the reaction of the dilithium salt of 1,2-C(2)B(10)H(12) with two equivalents of 4-vinylbenzyl chloride gives disubstituted compound 4. The closo clusters were degraded using the classical method, KOH in EtOH, to afford the corresponding nido species, which were isolated as tetramethylammonium salts. The crystal struc…

TetramethylammoniumQuenching (fluorescence)Organic ChemistrySubstituentGeneral ChemistryCrystal structurePhotochemistryMedicinal chemistryFluorescenceCatalysisDilithiumchemistry.chemical_compoundchemistryCarboranePhenyl groupta116Chemistry : A European Journal
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