Search results for "Borane"

showing 10 items of 278 documents

Evidence for an Intermediate in the Methylation of CB11H12−with Methyl Triflate: Comparison of Electrophilic Substitution in Cage Boranes and in Aren…

2013

The trideuteriomethylation of BH vertices in CB11H12− and its derivatives with CD3OTf (OTf=triflate, trifluoromethanesulfonate) yields a mixture of BCD3 and BCHD2 substitution products, thus demonstrating the intermediacy of a species with a long enough lifetime for hydrogen scrambling between the boron vertex and the methyl substituent. No such scrambling is observed if CD3OTf is used to methylate toluene. According to density functional theory calculations, the intermediate in BH vertex methylation is a three-center bonded σ adduct of a methyl cation to the BH bond and the proton scrambling occurs via a transition structure containing a distorted square-pyramidal methane attached axially …

Crystallographychemistry.chemical_compoundElectrophilic substitutionchemistryProtonSubstituentBoranesDensity functional theoryGeneral ChemistryAlkylationPhotochemistryTolueneTrifluoromethanesulfonateChemPlusChem
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Distinct Photophysics of the Isomers of B18H22 Explained

2012

The photophysics of the two isomers of octadecaborane(22), anti- and syn-B 18H 22, have been studied by UV-vis spectroscopic techniques and theoretical computational methods. In air-saturated hexane, anti-B 18H 22 shows fluorescence with a high quantum yield, Φ F = 0.97, and singlet oxygen O 2( 1Δ g) production (Φ Δ ∼ 0.008). Conversely, isomer syn-B 18H 22 shows no measurable fluorescence, instead displaying much faster, picosecond nonradiative decay of excited singlet states. Computed potential energy hypersurfaces (PEHs) for both isomers rationalize these data, pointing to a deep S 1 minimum for anti-B 18H 22 and a conical intersection (CI) between its S 0 and S 1 states that lies 0.51 e…

CzechPhotochemistryChemistryFoundation (engineering)Library science02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnology01 natural sciencesFluorescencelanguage.human_language0104 chemical sciencesInorganic ChemistryIsomerismlanguagemedia_common.cataloged_instanceSpectrophotometry UltravioletChristian ministryPhysical and Theoretical ChemistryEuropean unionBoranes0210 nano-technologymedia_commonInorganic Chemistry
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Synthesis of quadruped-shaped polyfunctionalized o-carborane synthons

2011

[EN] o-Carborane derivatives with precisely defined patterns of substitution have been prepared from 8,9,10,12-I-4-1,2-closo-C2B10H8 by replacing the iodine atoms, bonded to four adjacent boron vertices in the cluster, with allyl, and subsequently 3-hydroxypropyl groups. The resulting structures, comprising four pendant arms and two reactive vertices located on opposite sides of a central o-carborane core, can be envisaged as versatile precursors for dendritic growth

DendrimersIcosahedral CarboranesStereochemistryMolecular ConformationNeutron-Capture TherapySupramolecular Assemblieschemistry.chemical_elementBoranesCrystallography X-Ray010402 general chemistry01 natural sciencesCatalysisMolecular conformationDendrimerQUIMICA ANALITICAMaterials ChemistryCluster (physics)BoranesBoronta116CancerIodination010405 organic chemistryChemistryPolysubstituted FrameworksSynthonMetals and AlloysHalogenationGeneral Chemistry3. Good health0104 chemical sciencesSurfaces Coatings and FilmsElectronic Optical and Magnetic MaterialsC-HChemistryCrystallographyCeramics and CompositesCarboraneDerivativesIodineChemical Communications
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Synthesis, reactivity and complexation studies of N,S exo-heterodisubstituted o-carborane ligands. Carborane as a platform to produce the uncommon bi…

2008

The synthesis of N,S-heterodisubstituted 1-(2'-pyridyl)-2-SR-1,2-closo-C2B10H10 compounds (R = Et, 2; R = (i)Pr, 3) has been accomplished starting from 1-(2'-pyridyl)-l,2-closo-C2B10H11 (1), and their partial deboronation reaction leading to the structurally chiral [7-(2'-pyridyl)-8-SR-7,8-nido-C2B9H10]-derivatives (R = Et, [4]-; R = (i)Pr, [5]-) has been studied. Capillary electrophoresis combined with the chiral selector alpha-cyclodextrin has permitted the separation of the electrophoretically pure racemic [7-(2'-pyridyl)-8-SR-7,8-nido-C2B9H11]- ions into two peaks each one corresponding to the interaction of one enantiomer with the alpha-cyclodextrin. The N,S-heterodisubstituted o-carbo…

Denticity010405 organic chemistryLigandStereochemistryCoordination number010402 general chemistry01 natural sciences0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryPyridineCarboraneChelationReactivity (chemistry)EnantiomerDalton Trans.
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Photoluminescence in Carborane–Stilbene Triads : A Structural, Spectroscopic, and Computational Study

2016

A set of triads in which o- and m-carborane clusters are bonded to two stilbene units through Ccluster -CH2 bonds was synthesized, and their structures were confirmed by X-ray diffraction. A study on the influence of the o- and m- isomers on the absorption and photoluminescence properties of the stilbene units in solution revealed no charge-transfer contributions in the lowest excited state, as confirmed by (TD)DFT calculations. The presence of one or two B-I groups in m-carborane derivatives does not affect the emission properties of the stilbenes in solution, probably due to the rather large distance between the iodo substituents and the fluorophore. Nevertheless, a significant redshift o…

DiffractionFluorophorePhotoluminescencecarboranesalkenes010405 organic chemistryOrganic ChemistryGeneral Chemistry010402 general chemistryPhotochemistry01 natural sciencesCatalysis0104 chemical scienceschemistry.chemical_compoundchemistryExcited statedensity functional calculationsluminescenceCarboraneAbsorption (chemistry)Thin filmLuminescenceta116photophysicsChemistry: A European Journal
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Stability of Borane−Adduct Complexes:  A G-2 Molecular Orbital Study

1997

Complexation energies of H3BXHn and [H3BXHn-1]- complexes (X = N, O, F, P, S, and Cl) (n = 3, 2, 1) have been computed at the G-2 level of theory. The formation of H3BXH3 (X = N, P) is found to be more favored than the formations of H3BXH2 (X = O, S) and H3BXH (X = F, Cl). The qualitative features of the molecular orbital interaction (the correlation diagrams) of H3BNH3 (C3v symmetry group), H3BOH2 (Cs symmetry group), and H3BFH (Cs symmetry group) complexes are presented. These diagrams show that the σ character of the B−X bond decreases and the π character increases when the electronegativity of X increases and indicate that the B−X bond cannot be treated only in terms of the simplest mod…

ElectronegativityCrystallographychemistry.chemical_compoundchemistryStereochemistryMolecular orbitalWalsh diagramLewis acids and basesPhysical and Theoretical ChemistrySymmetry groupBoraneAffinitiesAdductThe Journal of Physical Chemistry A
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Interaction of half-sandwich alkylmolybdenum(III) complexes with B(C6F5)3. The X-ray structure of [CpMo(η4-C4H6)(μ-Cl)(μ-CH2)(O)MoCp][CH3B(C6F5)3]

2001

Abstract The reactions of the half-sandwich molybdenum(III) complexes CpMo(η 4 -C 4 H 4 R 2 )(CH 3 ) 2 , where Cpη 5 -C 5 H 5 and RH or CH 3 , with equimolar amounts of B(C 6 F 5 ) 3 have been investigated in toluene. EPR monitoring shows the formation of an addition product which does not readily react with Lewis bases such as ethylene, pyridine, or PMe 3 . The analysis of the EPR properties and the X-ray structure of a decomposition product obtained from dichloromethane, [CpMo(η 4 -C 4 H 6 )(μ-Cl)(μ-CH 2 )(O)MoCp][CH 3 B(C 6 F 5 ) 3 ], indicate that the borane attack has occurred at the methyl position.

EthyleneStereochemistrychemistry.chemical_elementBorane010402 general chemistry01 natural sciencesBiochemistryMedicinal chemistrylaw.inventionInorganic Chemistrychemistry.chemical_compoundlawPyridineMaterials Chemistry[CHIM.CRIS]Chemical Sciences/Cristallography[CHIM.COOR]Chemical Sciences/Coordination chemistryLewis acids and basesPhysical and Theoretical ChemistryElectron paramagnetic resonanceDichloromethaneMolybdenumEPR properties010405 organic chemistryOrganic ChemistryTolueneButadiene ligand0104 chemical sciences3. Good healthchemistryHalf-sandwichMolybdenumX-ray structure
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Inner-shell excitation spectroscopy of closo-carboranes

1997

Oscillator strength spectra in the region of B 1s and C 1s excitation of three isomeric carborane cage compounds [closo-1,2-orthocarborane, closo-1,7-metacarborane, closo-1,12-paracarborane (C2B10H...

Excitation spectroscopyOscillator strengthChemistryParticle acceleratorSpectral lineSurfaces Coatings and Filmslaw.inventionlawMaterials ChemistryCarboraneInner shellPhysical and Theoretical ChemistryAtomic physicsExcitation
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P-chirogenic secondary phosphine oxides : new synthesis and applications

2015

A new stereoselective synthesis of phosphinous acid boranes is described by hydrolysis of aminophosphines boranes prepared by reaction of the oxazaphospholidine complex derived from ephedrine with organolithium reagents.By reaction with a strong acid, the phosphinous acid boranes lead to the corresponding P-chirogenic secondary phosphine oxides in very good yields (90%) and with complete retention of the configuration at the phosphorus atom. The secondary phosphine oxides have been used in asymmetric hydrogenation and intramolecular Heck cyclisation using rhodium and palladium complexes, respectively. In a second part, a new synthesis of P-chirogenic ortho-halogenophenyl phosphine oxides is…

HomocouplingAcide phosphineux-boranePhosphinous acid boraneAsymmertric catalysisHomocouplage[CHIM.ORGA]Chemical Sciences/Organic chemistryP-chirogenic ligandOxyde de phosphine secondaire[CHIM.ORGA] Chemical Sciences/Organic chemistryO-halogénophosphineHétérocouplageCluster chiraux[ CHIM.ORGA ] Chemical Sciences/Organic chemistryCatalyse asymétriqueSecondary phosphine oxideHeterocouplingLigand P-chirogéniqueChiral cluster
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Measured and Calculated Oxidation Potentials of 1-X-12-Y-CB11Me10– Anions

2012

Cyclic voltammetry of 31 icosahedral carborane anions 1-X-12-Y-CB(11)Me(10)(-) at a Pt electrode in liquid SO(2) revealed a completely reversible one-electron oxidation even at low scan rates, except for the anions with Y = I, which are oxidized irreversibly up to a scan rate of 5.0 V/s, and the anion with X = COOH and Y = H, whose oxidation is irreversible at scan rates below 1.0 V/s. Relative reversible oxidation potentials agree well with RI-B3LYP/TZVPP,COSMO and significantly less well with RI-BP86/TZVPP,COSMO or RI-HF/TZVPP,COSMO calculated adiabatic electron detachment energies. Correlations with HOMO energies of the anions are nearly as good, even though the oxidized forms are subjec…

Horizontal scan rateIcosahedral symmetrySubstituentElectronIonInorganic ChemistryPt electrodechemistry.chemical_compoundCrystallographychemistryComputational chemistryCarboranePhysical and Theoretical ChemistryCyclic voltammetryInorganic Chemistry
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