Search results for "Borane"

showing 10 items of 278 documents

Thermochromic Fluorescence from B18H20(NC5H5)2: An Inorganic–Organic Composite Luminescent Compound with an Unusual Molecular Geometry

2017

BH(NCH) is a rare example of two conjoined boron hydride subclusters of nido and arachno geometrical character. At room temperature, solutions of BH(NCH) emit a 690 nm fluorescence. In the solid state, this emission is shifted to 620 nm and intensifies due to restriction of the rotation of the pyridine ligands. In addition, there is a thermochromicity to the fluorescence of BH(NCH). Cooling to 8 K engenders a further shift in the emission wavelength to 585 nm and a twofold increase in intensity. Immobilization in a polystyrene thin-film matrix results in an efficient absorption of pumping excitation energy at 414 nm and a 609 nm photostable fluorescence. Such fluorescence from polystyrene t…

ThermochromismMaterials scienceHydrideBoranes02 engineering and technology010402 general chemistry021001 nanoscience & nanotechnologyPhotochemistry01 natural sciencesFluorescenceAtomic and Molecular Physics and Optics0104 chemical sciencesElectronic Optical and Magnetic Materialschemistry.chemical_compoundchemistryPolystyrene0210 nano-technologySpectroscopyLuminescenceAbsorption (electromagnetic radiation)
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Synthesis, Characterization, and Properties of Weakly Coordinating Anions Based on tris-Perfluoro-tert-Butoxyborane

2017

A convenient method for the preparation of strongly Lewis acidic tris-perfluoro-tert-butoxyborane B(ORF)3 (1), (ORF = OC(CF3)3) was developed, and its X-ray structure was determined. 1 was used as a precursor, guided by density functional theory (DFT) calculations and volume-based thermodynamics, for the synthesis of [NEt4][NCB(ORF)3] (3) and [NMe4][FB(ORF)3] (5) and the novel large and weakly coordinating anion salts [Li 15-Crown-5][B(ORF)4] (2) and [NEt4][CN{B(ORF)3}2] (4). The stability of [B(ORF)4]− was compared with that of some related known weakly coordinating anions by appropriate DFT calculations.

Trisweakly coordinating anionssynthesis010405 organic chemistryboranes010402 general chemistry01 natural sciencesMedicinal chemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryComputational chemistryLewis acidsDensity functional theoryPhysical and Theoretical Chemistryta116Inorganic Chemistry
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Design of carborane molecular architectures via electronic structure computations

2009

10 pags, 9 figs

Work (thermodynamics)Renewable Energy Sustainability and the EnvironmentChemistrylcsh:TJ807-830lcsh:Renewable energy sourcesGeneral ChemistryElectronic structureAtomic and Molecular Physics and OpticsEnergy storageIonComputational chemistryChemical physicsExcited stateAtomCarboraneGeneral Materials ScienceSpin-½
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Towards purely inorganic clusters in medicine: Biocompatible divalent cations as counterions of cobaltabis(dicarbollide) and its iodinated derivatives

2021

Monovalent cations, Cs+, and alkylammonium ([NR4]+) salts have traditionally been used to precipitate the anions of boranes, carborane and metallocarborane clusters. In contrast, in the body and in living organisms in general, divalent cations have a special relevance. In this work, we isolate for the first time the cobaltabis(dicarbollide) salts of the biocompatible divalent cations of biological importance that can have application both in biology and in materials science. The preparation of Ca2+, Mg2+ and Fe2+ salts of anionic iodinated nido-[C2B9H12]− and cobaltabis(dicarbollide) as well as its di-, tetra- and octa-iodinated derivatives are reported. Ca2+ and Mg2+ are hard Lewis acids a…

X-ray contrastanionitDual-actionBoranesBiochemistryDivalentjodiInorganic Chemistrychemistry.chemical_compoundBone biomaterialsPolymer chemistryMaterials ChemistryAcetoneMoleculeLewis acids and basesPhysical and Theoretical Chemistrychemistry.chemical_classificationkalsiumChemistrydual-action biocompatibleOrganic ChemistrykationitSmall moleculeBiocompatibleX-ray contrastCarboraneCalciumMetallacarboranesCounterionbiomateriaalitIodine
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Stereoselective synthesis of o-bromo (or iodo)aryl P-chirogenic phosphines based on aryne chemistry.

2012

The efficient synthesis of chiral or achiral tertiary phosphines bearing an o-bromo (or iodo)aryl substituent is described. The key step of this synthesis is based on the reaction of a secondary phosphine borane with the 1,2-dibromo (or diiodo)arene, owing to the formation in situ of an aryne species in the presence of n-butyllithium. When P-chirogenic secondary phosphine boranes were used, the corresponding o-halogeno-arylphosphine boranes were obtained without racemization in moderate to good yields and with ee up to 99%. The stereochemistry of the reaction, with complete retention of the configuration at the P atom, has been established by X-ray structures of P-chirogenic o-halogenopheny…

[CHIM.ORGA]Chemical Sciences/Organic chemistry010405 organic chemistryChemistryStereochemistryArylOrganic ChemistrySubstituentBoranesDABCOBorane010402 general chemistry01 natural sciencesMedicinal chemistryAryne0104 chemical scienceschemistry.chemical_compoundRacemizationComputingMilieux_MISCELLANEOUSPhosphineThe Journal of organic chemistry
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Characterization of β-B-Agostic Isomers in Zirconocene Amidoborane Complexes

2009

The reaction of Cpx2ZrCl2 (Cpx = Cp, Cp*) with ammonia borane in presence of n-butyllithium yielded Cp2Zr(Cl)NH2BH3 and Cpx2Zr(H)NH2BH3. These derivatives are isoelectronic with the ethyl zirconocene chloride and hydride, respectively, and feature a chelating amidoborane ligand coordinating through a Zr−N bond and a Zr−H−B bridge. In solution, each of the complexes consists of an equilibrium mixture of two isomers differing in the orientation of the amidoborane ligand with respect to the Zr−X bond (X = H, Cl), while in the solid state, only one isomer was observed. Such isomers have not been characterized for any metal complexes containing the isoelectronic β-agostic ethyl ligand or any oth…

amidoboranesamidoboraanit
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CCDC 889025: Experimental Crystal Structure Determination

2015

Related Article: A. R. Popescu, I. Rojo, F. Teixidor, R. Sillanpää, C. Viñas|2015|Chem.-Eur.J.|21|8613|doi:10.1002/chem.201500307

bis(78-bis(diisopropylphosphino)-78-dicarba-nido-undecaborane)-aqua-magnesium acetonitrile solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Carboranylphosphinic Acids: A New Class of Purely Inorganic Ligands

2015

Purely inorganic carboranyl phosphinates were prepared, and the influence of the cluster on the reactivity of the phosphinate group was studied. Electron-withdrawal by the carboranyl carbon atoms, combined with space-filling efficiency and enhanced aromaticity of the cluster cage, renders the phosphorus more difficult to oxidize. This enables carboranyl phosphinates to survive harsh oxidizing conditions, a property which is uncommon in organic phosphinates.

carboranes010405 organic chemistryHydrogen bondOrganic Chemistryphosphonateschemistry.chemical_elementAromaticityGeneral ChemistryPhosphinatehydrogen bonding010402 general chemistry01 natural sciencesCatalysis0104 chemical scienceschemistryOxidizing agentCluster (physics)Organic chemistryReactivity (chemistry)ta116CarbonphosphinateshydrophobicityChemistry - A European Journal
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Poly-iodinated closo 1,2-C 2 B 10 and nido [7,8-C 2 B 9 ] − carborane frameworks: Synthesis and consequences

2015

Abstract The preparation of Cc-monosubstituted closo and nido carborane derivatives, mono-, di and tetraiodinated is reported. Some of these mono-to poly-iodinated nido carboranes are studied in terms of the acidity of the open face bridging proton, their chemical shift position in the 1H NMR, and the lesser tendency to η5-coordination in parallel to a larger number of iodo groups.

carboranesSolvent freeStereochemistryChemistryOrganic ChemistryHalogenationsolvent freeBiochemistryInorganic ChemistryiodinationMaterials ChemistryProton NMRCarboranePhysical and Theoretical Chemistryta116acidityJournal of Organometallic Chemistry
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Synthesis of Globular Precursors

2015

o-Carborane (C2 B10 H12 ) was adapted to perform as the core of globular macromolecules, dendrons or dendrimers. To meet this objective, precisely defined substitution patterns of terminal olefin groups on the carborane framework were subjected to Heck cross-coupling reactions or hydroboration leading to hydroxyl terminated arms. These led to new terminal groups (chloro, bromo, and tosyl leaving groups, organic acid, and azide) that permitted ester production, click chemistry, and oxonium ring opening to be performed as examples of reactions that demonstrate the wide possibilities of the globular icosahedral carboranes to produce new dendritic or dendrimer-like structures. Polyanionic speci…

carboranesStereochemistrydendronsOrganic ChemistryGeneral ChemistryCatalysismultibranched compoundsHydroborationchemistry.chemical_compoundpolyanionsNucleophileTosylchemistryDendrimerClick chemistrycross-couplingCarboraneAzideOxonium ionta116Chemistry: A European Journal
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