Search results for "Borane"

showing 10 items of 278 documents

CCDC 762079: Experimental Crystal Structure Determination

2010

Related Article: Duc Hanh Nguyen, H.Laureano, S.Juge, P.Kalck, J.-C.Daran, Y.Coppel, M.Urrutigoity, M.Gouygou|2009|Organometallics|28|6288|doi:10.1021/om900684w

((Borane)-diphenyl-((5H-benzo[b]phosphindol-5-yl)methyl)phosphine)-(eta^2^eta^2^-cycloocta-15-diene)-rhodium tetraphenylborateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 1824869: Experimental Crystal Structure Determination

2018

Related Article: María Frutos, Mar Gómez-Gallego, Elena A. Giner, Miguel A. Sierra, Carmen Ramírez de Arellano|2018|Dalton Trans.|47|9975|doi:10.1039/C8DT02296H

(1-(3-methyl-4-phenyl-123-triazol-3-ium-15-diyl)-12-dicarba-closo-dodecaborane(11))-chloro-gold(i)Space GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 768725: Experimental Crystal Structure Determination

2011

Related Article: F.Chaux, S.Frynas, H.Laureano, C.Salomon, G.Morata, M.-L.Auclair, M.Stephan, R.Merdes, P.Richard, M.-J.Ondel-Eymin, J.-C.Henry, J.Bayardon, C.Darcel, S.Juge|2010|Comptes Rendus Chimie|13|1213|doi:10.1016/j.crci.2010.06.001

(Borane)(phenyl)(2-methoxyphenyl)(35-dimethylphenyl)phosphineSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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CCDC 952664: Experimental Crystal Structure Determination

2013

Related Article: Naima Khiri-Meribout, Etienne Bertrand, Jérôme Bayardon, Marie-Joëlle Eymin, Yoann Rousselin, Hélène Cattey, Daniel Fortin, Pierre D. Harvey, and Sylvain Jugé|2013|Organometallics|32|2827|doi:10.1021/om400229p

(SS)-(-)-517-bis((Ferrocenyl(phenyl)phosphinoborane))-25262728-tetrapropoxycalix[4]arene dichloromethane solvateSpace GroupCrystallographyCrystal SystemCrystal StructureCell ParametersExperimental 3D Coordinates
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Sulfur, tin and gold derivatives of 1-(2'-pyridyl)-ortho-carborane, 1-R-2-X-1,2-C2B10H10 (R = 2'-pyridyl, X = SH, SnMe3 or AuPPh3).

2004

Reaction of the lithium salt of 1-(2'-pyridyl)-ortho-carborane, Li[1-R-1,2-C(2)B(10)H(10)](R = 2'-NC(5)H(4)), with sulfur, followed by hydrolysis, gave the mercapto-o-carborane, 1-R-2-SH-1,2-C(2)B(10)H(10) which forms chiral crystals containing helical chains of molecules linked by intermolecular S-H...N hydrogen bonds. The cage C(1)-C(2) and exo C(2)-S bond lengths (1.730(3) and 1.775(2)[Angstrom], respectively) are indicative of exo S=C pi bonding. The tin derivative 1-R-2-SnMe(3)-1,2-C(2)B(10)H(10), prepared from Li[1-R-1,2-C(2)B(10)H(10)] and Me(3)SnCl, crystallises with no significant intermolecular interactions. The pyridyl group lies in the C(1)-C(2)-Sn plane, oriented to minimise th…

010405 organic chemistryChemistryHydrogen bondStereochemistryIntermolecular forcechemistry.chemical_elementCrystal structure010402 general chemistry01 natural sciences3. Good health0104 chemical sciencesInorganic ChemistryBond lengthCrystallographyTrigonal bipyramidal molecular geometryCarboraneMoleculeTinDalton transactions (Cambridge, England : 2003)
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Diferratricarbaboranes of thesubcloso-[(η5-C5H5)2Fe2C3B8H11] Type, the First Representatives of the 13-Vertex Dimetallatricarbaborane Series

2003

Treatment of the [2-Cp-9-tBuNH-closo-2,1,7,9-FeC 3 B 8 H 1 0 ] (1) ferratricarbollide (Cp = η 5 -C 5 H 5 -) with Na + C 1 0 H 8 - in 1,2-dimethoxyethane (DME) at room temperature produced an air-sensitive transient anion with a tentatively identified nido-[tBUNH-CpFeC 3 B 8 H 1 0 ] 2 - constitution. In-situ reaction of this low-stability ion with [CpFe(CO) 2 I] or [CpFe(CO) 2 ] 2 generated three violet diferratricarbaboranes identified as paramagnetic subcloso complexes [4,5-Cp 2 - -4,5,1,6,7-Fe 2 C 3 B 8 H 1 1 ] (2; yield 2%), [4,5-Cp 2 - -4,5,1,7,12-Fe 2 C 3 B 8 H 1 1 ] (3; yield 2%), and [7-tBuNH-4,5-Cp 2 - -4,5,1,7,12-Fe 2 C 3 B 8 H 1 0 ] (4; yield 14%). These first representatives of t…

010405 organic chemistryChemistryStereochemistryOrganic ChemistryInfrared spectroscopyBoranesGeneral Chemistry010402 general chemistryMass spectrometry01 natural sciencesCatalysis3. Good health0104 chemical sciencesIonlaw.inventionVertex (geometry)CrystallographyParamagnetismlawYield (chemistry)Electron paramagnetic resonanceChemistry - A European Journal
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Sequential Nucleophilic−Electrophilic Reactions Selectively Produce Isomerically Pure Nona‐ B ‐Substituted o ‐Carborane Derivatives

2003

Nine equal substituents on the intensively studied o-carborane have been obtained for the first time by a combined nucleophilic-electrophilic reaction sequence. Iodine and methyl groups have been introduced to prove the generality of the method. (© Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)

010405 organic chemistryChemistrychemistry.chemical_element010402 general chemistryIodine01 natural sciences0104 chemical sciences3. Good healthInorganic ChemistryReaction sequenceNucleophileElectrophileCarboraneOrganic chemistryBoronEuropean Journal of Inorganic Chemistry
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Triorganotin( iv ) cation-promoted dimethyl carbonate synthesis from CO 2 and methanol: solution and solid-state characterization of an unexpected di…

2018

Two novel C,N-chelated organotin(IV) complexes bearing weakly coordinating carborane moieties were prepared by the reaction of the corresponding C,N-chelated organotin(IV) chloride (i.e. LCNR2SnCl, R = n-Bu (1) and Ph (2); LCN = 2-(N,N-dimethylaminomethyl)phenyl)) with monocarba-closo-dodecaborate silver salt (AgCB11H12; Ag·3). Both products of the metathesis, [LCN(n-Bu)2Sn]+[CB11H12]− (4) and [LCNPh2Sn]+ [CB11H12]− (5), respectively, were characterized by both multinuclear NMR spectroscopy and elemental analysis. The instability of 4 and 5 towards water is discussed. The solid-state structure of LCN(n-Bu)2SnOH·B(C6F5)3 (4a) as a model compound with a Sn–O(H)⋯B linkage is also reported. The…

010405 organic chemistryInfrared spectroscopyGeneral ChemistryNuclear magnetic resonance spectroscopy010402 general chemistryMetathesis01 natural sciencesMedicinal chemistryCatalysis0104 chemical sciencesCatalysischemistry.chemical_compoundchemistryMaterials ChemistryCarborane[CHIM]Chemical Sciences[CHIM.COOR]Chemical Sciences/Coordination chemistryMethanolDimethyl carbonateStoichiometryComputingMilieux_MISCELLANEOUS
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A P-chirogenic β-aminophosphine synthesis by diastereoselective reaction of the α-metallated PAMP–borane complex with benzaldimine

2004

International audience; The diastereoselective synthesis of a P-chirogenic β-aminophosphine ligand with carbon–carbon bond formation of the ethano bridge in a 3:1 ratio via reaction of an α-metallated P-chirogenic phosphine borane with a benzaldimine is described. The diastereoselectivity is attributed to a transition state where the lithium cation chelates the phosphine borane carbanion and the nitrogen of the imine and the attack of the C@N occurs on the face opposite to the P–B bond, due to its interaction with the antibonding P–B bond. The major diastereoisomeric β-aminophosphine borane was then separated and decomplexed into the corresponding β-aminophosphine under neutral conditions a…

010405 organic chemistryLigandOrganic ChemistryImineEnantioselective synthesisAsymmetric synthesisBoranesAminophosphineBoraneChiral phosphorous010402 general chemistryAntibonding molecular orbital01 natural sciencesMedicinal chemistryCatalysis0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundchemistryBoraneOrganic chemistry[CHIM.COOR]Chemical Sciences/Coordination chemistryPhysical and Theoretical ChemistryPhosphineCarbanionTetrahedron: Asymmetry
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Recent studies on RR′S·C2B9H11 charge-compensated ligands

2002

Abstract In this paper we report the synthesis of three new carborane derivatives of the series 7,8-R,R′-10-L-7,8-C2B9H9 (R=R′=H, L=SEtPh; R=CH3, R′=H, L=SMe2 and L=SEt2) along with the enhanced characterization of formerly described compounds 7,8-R,R′-10-L-7,8-C2B9H9 (R=R′=H, L=SMe2 (1), L=SEt2 (2) and L=S(CH2)4 (3)). They have been fully characterised using 1H-, 11B- and 13C-NMR spectroscopy. Their bridging proton resonances have been located for the first time. Individual sulfonium substituent contributions have been calculated that have permitted to establish a rule to predict its position in the 1H-NMR spectrum. The crystal structures of 1 and 3 have been resolved for the first time. T…

010405 organic chemistryLigandSulfoniumOrganic ChemistryThermal decompositionSubstituentCrystal structure010402 general chemistry01 natural sciencesBiochemistry0104 chemical sciencesInorganic Chemistrychemistry.chemical_compoundCrystallographychemistryComputational chemistryMaterials ChemistryCarboranePhysical and Theoretical ChemistrySpectroscopyIsomerizationJournal of Organometallic Chemistry
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