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  • Inorganic Chemistry  (34)
  • Cluster  (2)
  • (Borole)dicarbonyl(phosphane)cobalt cation, hydride addition  (1)
  • Wiley-Blackwell  (36)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 23-29 
    ISSN: 0009-2940
    Keywords: Diboracycloalkanes ; Diboracycloalkenes ; Trimethylenemethane, borylation of the dianion of ; Allylboranes, B - C bond length ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Syntheses of New Organoboron Rings with two Boron Atoms by Borylation of the Trimethylenemethane DianionBorylation of Li2[C(CH2)3] (1) provides a versatile starting point for the synthesis of 5-, 6-, 7-, and 8-membered ring systems with two boron atoms and leads to 1,5-bis(dialkylamino)-3,7-dimethylene-1,5-diboracyclooctanes 2a, b (a: R=Et; b: R=iPr), 1,3-bis(dialkylamino)-5-methylene-1,3-diboracyclohexanes 8a, b, 1,3-bis(diethylamino)-5-methyl-1,3-dibora-4-cyclo-hexene (10), and 1,4-bis(dialkylamino)-6-methylene-1,4-dibora-2-cycloheptenes 11a, b. The compounds 2b, 8b, and the 2,3-biboratafulvene derivative [Li(TMEDA)]2[CH2C(CHB)2-(NiPr2)2] are characterized by X-ray diffraction analysis. It is shown that for trigonal boron B - C(allyl) bond distances (typically 160 ± 1 pm) are significantly larger than B - C(alkyl) distances (typically 158 + 1 pm).
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  • 2
    ISSN: 0009-2940
    Keywords: Rhodium(I) phosphane complexes ; 14-Electron intermediates ; MO theory, applied ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bis(di-tert-butylphosphanyl)methane Complexes of Rhodium: Geometry, Electronic Structure, and Derivatives of the 14-Electron Fragment [Rh(dtbpm)Cl]. Molecular Structure of Rh(dtbpm)Cl(PMe3)14-Electron fragments [M(PR3)2X] (M = Rh, Ir, X = halogen etc.) are considered to be an important class of highly reactive, coordinatively unsaturated intermediates in many metal-induced stoichiometric or catalytic transformations of organic substrates. As available theoretical data suggest a slightly preferred T-shaped groundstate geometry with a less symmetric cis rather than the usually implied trans phosphane arrangement for such tricoordinate d8-ML3-type systems with monodentate phosphanes PR3, the chemistry of η2-diphosphanylmethane complexes of rhodium with four-membered RhPCP-chelate rings and thus with enforced cis phosphane coordination and anomalously small cis P - Rh - P angles has been studied by theory and by experiment. MO calculations (EH) have been performed both for the model 14-electron system [Rh(dhpm)Cl] (dhpm = diphosphanylmethane, H2P - CH2 - PH2) and for the experimentally accessible fragment [Rh(dhbpm)Cl], where dtbpm is bis(di-tert-butylphosphanyl)-methane, (tBu)2P - CH2 - P(tBu)2. The electronic and geometric structure of these species is described. Employing the unusual ligand dtbpm, tailor-made for stabilizing mononuclear η2- and destabilizing dinuclear μ-diphosphanylmethane coordination, the chloro-bridged dimer [Rh(dtbpm)Cl]2, has been synthesized. In agreement with steric and electronic considerations, its chemistry is dominated by a facile dissociation to monomeric (presumably solvent coordinated) fragments [Rh(dtbpm)Cl], even in benzene, as suggested by molecular mass determinations. Accordingly, by using [Rh(dtbpm)Cl]2 as a starting material, a series of sterically very congested but nevertheless mononuclear, square-planar complexes Rh(dtbpm)Cl(L) (L = CO, PMe3, PPh3, PCy3, pyridine, acrylonitrile) with chelating dtbpm could be readily prepared and fully characterized. The relative stability of these potential alternative precursors of a [Rh(dtbpm)Cl] intermediate towards dissociation of ligands L is reported. The molecular structure of Rh(dtbpm)Cl(PMe3) as the first representative of this class of compounds has been determined by X-ray crystallography.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1079-1081 
    ISSN: 0009-2940
    Keywords: Iminoboranes ; Stannylenes ; Aminostannation ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Addition of Stannylenes to IminoboranesIminoboranes tBuB ≡ NR (R = tBu, Mes: 1 a, b) undergo aminostannation by the diaminostannylene Sn[N(SiMe3)2]2 (2b) to give (Me3Si)2N-B(tBu) = NR-Sn-N(SiMe3)2 (4a, b). The stannylene 4 b remains monomeric in the crystal (space group P21/n). The cyclic diaminostannylene [-Sn-N(tBu)-SiMe2-N(tBu)-] (3 b), instead, simply adds the boranes 1 a, b across one of its Sn-N bonds to form the bicyclo[2.2.0]hexene-type products 5a, b.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 2681-2686 
    ISSN: 0009-2940
    Keywords: 1,2,3,4-Diazadiboretidines ; Oxadiazadiborolidines ; Triazadiborolidines ; Diazadiboracyclohexanes ; Tetraazadiboracyclohexanes ; 1,2,5,6,3,4,7,8-Tetraazatetraborocane ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,2,3,4-Diazadiboretidines: Reactions of a Novel Class of Unsaturated Boron-Nitrogen Four-Membered Rings1,2,3,4-Diazadiboretidines [=B(tBu)-B(tBu)=NR-NR=] (R=Et, iPr: 2a, b) belong to the hitherto unknown class of head-head isomers of the known 1,3,2,4-diazadiboretidines (1). They are formed from the diborane(4) Cl-B(tBu)-B(tBu)-Cl and the hydrazines RHN-NHR in the presence of NEt3 via the partially unsaturated four-membered rings [-B(tBu)Cl-B(tBu)=NR-NHR-] (4a, b), which are transformed into 2a, b by the abstraction of HCl by means of the base LiNC9H18. Whereas the pure products 2a, b are instable, solutions of 2a, b in alkanes can be handled at 0°C without considerable decomposition. Reaction of 2a, b with the amine oxide Me3NO leads to insertion of an O atom, reaction with diazoalkane tBuCR′N2 (R′ = H, Me) to insertion of its β-N atom, and reaction with the azide PhCH2N3 to insertion of a nitrene N atom into the B-B bond of 2a, b with formation of five-membered rings 5a, b or 6a, b or 7a, b, respectively. Six-membered rings 8a, 9a, 10a, respectively, are the products of the insertion of the C≡C unit of 3-hexyne, the N=N unit of EtO2C-N=N-CO2Et, or the unsaturated C atoms of two molecules of C≡NtBu into the B-B bond of 2a. The condensation of the diaminodiborane(4) Cl-B(NMe2)-B(NMe2)-Cl with the hydrazine EtHN-NHEt in the presence of NEt3 yields the corresponding eight-membered ring [-B(NMe2)-B(NMe2)-NEt-NEt-]2 (11), which crystallizes in a twist conformation with symmetry group D2.
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  • 5
    ISSN: 0009-2940
    Keywords: Diastereoselective synthesis ; Homoallylic alcohols ; 1,3-Diols, homoallylic ; β1-Hydroxyalkyl ketones ; 2,5-Dihydro-1H1-boroles ; 1,2-Oxaborolanes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1-Phenyl-3-borolenes CH2CR1=CR1CH2BPh) (1a: R1=H; b: R1=Me) react with aldehydes R2CHO to give cis-1,2-oxaborolanes CH2CR1[CR1(=CH2)]CR2R3OBPh (2, R2 = e.g. Me, Ph, CH=CH2, tBu, CCl3, R3 = H). Yields are nearly quantitative. Stereoselectivities usually are 100% (but only 95% for R2=CH=CH2, 97% for R2=Me). Oxidation with NaOH/H2O2 in THF affords homoallylic anti-1,3-diols HOCR2R31-CR1[CR1(=CH2)]CH2OH (3). An X-ray diffraction analysis of 3a (R2=p1-tolyl) proves the assigned stereochemistries. Ketones R2R3CO react analogously. Ketenes R2CCO form 5-alkylidene-4-vinyl-1,2-oxaborolanes (4), which tend to undergo double-bond migration. Oxidation produces two types of β1-hydroxylalkyl ketones R22CHCOC[(E)=CHMe]CH2OH (5) and R22CHCOCMe[CMe=CH2]CH2OH (6).
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1397-1402 
    ISSN: 0009-2940
    Keywords: 2-Boraindanes ; 2-Benzoboroles, 1,3-dihydro- ; 2-Benzoborole-1,3-diides, 1,3-dihydro- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 2-Boraindanes and 2-(Dialkylamino)1-2-benzoborole Dianionsortho1-Xylene reacts with the Lochmann-Schlosser base to produce a mixture of the potassium derivatives K2[1,2-C6H4(CH2)2] (2) and K[2-MeC6H4CH2] (3). Condensation of 1 + 2 with BCl2(NR2) (R=Me, Et, iPr) affords 2-(dialkylamino)1-2-boraindanes (1a-c) (50%). Treatment of 1a, b with LiTMP/TMEDA in THF yields dilithio derivatives [Li(tmeda)]2[C6H4(CH)2BNR2] (8a, b) (40%) which show tripledecked structures consisting of an aromatic 10′-electron 2-benzoborole dianion and two [Li-(tmeda)]+ units facially bound to the borole ring. 1a reacts with HCl/Et2O/hexane to give C6H4(CH2)2BCl · OEt2 (1d · OEt2) (76%) which decomposes in vacuo to give the chloro derivative 1d. The methyl derivative C6H4(CH2)2BMe (1e) is obtained from 1a by treatment with LiMe/Et2O at -78°C and subsequently with HCl/Et2O at -78°C (41%). 1a, b react with MeOH at -78°C to give solid adducts C6H4(CH2)2BOMe · NHR2 (12a, b) while 1c affords C6H4(CH2)2BOMe (1f). Subsequent ring-opening produces 2-MeC6H4CH2B(OMe)2 (13). With the exception of 1b the 2-boraindanes 1 are crystalline solids. The silylation of the 2-benzoborole dianions and various (2-methylbenzyl)borane derivatives is also described.
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 99-103 
    ISSN: 0009-2940
    Keywords: Tri-tert-butylazadiboriridine ; (Hydroboryl)(methoxyboryl)amine ; 2,3-μ-Hydro-1,2,3-azoniadiborata-l-cyclopropenes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The B—B bond of tri-tert-butylazadiboriridine [—NR—BR—BR—] (R = tBu; 1) is oxidized by MeOH to give the (hydroboryl)(methoxyboryl)amine H—BR=NR-BR(OMe) (2a). μ-2,3-Hydroazoniadiborata-1-cyclopropenes [=NR—BR(X)—μH—BR=] (3a, 3c-e) are formed by the action of the acids HX upon 1. A similar hydrogen bridge as in 3a-e is formed during the hydroboration of 1 by catecholborane, yielding 3f. A B atom is identified in the products 3a-f to be planarly coordinated by four atoms, two of which are forming a BHB three-center bond with that B atom. This is a novel bonding situation in boron chemistry. The structures of the products are deduced from 1H-, 11B-, and 13C-NMR spectra and are confirmed by X-ray structural analyses of 2a, 3a, and 3c.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 128 (1995), S. 493-497 
    ISSN: 0009-2940
    Keywords: Organoaluminium compounds ; Alanes, 2-[(dimethylamino)methyl]phenyl- ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of LiAr (Ar = 2-[(dimethylamino)methyl]phenyl) with AlCl3, MeAlCl2, and Me2AlCl in a 1:1 ratio yields the corresponding organoaluminium compounds ArAlCl2, ArAl(Cl)Me, and ArAlMe2 (1-3). The alanes Ar2AlCl and Ar2AlMe (4 and 5) were synthesized from AlCl3 and MeAlCl2 with two equivalents of LiAr. The products ArAl(Cl)R [R = tBu, C(SiMe3)3] 6 and 7 are formed by the reaction of LiR with 1. The Lewis acid 1 adds the bases iPrNH2 and THF to yield the adducts 1 · iPrNH2 and 1 · THF. The structures of the products were deduced from the 1H-, 13C-, and 27Al-NMR spectra and were confirmed by X-ray structural determinations of 5 and 1 · iPrNH2.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 130 (1997), S. 1223-1229 
    ISSN: 0009-2940
    Keywords: Tripodal ligands ; O ligands ; Cabalticenium cation ; Sodium coordination ; Ligand profile ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The lithium and sodium compounds A[P(O)R2] (A+ = Li+, Na+; R = OPh, OiPr) have been prepared in situ from Hp(O)R2 and butyllithium or sodium hydride. They react with the cyclopentadienyl complexes [(C5H5)MI2(CO)] (M = Co, Rh), [(C5Me5)CoCl2]2, and [(C5H5)CoI2]n to yield alkali metal salts AL of tridentate oxygen ligands (A+ = Li+, Na+; L- = [(C5R′5]M{P(O)R2}3]-, R′ = H, Me; M = Co, Rh; R = OPh, OiPr) (2). For the ligand LCo, OPh = [(C5H5)-Co{P(O)(OPh)2}3]-, an alternative synthesis has been developed, starting from [(C5H5)2Co]PF6. The structure of the sodium salt NaLCo, OPh (2d) has been determined by X-ray diffraction. The ligand LCo, Oph-, with a cone angle TH of about 200°, completely blocks one half of the coordination sphere around the sodium centre. The ligand profile has been calculated to allow appraisal of the angular encumbrance of the ligand.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 975-980 
    ISSN: 0009-2940
    Keywords: Niobium complexes ; Cyclopentadienyl derivatives ; Butadiene derivatives ; Acetylene derivatives ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: (Butadiene)(cyclopentadienyl)niobium ComplexesThe known bis(butadiene)(cyclopentadienyl)niobium complex (C5H4R)Nb(C4H6)2 (1, R=H) exists in solution as a 1 : 1 mixture of a bis(cis-butadiene) isomer 1a and a (cis-butadiene)(trans-butadiene) isomer 1b. In solution the barrier to isomerisation is 80 ± 2 kJ/mol. New derivatives 2 (R=Me) and 3 (R=SiMe3) of 1 are described. One of the butadiene ligands in 1 - 3 is readily substituted with CO, CNtBu, P(OMe)3, and PMe3. CpNb(PMe3)2(C4H6) (7) reacts with disubstituted acetylenes to form acetylene complexes CpNb(PMe3)(C4H6)(RC=CR') (8: R, R'=Ph, 9: R=Me, R'=Ph, and 10: R=Ph, R'=SiMe3), The structure of 9 resembles that of bent metallocene derivatives with the acetylene acting as a 2-e ligand.
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