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  • Inorganic Chemistry  (34)
  • (Borole)dicarbonyl(phosphane)cobalt cation, hydride addition  (1)
  • Wiley-Blackwell  (34)
  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 17-23 
    ISSN: 0009-2940
    Keywords: (Borole)nickel complexes ; Nucleophilic substitution at boron ; 1H-Borole ; Dihydro-1H-borolediide ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Derivatives of Borole, XVI1), - Bis(borole)nickel Complexes2)The dilithium 1-(dialkylamino)dihydroborolediides Li2[C4H4-BNR2] 2a, b: R = Me, Et) react with NiCl2 · DME to give bis(borole)nickel complexes Ni(C4H4BNR2)2. Nucleophilic substitution reactions are used to produce a large variety of derivatives Ni(C4H4BR)2 1 (e.g. R = H, tBu, F, Cl, Br, I, OH, OMe). Treatment of Ni(C4H4BCl)2 (tg) with LiO(CH2)3OLi in THF produces a polymer and a dinuclear complex (μ-{η5:η5-[(CH2)3(OBC4H4)2]}2Ni2 (3) which crystallizes from CH2Cl2 as solvate 3 · CH2Cl2. The complexes 1g and 3 · CH2Cl2 are characterized by X-ray diffraction work. Barriers to internal ring-ring rotation are measured by variable-temperature NMR spectroscopy. The B - H bond of Ni(C4H4BH)2 (1a) is remarkably inert and does not react with H2O or with carboxylic acids in THF at room temperature. With PhCHO slow formation of the benzyloxy compound Ni(C4H4BOCH2Ph)2 (1 m) is observed at 100°C. For typical complexes such as the phenyl derivative 1e cyclic voltammetry in CH2Cl2 reveals an irreversible oxidation at 1.32 and a quasi-reversible reduction at -1.37 V vs. SCE.
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  • 2
    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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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 2025-2026 
    ISSN: 0009-2940
    Keywords: Aza-nido-decaborane(12) ; (1H-Triazen-1,3-diyl)-aza-arachno-decaborane(13) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: 1,3-Addition of Azides to Azadecaborane: 6-Azadecaborane-4,9-diyltriazenesnido-NB9H12 (1) reacts with azides RN3 to form a coordinative B-N bond between B9 and N1 of RN3, accompanied by the α-addition of the B4-H bond of 1 to the N3 atom of RN3. The products 2a, b (R = H, CH2Ph, respectively) thus contain an azadecaborane skeleton and a five-membered unsaturated B2N3 ring with a common B-B edge. The product 2a crystallizes in the space group Pna21.
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 129 (1996), S. 833-836 
    ISSN: 0009-2940
    Keywords: Oxotitanium(IV) porphyrinate ; Peroxotitanium(IV) porphyrinate ; Photochemistry ; Singlet oxygen ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The syntheses of oxotitanium(IV) meso-tetrakis(2,3,4,5,6-pentafluorophenyl)porphyrinate O=Ti(TPPF20) (1), oxotitanium(IV) meso-tetrakis(2,6-difluorophenyl)porphyrinate O=Ti-(TPPF8) (3), and oxotitanium(IV) meso-tetrakis(2,6-dichlorophenyl)porphyrinate O=Ti(TPPCl8) (5) from titanium tetrachloride and the corresponding porphine are described. The structure of 1 was determined by single-crystal X-ray diffraction. The reaction of oxotitanium porphyrinates with aqueous hydrogen peroxide leads to the corresponding light-sensitive peroxotitanium(IV) complexes: Ti(O2)(TPPF20) (2), Ti(O2)-(TPPF8) (4), Ti(O2)(TPPCl8) (6). All complexes are efficient and stable photosensitizers for the generation of singlet oxygen.
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  • 5
    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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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 124 (1991), S. 2209-2216 
    ISSN: 0009-2940
    Keywords: Tetrazatetraborocanes ; Boron-nitrogen ring compounds ; [2 + 3] Cycloadditions ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Eight-Membered BN Rings (RBNR')4 from Four-Membered BN Rings (RBNtBu)2 by an Exchange NtBu/NR'Reactions of the four-membered BN ring compounds (RBNtBu)2 (1a - e: R = Me, Et, iPr, iBu, Pr) with azides R'N3 (R' = PhCH2, Pr, iBu, Ph) and with the nitrone PhHC=N(Me)=O are studied. The five-membered ring [=(Me)B=N(tBu)-N=N-(PhCH2)N=] (2a) is formed from the four-membered ring 1a and PhCH2N3 in the ratio 1:2. An exchange of NtBu for NR' with elimination of tBuN3 is observed, however, in the reaction of the ring compounds 1b -d with R'N3. Instead of four-membered BN rings, the six-membered BN ring (RBNR')3 (3a: R/R' = Et/PhCH2) and the eight-membered BN rings (RBNR')4 (4a -h: R/R' = iPr/PhCH2, iBu/PhCH2, iPr/Pr, iBu/Pr, iPr/iBu, iBu/iBu, Et/Ph, iBu/Ph) are formed, respectively. The NMR spectra reveal diastereotopic methylene protons (Et, Pr, iBu, PhCH2) and methyl groups (iPr, iBu) and thus elucidate the tub-like structure of the eight-membered rings. 3a and 4a crystallize in the space group P2,/c. The reaction of the four-membered rings 1c - e with the nitrone gives five-membered rings [=(R)B=N(tBu)=B(R)=N(Me) - O=] (5c - e). Both of the reactions of the four-membered rings with azides and with the nitrone can be rationalized in terms of a similar sequence of reaction steps.
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  • 7
    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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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 1073-1078 
    ISSN: 0009-2940
    Keywords: Iminoboranes ; Silylenes ; Azasilaboriridin ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Addition of Silylenes to Iminoboranes[1]Photolytically generated silylenes SiMe2 and SiMes2 are treated with iminoboranes XB≡NtBu [X = tBu, Me3Si(tBu)N, iPr2N: 1a-c]. The products from SiMe2 and 1a are the four-and six-membered rings [-B(tBu)=N(tBu)-SiMe2-SiMe2-] (3a) and [-B(tBu)=N(tBu)—B(tBu)N(tBu)-SiMe2-SiMe2-] (4a), depending on the conditions of the photolysis. SiMe2 reacts with 1b to give the six-membered ring [-BX=N(tBu)-SiMe2-BX=N(tBu)-SiMe2-] (4b). From SiMes2 and 1a,c the three-membered rings [-BX=N(tBu)-SiMes2-] are formed (2a: space group Pbca; 2c: space group P1): SiMes2 reacts with 1b to yield the unexpected four-membered BNSiN ring [B(Mes)N(tBu)-Si(Mes)(SiMe3)-N(tBu)] (5: space group P1).
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 125 (1992), S. 2351-2357 
    ISSN: 0009-2940
    Keywords: (Borole)dicarbonylcobalt anions, methylation, protonation ; (Boracyclopentenyl)dicarbonyl(phosphane)cobalt complexes, hydride abstraction ; (Borole)dicarbonyl(phosphane)cobalt cation, hydride addition ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Derivatives of Borole, XIX[1]. - (Borole)dicarbonylcobaltate Ions: Synthesis, Structure, and Reactivity[3]Reduction of the dinuclear (borole)carbonylcobalt complexes [(3,4-R2C4H2BPh)Co(CO)2]2 (3a: R = H, b: R = Me) with Na/Hg in THF at -30°C affords the anions [(3,4-R2C4H2BPh)-Co(CO)2]- (2a,b-) which can be isolated as [Na([15]crown-5)]+ salts. The structural data of PPh4 · 2a indicate a strong Co - C(CO) interaction and relatively weak cobalt-to-boron bonding. Methylation of the anions 2a,b- gives labile metal alkyl complexes (3,4-R2C4H2BPh)Co(CO)2Me while protonation and subsequent addition of phosphanes afford boracyclopentenyl complexes as e.g. (C4H5BPh)Co(CO)2(PMe3) (5a). The latter reacts with Ph3CBF4 to give the salt [(C4H4BPh)Co(CO)2-(PMe3)]BF4 (6 · BF4). At -80CC cation 6+ undergoes hydride addition at the carbonyl carbon to give the formyl species (C4H4BPh)Co(CO)(CHO)(PMe3) (7) which transforms to the hydride (C4H4BPh)CoH(CO)(PMe3) (8). At room temperature the same reaction produces 5a. Deuteration studies show that the oxidative formation of 6+ from 5a and the formation of 5a by addition of hydride to 6+ are nonstereospecific processes.
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  • 10
    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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