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  • Electronic Resource  (7)
  • Iminoboranes  (5)
  • (Hydroboryl)(methoxyboryl)amine  (1)
  • 1,2,5,6,3,4,7,8-Tetraazatetraborocane  (1)
  • 1
    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.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 122 (1989), S. 479-480 
    ISSN: 0009-2940
    Keywords: Azaborane clusters ; Aza-arachno-heptaborane(10) anions ; Iminoboranes ; Pentaborane(9) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Aza-arachno-heptaboranes, a Novel Class of AzaboranesIn the presence of 2,6-lutidine (Lu), iminoboranes RB≡NR′ (1a-c, R/R′ = iPr/tBu, tBu/tBu,tBu/SiMe3) are added to B5H9 to give [LuH][R′NB6H8R] (2a-c). A monocapped trigonal prism for the arachno-NB6 skeleton of 2a-c is deduced from 11B-NMR data.
    Type of Medium: Electronic Resource
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  • 3
    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).
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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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.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1787-1790 
    ISSN: 0009-2940
    Keywords: Iminoboranes ; Azadiboriridines ; Diaza-arachno-octaborane ; arachno-Nonaborate(1 -) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of the Boron Hydrides B3H7 and B5H9 with the Unsaturated Boron-Nitrogen Compounds NBtBu2 and NB2tBu3THF · B3H7 reacts with RB≡NR (1, R = tBu) to yield the μ-amino-diborane(6) B2H4R(NHR) (5), which crystallizes in the triclinic space group Pī. The reaction of B3H7 with the azadiboriridine NB2tBu3 (2, R = tBu) leads to the known NB2R3 · BH3 (4) and the novel (NB2R3)2B2H4 (6). Product 6 is considered to represent a diaza-arachno-octaborane derivative. The iminoborane 1 reacts with B5H9 in the presence of lutidine (L) to give the ionic product [L - BR = NHR][B9H14] (7); our earlier report on the formation of the aza-arachno-heptaborate [LH][NB6H8R2] has to be revised. The products from the reaction of B5H9 with NB2R3 are 4 and 6.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    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.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 126 (1993), S. 1571-1577 
    ISSN: 0009-2940
    Keywords: Iminoboranes ; Tantalum complexes, cyclic carbene- ; Azaboratantalacyclobutanes ; Azaboratantalacyclobutenes ; Diazoniadiboratatantalacyclohexadienes ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Further Reactions of Iminoboranes RB≡NR' with Neopentylidenetantalum ComplexesThe azaboratantalacyclobutanes [-NR≡-BR-CH(tBu)-Ta-CpCl2-] (3b, d, f, h-1; R/R′=Pr/tBu, iPr/tBu, iPr/iPr, tBuCH2/tBuCH2, Me3SiCH2/Me3SiCH2, tBu/Me, tBu/iPr, tBu/SiMe3) are formed from the corresponding iminoboranes RB≡NR′ and the neopentylidenetantalum complex [tBuHC=TaCpCl2] (2a) by [2 + 2] cycloaddition. The elimination of HCl from 3b, d, f, h and from the four known azaboratantalacyclobutanes 3a, c, e, g [R/R'equals;Et/tBu, Bu/tBu, Ph/tBu, iBu/iBu] gives the azaboratantalacyclobutenes [-NR′-BR-C(tBu)=TaCpCl-] (4a-h). X-Ray structural analyses of 4e, f show these cyclic carbenetantalum complexes to contain short Ta-C and Ta-N bonds and perhaps some transannular Ta-B interaction. The complex [tBuHC=TaCl3(THF)2] (2b) adds iminoboranes RB≡NtBu with unbranched alkyl groups (R=Et, Pr, Bu) in a 1:2 molar ratio to yield the diazoniadiboratatantalacyclohexadienes 5a-c; the product 5a adopts a non-planar ring structure in the crystal. The 1:2 reaction of 2b with tBuB≡NMes, instead, results in the cyclobutane [-N(Mes)-B(tBu)-N(Mes)-TaCl3(THF)-] (7m).
    Additional Material: 1 Ill.
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