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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 103 (1970), S. 2003-2005 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 104 (1971), S. 1136-1146 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation and Properties of CyclopentadienyldiethylboraneCyclopentadienyldiethylborane, Et2BCp (6), can be liberated from its easily available amine addition compounds 2a, 2b by the action of BF3. According to the 1H n.m.r. spectra of 2a, 2b, and 6, only one tautomeric species is present, with the boron atom in a vinylic position: a 1.5-sigmatropic hydrogen shift occurs during the formation of 2a and 2b. Diels-Alder dimers are formed from 6 already at room temperature with the aid of Lewis acids as catalysts. The synthesis and properties of the methylcyclopentadienyl compound 7 correspond to those of 6. The reaction of 6 with LiBu, Na[BHEt3], or FeCl2, yields LiCp, NaCp, or FeCp2, respectively. A 1:1 addition compound is formed from 6 and Na.
    Notes: Cyclopentadienyldiäthylboran, Ät2BCp (6), läßt sich mit Hilfe von BF3 aus seinen einfach zugänglichen Amin-Addukten 2a und 2b in Freiheit setzen. Aus den 1H-NMR-Spektren folgt, daß sowohl das gesättigte B-Atom in 2a und 2b als auch das ungesättigte B-Atom in 6 an ein vinylisches C-Atom gebunden sind und daß jeweils nur ein Tautomeres vorliegt: bei der Bildung von 2a und 2b vollzieht sich eine 1.5-sigmatrope H-Verschiebung. Schon bei Raumtemperatur unterliegt 6 einer von Lewis-Säuren katalysierten Diels-Alder-Dimerisierung. Darstellung und Eigenschaften der Methylcyclopentadienylverbindung 7 entsprechen denen von 6. Die Reaktion von 6 mit LiBu bzw. Na[BHät3] führt zu LiCp bzw. NaCp, die Reaktion mit FeCl2 zu FeCp2. Aus Na und 6 entsteht ein 1:1-Addukt.
    Additional Material: 2 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 101 (1968), S. 2881-2888 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Pentafluorphenylbor-[p-methoxy-phenylimid], C6F5B ≡ NC6H4OCH3 (1), reagiert mit Phenylacetylen zu 6-Methoxy-4-phenyl-2-pentafluorphenyl-2.1-borazaronaphthalin (6-Methoxy-4-phenyl-2-pentafluorphenyl-1.2-benzazaborin) (2). Das gleiche Produkt entsteht erwartungsgemäß auch, wenn man die zur Bereitung von 1 nötige thermische Abspaltung von HCl aus C6F5B(NHC6H4OCH3)Cl in Gegenwart von Phenylacetylen ausführt. Bei Zusatz von Triäthylamin erhält man nicht 2, sondern unter Substitution von Chlorid am Boramidchlorid durch die Phenylacetylid-Gruppe das zu 2 isomere Pentafluorphenylborphenylacetylid-p-anisidid, C6F5B(C2C6H5)(NHC6H4OCH3) (6). Aus vier Arylboridchlorid-Arylaminen Ar′BCl2 · H2NAr, bei denen die entsprechenden Borimide nicht bekannt sind, wurden in Gegenwart von Phenylacetylen 2 Mol HCl abgespalten und dabei in guten Ausbeuten entsprechende 2.1-Borazaronaphthaline (1.2-Benzazaborine) (7-10) erhalten.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 101 (1968), S. 2870-2873 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Die bei der thermischen Abspaltung von 2 Mol Halogenwasserstoff aus Boran-Aminen R′BHal2·H2NR gebildeten Borimide R′B ≡ NR reagieren mit 3.4-Dihydro-isochinolin-N-phenylimin (1) als 1.3-dipolarem Agens zu den entsprechenden 3-Bora-1.2.4-triazolidinen (Hexahydro-1.2.4.3-triazaborolo[5.1-α]isochinolinen) (2--5).
    Type of Medium: Electronic Resource
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  • 5
    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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  • 6
    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.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 123 (1990), S. 747-750 
    ISSN: 0009-2940
    Keywords: Methylenoboranes / (2 + 2)-Cycloadditions / Boraheterocycles / 1,3-Sigmatropic methyl shift ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A 1.3-Methyl Shift along the Unsaturated BCSi SkeletonThe synthesis of the methoxy[tris(trimethylsilyl)methyl]boranes X-(MeO)B-C(SiMe3)3 (1a-d; X = Cl, Br, Ph, PhCH2) is described. The methylenoboranes Me-B=C(SiMe2Hal) (3a, b), the 2,3-dihydro-1H-1-sila-3-boraindene species 6, and the 1,2,3,4-tetrahydro-1-sila-3-boranaphthalene species 7 are formed by the thermal elimination of MeOSiMe3 from 1a/b or 1c or 1d, respectively. The boranes 3a, b undergo cyclodimerization at the B=C bond at 25 and 69°C, respectively, the diboretanes 4a, b being formed. The oxaboretanes 5a, b are isolated from the reaction of 3a, b with Ph2CO. The thermal elimination of MeOSiMe3 from Me′-(MeO)B-C(SiMe3)3 (1g;; Me′ = CD3) and subsequent addition of Ph2CO gives the oxboretanes 5g′/5g″ in the ratio of 1:6, showing that an equilibrium Me′-B=C(SiMe32 ⇄ Me - B=C(SiMe3(SiMe2Me′) with a statistical distribution of Me′ among seven methyl places is established in the hot tube before Ph2CO finally attacks the double bond. All these results are in accord with the primary formation of the methyleneboranes X-B=C(SiMe3)2 from 1a-d, followed by a 1,3-shift of Me along the unsaturated BCSi skeleton and the subsequent transformation into the isolated products.
    Type of Medium: Electronic Resource
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  • 8
    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.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 9
    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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  • 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.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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