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  • 1
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Inorganic chemistry 32 (1993), S. 5053-5057 
    ISSN: 1520-510X
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Springer
    Structural chemistry 5 (1994), S. 51-55 
    ISSN: 1572-9001
    Keywords: X-ray diffraction ; monoclinic twinning ; crystal structure determination ; dioxaborolane ; tetramethylurea adduct
    Source: Springer Online Journal Archives 1860-2000
    Topics: Chemistry and Pharmacology
    Notes: Abstract The title compound crystallizes in the monoclinic space groupP21/c. Twinning occurs between domains sharing thehk0 zone. The indices of imprecise intensity data were interpreted successfully. A subset of these data could be corrected and used in structure determination together with single-crystal intensity data of the predominant domain, whereas the remaining superposition data were excluded from refinement. Structure solution converged at satisfactory values ofR=0.082,R w=0.074. The structure consists of isolated Lewis acid base adducts.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 104 (1992), S. 372-373 
    ISSN: 0044-8249
    Keywords: Chemistry ; General Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    New York, NY [u.a.] : Wiley-Blackwell
    Heteroatom Chemistry 1 (1990), S. 479-484 
    ISSN: 1042-7163
    Keywords: Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The reaction of appropriate amounts of BH3 with diazadiboretidines (RBNtBu)2 (1a-e; R = Et, Pr, Bu, tBu, tBu(Me3Si)N) transforms them into cyclic diazapentaboranes either of the type [—RB—(H2)—BR—NtBu—BH—NtBu—] (2a-c), of the type [—HB—(H2)—BR—NtBu—BH—NtBu—] (3a-d), or of the type [—HB—(H2)—BH—NtBu—BH—NtBu—] (4), or into an acyclic product RBH—NtBu—BH—NtBu—BHR (2e). The structure of 3c is characterized by a planar N2B3 ring skeleton with an unsymmetrical double-hydrogen bridge.
    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 124 (1991), S. 2435-2441 
    ISSN: 0009-2940
    Keywords: Azadiboriridine ; nido-Diazahexaborane ; Azadiboroline ; closo-Azadicarbadilithiaheptaborane ; Diazatriborolidine ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Reactions of the Azadiboriridines: Formation of Clusters and Ring Expansions*Nine bis(haloboryl)amines 1 were synthesized by haloboration of iminoboranes RB = NR” with dihaloboranes R'BHal2 [R/R'/R” = Et/iPr/tBu (1b), Et/sBu/tBu (c), iPr/iPr/iPr (d), iPr/tBu/iPr (e), tBu/Me/tBu (g), tBu/Et/tBu (h), tBu/Et/SiMe3 (k), tBu/tBu/SiMe3 (1), tBu/Cl/tBu n)]. The borane 1n can be transformed into 1o (R' = NMe2) by the reaction with Me3SiNMe2; an equilibrium between 1o and the four-membered ring 1o' is observed, 1o' being formed from 1o by intramolecular B - N coordination. On reduction with lithium, the nido-diazahexaboranes 3b-e, g, h are formed from the corresponding bis-(haloboryl)amines 1. In the case of 3e, g, h, the ligands R and R' are unsymmetrically distributed to axial and equatorial positions of the fragment structure derived from the pentagonal bipyramid. In particular cases, azadiboriridines of type 2 are either isolated or proven as intermediates on the way from 1 to 3. The three-membered ring of the known azadiboriridines 2i, m (R/R'/R” = tBu/iPr/tBu, tBu/tBu/tBu) is expanded to the five-membered ring of the corresponding azadiborolines 4i, m by the reaction with 3-hexyne. The products 4i, m are reduced to the dilithium azadiborolinates 5i, m by the action of lithium; the molecular structure of a closo-azadicarbadili-thiaheptaborane is recognized in crystals of 5i. The threemembered ring of 2m is also expanded by the reaction with the iminoborane EtB ≡ NtBu giving the diazatriborolidin 6m, which crystallizes in the space group Pca21
    Additional Material: 1 Ill.
    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. 97-102 
    ISSN: 0009-2940
    Keywords: Aza-nido-decaborane(12) ; Aza-arachno-undecaborate(1  - ) ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Novel Syntheses of the Aza-nido-decaborane SkeletonThe known nido-NB9H12 (3) can be synthesized by thermolysis of either arachno-B9H13(NH3) (4) in xylene (11%) or arachno-B10H12(N3)(NH2) (5) in diglyme (100%). The deprotonation of 5 yields the anion arachno-[NB10H13(N3)]- (6), whose skeleton is derived from the closed 13-vertex deltahedron. On protonation, a degradation of 6 is observed to give nido-NB9H11(N3) (7), which crystallizes in the monoclinic space group P21/c. The borane 3 is attacked by Et3N · BH3 with evolution of H2 and formation of the 6-BH2  -  NEt3 derivative of 3 (8). Both nido-species 8 and 7 add the isonitrile CNtBu at the position 9 to yield the arachno-products 9 and 10, respectively. The adduct 11 is formed from 7 and the azadiboriridine (- tBuB  -  BtBu  -  NtBu  - ).
    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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