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  • 1975-1979  (12)
  • 1976  (12)
  • Chemistry  (12)
  • Alanes
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  • 1975-1979  (12)
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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 884-895 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Boron, LXXIV: Stabilisation of Diborylamines: (Borolanylamino)boranes and (Diazaborolidinylamino) boranesThe thermal decomposition of diborylamines into a borane and a borazine derivative becomes considerably more difficult when the boron atoms of diborylamines are incorporated into a five-membered ring system. This type of diborylamines is represented by (1-borolanylamino)-boranes as well as by (1,3-dimethyl-1,3,2-diazaborolidin-2-Ylamino)boranes whose structure and bonding are discussed on the basis of spectroscopic data.
    Notes: Durch Einbau der Boratome eines Diborylamins in ein fünfgliedriges Ringsystem wird die thermische Zersetzung der Diborylamine in ein Boran-und ein Borazin-Derivat beträchtlich erschwert. (1-Borolanylamino)borane und (1,3-Dimethyl-1,3,2-diazaborolidin-2-ylamino)borane repräsentieren diese Diborylamin-Typen, deren Struktur und Bindungsverhältnisse aufgrund spektroskopischer Daten diskutiert werden.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Nuclear Magnetic Resonance Studies on Boron Compounds, X: 11B, 14N, and 1H N. M. R. Studies on Boryl-substituted Thiophene, Furan, and N Methylpyrrole and Related Systems: Interaction of sp2-Boron Atoms with π-Systemδ11B data of R3-nBXn (R=alkyl; X = N(CH3)2, Cl, Br; n = 0, 1, 2) and R3-n′BXn(R = phenyl, 2- and 3-thienyl, 1-methyl-2-pyrrolyl, 2-furyl, cyclopentadienyl, vinyl, cyclopropyl; X = alkyl, N(CH3)2,Cl, Br; n = 0, 1, 2) are reported. A comparison of the two series points to increasing π-back-bonding from the ring systems to boron in the series phenyl 〈 3-thienyl 〈 2-thienyl 〈 1-methyl-2-pyrrolyl 〈 2-furyl, which is compatible with the decrease of „aromaticity“ of the cyclic systems. The influence of the conjugated double-bond system in the cyclopentadienyl group leads to a high field shift of the 11B resonance relative to that of the vinylboranes. Preparative methods for the synthesis of the five-membered heteroaromatic rings borylated in the 2-position are reported.
    Notes: Es werden die δ11B-Daten einer Reihe von Boranen des Typs R3-nBXn(R = Alkyl; X = N(CH3)2,Cl, Br; n = 0, 1, 2) und R′3-nBXn(R = Phenyl, 2- und 3-Thienyl, 1-Methyl-2-Pyrrolyl, 2-Furyl, Cyclopentadienyl, Vinyl, Cyclopropyl; X = Alkyl, N(CH3)2, Cl Br; n = 0, 1, 2)mitgeteilt. Der Vergleich beider Reihen läßt eine Zunahme der π-Rückbindung vom Ringsystem zum B-Atom in der Reihe Phenyl 〈 3-Thienyl 〈 2-Thienyl 〈 1-Methyl-2-pyrrolyl 〈 2-Furyl erkennen, die mit der Abnahme der „Aromatizität“ der Ringsysteme in Einklang Steht. Bei den Cyclopentadienylboranen führt das konjugierte Doppelbindungssystem, verglichen mit den Vinylboranen, zu einer Hochfeldverschiebung von δ11B. Präparative Methoden zur Darstellung der in 2-Stellung borylierten Heteroaromaten werden mitgeteilt.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 3247-3249 
    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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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für die chemische Industrie 88 (1976), S. 231-232 
    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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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 2266-2290 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Boron-Halogen Bond in Methylhalogenoboranes: Photoelectron Spectra and ab initio CalculationsHe(I) photoelectron (p.e.) spectra of the methylhalogenoboranes (CH3)3-nBXn (X = F, Cl, Br; n = 1,2) are discussed in comparison with known p.e. spectra of the trihalogenoboranes BX3 and of trimethylborane B(CH3)3 on the basis of ab initio calculations. Correlations of orbital and ionization energies, of π-charge densities and 11B chemical shifts as well as calculated and measured dipole moments give insight into the electronic structure of tricoordinate boron compounds with substituents such as X = F, Cl OCH3 SCH3, N(CH3)2, and CH3.
    Notes: Die He(I)-Photoelektronen(PE)-Spektren der Methylhalogenborane (CH3)3-nBXn (X = F, Cl, Br; n = 1,2) werden mit den bekannten PE-Spektren der Trihalogenborane BX3 und des Trimethylborans B(CH3)3 an Hand von ab initio-Rechnungen vergleichend diskutiert. Korrelationen von Orbital-und Ionisierungsenergien, von π-Ladungsdichten und 11B-Kernresonanzverschiebungen sowie von berechneten und gemessenen Dipolmomenten vermitteln Einblicke in die Bindungsverhältnisse dreifach koordinierter Bor-Verbindungen mit den Substituenten X = F, Cl, OCH3, SCH3, N(CH3)2 und CH3.
    Additional Material: 9 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 1089-1094 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Crystal and Molecular Structure of 3,6-Dichloro-1,2,4,5-tetramethyl-1,2,4,5-tetraaza-36-diphosphacyclohexaneThe title compound 2a crystallizes in the monoclinic system with space group P21/c. The unit cell contains two molecules of 2a The lattice parameters were determined as a = 747.3 ± 0.2, b = 648.2 ± 0.2, c = 1449.3 ± 0.5pm, and β = 128.98 ± 0.02°. The molecule has almost the symmetry of the point group C2h It exists in a flattened chair form with the Cl-atoms and the CH3-groups in equatorial positions. The PCl bond lengths of 207.0 pm are shorter than in ClP[N(CH3)2]2. The PN bond length (168.3 pm) lies well below the PN single bond distance. The NN bond length was determined as 146.2 pm. All intermolecular distances show no anomalies. Finally the R value was 0.0915.
    Notes: 3,6-Dichlor-1,2,4,5-tetramethyl-1,2,4,5-tetraaza-3,6-diphosphacyclohexan (2a) kristallisiert monoklin in der Raumgruppe P21/c mit zwei Molekülen 2a in der Elementarzelle, deren Gitterkonstanten zu a = 747.3 ± 0.2, b = 648.2 ± 0.2, c= 1449.3 ± 0.5 pm und β = 128.98 ± 0.02° ermittelt wurden. Das Molekül besitzt nahezu die Zentrosymmetrie der Punktgruppe C2h; es liegt in einer abgeflachten Sesselform vor mit den Cl-Atomen und den CH3-Gruppen in äquatorialen Positionen. Die PCl-Bindungen sind mit 207.0 pm kürzer als in ClP[N(CH3)2]2; auch der PN-Bindungsabstand liegt mit 168.2 pm erheblich unter dem der Einfachbindung. Die NN-Bindungslänge wurde zu 146.2 pm ermittelt. Alle intermolekularen Abstände weisen keine Anomalien auf. Der R-Wert war zuletzt 0.0915.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 2572-2580 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Boron, LXXVI: N-Functional Aminoboranes: Preparation and Association Behaviour of [Dimethyl(thiophosphoryl)amino]boranes[Dimethyl(thiophosphoryl)amino]boranes of the types [(CH3)2P(S)- NR]3B and [(CH3)2-P(S)-NR]2BX are monomeric. However, the compounds (CH3)2P(S)- NR- BX2 (X = F, Cl, Br) exist in solution in an equilibrium of monomers and dimers, while the aminoboranes of type Cl2P(S)-NCH3 - BX2 (X = CH3, Br) do not associate. 11B n. m. r. data and the monomer/dimer distribution suggests S → B coordination rather than N → B coordination. All [(thiophosphoryl)amino] dihalogenoboranes decompose readily into (CH3)2P(S)X and (RNBX)3.
    Notes: [Dimethyl(thiophosphoryl)amino] boranedes Typs[(CH3)2P(S)-NR]3Bund [(CH3)2P(S)-NR]2-BX sind monomer. Hingegen liegen die Verbindungen (CH3)2P(S)-NR-BX2 (X = F, Cl, Br) in Lösung in einem Monomeren-Dimeren-Gleichgewicht vor, während Cl2P(S)-NCH3- BX2-Verbindungen (X = CH3, Br) nicht assoziieren. 11B-NMR-Daten und die Abhängigkeit des Monomeren/Dimeren-Verhältnisses von X legen eher eine S → B- als eine N → B-Koordination in den Dimeren nahe. Alle [(Thiophosphoryl)amino]dihalogenborane zersetzen sich leicht in (CH3)2P(S)X und (RNBX)3.
    Additional Material: 2 Tab.
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  • 8
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: I. R. Laser-specific Reactions of Boron Compounds, VMercaptoboranes from the Reaction of Diborane with Hydrogen SulfideThe new and unstable compounds HB(SH)2 (1) and HB(SD)2 are formed by CO2-laser irradiation of a gaseous mixture of B2H6 and H2S or D2S, respectively. In addition, μ-mercapto-diborane, HSB2H5 (2), has been obtained. None of these compounds is produced in the thermal reaction of B2H6 and H2S.
    Notes: Die neuen, instabilen Verbindungen HB(SH)2 (1) und HB(SD)2 bilden sich bei der CO2-Laserbestrahlung eines Gasgemisches von B2H6 und H2S bzw. D2S. Außerdem wurde μ-Mercaptodiboran, HSB2H5 (2), erhalten. Keine dieser Verbindungen entsteht bei der thermisch angeregten Reaktion von B2H6 mit H2S.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 2581-2587 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Crystal and Molecular Structure of a Triazadiphospholidine: 3,5-Dichloro-1,2,4-trimethyl-1,2,4,3,5-triazadiphospholidineThe title compound 1a crystallizes in the monoclinic system, space group C 2/c. The structure was determined by Patterson and Fourier methods and refined to R = 0.053. Some of the hydrogen atoms were located by a difference Fourier synthesis and the remaining ones obtained by symmetry operations.  - The P2N3 ring system is nonplanar, its point group symmetry being C2 (H atoms excluded). The planar-coordinated imino nitrogen atom is contrasted by flat pyramids of the hydrazino nitrogen atoms. The N—P—N bond angles of 92.7° imply that phosphorus uses p-orbitals for endocyclic bonding. The P—Cl bonds (2.20 Å) are rather long. The small N — P — N angle and the elongation of the N — N bond to 1.50 Å show the ring strain in this five—membered ring system.
    Notes: Die Titelverbindung 1a kristallisiert im monoklinen System, Raumgruppe C2/c. Über Patterson und Fourier-Methoden wurde die Struktur bis R = 0.053 verfeinert. Ein Teil der Lagen von H-Atomen konnte der Differenz-Fourier-Synthese entnommen werden. Die übrigen wurden durch Symmetrieoperationen gewonnen.  -  Das P2N3-Ringsystem ist aplanar, Molekülsymmetrie C2 (ohne H-Atome). Dem planar koordinierten Iminostickstoff stehen abgeflachte Pyramiden der beiden Hydrazin—N—Atome gegenüber. Der N—P—N-Winkel von 92.7° legt nahe, daß der Phosphor für die endocyclischen Bindungen nur ρ-Bahnfunktionen betätigt. Die P—Cl-Bindungen sind mit 2.20 Å relativ lang. Der kleine N—P—N-Bindungswinkel und die auf 1.50 Å aufgeweitete N— N-Bindung belegen die Ringspannung in diesem Fünfringsystem.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 3480-3485 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: N. M. R. Spectroscopic Investigations on Boron Compounds. XI14N- and 11B-Nuclear Magnetic Resonance Studies on Borazines14N and 11B chemical shifts of 30 borazines can be interpreted in terms of delocalised pz electron pairs of the nitrogen atoms in the ring system. Calculated π charge densities at the N-atoms correlate linearly with δ14N. Substituents effects are discussed.
    Notes: Die 14N- und 11B-chemischen Verschiebungen von 30 Borazinen lassen sich im Sinne einer Delokalisierung der pz-Elektronenpaare der Stickstoffatome im Ringsystem interpretieren. Berechnete π-Elektronendichten an den N-Atomen korrelieren linear mit δ14N. Substituenten. effekte werden diskutiert.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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