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  • Wiley-Blackwell  (45)
  • 1975-1979  (45)
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  • Wiley-Blackwell  (45)
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  • 1
    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.
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 1086-1094 
    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, XII. 1H-, 11B-, 13C-, and 14N-Nuclear Magnetic Resonance Studies on Alkinylboranesπ-Back bonding of the CC-triple bond to boron accounts for δ11 B and δ13C of alkinylboranes (1 - 20, tables 1, 2). δs14 N-data support this interpretation. The diamagnetic anisotropy of the CC-triple bond is responsible for an additional high field shift of δ11B compared with those of alkenylboranes. - The magnitude and sign of the coupling constant 1J(13C11 B) in (C2H5)2 N - B-(C≡CH)2 has been determinded by means of double resonance measurements 1H{11B}. δ1 H of the ethinylic protons depends on anisotropic and mesomeric effects.
    Notes: δ11 B- und δ13C-Werte von Alkinylboranen (1-20, Tab. 1, 2) legen eine π-Rückbindung der CC-Dreifachbindung zum Bor-Atom nahe. δ14 N-Daten stützen diese Interpretation. δ11 B ist infolge des Anisotropieeffektes der benachbarten Dreifachbindung stärker hochfeldverschoben als in Alkenylboranen. - Größe und Vorzeichen der Kopplungskonstante 1J (13C11B) in (C2H5)2N - B(C≡CH)2 wurden mit Hilfe von Doppelresonanzmessungen 1H{11B} bestimmt. δ1 H der Ethinylprotonen wird vom Anisotropieeffekt und vom mesomeren Effekt kontrolliert.
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 2790-2801 
    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, LXXXVII. B,Si-Functional (Silylamino)boranes: a Contribution to the SiN-Cleavage by Boron Halides(Silylamino)boranes are virtually inert towards transsilylation or BN-cleavage by chloromethylsilanes. However, B- and/or Si-halogenated (silylamino)boranes are easily obtained from Si-halogenated disilazanes and boron halides, and, especially, from nonamethylcyclotrisilazane 14 and boron halides. Information concerning the degradation of this ring system have been obtained from several intermediates formed in the reaction of 14 with (CH3)2BBr.
    Notes: (Silylamino)borane sind weitgehend inert gegenüber einer Umsilylierung bzw. BN-Spaltung durch Chlormethylsilane. Hingegen erhält man B- und/oder Si-halogenierte (Silylamino)borane aus Si-halogenierten Disilazanen und Borhalogeniden oder besonders einfach aus Nonamethylcyclotrisilazan 14 und Borhalogeniden. Verschiedene Zwischenprodukte, die bei der Reaktion von 14 und (CH3)2BBr gebildet werden, geben Hinweise auf den Abbau dieses Ringsystems.
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  • 4
    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, XIV. Indirect Nuclear Spin-Spin Coupling of 11B with other Directly Bonded NucleiCoupling constants 1J(11BX) and chemical shifts δ11 B and δX are reported for X = 1H, 13C, 15N, 19F, 29Si, 31P, 77Se, 119Sn, and 207Pb. The signs of 1J(11B29Si)(negative) and 1J(11B31P) (positive) in compounds of tervalent boron have been determined by double resonance experiments 1H-{11B} and 13C-{X}. With the exception of X = 19F, the magnitude and sign of 1J(11BX) can be interpreted by assuming a dominating Fermi contact term in the coupling mechanism. The possible influence of the spin-dipole and the orbital term on the magnitude of the coupling is discussed.
    Notes: Kopplungskonstanten 1J(11BX) mit X = 1H, 13C, 15N, 19F, 29Si, 31P, 77Se, 119Sn und 207Pb sowie chemische Verschiebungen δ11 B und δX wurden bestimmt. Die Vorzeichen von 1J(11B29Si) (negativ) und 1J(11B31P) (positiv) in Verbindungen des dreibindigen Bors folgten aus Doppel-resonanzexperimenten 1H-{11B} and 13C-{X}. Ausgenommen X = 19F, sind Größe und Vorzeichen von 1J(11BX) mit der Annahme zu erklären, daß der Fermi-Kontaktterm im Kopplungs-mechanismus dominiert. Der mögliche Einfluß des Spin-Dipol- und des Orbital-Terms auf die Größe der Kopplung wird diskutiert.
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  • 5
    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.
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  • 6
    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.
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  • 7
    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.
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  • 8
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 1643-1650 
    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, LXXX. Aminolysis of Dimethyltrithiadiborolane with Primary AminesPrimary amines react with 3,5-dimethyl-1,2,4,3,5-trithiadiborolane (1) by ring-opening followed by an intramolecular cyclocondensation to yield 1,2,4,3,5-dithiaazadiborolidines (2) and by an intermolecular cyclocondensation to give the six-membered 1,3,5,2,4,6-thiadiazatriborines (3) and borazines (4). The product distribution is influenced by steric and electronic effects of the amine.
    Notes: Primäre Amine reagieren mit 3,5-Dimethyl-1,2,4,3,5-trithiadiborolan (1) unter Ringöffnung und intramolekularer Cyclokondensation zu 1,2,4,3,5-Dithiaazadiborolidinen (2) bzw. intermolekular zu den sechsgliedrigen 1,3,5,2,4,6-Thiadiazatriborinen (3) und Borazinen (4). Die Produktverteilung wird von sterischen und elektronischen Effekten des Amins beeinflußt.
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  • 9
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 2783-2789 
    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, LXXXVI. Phenyl-substituted Diborylamines[(C6H5)2B]2NH results not only by SiN-cleavage of hexamethyldisilazane with (C6H5)2 BBr but also by an exchange process from (C5H5)2B—NH—Si(CH3)3 or (C6H5)2B—NH—B(CH3)2. In contrast, (C6H5)2B—NCH3—Si(CH3)3is quite stable. At ≈ 50°C (C6H5)2B—NCH3—B(CH3)2 decomposes with phenyl group migration to yield dimethylphenylborane and the borazine 5.
    Notes: [(C6H5)2B]2NH entsteht nicht nur durch SiN-Spaltung von Hexamethyldisilazan mit (C6H5)2 BBr, sondern auch in einem Umordnungsprozeß aus (C6H5)2B—NH—Si(CH3)3 oder (C6H5)2B—NH—B(CH3)2. Im Gegensatz dazu ist (C6H5)2B—NCH3—Si(CH3)3stabil. (C6H5)2B—NCH3—B(CH3)2 zersetzt sich bei ≈ 50°C unter Phenylgruppenwanderung in Dimethylphenylboran und das Borazin 5.
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  • 10
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 110 (1977), S. 2607-2623 
    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, LXXXV Diorganyl(phosphinoamino)boranes: Synthesis, Structure, and AssociationThe preparation of (phosphinoamino)boranes by various methods is described, and the selective cleavage of (silylamino)phosphines by boron halides is shown to depend on the substituents at the boron atom. In case of the system (C6H5)2P—NCH3—Si(CH3)3/BCl3 borontrichloride adds to the P-atom in the first step followed by (CH3)3SiCl elimination which obeys a first order rate law. Most of the (phosphinoamino)boranes are monomeric at room temperature and in solution but (CH3)2P—NCH3—B(CH3)2 associates with BP coordination at low temperature. Rotation at the BN bond is strongly restricted mainly due to steric hindrance. In these cases a long range coupling 4JPNBCH is observed which can be explained by the π-bond model. Thermally the (phosphinoamino)boranes decompose with formation of borazine and phosphine derivatives.
    Notes: Zur Darstellung von (Phosphinoamino)boranen werden verschiedene Verfahren beschrieben, wobei u. a. gezeigt wird, daß (Silylamino)phosphine durch Borhalogenide in Abhängigkeit von den Substituenten am Boratom selektiv gespalten werden. Im Falle des Systems(C6H5)2P—NCH3—Si(CH3)3/BCl3 wird im 1. Schritt Borchlorid am P-Atom addiert, dann schließt sich eine (CH3)3SiCl-Eliminierung an, die einem Geschwindigkeitsgesetz 1. Ordnung gehorcht. Die meisten (Phosphinoamino)borane sind bei Raumtemperatur und in Lösung monomer, jedoch assoziiert z. B. (CH3)2P—NCH3—B(CH3)2 unter BP-Koordination in der Kälte. Die Rotation um die BN-Bindung ist (hauptsächlich aus sterischen Gründen) stark gehindert. In diesen Fällen beobachtet man eine Fernkopplung 4JPNBCH′, die mit Hilfe des π-Bindungsmodells interpretiert wird. Die (Phosphinoamino)borane zersetzen sich thermisch in Borazine und Phosphinderivate.
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