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  • 11
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions to the Chemistry of Transition Metal Diolefin Complexes. IV. Synthesis of Cobalt Coordination Compounds of Butadiene-d6The synthesis and characterization of two cobalt complexes of butadiene-1, 3-d6 with the empirical formula CoC12D19 and CoC12D18H will be described. The results of the mass spectroscopy and the 1H-NMR studies lead to the proposed structure:.1(π-butadiene-1, 3-d6)(π-3-methyl-d3-heptadienyl-d10)cobalt.2(π-butadiene-1, 3-d6)(π-3-methyl-d2-heptadienyl-d10)cobalt. .The mechanism of synthesis of the named complexes will be reported.
    Notes: Die Darstellung und Charakterisierung von zwei Kobaltkomplexen des perdeuterierten Butadiens mit den Summenformeln CoC12D19 (1) bzw. CoC12D18H (2) wird beschrieben. Die Ergebnisse der Massenspektroskopie und der 1H-NMR-Studien führen zu folgenden Strukturvorschlägen:.1(π-Butadien-1, 3-d6)(π-3-methyl-d3-heptadienyl-d10)kobalt.2(π-Butadien-1, 3-d6)(π-3-methyl-d2-heptadienyl-d10)kobalt..Der Mechanismus zur Bildung der beiden π-Komplexe wird beschrieben.
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  • 12
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 440 (1978), S. 45-51 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Correlation of Tolman's Cone Angles with 1J(31p—1H) of Phosphonium FluorosulfonatesA 1H-n.m.r. study of three series of phosphonium salts [HPR3-nHn]X, and [HPPh2R1-nHn]X and (R = aliphatic substituent and H, X = SO3 F) gives a good relationship between increasing values of 1J(31P—1H) versus decreasing size of substituted phosphines. A method to obtain Tolman's cone angle is described.
    Notes: Die 1H-NMR-Untersuchung dreier Reihen von Phosphoniumsalzen [HPR3-nHn]X, [HPPhR2-nHn]X und [HPPh2R1-nHn]X (R = aliphat. Rest und H, X = SO3F) ergab einen inversen Zusammenhang von Werten der 1J(31p—1H)-Kopplungskonstante und Raumbedarf der Phosphine. Es wird eine Methode zur Bestimmung Tolmanscher Kegelwinkel auf der Basis von 1J(31p—1H)-Werten angegeben.
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  • 13
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 463 (1980), S. 123-131 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Association Behaviour of Strannatranes1-Alkylstannatranes (R = Me, Et, Bu, Phenyl) associate in unpolar solvents to relatively stable trimeric units. In aqueous solution 1-methylstannatran displays no autoassociation. 1-t-Butylstannatran, 1-o-tolylstannatran, and 1-alkylthiostannatranes are monomeric in all kinds of solvents. The association behaviour is characterized by molecular mass estimation and 1H-, 13C-, and 119Sn-NMR measurements.
    Notes: Es wird über einige neue Stannatrane und Thiostannatrane berichtet und gezeigt, daß die 1-Alkylstannatrane in unpolaren Lösungsmitteln zu relativ stabilen trimeren Einheiten assoziieren. In wäßriger Lösung zeigt 1-Methylstannatran keine Selbstassoziation. 1-t-Butylstannatran, 1-o-Tolylstannatran und 1-Alkylthiostannatrane sind in allen Lösungsmitteln monomer. Das Assoziationsverhalten wird durch Molekulargewichtsbestimmung und 1H-, 13C- und 119Sn-NMR-Messungen charakterisiert.
    Additional Material: 5 Ill.
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  • 14
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 495 (1982), S. 115-119 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Alkali Phosphorus Compounds and their Reactivity. 79. NMR Investigations of Alkali Organophosphides. IThe 31C and 31P NMR spectra display a further separation of ion-pairs of alkali-organophosphides in THF solution after addition of cryptandes . An exception presents LiP(Ph)2, T1—13C-NMR measurements suggest a tetrameric structure in THF.
    Notes: Anhand der 13C- und 31P-NMR-Daten läßt sich zeigen, daß sich die Ionenpaare der Alkali-organophosphide in THF durch Zugabe von Kryptanden entsprechend weiter trennen lassen. Eine Ausnahme bildet LiP(Ph)2, das aufgrund von T1—13C-NMR-Messungen eine tetramere Struktur in THF aufweist.
    Additional Material: 2 Tab.
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  • 15
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 494 (1982), S. 189-195 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Intramolecular Mobility of Phosphin-3η-allyl Palladium Chloride ComplexesThe diastereomers of the complexes cis- and trans-2.3-diphenyl-1.3-oxaphosphorinan-3η-allyl palladiumchloride interchange. The activation parameters of the diastereomerization are estimated by line-shape analysis of the 31P - NMR signals.The exchange of allyl protons is described by 16 permutations involved in three graphes of the proposed seven modes of intramolecular movement.The cross-peaks in the 2D-exchange-1H - NMR spectrum display the exchanging protons.The results suggest a π-σ-transition together with a trigonal-bipyramidal arrangement of ligands in the transition state.
    Notes: Die Diastereomere der Komplexe cis- und trans-2,3-Diphenyl-1,3-oxa-phosphorinan-3η-allylpalladiumchlorid wandeln sich ineinander um. Die Aktivierungsparameter für diese Diastereomerisierung werden durch Linienformanalyse der 31P-NMR-Signale bestimmt.Der Positionswechsel der Allylprotonen wird durch 16 Permutationen beschrieben und in je drei Graphen den sieben vorgeschlagenen intramolekularen Bewegungsmechanismen zugeordnet. Aus den cross-peaks im 2D-Austausch-1H - NMR-Spektrum werden die miteinander im Positionswechsel befindlichen Protonen bestimmt.Die Ergebnisse sprechen für einen π-σ-Übergang mit trigonalbipyrymidaler Ligandenanordnung im Übergangszustand.
    Additional Material: 2 Ill.
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  • 16
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 450 (1979), S. 70-78 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: NMR Investigations on Dimeric Dialkylthallium Compoounds with (TIX)2 Four-membered Ring StructureNMR investigations on dimeric dialkylthallium amides and on dimethylthallium diphenylphosphide indicate a significant influence of the largeness of the bridging groups on the binding strength in the (TIX)2-four-membered ring structure. Exchange reactions among different dimeric dialkylthallium compounds give evidence of a dimer-monomer equilibrium, which is of fundamental importance for the reactivity and the reaction mechanisms of these compounds.
    Notes: NMR-Untersuchungen an dimeren Dialkylthalliumamiden und am Dimethylthalliumdiphenylphosphid indizieren einen signifikanten Einfluß der Größe der Brückengruppen auf die Bindungsstärke in den (TIX)2-Vierringen. Austauschreaktionen zwischen unterschiedlichen dimeren Dialkylthalliumverbindungen beweisen ein Dimer-Monomer-Gleichgewicht, das von grundsätzlicher Bedeutung für die Reaktivität und die Reaktionsmechanismen dieser Verbindungen ist.
    Additional Material: 3 Ill.
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  • 17
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 494 (1982), S. 144-150 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Synthesis and Properties of Trinorbornyl Boron CompoundsTris(1-norbornyl), Tris(2-norbornyl), and Tris(7-norbornyl) boron were synthesized from boron trifluoride diethylether and 1-norbornyl lithium or 2- and 7-norbornyl magnesium halides respectively. The compounds were characterized by the IR-, 13C-, 11B-NMR, and mass spectra. Furthermore 1-norbornyl lithium was isolated in the crystalline state and investigated in detail.
    Notes: Tris(1-norbornyl)-, Tris(2-norbornyl)- und Tris(7-norbornyl)bor1 wurden aus Bortrifluorid-diethylether und 1-Norbornyllithium bzw. 2- und 7-Norbornylmagnesiumhalogeniden synthetisiert. Eine nähere Charakterisierung erfolgte durch IR-, 13C- und 11B-NMR- sowie Massenspektren. 1-Norbornyllithium wurde in kristalliner Form erhalten; die Verbindung liegt in Benzol tetramer vor. Das 13C-NMR-Spektrum wird angegeben.
    Additional Material: 1 Ill.
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  • 18
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 525 (1985), S. 35-40 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: NMR-Studies of 1,2-Bis(alkylphosphino)benzenes and their Anions7Li, 13C, and 31P magnetic resonance spectroscopy, including studies of spin-lattice relaxation times, have been used to investigate the structure of 1,2-bis-(alkylphosphino)benzenes and their dilithiated species in THF and Et2O solutions. A phosphorus inversion barrier of 100-110 kJ/mol has been determined for the diastereomeric bisphosphines. The chemical shifts of the diphosphides demonstrate the delocalization of the negative charge of the anions in the aromatic ring. 7Li-31P-nuclear spin couplings and T1 measurements for 13C nuclei indicate that all lithiated species are dimers with intermolecular P-Li-P-bridges.
    Notes: 7Li-, 13C- und 31P-NMR, einschließlich Spin-Gitter-Relaxationszeitmessungen, wurden zur Strukturaufklärung von 1,2-Bis(alkylphosphino)benzenen und ihren dilithiierten Spezies in THF und Et2O-Lösungen angewendet. An den diastereomeren Bisphosphinen läßt sich eine Phosphorinversionsbarriere von 100-110 kJ/mol bestimmen. Die chemischen Verschiebungen der Diphosphide demonstrieren die Delokalisierung der negativen Ladung des Anions in den aromatischen Ring.7Li-31P-Kernspinkopplungen und T1-Messungen der 13C-Kerne zeigen, daß alle lithiierten Spezies unter Ausbildung intermolekularer P-Li-P-Brücken dimer vorliegen.
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  • 19
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 334 (1992), S. 179-180 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Lanthanide-Complexes with Rapid Z/E-Isomerisation of the 3-Acetyltetramic Acid Ligand
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  • 20
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    Journal für Praktische Chemie/Chemiker-Zeitung 338 (1996), S. 642-646 
    ISSN: 0941-1216
    Keywords: Chemistry ; Organic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Novel Cu(II) complexes derived from N,N′ P-ethylene-bis-(1′,5′,5′-trimethyltetramic acid-3′-acetiminato)copper(II) aCu [1] were evaluated as contrast agents for NMR microscopy and therefore tested for penetration into living cells (Xenopus laevis oocytes). By in vitro 1H NMR relaxation (T1) and atomic absorption spectroscopy measurements (AAS) we confirmed, that independent of the complex isomers (Z/Z, Z/E, E/E, E/Z) compounds with alkyl substituents in R1 - R5 exclusively were able to penetrate the plasma membranes. It is noteworthy that compounds containing the tetramic acid moieties from both a penetrating and a non-penetrating complex most likely were accumulated in the plasma membrane and/or plasma membrane-associated vesicles, which was concluded from in vitro NMR measurements combined with AAS trace analyses. In this context the crystal and molecular structure of the ‘chimerical’ C17H22N4O4Cu · 3H2O kCu · 3H2O were determined by x-ray analysis. The x-ray structural parameters are discussed in detail.
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