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  • 1
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 151 (1926), S. 221-238 
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Es wird eine neue Methode zur Trennung von Tantal und Niob beschrieben. Dieselbe beruht auf hydrolytischer Differentialspaltung von Tantaloxal- und Nioboxalsäure in Gegenwart von Gerbsäure in schwach saurer Lösung. Die Methode besitzt die folgenden Vorteile: Die Färbung des Tantalniederschlages zeigt auf den ersten Blick, ob er niobfrei oder niobhaltig ist, es werden keine Platingefäße benutzt, und der erreichbare Genauigkeitsgrad steht nicht viel hinter dem für die Trennung der gewöhnlicheren Elemente zurück.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 141 (1924), S. 231-283 
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 169 (1928), S. 321-335 
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Wenn Tantaloxyd mit Kaliumcarbonat geschmolzen und die Auflösung der Schmelze mit Chlornatrium gesättigt wird, fällt 4:3 Natriumtantalat. Nioboxyd, auf gleiche Weise behandelt, ergibt 7:6 Natrinmniobat. Die Niederschläge bilden ein schweres, weißes, mikrokristallinisches Pulver. Die Filtrate enthalten einige Milligramm Erdsäure, welche mittels Neutralisation des Carbonats zu Bicarbonat in heißer Lösung zur Ausflockung gelangen.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 109 (1976), S. 306-313 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Formation and Structure of the Pentabromocarbonate Anion [CBr5⊖]n - On the Oxidation of En-aminesOxidation of enamines 5 with tetrabromomethane yields stable crystalline pentabromocarbonates 6, which may easily be converted into the corresponding perchlorates 7. From the pentabromocarbonates, tetrabromomethane cannot be extracted either by organic solvents or by heating in vacuo; with silver nitrate, however, silver bromide can be precipitated from tetraphenylphosphonium pentabromocarbonate (9). If labelled 9 - prepared from tetraphenylphosphonium [82Br]bromide and tetrabromomethane - is treated with silver nitrate, all the activity is found in the silver bromide precipitate. This is clear evidence against a trigonal bipyramidal structure of the pentabromocarbonate anion CBr5⊖]n.
    Notes: Bei der Oxidation von Enaminen 5 mit Tetrabrommethan entstehen stabile kristalline Pentabromocarbonate 6, die sich leicht in die entsprechenden Perchlorate 7 überführen lassen. Aus den Pentabromocarbonaten kann Tetrabrommethan weder durch Extraktion mit organischen Solventien noch durch Erhitzen i. Vak. abgespalten werden, mit Silbernitrat kann jedoch aus Tetraphenylphosphonium-pentabromocarbonat (9)Silberbromid ausgefällt werden. Bei der Umsetzung von markiertem 9 - dargestellt aus [82Br] Tetraphenylphosphoniumbromid und Tetrabrommethan - mit Silbernitrat findet man die Gesamtaktivität im Silberbromid-Niederschlag. Dies spricht gegen die Struktur einer trigonalen Bipyramide für das CBr5⊖]n-Anion.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 108 (1975), S. 1285-1292 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: On the Thermal of Rearrangement of Methylenecyclobutane - A MO-StudyA MO-model by the semiempirical MINDO/2 method explains the experimental stereochemistry in the thermal rearrangement of methylenecyclobutane: 1. Retention of configuration at the migrating carbon atom due to “subjacent orbital control” as it has been suggested previously by Berson and Salem. 2. Antarafacial participation of the allyl unit due to Jahn-Teller instability in the diradical transition state. The quantumchemical studies suggest that the mechanism of the reaction depends on substituents.
    Notes: Ein MO-Modell nach der semiempirischen MINDO/2 Methode erklärt die Stereochemie in der 1,3-sigmatropen Umlagerung von Methylencyclobutan: 1. Retention der Konfiguration am wandernden Kohlenstoffatom durch „subjacent orbital control“ nach dem Konzept von Berson und Salem. 2. Antarafaciale Beteiligung der Allyleinheit als Konsequenz des Jahn-Teller-Effektes im Diradikal-Übergangszustand. Die quantenchemischen Rechnungen weisen darauf hin, daß der Mechanismus der Reaktion von Substituenten abhängt.
    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 91 (1958), S. 2103-2108 
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Bildung und Verhalten von Silicophosphorsäure-Derivaten werden untersucht. Im besonderen wird gezeigt, daß Phosphorsäure ester durch Monokieselsäureabkömmlinge wie Silanole und Alkoxysilane unter Entstehung von Verbindungen mit der typischen -Gruppe gespalten werden.
    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. 271-274 
    ISSN: 0009-2940
    Keywords: Phosphacumulenes ; Cumulenes ; Calculations, MNDO, SCF ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: The title compound phosphabutatriene possesses two energetically closely spaced frontier orbitals, as in methylenephosphane and in phosphaallene. They are built up from the π system or the s̰ orbital of phosphorus by interaction with neighboring π bonds. The extension of these frontier orbitals over all (heavy) atoms makes self-dimerization to different cyclobutane derivatives feasible. Substituent effects on the ordering of s̰ and π are analyzed. Vibrational analyses indicate P=C vibrations of low intensity which decrease with increasing length of the heterocumulene chain. The analysis is extended to the two next higher homologs, which are hitherto experimentally unknown.
    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 123 (1990), S. 971-973 
    ISSN: 0009-2940
    Keywords: Calculations ; Jahn-Teller distortion ; Nitrenium ; Phosphenium ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Ab initio calculations at SCF, MCSCF, and ACPF level were performed on a series of the phosphenium- and nitreniumcation family. These show that they possess an allylic π-system with 4 electrons, which is distorted from planarity when the terminal groups of the allylic system are PR2 (R — H) fragments. The distortion is such as to adopt C2 symmetry, and is the consequence of Jahn-Teller distortion via mixing of the energy highest π2 orbital with an energetically low lying δ* orbital. The latter interaction is only operative if a symmetry breaking from C2v to C2 symmetry occurs. The importance of Jahn-Teller distortion on the biradical character in these systems is investigated by correlation calculations.
    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 123 (1990), S. 1653-1654 
    ISSN: 0009-2940
    Keywords: Iminophosphines ; s̰-Push-pull substitution ; Nitrogen inversion ; cis/trans Isomerization ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A combination of α-electron-withdrawing/-releasing substituents (push-pull substitution) at iminophosphanes considerably lengthen (shorten) the central PN bond as revealed by ab initio calculations on model geometries; they also stress the importance of the energy barrier to inversion at nitrogen.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 10
    ISSN: 0009-2940
    Keywords: 1,3-Diaza-2-phosphaallyllithium ; Calculations, ab initio ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: Monomer and Dimer 1,3-Diaza-2-phosphaallyllithium Complexes: Structures and Ambident Reactivity*Metallation of the NH-functional amino(imino)phosphanes Mes*NPNHR (R = CPh3, Ad, tBu) 1a-c yields the 1,3-diaza-2-phosphaallyllithium compounds 2a-c. The crystal structure shows an ether-stabilized monomer of 2a and a solvent-free dimer with an eight-membered ring in the case of 2b, c. The reaction of 2b with chlorodiphenylphosphane yields, dependent on the reaction conditions, (phosphanylamino)iminophosphane 3 or bis(imino)phosphanylphosphorane 4. The structural and reactivity is discussed on the basis of ab initio calculations.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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