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  • Articles  (32)
  • Inorganic Chemistry  (29)
  • Atomic, Molecular and Optical Physics  (3)
  • 42.75
  • Surface physics, nanoscale physics, low-dimensional systems
  • 1970-1974  (15)
  • 1915-1919  (17)
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  • Articles  (32)
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  • 1
    Electronic Resource
    Electronic Resource
    Padé approximants to physical properties via inner projections (1973)
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 7 (1973), S. 133-134 
    Details
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/qua.560070114
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  • 2
    Electronic Resource
    Electronic Resource
    Molecular-orbital calculations on transition metal complexes, charge-transfer spectra and the sequence of metal and ligand orbitals (1972)
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 6 (1972), S. 859-880 
    Details
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: An outline is given of a semi-empirical scheme for molecular-orbital calculations on transition-metal complexes according to a revised INDO procedure. To judge the reliability of the results of the calculations, the charge-transfer transitions of a number of complexes have been calculated and compared with experimental data. Both for the excitation energies and for the oscillator strengths the agreement is very satisfactory. With respect to the sequence of occupied metal and ligand orbitals it was found that for closed-shell d6 and d8 systems the molecular orbitals which are mainly composed of metal d orbitals have a lower energy than the orbitals built up from ligand p orbitals. Calculations by the extended Hückel method and other similar schemes give the d orbitals as the highest occupied ones as a result of a bad approximation of the diagonal elements of the Fock matrix. The consequences for the interpretation of photo-electron spectra of transition-metal complexes are discussed.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/qua.560060506
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  • 3
    Electronic Resource
    Electronic Resource
    Molecular integrals over generalized gaussian basis sets (1974)
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 8 (1974), S. 179-191 
    Details
    ISSN: 0020-7608
    Keywords: Computational Chemistry and Molecular Modeling ; Atomic, Molecular and Optical Physics
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Notes: A method is given for obtaining the common molecular integrals over generalized gaussian functions: \documentclass{article}\pagestyle{empty}\begin{document}$$ \chi_i = x^{\lambda_i}_i \exp \big\{ - \big(\alpha_i x^2_i + \alpha^{\prime}_i x^{\prime 2}_i + \alpha^{\prime\prime}_i x^{\prime\prime 2}_i\big)\big\} $$\end{document}The present algorithms are expected to be more efficient than those given in earlier work by the same author.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/qua.560080205
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  • 4
    Electronic Resource
    Electronic Resource
    Notiz über ein einfaches Verfahren zur Darstellung von 3,4-Bismethylencyclobuten (1973)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 106 (1973), S. 3461-3462 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19731061031
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  • 5
    Electronic Resource
    Electronic Resource
    [2.2]Paracyclophane durch Addition von Acetylenderivaten an 1,2,4,5-Hexatetraen (1974)
    Weinheim : Wiley-Blackwell
    Berichte der deutschen chemischen Gesellschaft 107 (1974), S. 1891-1902 
    Details
    ISSN: 0009-2940
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Preparation of [2.2]Paracyclophanes by Addition of Acetylene Derivatives to 1,2,4,5-HexatetraeneThe tetrasubstituted [2.2]paracyclophanes 4a - e are formed by cycloaddition of the symmetrical acetylene derivatives 2a - e to 1,2,4,5-hexatetraene (1), and their constitution and configuration is established by spectroscopic methods, degradation and pyrolysis experiments. The tetramethyl ester 4a is reduced to the tetraalcohol 4g, and the tetracarboxylic acid 4c is converted to the bisanhydride 4f and [2.2] paracyclophanes (4h), respectively. All possible disubstituted [2.2] paracyclophanes 6 are obtained when methyl propiolate (5a) is added to. 1, whereas further symmetrical and unsymmetrical acetylene derivatives do not react with 1.
    Notes: Die tetrasubstituierten [2.2]Paracyclophane 4a - e werden durch Cycloaddition der symmetrischen Acetylenderivate 2a - e an 1,2,4,5-Hexatetraen (1) dargestellt und ihre Konstitution und Konfiguration durch spektroskopische Methoden. Abbau- und Pyrolyseversuche bewiesen. Der Tetramethylester 4a wird zum Tetraalkohol 4g reduziert und die Tetracarbonsäure 4c in das Bisanhydrid 4f bzw. [2.2] Paracyclophan (4h) übergeführt. Bei der Anlagerung von Propiolsäure-methylester (5a) an 1 werden alle isomeren disubstituierten [2.2]paracyclophanes 6 erhalten. Weitere symmetrische und unsymmetrische Acetylenderivate reagieren nicht mit 1.
    Additional Material: 3 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/cber.19741070613
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  • 6
    Electronic Resource
    Electronic Resource
    Kristallisationsvorgänge in ternären Systemen aus Chloriden von einwertigen und zweiwertigen Metallen. I (1917)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 99 (1917), S. 50-66 
    Details
    ISSN: 0863-1786
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Additional Material: 11 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19170990107
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  • 7
    Electronic Resource
    Electronic Resource
    Metallkomplexe mit anionischen Liganden von Elementen der 4. Hauptgruppe. IV. Homogene und heterogene Übergangsmetall(0)-Komplexe der Liganden Dichlorbrom-, Dibromchlor- und Tribromstannid (1974)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 405 (1974), S. 95-100 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Metal Complexes with Anionic Ligands of Elements of the Main Group IV. IV. Homogenous and Heterogenous Transition Metal Complexes of the Dichlorobromo-, Dibromochloro-, and Tribromostannide LigandsMonosubstituted complexes of the type [M(CO)5SnBr3-nCln]- are formed if the hexacarbonyls of chromium, molybdenum, and tungsten are reacted with halogenostannide ions SnBr3-nCln- (n = 0, 1, 2). The reactions of dibenzene chromium and this stannide ions yield homogenous hexakis(trihalogenostannide)chromate(0) complexes [Cr(SnBr3-nCln)6]6- (n = 1, 2). Both types of chromate(0) ions are isolated as salts with the cation [N(C2H5)4]+. The behaviour of SnBr3-nCln- (n = 0-3) as ligands is discussed, the i. r. spectra of their metalcarbonyl derivatives are reported.
    Notes: SnBr3-nCln--Ionen (n = 0-2) reagieren mit den Hexacarbonylen von Chrom, Molybdän und Wolfram zu den anionischen Monosubstitutionsprodukten [M(CO)5SnBR3-nCln]-. Sie warden den analogen Trichlorstannido-carbonylmetallat(0)-Komplexen gegenübergestellt. Die homogenen Hexakis(halogenstannido)-chromat(0)- Komplexe [Cr(SnBr3-nCln)]6- (n = 1, 2) bilden sich als Tetraäthylammoniumsalze bei den Umsetzungen mit Dibenzolchrom. Das komplexchemische Verhalten von Trihalogenstannido-Liganden wird diskutiert, die Infrarot-Spektren warden mitgeteilt.
    Additional Material: 1 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19744050110
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  • 8
    Electronic Resource
    Electronic Resource
    Zur Chemie in Schmelzlösungen. VI. Präparative Darstellung von Übergangsmetall-Manganaten in Salzschmelzen (1971)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 386 (1971), S. 288-296 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Transition metal manganates with spinel structure are prepared by joint decomposition of MnSO4 and MeSO4 (Me = Co, Zn, Cu, Ni) about 1000°C in the fused sodium potassium sulfate eutectic. Complete series of mixed oxides MexMn3-xO4+γ have been observed within the limits: Co: 0 〈 x 〈 3; Zn: 0 〈 x 〈 1,5; Cu: 0 〈 x 〈 1; Ni: 0 〈 x 〈 1. The compounds Co2.2Mn0.8O4 to Co1.9Mn1.1O4, ZnMn2O4, Zn1.25Mn1.75O4 may be prepared in high yield and as single-phase compounds. The oxygen deficit of the manganates has the limits 0,02 〉 γ 〉 -0.08. The lattice constants of the spinels are compared with literature dates.
    Notes: Durch gemeinsame Zersetzung von MnSO4 und MeSO4 (Me = Co, Zn, Cu, Ni) in der eutektischen K—Na-Sulfat-Schmelze bei Temperaturen um 1000°C sind grobkristalline Übergangsmetall-Manganate darstellbar. Dabei wurden lückenlose Reihen im Spinellgitter kristallisierender Mischoxide MexMn3-xO4+γ in folgenden Grenzen erhalten: Co: 0 〈 x 〈 3; Zn: 0 〈 x 〈 1,5; Cu: 0 〈 x 〈 1; Ni: 0 〈 x 〈 1. Folgende Verbindungen lassen sich mit definierter Zusammensetzung in guter Ausbeute darstellen: Co2,2Mn0,8O4 bis Co1,9Mn1,1O4, ZnMn2O4 und Zn1,25Mn1,75O4. Das Sauerstoffdefizit der Manganate lag zwischen 0,02 〉 γ 〉 -0,08. Die Gitterkonstanten der Spinelle werden mit Literaturangaben verglichen.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19713860307
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  • 9
    Electronic Resource
    Electronic Resource
    Relationship between V4+ and Mo6+ Contents in V2O5 doped with MoO3 (1973)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 399 (1973), S. 170-174 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Zusammenhang zwischen der V4+ und Mo6+-Konzentration in mit MoO3 dotiertem V2O5Der V4+-Gehalt von mit MoO3 dotiertem V2O5 wird durch spektrophotometrische Messung bestimmt. Der Einfluß des Sauerstoffdruckes wird untersucht. Bis zu ungefähr 3,5 At.-% Mo/(Mo+V) ist der V4+-Gehalt gleich dem Mo6+-Gehalt für an der Luft gesinterte Proben. Bei Zunahme des Sauerstoffdrucks erfolgt eine Abnahme des V4+-Gehalts für die mit 5, 10 und 33 At.-% Mo dotierten Proben.
    Notes: The V4+ content in V2O5 doped with MoO3 is measured by a spectroscopic method. The influence of the oxygen pressure is also considered. Up to roughly 3.5 at.-% Mo/(Mo+V) the V4+ fraction is equal to the Mo6+ fraction for samples sintered in air. Increase of PO2 gives a decrease in the measured values of the V4+ fraction for the 5, 10 and 33 at.-% Mo-doped samples.
    Additional Material: 2 Ill.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19733990205
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  • 10
    Electronic Resource
    Electronic Resource
    Fluoraustauschreaktionen an Metalltrifluorphosphin-Komplexen. IV. Zur Kenntnis der Reaktionen von Nitrosyl-trifluorphosphin-Komplexen von Eisen und Kobalt mit Alkoholat- und Hydroxid-Ionen (1973)
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 402 (1973), S. 16-28 
    Details
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Fluorine Exchange in Trifltiorophosphinemetal Complexes. IVThe Reaction of Nitrosyltrifluorophosphirie Complexes of Iron and Cobalt with Alkoxid- and Hydroxid-IonsFe(NO)2(PF3)2, 1, and Co(NO)(PF3)3, 2, react with alcoxids and phenoxid by a complete F/OR-exchange to the corresponding phosphite complexes Fe(NO)2P(OR)3)2 and Co(NO)(P(OR)3)3, (R = CH3, C2H5, n-C3H7, i-C3H7, n-C4H9, C6H5), 3-13. The nitrosyltrifluorophosphine complexes 1 and 2 change only one or two fluorine atoms against OH--ions to give difluorophosphito complexes: The reaction of 1 with a diisopropylamine/water mixture yields the bis(difluorophosphito) complex [Fe(NO)2(PF2O)2]2-, 15, with 2 under identical conditions [Co(NO)(PF3)2 PF2O]-, 14, is obtained; 1 and 2 react with Ba(OH)2 in THF to give [Fe(NO)2(PF3)PF2O]- resp. 14, the latter reacts under harder conditions partially to [Co(NO)(PF3)(PF2O)2]2-. These difluorophosphito complexes, which are isolated as salts with the cations [(i-C3H7)2NH2]+ and Ba2+, can be alkylated to the corresponding difluorethoxyphosphine derivates of 1 and 2, Fe(NO)2 (PF3)2-n(PF2OC2H5)n (n = 1,2) and Co(NO)(PF3)2PF2OC2H5. All compounds are characterised by IR and mass spectra.
    Notes: Fe(NO)2(PF3)2, 1, und Co(NO)(PF3)3, 2, tauschen bei der Umsetzung mit Alkoholaten und Phenolat sämtliche Fluoratome gegen RO-Gruppen aus unter Bildung der entsprechenden Phosphitkomplexe Fe(NO)2(P(OR)3)2 bzw. Co(NO)(P(OR)3)3 (R = CH3, C2H5, n-C3H7, i-C3H7, n-C4H9, C6H5), 3-13. Beide Nitrosyl-trifluorphosphin-Komplexe gehen maximal nur einen zweifachen F/OH-Austausch zu Difluorphosphito-Komplexen ein: In einem Diisopropylamin/Wasser-Gemisch liefert 1 den Bis(difluorphosphito)-Komplex[Fe(NO)2(PF2O)2] 2-, 15, 2 unter gleichen Bedingungen [Co(NO)(PF3)2PF2O- 14; die Umsetzung von 1 und 2 mit Ba(OH)2 in Tetrahydrofuran führt zu [Fe(NO)2(PF3) PF2O]- bzw. 14, welches sich unter drastischen Bedingungen teilweise zu [Co(NO)(PF3) (PF2O)2]2- umsetzt. Diese Difluorphosphito-Komplexe, die als Salze mit den Kationen [(i-C3H7)2NH2]+ bzw. Ba2+ anfallen, können zu den entsprechenden Difluoräthoxy-Derivaten von 1 und 2, Fe(NO)2 (PF3)2-n(PF2OC2H5)n (n = 1, 2) bzw. Co(NO)(PF3)2PF2OC2H5, alkyliert werden. Sämtliche Verbindungen werden anhand der IR- und Massenspektren charakterisiert.
    Additional Material: 8 Tab.
    Type of Medium: Electronic Resource
    URL: http://dx.doi.org/10.1002/zaac.19734020103
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