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  • Chemistry  (3)
  • ATOMIC AND MOLECULAR PHYSICS  (2)
  • Biochemistry and Biotechnology
  • General Chemistry
  • 1975-1979  (5)
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  • Chemistry  (3)
  • ATOMIC AND MOLECULAR PHYSICS  (2)
  • Biochemistry and Biotechnology
  • General Chemistry
  • Inorganic Chemistry  (3)
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  • 1
    Publication Date: 2011-08-17
    Description: It is shown through the use of transformation theory that unique semiclassical atomic scattering states which obey the asymptotic conditions of formal scattering theory can be derived by transforming 'nontraveling' atomic states, ie., states whose coordinate variables are referred to a stationary origin, to frames at rest with respect to the incoming or outgoing particles. An overview of the problem of properly defining such scattering states is presented. The operator which carries out the necessary transformation from inertial to noninertial frames is derived and its properties are discussed. The relation of this transformation operator to the 'translation factor' discussed in the literature is presented. The application of this operator to transform the time-dependent Schroedinger equation from an inertial to a noninertial frame is presented and shown to introduce new terms in the resulting equation. The implications of these new terms to scattering problems are discussed.
    Keywords: ATOMIC AND MOLECULAR PHYSICS
    Type: Physical Review A - General Physics; vol. 15
    Format: text
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  • 2
    Publication Date: 2011-08-17
    Description: Ab initio calculations are presented of inelastic energy loss and ionization phenomena associated with Ar(+)-Ar collisions at small distances of closest approach and for laboratory collision energies ranging from several keV to several hundred keV. Outer-shell excitations are handled statistically; inner-shell excitations are calculated from the viewpoint of quasidiabatic molecular orbital promotion. Auger electron yield, average state of ionization, and average inelastic energy loss are calculated per collision as a function of distance of closest approach of the collision partners for several laboratory collision energies. Average charge-state probabilities per collision partner are calculated as a function of the average inelastic energy loss per atom. It is shown that the structure in the data is due to the underlying structure in the inner-shell independent-electron quasimolecular promotion probabilities.
    Keywords: ATOMIC AND MOLECULAR PHYSICS
    Type: Physical Review A - General Physics; vol. 15
    Format: text
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  • 3
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 418 (1975), S. 243-246 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: P2J3 - a New Complex LigandP2J4 and Na2Cr(CO)5 react in benzene to the monomeric diamagnetic complex (CO)4CrP2J3. The 31P-nmr spectrum shows the presence of different bonded phosphorus atoms. The exchange of one iodine atom between the P atoms leads to a temperature dependent equilibrium with a symmetrical transition state. Triphenyl- and tricyclohexylphosphine react with (CO)4CrP2J3 to (CO)4CrPJ2 · P(C6H5)3 resp. (CO)4CrPJ2 · P(C6H11)3, probably of dimeric nature.
    Notes: P2J4 und Na2Cr(CO)5 reagieren in Benzol zu dem monomeren, diamagnetischen Komplex (CO)4CrP2J3. Das 31P-NMR-Spektrum zeigt die Anwesenheit unterschiedlich gebundener Phosphoratome. Der Austausch eines Jodatoms zwischen den P-Atomen führt zu einem temperaturabhängigen Gleichgewicht, in dem ein symmetrischer Übergangszustand auftritt. Triphenyl- und Tricyclohexylphosphin reagieren mit (CO)4CrP2J3 zu (CO)4 · P(C6H5)3 bzw. (CO)4 CrPJ2 · P(C6H11)3, wahrscheinlich dimerer Natur.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 415 (1975), S. 97-103 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Experiments on the Oxidative Addition of Thionylhalides to Transition Metal ComplexesThe complexes [(C6H5)3P]4Pd and [(C6H5)3P]2Ni(NO)Cl react with SOX2 to trans [(C6H5)3P]2PdX2 (X = Cl, Br) resp. to [(C6H5)3PX][NiX3] (X = Cl). Furthermore (C6H5)3PO and (C6H5)3PS are formed. In contrast SOCl2 is added oxidatively by [(C6H5)3P]2Ir(CO)Cl to the complex [(C6H5)3P]2Ir(CO)(Cl2)SOCl.
    Notes: Die Komplexe [(C6H5)3P]4Pd und [(C6H5)3P]2Ni(NO)Cl reagieren mit SOX2 zu trans-[(C6H5)3P]2PdX2 (X = Cl. Br) bzw. [(C6H5)3PX][NiX3] (X = Cl). Weiterhin bilden sich (C6H5)3PO und (C6H5)3PS. Im Gegensatz dazu wird SOCl2 durch [(C6H5)3P]2 Ir(CO)Cl oxydativ zu dem Komplex [(C6H5)3P]2 Ir(CO)(Cl2)SOCl addiert.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 432 (1977), S. 160-166 
    ISSN: 0044-2313
    Keywords: Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: The Use of Elemental Phosphorus as Ligand in Iron CarbonylsWhite phosphorus and Fe2(CO)9 react in benzene at room temperature to the monomeric diamagnetic complex [(CO)4Fe]3P4. The Mössbauer spectrum proves the presence of penta- and hexacoordinated Fe atoms in the ratio 1:2. The i.r. spectrum also suggests different bonded Fe(CO)4 groups. As the 31P-n.m.r. spectrum shows, the 4 P atoms are equivalent. It is supposed that one Fe(CO)4 group fluctuates between the P atoms. At 70°C P4 and Fe2(CO)9 react to the polymeric diphosphorous complex [(CO)3FeP2]n. Its synthesis succeeds also with Fe(CO)5 and P4 under u.v. irradiation. Additionally [(CO)4Fe]3P4 can be decomposed to [(CO)3FeP2]n by warming or irradiation. The Mössbauer spectrum of this complex shows equivalent Fe atoms with the coordination number 6. Possible structures are discussed.
    Notes: Weißer Phosphor und Fe2(CO)9 reagieren in Benzol bei Raumtemperatur zu dem monomeren, diamagnetischen Komplex [(CO)4Fe]3P4. Das Mössbauerspektrum belegt die Anwesenheit fünffach und sechsfach koordinierter Fe-Atome im Verhältnis 1:2. Auch das IR-Spektrum legt unterschiedlich gebundene Fe(CO)4-Gruppen nahe. Wie das 31P-NMR-Spektrum zeigt, sind alle 4 P-Atome äquivalent. Es wird angenommen, daß eine Fe(CO)4-Gruppe zwischen den P-Atomen fluktuiert. Bei 70°C setzen sich P4 und Fe2(CO)9 zu dem polymeren Diphosphorkomplex [(CO)3FeP2]n um. Dessen Synthese gelingt auch aus Fe(CO)5 und P4 unter UV-Bestrahlung. Ebenso kann [(CO)4Fe]3P4 durch Erwärmen oder Belichten in [(CO)3FeP2]n zersetzt werden. Das Mössbauerspektrum dieses Komplexes zeigt äquivalente Fe-Atome mit der Koordinationszahl 6. Mögliche Strukturen werden diskutiert.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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