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  • 1
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 40 (1991), S. 829-846 
    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: Ab initio averaged relativistic effective core potentials (AREP), spin-orbit (SO) operators, and valence basis sets are reported for the elements Fr through Pu in the form of expansions in Gaussian-type functions. Gaussian basis sets with expansion coefficients for the low-energy states of each atom are given. Atomic orbital energies calculated under the j-j coupling scheme within the self-consistent field approximation and employing the AREP'S in their unaveraged form (REP'S) agree to within 10% of orbital energies due to numerical all-electron Dirac-Fock calculations. The accuracy of the AREP'S and so operators is also shown to be good through comparisons of calculated so splitting energies with all-electron Dirac-Fock results.
    Additional Material: 4 Tab.
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 41 (1992), S. 733-747 
    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: Hartree-Fock-Roothaan studies are reported for low-lying electronic states of metallic beryllium as modeled by a moiety of 135 beryllium atoms. The system corresponds to 16 coordination shells of a central Be with internuclear separations derived from the lattice constants of the bulk metal. The calculations become tractable by use of the full D3h symmetry of the system at both the integrals and self-consistent-field stages and by employing ab initio effective potentials for the 1s electrons of each beryllium atom. Ionization potentials, binding energies, orbital energies, electric field gradients, nuclear-electrostatic potentials, diamagnetic shielding constants, second moments, and Mulliken populations are calculated for selected electronic states. The calculated ionization potential for the lowest state agrees to within 10% of the experimental bulk work function. A density-of-states analysis for that state is reported and compared with band structure calculations.
    Additional Material: 5 Ill.
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 55 (1995), S. 393-410 
    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: Ab initio self-consistent-field calculations are reported for electronic states of beryllium clusters comprised of 93, 105, 111, and 123 atoms. The respective clusters correspond to coordination shells 12-15 of a central Be atom with internuclear separations derived from the lattice constants of the bulk metal. Ab initio effective core potentials have been employed to replace the 1 s electrons, thereby reducing the complexity of the calculations. In addition, use of the full D3h point group symmetry of the clusters results in a substantial reduction of the numbers of two-electron integrals that must be computed and processed. Binding energies, orbital energies, electric field gradient, nuclear-electrostatic potential, diamagnetic shielding constant, second moments, and Mulliken populations are calculated for selected electronic states. Calculated binding energies when compared among the different clusters as well as to smaller and larger fragments from earlier studies provide evidence for the onset of convergence to the Hartree-Fock limit of the bulk. Lowest-state ionization potentials are consistently above and agree to within 14% of the experimental workfunction. The net charge on the central beryllium atom decreases toward zero. The variability of observed bulklike behavior for the different properties indicates that the transition between cluster and bulklike behavior is not sharp and depends on the quantity of interest. © 1995 John Wiley & Sons, Inc.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    New York, NY : Wiley-Blackwell
    International Journal of Quantum Chemistry 38 (1990), S. 225-240 
    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: Ab initio self-consistent field calculations are reported for electronic states of beryllium clusters comprised of 81 and 87 atoms. The clusters correspond to the tenth and eleventh coordination shells of a central Be with internuclear separations derived from the lattice constants of the bulk metal. Ab initio effective core potentials have been employed to replace the 1s electrons, therey reducing the complexity of the calculations. In addition, the use of the full D3h point group symmetry of the clusters results in a substantial reduction of the number of two-electron integrals that must be computed and processed. Binding energies, orbital energies, electric field gradient, nuclear-electrostatic potential, diamagnetic shielding constant, second moments, and Mulliken populations are calculated for selected electronic states. Systematic trends toward bulk behavior with increasing cluster size, as found in earlier cluster studies, continue to appear for the electric field gradient and quadrupole moment of Be81. Anomalous behavior, however, is observed in Be87. This is attributed to distortional effects due to the addition of atoms in planes above and below the Be81 cluster along the principal axis of symmetry.
    Additional Material: 4 Ill.
    Type of Medium: Electronic Resource
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  • 5
    ISSN: 0044-2313
    Keywords: Oxoniobates ; manganese oxoniobate, MnNb2O6 ; chemical vapour transport ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions on the Thermal Behaviour of Oxoniobates of the Transition Metals. II. The Chemical Vapour Transport of MnNb2O6 with Cl2 or NH4Cl. Experiments and CalculationsCrystals of MnNb2O6 were obtained by chemical transport reactions in a temperature gradient (1020°C → 960 °C) using Cl2 (added as PtCl2) or NH4Cl as transport agent. As a result of thermodynamic calculations the evaporation and deposition of MnNb2O6 in the presence of Cl2 can be expressed by the endothermic equilibrium (1).The endothermic reaction (2) is responsible for the migration of MnNb2O6 if NH4Cl is used as transport agent.Assuming ΔH°298(MnNb2O6, s) = -567.6 kcal/mol a satisfying agreement between thermodynamic calculations and experimental results can be reached.
    Notes: Kristalle von MnNb2O6 ließen sich mit Cl2 (Zusatz von PtCl2) oder NH4Cl als Transportmittel im Temperaturgefälle (1020°C → 960° C) abscheiden. Wie thermodynamische Modellrechnungen zeigen, ist für den Transport mit Cl2 das endotherme Gleichgewicht (1) bestimmend.Bei Zugabe von NH4Cl ist die endotherme Reaktion (2) für die Wanderung von MnNb2O6 im Temperaturgradienten verantwortlich.Experimente und Modellrechnungen stimmen gut überein, wenn δBH°298(MnNb2O6, f) zu -567, 6 kcal/mol abgeschätzt wird.
    Additional Material: 1 Ill.
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 612 (1992), S. 63-71 
    ISSN: 0044-2313
    Keywords: Oxoniobates ; cobalt niobate ; chemical vapour transport ; thermodynamical calculations ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions on the Thermal Behaviour of Oxoniobates of the Transition Metals. IV The Chemical Vapour Transport of CoNb2O6 with Cl2, NH4Cl, or HgCl2. Experiments and CalculationsWell shaped crystals of CoNb2O6 were obtained by CVT using Cl2 (added as PtCl2), NH4Cl or HgCl2 as transport agents (1020°C → 960°C). As a result of thermodynamic calculations the evaporation and deposition of CoNb2O6 in the presence of Cl2 can be expressed by the heterogenous endothermic equilibrium (1). The endothermic reaction (2) is responsible for the CVT of CoNb2O6 if NH4Cl is used as transport agent: The unfavourable site of the equilibrium (3) causes the small transport effect using HgCl2 as transport agent. Assuming ΔBH°298(CoNb2O6,s) = -524.7 kcal/mol a satisfying agreement between thermodynamical calculation and experimental results can be reached.
    Notes: Gut ausgebildete Kristalle von CoNb2O6 ließen sich mit Cl2 (Zusatz von PtCl2), NH4Cl oder HgCl2 als Transportmittel im Temperaturgefälle (1020°C → 960°C) erhalten. Mit Cl2 sowie mit NH4Cl konnten hohe, mit HgCl2 dagegen nur geringe Transportraten erzielt werden.Thermodynamische Modellrechnungen zeigen, daß der Transport in Gegenwart von Cl2 durch das heterogene endotherme Gleichgewicht (1) gut beschrieben werden kann. Bei Zugabe von NH4Cl ist die endotherme Reaktion (2) für die Wanderung von CoNb2O6 im Temperaturgradienten verantwortlich.Infolge der ungünstigen Lage des Gleichgewichts (3) ist HgCl2 als Transportmittel weniger geeignet.Experimente und Modellrechnungen zeigen eine gute Übereinstimmung, wenn ΔBH°298(CoNb2O6,f) zu - 524,7 kcal/mol abgeschätzt wird.
    Additional Material: 8 Ill.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    Weinheim : Wiley-Blackwell
    Zeitschrift für anorganische Chemie 614 (1992), S. 47-52 
    ISSN: 0044-2313
    Keywords: Oxoniobates ; nickel oxoniobate, NiNb2O6 ; chemical vapour transport ; Chemistry ; Inorganic Chemistry
    Source: Wiley InterScience Backfile Collection 1832-2000
    Topics: Chemistry and Pharmacology
    Description / Table of Contents: Contributions on the Thermal Behaviour of Oxoniobates of the Transition Metals. V. Chemical Vapour Transport of NiNb2O6 with Cl2 or NH4Cl. Experiments and CalculationsWell shaped crystals of NiNb2O6 were obtained by CVT using Cl2 (added as PtCl2) or NH4Cl as transport agents (1020°C → 960°C). As a result of thermodynamic calculations the migration of NiNb2O6 in the temperature gradient in the presence of Cl2 can be expressed by the heterogenous endothermic equilibrium (1).\documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm NiNb}_{\rm 2} {\rm O}_{{\rm 6, s}} + 4{\rm Cl}_{{\rm 2, g}} = {\rm NiCl}_{{\rm 2, g}} + 2{\rm NbOCl}_{\rm 3} + {\rm 2O}_{{\rm 2, g}} {\rm \qquad (1)} $$\end{document}Assuming ΔBH298o(NiNb2O6, s) = -524.4 kcal/mol a satisfying agreement between thermodynamical calculation and experimental results can be reached.NH4Cl is less suitable as transport agent, because Ni2+ is partly reduced to the metal by NH3. The additionally H2O produced by this reduction leads to a less favourable equilibrium position of (2) and to low deposition rates.\documentclass{article}\pagestyle{empty}\begin{document}$${\rm NiNb}_{\rm 2} {\rm O}_{{\rm 6, s}} + 8{\rm HCl}_{\rm g} = {\rm NiCl}_{{\rm 2, g}} + 2{\rm NbOCl}_{{\rm 3, g}} + {\rm 2H}_{\rm 2} {\rm O}_{\rm g} {\rm \qquad (2)} $$\end{document}.
    Notes: Gut ausgebildete Kristalle von NiNb2O6 ließen sich mit cl2 (Zusatz von PtCl2) oder NH4Cl als Transportmittel im Temperaturgefälle (1020°C→960°C) abscheiden. Begleitende thermodynamische Modellrechnungen zeigen, daß der Transport bei Zugabe von Cl2 durch das heterogene endotherme Gleichgewicht (1)\documentclass{article}\pagestyle{empty}\begin{document}$$ {\rm NiNb}_{\rm 2} {\rm O}_{{\rm 6, f}} + 4{\rm Cl}_{{\rm 2, g}} = {\rm NiCl}_{{\rm 2, g}} + 2{\rm NbOCl}_{\rm 3} + {\rm 2O}_{{\rm 2, g}} {\rm \qquad (1)} $$\end{document}beschrieben werden kann. Experimente und Modellrechnungen sind in guter Übereinstimmung, wenn ΔBH298o(NiNb2O6, f) zu -524,4 kcal/mol abgeschätzt wird.NH4Cl ist als Transportmittel wenig geeignet, da Ni2+ zum Teil durch NH3 zum Metall reduziert wird; dadurch zusätzlich entstehendes H2O führt zu einer ungünstigen Gleichgewichtslage der Transportreaktion (2) und dementsprechend niedrigen Transportraten.\documentclass{article}\pagestyle{empty}\begin{document}$${\rm NiNb}_{\rm 2} {\rm O}_{{\rm 6, f}} + 8{\rm HCl}_{\rm g} = {\rm NiCl}_{{\rm 2, g}} + 2{\rm NbOCl}_{{\rm 3, g}} + {\rm 2H}_{\rm 2} {\rm O}_{\rm g} {\rm \qquad (2)} $$\end{document}.
    Additional Material: 3 Ill.
    Type of Medium: Electronic Resource
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