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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of chemical & engineering data 15 (1970), S. 52-56 
    ISSN: 1520-5134
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 2
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of chemical & engineering data 7 (1962), S. 74-74 
    ISSN: 1520-5134
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 3
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of chemical & engineering data 7 (1962), S. 229-231 
    ISSN: 1520-5134
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology , Process Engineering, Biotechnology, Nutrition Technology
    Type of Medium: Electronic Resource
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  • 4
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 81 (1959), S. 5028-5030 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 5
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of the American Chemical Society 80 (1958), S. 4129-4132 
    ISSN: 1520-5126
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 6
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 91 (1989), S. 4909-4911 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The dissociation equilibrium AlBr=Al+Br was studied by effusion beam mass spectrometry over the range 1970 to 2260 K and the dissociation energy D00(AlBr) was derived as 4.41±0.06 eV. This value is in general agreement with other fragmentary thermochemical results, but it is lower than a value derived from a short extrapolation of vibrational levels in the excited 1π state, doubtless because of a potential maximum of about 0.22 eV in that state. A Birge–Sponer extrapolation of the ground state vibrational levels, when corrected for degree of ionicity, yields a D00 value in close accord with the experimental result, but an electrostatic model calculation falls short by 0.45 eV.
    Type of Medium: Electronic Resource
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  • 7
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 89 (1988), S. 5825-5828 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: Mass spectrometry was used to identify and to thermochemically characterize the gaseous fluorides RuF4 , RuF3 , RuF2 , and RuF generated by fluorination of Ru powder in a platinum effusion cell. Reaction enthalpies and bond dissociation energies were derived from equilibrium measurements involving these species, yielding the following results in kJ mol−1 : D°(F3 Ru–F)=361; D°(F2 Ru–F)=339; D°(FRu–F)=464; and D°(Ru–F)=402. The results show that the +4 oxidation state dominates the high temperature chemistry of the Ru–F system. Results are compared with the properties of the neighboring Mo–F system.
    Type of Medium: Electronic Resource
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  • 8
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 86 (1987), S. 2949-2954 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: High temperature gaseous equilibria involving the molecular species UBr, UBr2, UBr3, UBr4, and UBr5 were studied by mass spectrometry over wide temperature ranges; reaction enthalpy data were derived primarily from second-law analysis. From this information, the individual bond dissociation energies and the standard enthalpies of formation of the U–Br species were derived with an accuracy of about 8 kJ mol−1. The derived bond dissociation energies at 298 K in kJ mol−1 are as follows: D °(U–Br)=377; D °(BrU–Br)=435; D °(Br2U–Br)=430; D °(Br3U–Br)=348; and D °(Br4U–Br)=166. Trends in these values are similar to those found in the U–Cl system, but quite different from those of the U–F system. Absolute entropies evaluated from the equilibrium data indicate significant electronic contributions for the lighter species, decreasing markedly on approaching UBr5. Trends in the bond dissociation energies and electronic entropies of the fluorides, chlorides, and bromides are discussed.
    Type of Medium: Electronic Resource
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  • 9
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 1158-1164 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The gaseous species ThF, ThF2, ThF3, and ThF4 were generated in a heated effusion beam source, and were identified and characterized by mass spectrometry. An oxygen impurity in the sample also led to the characterization of the gaseous oxyfluoride ThOF. Reaction equilibria involving these species were studied over large temperature ranges, leading to the derivation of both enthalpy and entropy data for these species. The vapor pressure and vaporization thermodynamics of ThF4(s) were also determined. Derived bond dissociation energies in ThF4 oscillate about a mean value of 670±25 kJ mol−1, with a distinct pattern similar to other metal tetrafluorides. Absolute entropies calculated from the equilibrium data indicate moderate electronic level contributions for the odd-electron molecules ThF and ThF3, but not for the even-electron species ThF2 and ThF4. Furthermore, the experimental entropy of ThF4 is compatible with a regular tetrahedral configuration, rather than the distorted configuration of lower symmetry found earlier for UF4 and UCl4. Thermochemical properties of the Th–F species are presented and the comparison with the corresponding uranium fluorides is discussed.
    Type of Medium: Electronic Resource
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  • 10
    Electronic Resource
    Electronic Resource
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 93 (1990), S. 5983-5989 
    ISSN: 1089-7690
    Source: AIP Digital Archive
    Topics: Physics , Chemistry and Pharmacology
    Notes: The sublimation of ThBr4(s) was studied by the torsion-effusion and mass spectrometric methods in the range 600–750 K; only monomeric ThBr4 vapor was observed, and the pertinent thermodynamic parameters were derived. The gaseous lower-valent species ThBr3, ThBr2, and ThBr were identified in the bromination of Th(s) at 1500 to 2000 K, and several reaction equilibria involving these species were studied by mass spectrometry over wide temperature ranges for second law analysis. Reaction enthalpies, bond dissociation energies, and standard enthalpies of formation were derived from the results. Unlike ThF4 and ThCl4, the sublimation entropy indicates that ThBr4 may have a distorted tetrahedral structure. Bond dissociation energies and related thermodynamic properties are discussed and compared with values in other thorium and uranium halides.
    Type of Medium: Electronic Resource
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