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  • 1
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Inorganic chemistry 26 (1987), S. 2232-2234 
    ISSN: 1520-510X
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
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  • 2
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 98 (1993), S. 3627-3636 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The microwave spectrum of toluene⋅SO2 was observed with a pulsed beam Fourier-transform microwave spectrometer. The spectrum displays a-, b-, and c-dipole transitions. The transitions occur as doublets arising from the internal rotation of the methyl group. The transitions were assigned using the principal-axis method (PAM) internal rotation Hamiltonian with centrifugal distortions. Assuming a threefold symmetry for the internal rotation potential, the barrier height was determined as V3=83.236(2) cm−1. The torsional–rotational spectra of toluene-CD3⋅SO2 and toluene-d8⋅SO2 were also assigned. Additional small splittings of the c-dipole transitions for the normal species and toluene-CD3⋅SO2 suggest a reorientation tunneling motion of SO2 with respect to the aromatic plane. The moment of inertia data show that the two monomer units are separated by Rcm=3.370(1) A(ring), with the SO2 located above the aromatic ring. The projection of the C2 axis of SO2 on the aromatic plane makes an angle of τ=47.0(1)° with the C3 axis of toluene. The dipole moment of the complex is μT=1.869(27) D.
    Materialart: Digitale Medien
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  • 3
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 96 (1992), S. 1784-1792 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The rotational spectrum of the cyclopropane-sulfur dioxide complex was observed by Fourier transform microwave spectroscopy. The spectrum exhibited a- and c-dipole selection rules with the c-dipole transitions split into doublets of unequal intensity separated by about 150 kHz. The structure has Cs symmetry with the sulfur and carbon atoms all lying in the ac plane; the oxygen and hydrogen atoms straddle the plane. The sulfur dioxide plane is nearly parallel to a C–C bond edge. The distance from the center of mass of the SO2 to the C–C bond center is 3.295 A(ring). The dipole moment of the complex is 1.681(1) D, with components μa=0.815(1) D and μc=1.470(1) D. The splittings in the spectrum arise from an internal rotation of the cyclopropane subunit about its local C2 axis which lies nearly along the line connecting the centers of mass.
    Materialart: Digitale Medien
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  • 4
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 6947-6955 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: Thirty-three a- and c-dipole transitions of the acetylene–SO2 van der Waals complex have been observed by Fourier transform microwave spectroscopy and fit to rotational constants A=7176.804(2) MHz, B=2234.962(1) MHz, C=1796.160(1) MHz. The complex has Cs symmetry with the C2H2 and SO2 moieties both straddling an a–c symmetry plane (i.e., only the S atom lies in the plane). The two subunits are separated by a distance Rcm=3.430(1) A(ring) and the C2 axis of the SO2 is tilted 14.1(1)° from perpendicular to the Rcm vector, with the S atom closer to the C2H2. The dipole moment of the complex is 1.683(5) D. The deuterium nuclear quadrupole hyperfine structure was resolved for several transitions in both C2HD⋅SO2 and C2D2⋅SO2. A lower limit for the barrier to internal rotation of the C2H2 was estimated to be 150 cm−1 from the absence of tunneling splittings. The binding energy was estimated by the pseudo-diatomic model as 2.1 kcal/mol. A distributed multipole analysis was investigated to rationalize the structure and binding of the complex.
    Materialart: Digitale Medien
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  • 5
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 94 (1991), S. 6956-6963 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The microwave spectrum of (SO2)2 has been reinvestigated using a pulsed beam Fourier-transform microwave spectrometer. Several new a-type transitions for the normal species and the a-type spectra of eight isotopically substituted species were measured. The spectra indicate that the SO2 dimer undergoes a high-barrier tunneling motion. Based on the analysis used for (H2O)2 by Coudert and Hougen [J. Mol. Spectrosc. 130, 86 (1988)], the internal motion is identified as a geared interconversion motion similar to that displayed by (H2O)2. From the analysis of the moments of inertia of the various isotopic species, an ac plane of symmetry is established for the dimer and the tilt angles of the C2 axes of each subunit relative to the line joining their centers of mass were determined. From Stark effect measurements, μa was redetermined and μc was shown to be nearly zero. Electrostatic calculations using distributed multipoles were carried out to explore the structure of this dimer.
    Materialart: Digitale Medien
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  • 6
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The microwave spectra of the complex between ethylene and sulfur dioxide and nine of its isotopic species have been observed in a Fourier transform microwave spectrometer. The spectra exhibit a and c dipole selection rules; transitions of the normal species and several of the isotopically substituted species occur as tunneling doublets. The complex has a stacked structure with Cs symmetry; the C2H4 and SO2 moieties both straddle the mirror plane with the C2 axis of SO2 crossed at 90 ° to the carbon–carbon bond axis (i.e., only the S atom lies in the symmetry plane). The distance between the centers of mass (Rcm) of C2H4 and SO2 is 3.504(1) A(ring) and the deviation of their planes from perpendicular to Rcm is 21(2) ° and 12(2) °, respectively. The tunneling splittings arise from a rotation of the ethylene subunit in its molecular plane. The barrier to internal rotation is 30(2) cm−1. The dipole moment of the complex is 1.650(3)D. The deuterium nuclear quadrupole coupling constants for C2H3D⋅SO2 are χaa=−0.119(1) MHz, χbb=0.010(1) MHz, and χcc=0.109(1) MHz. The binding energy is estimated to be 490 cm−1 from the pseudo-diatomic approximation. A distributed multipole electrostatic model is explored to rationalize the structure and binding energies.
    Materialart: Digitale Medien
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  • 7
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 90 (1989), S. 6949-6955 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The complexes of PF3 with Ar and Kr, were studied by Fourier transform microwave spectroscopy. The force constants and amplitudes of vibration for the van der Waals modes of the complexes and the average moments of inertia and structural parameters were estimated from the centrifugal distortion constants. The distance (Rc.m. )ave between the rare-gas atom and the center of mass of PF3 is 3.959 A(ring) for the Ar complex and 4.077 A(ring) for Kr while the angle (θc.m. )ave between the Rc.m. vector and the C3 axis of the PF3 is 69.30° and 67.25°, respectively. The dipole moments of both complexes and of free PF3 were determined. The induced dipole components estimated for the rare gas using electric fields from ab initio calculations of PF3 agree with the experimental values for a conformation with the rare gas over a PF2 face. The PF2 face conformation is also consistent with the observed and ab initio estimates of the 83 Kr nuclear quadrupole coupling constant for the 83 Kr–PF3 species.
    Materialart: Digitale Medien
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  • 8
    Digitale Medien
    Digitale Medien
    College Park, Md. : American Institute of Physics (AIP)
    The Journal of Chemical Physics 97 (1992), S. 2996-3006 
    ISSN: 1089-7690
    Quelle: AIP Digital Archive
    Thema: Physik , Chemie und Pharmazie
    Notizen: The microwave spectrum of the benzene⋅SO2 complex was observed with a pulsed beam Fourier-transform microwave spectrometer. The spectrum was characteristic of an asymmetric-top with a- and c-dipole selection rules. In addition to the rigid-rotor spectrum, many other transitions were observed. The existence of a rich spectrum arose from torsional–rotation interactions from nearly free internal rotation of benzene about its C6 axis. Transitions from torsional states up to m=±5 were observed. The principal-axis method (PAM) internal rotation Hamiltonian with centrifugal distortion was used to assign the spectrum. Assuming six-fold symmetry for the internal rotation potential, the barrier height was determined as V6=0.277(2) cm−1. The spectrum of C6D6⋅SO2 was also assigned. Analysis of the moments of inertia indicated that the complex has a stacked structure. The distance Rcm separating the centers of mass of benzene and SO2, as well as the tilt angles of the benzene and SO2 planes relative to Rcm were determined. The values obtained were Rcm=3.485(1) A(ring), θC6H6=±12(1)° and θSO2=44(6)°. While SO2 is certainly tilted with the sulfur end towards benzene, the sign of the benzene tilt angle could not be unambiguously determined. The dipole moment of C6H6⋅SO2 was determined as μa=1.691(2) D, μc=1.179(2) D, and μT=2.061(2) D.
    Materialart: Digitale Medien
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  • 9
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    Journal of the American Chemical Society 109 (1987), S. 7222-7223 
    ISSN: 1520-5126
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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  • 10
    Digitale Medien
    Digitale Medien
    s.l. : American Chemical Society
    The @journal of physical chemistry 〈Washington, DC〉 90 (1986), S. 3092-3097 
    Quelle: ACS Legacy Archives
    Thema: Chemie und Pharmazie , Physik
    Materialart: Digitale Medien
    Bibliothek Standort Signatur Band/Heft/Jahr Verfügbarkeit
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