Microwave and ab initio studies of rare gas-methane van der Waals complexes

被引:19
作者
Liu, YQ [1 ]
Jäger, W [1 ]
机构
[1] Univ Alberta, Dept Chem, Edmonton, AB T6G 2G2, Canada
关键词
D O I
10.1063/1.1691743
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
Rotational spectra of the weakly bound Kr-methane van der Waals complex were recorded using a pulsed molecular beam Fourier transform microwave spectrometer in the range from 3.5 to 18 GHz. Spectra of 25 isotopomers of Kr-methane were assigned and analyzed. For isotopomers containing CH4, (CH4)-C-13, and CD4, two sets of transitions with K=0 and one with K=1 were recorded, correlating to the j=0, 1, and 2 rotational levels of free methane, respectively (j is the rotational angular momentum quantum number of the methane monomer). For isotopomers containing CH3D and CHD3, two K=0 components were recorded, correlating to the j(k)=0(0) and 1(1) rotational levels of free methane (k corresponds to the projection of j onto the C-3 axis of CH3D and CHD3). The obtained spectroscopic results were used to derive van der Waals bond distance R, van der Waals stretching frequency nu(s), and the corresponding stretching force constant k(s). Nuclear spin statistical weights of individual states were obtained from molecular symmetry group analyses and were compared with the observed relative transition intensities. The tentatively assigned j=2 transitions were more intense than predicted from symmetry considerations. This is attributed to a relatively large effective dipole moment of this state, supported by ab initio dipole moment calculations. Ab initio potential energy calculations of Kr-CH4 and Ar-CH4 were done at the coupled cluster level of theory, with single and double excitations and perturbative inclusion of triple excitations, using the aug-cc-pVTZ basis set supplemented with bond functions. The theoretical results show that the angular dynamics of the dimer does not change significantly when the binding partner of methane changes from Ar to Kr. The dipole moment of Ar-CH4 was calculated at various configurations, providing a qualitative explanation for the unsuccessful spectral searches for rotational transitions of Ar-CH4. (C) 2004 American Institute of Physics.
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页码:9047 / 9059
页数:13
相关论文
共 64 条
[1]   THE PAIRWISE INTERACTION OF METHANE AND HYDROGEN BROMIDE - PROPERTIES OF THE WEAKLY BOUND DIMER CH4...HBR FROM MICROWAVE SPECTROSCOPY [J].
ATKINS, MJ ;
LEGON, AC ;
WALLWORK, AL .
CHEMICAL PHYSICS LETTERS, 1992, 192 (04) :368-374
[2]   FABRY-PEROT CAVITY PULSED FOURIER-TRANSFORM MICROWAVE SPECTROMETER WITH A PULSED NOZZLE PARTICLE SOURCE [J].
BALLE, TJ ;
FLYGARE, WH .
REVIEW OF SCIENTIFIC INSTRUMENTS, 1981, 52 (01) :33-45
[3]   FAR INFRARED COLLISION-INDUCED ABSORPTION IN GASEOUS METHANE .2. DETERMINATION OF OCTUPOLE AND HEXADECAPOLE MOMENTS [J].
BIRNBAUM, G ;
COHEN, ER .
JOURNAL OF CHEMICAL PHYSICS, 1975, 62 (09) :3807-3812
[4]   CALCULATION OF SMALL MOLECULAR INTERACTIONS BY DIFFERENCES OF SEPARATE TOTAL ENERGIES - SOME PROCEDURES WITH REDUCED ERRORS [J].
BOYS, SF ;
BERNARDI, F .
MOLECULAR PHYSICS, 1970, 19 (04) :553-&
[5]  
BROOKS MD, 1994, J CHEM PHYS, V100, P7051
[6]  
Bunker P. R., 1998, MOL SYMMETRY SPECTRO
[7]   ON THE ROLE OF BOND FUNCTIONS IN INTERACTION ENERGY CALCULATIONS - AR-CENTER-DOT-CENTER-DOT-CENTER-DOT-HCL, AR-CENTER-DOT-CENTER-DOT-CENTER-DOT-H2O, (HF)(2) [J].
BURCL, R ;
CHALASINSKI, G ;
BUKOWSKI, R ;
SZCZESNIAK, MM .
JOURNAL OF CHEMICAL PHYSICS, 1995, 103 (04) :1498-1507
[8]   THE ROTATIONAL SPECTRUM, NUCLEAR SPIN-SPIN COUPLING, NUCLEAR-QUADRUPOLE COUPLING, AND MOLECULAR-STRUCTURE OF KRHF [J].
BUXTON, LW ;
CAMPBELL, EJ ;
KEENAN, MR ;
BALLE, TJ ;
FLYGARE, WH .
CHEMICAL PHYSICS, 1981, 54 (02) :173-181
[9]   KR-83 AND XE-131 NUCLEAR-QUADRUPOLE COUPLING AND QUADRUPOLAR SHIELDING IN KRHCL AND XEDCL [J].
CAMPBELL, EJ ;
BUXTON, LW ;
KEENAN, MR ;
FLYGARE, WH .
PHYSICAL REVIEW A, 1981, 24 (02) :812-821
[10]   KR-83 NUCLEAR-QUADRUPOLE COUPLING, MICROWAVE-SPECTRUM, AND STRUCTURE OF KRHCN [J].
CAMPBELL, EJ ;
BUXTON, LW ;
LEGON, AC .
JOURNAL OF CHEMICAL PHYSICS, 1983, 78 (06) :3483-3493