THE STRUCTURE AND INTERNAL DYNAMICS OF CO-CO-H2O DETERMINED BY MICROWAVE SPECTROSCOPY

被引:13
作者
PETERSON, KI
SUENRAM, RD
LOVAS, FJ
机构
[1] UNIV RHODE ISL, DEPT CHEM, KINGSTON, RI 02881 USA
[2] NIST, DIV MOLEC PHYS, GAITHERSBURG, MD 20899 USA
关键词
D O I
10.1063/1.468981
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
The rotational spectra of CO-CO-H2O, CO-CO-HDO, 13CO-CO-H2O, and 13CO-13CO-H 2O have been measured using a pulsed-molecular-beam Fabry-Perot Fourier-transform microwave spectrometer. The complex exhibits internal motion involving an exchange of the CO subunits as well as an hydrogen exchange. In the normal species this is indicated in the spectrum by transition doublets separated by a few hundred kHz and an effective shift of alternating transitions which prevents a good semirigid rotor fit. The other isotopically substituted complexes have spectra in which the transitions are either singlet, doublet or quartets depending on the appropriate spin weights or because of dampening of the internal motion. All the spectra are mutually consistent with a tunneling path with four isoenergetic states. By treating the tunneling frequency of the CO interchange as a vibrational frequency, the rotational constants of two internal rotor states and a tunneling frequency could be determined. The tunneling frequency in CO-CO-H2O is 372 kHz and the ground state rotational constants are A = 4294.683(70) MHz, B = 1685.399(35) MHz, C = 1205.532(35) MHz. The tunneling frequency corresponding to the hydrogen exchange is not determined but the observed transition splittings are comparable to those found for other van der Waals complexes containing a water subunit. The dipole moments determined for CO-CO-HDO are μa=4.790(87) ×10-30 C m [1.436(26) D], μb = 1.79(12)×10-30 C m [0.533(35) D], and μc=1.10(37) ×10-30 C m [0.33(11) D]. The general structure of the complex is found to be cyclic. The CO-CO configuration is approximately T-shaped with the carbon atom of one subunit directed toward the molecular axis of the other subunit. The H2O subunit has a hydrogen atom directed toward the CO subunits but not in the expected linear hydrogen bonded configuration. The uncertainties given in parentheses are one standard deviation. © 1995 American Institute of Physics.
引用
收藏
页码:7807 / 7816
页数:10
相关论文
共 29 条
[1]   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
[2]  
Bunker P. R., 2006, MOL SYMMETRY SPECTRO
[3]   AN ABINITIO CALCULATION OF THE LOW ROTATION VIBRATION ENERGIES OF THE CO DIMER [J].
BUNKER, PR ;
JENSEN, P ;
ALTHORPE, SC ;
CLARY, DC .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1993, 157 (01) :208-219
[4]   MOLECULAR FORCE-FIELD AND STRUCTURE OF WATER - RECENT MICROWAVE RESULTS [J].
COOK, RL ;
DELUCIA, FC ;
HELMINGER, P .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1974, 53 (01) :62-76
[5]   NEW MEASUREMENTS OF MICROWAVE TRANSITIONS IN THE WATER DIMER [J].
COUDERT, LH ;
LOVAS, FJ ;
SUENRAM, RD ;
HOUGEN, JT .
JOURNAL OF CHEMICAL PHYSICS, 1987, 87 (11) :6290-6299
[6]   INFRARED AND MICROWAVE INVESTIGATIONS OF INTERCONVERSION TUNNELING IN THE ACETYLENE DIMER [J].
FRASER, GT ;
SUENRAM, RD ;
LOVAS, FJ ;
PINE, AS ;
HOUGEN, JT ;
LAFFERTY, WJ ;
MUENTER, JS .
JOURNAL OF CHEMICAL PHYSICS, 1988, 89 (10) :6028-6045
[7]  
Gordy W., 1984, MICROWAVE MOL SPECTR, V3rd
[8]   ROTATIONAL SPECTRUM AND STRUCTURE OF THE AR2-HF TRIMER [J].
GUTOWSKY, HS ;
KLOTS, TD ;
CHUANG, C ;
SCHMUTTENMAER, CA ;
EMILSSON, T .
JOURNAL OF CHEMICAL PHYSICS, 1985, 83 (09) :4817-4818
[9]   MOLECULAR-STRUCTURES OF GAS-PHASE POLYATOMIC-MOLECULES DETERMINED BY SPECTROSCOPIC METHODS [J].
HARMONY, MD ;
LAURIE, VW ;
KUCZKOWSKI, RL ;
SCHWENDEMAN, RH ;
RAMSAY, DA ;
LOVAS, FJ ;
LAFFERTY, WJ ;
MAKI, AG .
JOURNAL OF PHYSICAL AND CHEMICAL REFERENCE DATA, 1979, 8 (03) :619-721
[10]   IR SPECTROSCOPY OF (CO)(2) USING CONCENTRATION-FREQUENCY DOUBLE-MODULATION IN A SUPERSONIC JET EXPANSION [J].
HAVENITH, M ;
PETRI, M ;
LUBINA, C ;
HILPERT, G ;
URBAN, W .
JOURNAL OF MOLECULAR SPECTROSCOPY, 1994, 167 (02) :248-261