THE STRUCTURE OF AN ($H_{2}O-HCN$)-ArTRIMER

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1993

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Ohio State University

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Rotational spectra are being observed for an (H2OHCN)-Ar trimer with a Balle/Flygare Fourier transform microwave spectrometer. Thus far, two sets of closely related transitions have been assigned to the parent isotopic species, each with both a and bdipole transitions and with 14N hfs corresponding to = 0.647 MHz and χbb=−2.900 MHz. There is no hfs attributable to H---H interactions in the H2O. A fit of the line centers, including centrifugal distortion, gives rotational constants (A, B, and C) for species 1 of 3535.64, 1845.07, and 1219.30 MHz, and for species II of 3508.55, 1897.09, and 1228.82 MHz. The structure is roughly T-shaped consisting of the linear, pseudoplanar H2OHCN dimer1 with an argon alongside. The a-dipole transitions are stronger than the b-dipole in species II but the reverse is found in species I. This suggests that the effective orientation of the H2O differs in the two species. Further work is underway and will be reported.

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  1. H. S. Gutowsky, T. C. Germann, J. D. Augspurger, and C. E Dykstra. J. Chem. Phys. 96, 5808 (1992).

Author Institution: Noyes Chemical Laboratory, University of Illinois; Department of Chemistry, Indiana University-Purdue University

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