ROTATIONALLY-RESOLVED ELECTRONIC SPECTRA FOR THE CH-Ne and CD-Ne VAN DER WAALS COMPLEXES

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1993

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Ohio State University

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CH/D-Ne complexes were generated in a free-jet expansion, and detected by laser excitation of bands associated with the CH/DA2ΔX2Π and B2ΣX2Π transitions. The monomer B-X 0-0 and 1-0 transitions were each accompanied by four strong features of the complex. Rotational analysis of the origin band yielded rotational constants of (CH-Ne) B=0.117 and B=0.149cm−1. Hence the van der Waals bond lengthens on excitation to the B state. Two strong complex features were seen in conjunction with the monomer AX0−0 transition. The rotational structures of these features were much more congested than those of the BX bands. A preliminary analysis yields an A state rotational constant which is slightly larger than that of the ground state, implying that the intermolecular bond shortens on excitation to the A state. Results from detailed analyses of the AX and BX systems will be presented.

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Author Institution: Department of Chemistry, Emory University

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