I-UNCOUPLING AND ROTATIONAL STRUCTURE IN VIBRATIONALLY AUTOIONIZING RYDBERG STATES OF HCO CONVERGING TO THE (010) LIMIT

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1999

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Ohio State University

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We have obtained (1+1) double resonance spectra autoionizing high Rydberg states of HCO. Scans originate from 3pπ2ΠN=0−5 intermediate states. These spectra cover Rydberg states of binding energies ranging from 650 to 400cm−1, converging to the (010) fundamental of HCO+. Using our highly accurate ionization thresholds and by applying the Rydberg model, simulations which neglect coupling are found to reasonably represent the experimental spectra within a minimal quantum defect basis. Analysis based on Multichannel Quantum Defect Theory, which includes coupling, is underway.

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Author Institution: Department of Chemistry, Purdue University

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