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• W1527832579 abstract "The pure rotational transitions of HN2+ and DN2+ in the first excited vibrational states for all the fundamental vibrational modes have been observed in the range of 300–750 GHz. The molecular constants determined are much more accurate compared with those obtained from the infrared spectroscopy. The equilibrium rotational constants, Be = 46832.45 (71) MHz for HN2+ and Be = 38708.38 (58) MHz for DN2+, have been determined by correcting for the higher-order vibration–rotation interaction effects, γij, obtained by an infrared investigation. The equilibrium bond lengths are derived from these equilibrium rotational constants: re(H–N) = 1.03460 (14) Å and re (N–N) = 1.092698 (26) Å." @default.
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• W1527832579 date "2005-11-01" @default.
• W1527832579 modified "2023-09-27" @default.
• W1527832579 title "Submillimeter-wave spectroscopy of HN2+ and DN2+ in the excited vibrational states" @default.
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• W1527832579 doi "https://doi.org/10.1016/j.jms.2005.09.004" @default.
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