Note: Cold spectra of the electronic transition A(2)Σ(+)-X(2)Π of N2O(+) radical: High resolution analysis of the bands 000-100, 100-100, and 001-101.

In this note, three vibrational bands of the electronic transition A(2)Σ(+)-X(2)Π of the N2O(+) radical (000-100, 100-100, and 001-101) were theoretically analysed. Starting from Hamiltonian models proposed for this kind of molecule, their parameters were calculated using a Levenberg-Marquardt fit procedure in order to reduce the root mean square deviation from the experimental transitions below to 0.01 cm(-1). The main objective of this work is to obtain new and reliable values for rotational constant B″ and the spin-orbit interaction parameter A of the analysed vibrational levels of the X(2)Π electronic state of this molecule.

High resolution analysis of three bands of the electronic transition A²Σ⁺-X²Π of N2O⁺ radical: 100-000, 000-001, and 001-001.

In this article three vibrational bands of the electronic transition A(2)Σ(+)-X(2)Π of the N2O(+) radical (100-000, 000-001, and 001-001) are analysed through high resolution Fourier transform spectroscopy. The N2O(+) radical was produced by Penning ionization of N2O by colliding with metastable atoms of He(2(3)S) in a reaction chamber. The spectra was recorded in a spectral range of 24,500-30,000 cm(-1) and obtained from 200 coadded interferograms recorded at an apodized resolution of 0.08 cm(-1). Through a recursive way, the wavenumbers of the correspondent rotational transitions were reduced into molecular constants, improving the values previously reported. New values for the first vibrational energies ν1', ν3", and ν3' are also obtained and compared with previous values reported in the literature.