Yu. G. Borkov, O. N. Sulakshina, V. I. Serdyukov, L. N. Sinitsa
{"title":"5200-5500 сm-1 光谱区 14N18O 光谱分析","authors":"Yu. G. Borkov, O. N. Sulakshina, V. I. Serdyukov, L. N. Sinitsa","doi":"10.1134/S1024856024010159","DOIUrl":null,"url":null,"abstract":"<p>The absorption spectrum of <sup>14</sup>N<sup>18</sup>O molecule in the 5200–5500 сm<sup>−1</sup> region was recorded for the first time using a Bruker IFS 125M Fourier spectrometer with a spectral resolution of 0.0056 сm<sup>−1</sup>. The analysis of the spectrum made it possible to detect the vibrational–rotational lines of the 3–0 band of the main transitions in the X<sup>2</sup>Π electronic state of the <sup>14</sup>N<sup>18</sup>O molecule. For the main <sup>2</sup>Π<sub>1/2</sub>–<sup>2</sup>Π<sub>1/2</sub> and <sup>2</sup>Π<sub>3/2</sub>–<sup>2</sup>Π<sub>3/2</sub> transitions, positions of 102 lines from a Λ-doublet were recorded in three branches. The positions and relative intensities of each component of the doublet were determined for 61 resolved doublets. The maximal rotational quantum number <i>J</i> was 29.5. The experimental line positions in the 3–0 band confirm the calculated data presented in HITRAN database. The frequencies of recorded transitions, weighted in accordance with experimental uncertainties, were processed, and the spectroscopic constants were determined for the vibrational state <span>\\({v}\\)</span> = 3. With the found spectroscopic constants, we predicted the rotational energy values up to <i>J</i> = 35.5 for the vibrational state <span>\\({v}\\)</span> = 3 and transition frequencies in the 3–3 and 3–0 vibrational bands for the <sup>2</sup>Π<sub>1/2</sub> and <sup>2</sup>Π<sub>3/2</sub> electronic states. The calculation results agree with the data given in HITRAN within the error specified in this database.</p>","PeriodicalId":46751,"journal":{"name":"Atmospheric and Oceanic Optics","volume":null,"pages":null},"PeriodicalIF":0.9000,"publicationDate":"2024-03-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Analysis of 14N18O Spectrum in the 5200–5500 сm−1 Spectral Region\",\"authors\":\"Yu. G. Borkov, O. N. Sulakshina, V. I. Serdyukov, L. N. Sinitsa\",\"doi\":\"10.1134/S1024856024010159\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p>The absorption spectrum of <sup>14</sup>N<sup>18</sup>O molecule in the 5200–5500 сm<sup>−1</sup> region was recorded for the first time using a Bruker IFS 125M Fourier spectrometer with a spectral resolution of 0.0056 сm<sup>−1</sup>. The analysis of the spectrum made it possible to detect the vibrational–rotational lines of the 3–0 band of the main transitions in the X<sup>2</sup>Π electronic state of the <sup>14</sup>N<sup>18</sup>O molecule. For the main <sup>2</sup>Π<sub>1/2</sub>–<sup>2</sup>Π<sub>1/2</sub> and <sup>2</sup>Π<sub>3/2</sub>–<sup>2</sup>Π<sub>3/2</sub> transitions, positions of 102 lines from a Λ-doublet were recorded in three branches. The positions and relative intensities of each component of the doublet were determined for 61 resolved doublets. The maximal rotational quantum number <i>J</i> was 29.5. The experimental line positions in the 3–0 band confirm the calculated data presented in HITRAN database. The frequencies of recorded transitions, weighted in accordance with experimental uncertainties, were processed, and the spectroscopic constants were determined for the vibrational state <span>\\\\({v}\\\\)</span> = 3. With the found spectroscopic constants, we predicted the rotational energy values up to <i>J</i> = 35.5 for the vibrational state <span>\\\\({v}\\\\)</span> = 3 and transition frequencies in the 3–3 and 3–0 vibrational bands for the <sup>2</sup>Π<sub>1/2</sub> and <sup>2</sup>Π<sub>3/2</sub> electronic states. The calculation results agree with the data given in HITRAN within the error specified in this database.</p>\",\"PeriodicalId\":46751,\"journal\":{\"name\":\"Atmospheric and Oceanic Optics\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":0.9000,\"publicationDate\":\"2024-03-23\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Atmospheric and Oceanic Optics\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://link.springer.com/article/10.1134/S1024856024010159\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"OPTICS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Atmospheric and Oceanic Optics","FirstCategoryId":"1085","ListUrlMain":"https://link.springer.com/article/10.1134/S1024856024010159","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"OPTICS","Score":null,"Total":0}
Analysis of 14N18O Spectrum in the 5200–5500 сm−1 Spectral Region
The absorption spectrum of 14N18O molecule in the 5200–5500 сm−1 region was recorded for the first time using a Bruker IFS 125M Fourier spectrometer with a spectral resolution of 0.0056 сm−1. The analysis of the spectrum made it possible to detect the vibrational–rotational lines of the 3–0 band of the main transitions in the X2Π electronic state of the 14N18O molecule. For the main 2Π1/2–2Π1/2 and 2Π3/2–2Π3/2 transitions, positions of 102 lines from a Λ-doublet were recorded in three branches. The positions and relative intensities of each component of the doublet were determined for 61 resolved doublets. The maximal rotational quantum number J was 29.5. The experimental line positions in the 3–0 band confirm the calculated data presented in HITRAN database. The frequencies of recorded transitions, weighted in accordance with experimental uncertainties, were processed, and the spectroscopic constants were determined for the vibrational state \({v}\) = 3. With the found spectroscopic constants, we predicted the rotational energy values up to J = 35.5 for the vibrational state \({v}\) = 3 and transition frequencies in the 3–3 and 3–0 vibrational bands for the 2Π1/2 and 2Π3/2 electronic states. The calculation results agree with the data given in HITRAN within the error specified in this database.
期刊介绍:
Atmospheric and Oceanic Optics is an international peer reviewed journal that presents experimental and theoretical articles relevant to a wide range of problems of atmospheric and oceanic optics, ecology, and climate. The journal coverage includes: scattering and transfer of optical waves, spectroscopy of atmospheric gases, turbulent and nonlinear optical phenomena, adaptive optics, remote (ground-based, airborne, and spaceborne) sensing of the atmosphere and the surface, methods for solving of inverse problems, new equipment for optical investigations, development of computer programs and databases for optical studies. Thematic issues are devoted to the studies of atmospheric ozone, adaptive, nonlinear, and coherent optics, regional climate and environmental monitoring, and other subjects.