中国物理B ›› 2014, Vol. 23 ›› Issue (12): 123301-123301.doi: 10.1088/1674-1056/23/12/123301

• ATOMIC AND MOLECULAR PHYSICS • 上一篇    下一篇

Infrared diode laser spectroscopy of O2–N2O van der Waals complex in the ν1 symmetric stretch region of N2O

李松a b, 郑锐c, 段传喜a   

  1. a College of Physical Science and Technology, Central China Normal University, Wuhan 430079, China;
    b College of Physical Science and Technology, Yangtze University, Jingzhou 434023, China;
    c School of Mathematics & Information Science, North China University of Water Resources and Electric Power, Zhengzhou 450011, China
  • 收稿日期:2014-04-16 修回日期:2014-07-15 出版日期:2014-12-15 发布日期:2014-12-15
  • 基金资助:

    Project supported by the National Natural Science Foundation of China (Grants Nos. 11174098, 11304023, and 11304095).

Infrared diode laser spectroscopy of O2–N2O van der Waals complex in the ν1 symmetric stretch region of N2O

Li Song (李松)a b, Zheng Rui (郑锐)c, Duan Chuan-Xi (段传喜)a   

  1. a College of Physical Science and Technology, Central China Normal University, Wuhan 430079, China;
    b College of Physical Science and Technology, Yangtze University, Jingzhou 434023, China;
    c School of Mathematics & Information Science, North China University of Water Resources and Electric Power, Zhengzhou 450011, China
  • Received:2014-04-16 Revised:2014-07-15 Online:2014-12-15 Published:2014-12-15
  • Contact: Duan Chuan-Xi E-mail:cxduan@phy.ccnu.edu.cn
  • Supported by:

    Project supported by the National Natural Science Foundation of China (Grants Nos. 11174098, 11304023, and 11304095).

摘要:

The rovibrational spectrum of O2–N2O van der Waals complex is measured in the v1 symmetric stretch region of N2O monomer using a tunable diode laser spectrometer. The complex is generated by a slit-pulsed supersonic expansion with gas mixtures of O2, N2O, and He. Both a- and b-type transitions are observed. The effective Hamiltonian for an open-shell complex consisting of a diatomic molecule in a 3Σ electronic state and a closed-shell partner is used to analyze the observed spectrum. Molecular constants in the vibrationally excited state are determined accurately. The band-origin of the spectrum is determined to be 1284.7504(25) cm-1, red-shifted from that of the N2O monomer by ~ 0.1529 cm-1.

关键词: rovibrational spectrum, van der Waals complex, intermolecular interactions

Abstract: The rovibrational spectrum of O2–N2O van der Waals complex is measured in the v1 symmetric stretch region of N2O monomer using a tunable diode laser spectrometer. The complex is generated by a slit-pulsed supersonic expansion with gas mixtures of O2, N2O, and He. Both a- and b-type transitions are observed. The effective Hamiltonian for an open-shell complex consisting of a diatomic molecule in a 3Σ electronic state and a closed-shell partner is used to analyze the observed spectrum. Molecular constants in the vibrationally excited state are determined accurately. The band-origin of the spectrum is determined to be 1284.7504(25) cm-1, red-shifted from that of the N2O monomer by ~ 0.1529 cm-1.

Key words: rovibrational spectrum, van der Waals complex, intermolecular interactions

中图分类号:  (Rotation, vibration, and vibration-rotation constants)

  • 33.15.Mt
33.20.Ea (Infrared spectra) 36.40.Mr (Spectroscopy and geometrical structure of clusters)