Study of the high resolution FTIR spectrum of CH2CD2 in the region of 1300-1450 cm−1: The ν12(A1) and 2ν10(A1) bands; Journal of Quantitative Spectroscopy and Radiative Transfer; Vol. 161

Chi tiết về thư mục
Parent link:Journal of Quantitative Spectroscopy and Radiative Transfer
Vol. 161.— 2015.— [P. 180-196]
Tác giả của công ty: Национальный исследовательский Томский политехнический университет (ТПУ) Физико-технический институт (ФТИ) Кафедра общей физики (ОФ)
Tác giả khác: Ulenekov (Ulenikov) O. N. Oleg Nikolaevich, Gromova O. V. Olga Vasilievna, Bekhtereva E. S. Elena Sergeevna, Beryozkin K. B. Kirill Borisovich, Sklyarova E. A. Elena Aleksandrovna, Maul C., Gericke К. Н., Bauerecker Z. (S.) H. Zigurd (Sigurd) Hermann
Tóm tắt:Title screen
The high resolution IR spectrum of the CH2double bond; length as m-dashCD2 ethylene isotopomer was recorded and analyzed in the region of 1300–1450 cm?1, where the strongly interacting bands ?12(A1) and 2?10(A1) are located (the band ?12 was analyzed earlier; transitions belonging to the 2?10 band were experimentally recorded and assigned in the present study for the first time). For description of the upper ro-vibrational energy levels obtained from the assigned transitions, the used Hamiltonian takes into account not only resonance interactions between the states (v12=1) and (v10=2), but interactions of the mentioned pair of vibrational states with the states (v7=v10=1) and (v7=2), as well. More than 1960 and 320 transitions with the values View the MathML source and View the MathML source were assigned to the bands ?12(A1) and 2?10(A1), respectively. A set of 59 spectroscopic parameters was obtained from a weighted least square fit procedure. This reproduces the 959 and 180 initial upper ro-vibrational energies of the vibrational states ?12(A1) and 2?10(A1) used in the fit with a View the MathML source and View the MathML source, respectively (in this case, only upper energies obtained from unblended and nonsaturated transitions of relatively high intensities have been taken into account). The ground state rotational parameters were improved in comparison with the parameters known in the literature.
Режим доступа: по договору с организацией-держателем ресурса
Ngôn ngữ:Tiếng Anh
Được phát hành: 2015
Những chủ đề:
Truy cập trực tuyến:http://dx.doi.org/10.1016/j.jqsrt.2015.04.008
Định dạng: Điện tử Chương của sách
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=641651

MARC

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200 1 |a Study of the high resolution FTIR spectrum of CH2CD2 in the region of 1300-1450 cm−1: The ν12(A1) and 2ν10(A1) bands  |f O. N. Ulenikov [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: p. 195-196 (52 tit.)] 
330 |a The high resolution IR spectrum of the CH2double bond; length as m-dashCD2 ethylene isotopomer was recorded and analyzed in the region of 1300–1450 cm?1, where the strongly interacting bands ?12(A1) and 2?10(A1) are located (the band ?12 was analyzed earlier; transitions belonging to the 2?10 band were experimentally recorded and assigned in the present study for the first time). For description of the upper ro-vibrational energy levels obtained from the assigned transitions, the used Hamiltonian takes into account not only resonance interactions between the states (v12=1) and (v10=2), but interactions of the mentioned pair of vibrational states with the states (v7=v10=1) and (v7=2), as well. More than 1960 and 320 transitions with the values View the MathML source and View the MathML source were assigned to the bands ?12(A1) and 2?10(A1), respectively. A set of 59 spectroscopic parameters was obtained from a weighted least square fit procedure. This reproduces the 959 and 180 initial upper ro-vibrational energies of the vibrational states ?12(A1) and 2?10(A1) used in the fit with a View the MathML source and View the MathML source, respectively (in this case, only upper energies obtained from unblended and nonsaturated transitions of relatively high intensities have been taken into account). The ground state rotational parameters were improved in comparison with the parameters known in the literature. 
333 |a Режим доступа: по договору с организацией-держателем ресурса 
461 |t Journal of Quantitative Spectroscopy and Radiative Transfer 
463 |t Vol. 161  |v [P. 180-196]  |d 2015 
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701 1 |a Gromova  |b O. V.  |c physicist  |c Professor of Tomsk Polytechnic University, Candidate of physical and mathematical sciences  |f 1982-  |g Olga Vasilievna  |3 (RuTPU)RU\TPU\pers\34333  |9 17839 
701 1 |a Bekhtereva  |b E. S.  |c physicist  |c Professor of Tomsk Polytechnic University, Doctor of physical and mathematical sciences  |f 1974-  |g Elena Sergeevna  |3 (RuTPU)RU\TPU\pers\34450  |9 17851 
701 1 |a Beryozkin  |b K. B.  |c physicist  |c technician Tomsk Polytechnic University  |f 1987-  |g Kirill Borisovich  |3 (RuTPU)RU\TPU\pers\34702  |9 18052 
701 1 |a Sklyarova  |b E. A.  |c physicist  |c associate Professor of Tomsk Polytechnic University, candidate of pedagogical Sciences  |f 1972-  |g Elena Aleksandrovna  |3 (RuTPU)RU\TPU\pers\34705  |9 18055 
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