High resolution FTIR spectroscopy of fluoroform 12CHF3 and critical analysis of the infrared spectrum from 25 to 1500 cm−1; Molecular Physics; Vol. 116, iss. 9

Bibliografiske detaljer
Parent link:Molecular Physics
Vol. 116, iss. 9.— 2018.— [P. 1091-1107]
Institution som forfatter: Национальный исследовательский Томский политехнический университет Исследовательская школа физики высокоэнергетических процессов
Andre forfattere: Albert S. Sieghard, Bekhtereva E. S. Elena Sergeevna, Bolotova I. B., Hollenstein Hans H. A., Quack M. Martin, Ulenekov (Ulenikov) O. N. Oleg Nikolaevich
Summary:Title screen
We report high-resolution ( 0.001 cm−1) Fourier Transform Infrared spectra of fluoroform (CHF3) including the pure rotational (far infrared or THz) range (28-65 cm−1), the ν3 fundamental ( = 700.099 cm−1), as well as the associated “hot' band 2ν3 − ν3 ( = 699.295 cm−1) and the 'atmospheric window' range 1100-1250 cm−1 containing the strongly coupled polyad of the levels ν2, ν5 and ν3 + ν6, at room temperature and at 120 K using the collisional cooling cell coupled to our Bruker IFS 125 HR prototype (ZP2001) spectrometer and Bruker IFS 125 HR ETH-SLS prototype at the Swiss Light Source providing intense synchrotron radiation. The pure rotational spectra provide new information about the vibrational ground state of CHF3, which is useful for further analysis of excited vibrational states. The ν3 fundamental band is re-investigated together with the corresponding 'hot' band 2ν3 − ν3 leading to an extension of the existing line lists up to 4430 transitions with = 66 for ν3 and 1040 transitions with = 43 for 2ν3 − ν3. About 6000 transitions were assigned to rovibrational levels in the polyad ν2/ν5/ν3 + ν6 with = 63 for ν2 ( = 1141.457 cm−1), = 63 for ν5 ( = 1157.335 cm−1) and = 59 for ν3 + ν6 ( = 1208.771 cm−1)( = in each case). The resonance interactions between the ν2, ν5 and ν3 + ν6 states have been taken into account providing an accurate set of effective hamiltonian parameters, which reproduce the experimental results with an accuracy close to the experimental uncertainties (with a root mean square deviation drms = 0.00025 cm−1). The analysis is further extended to the ν4 fundamental ( = 1377.847 cm−1) interacting with 2ν3 ( = 1399.394 cm−1). The results are discussed in relation to the importance of understanding the spectra of CHF3 as a greenhouse gas and as part of our large effort to measure and understand the complete spectrum of CHF3 from the far-infrared to the near-infrared as a prototype for intramolecular quantum dynamics and rovibrational energy redistribution.
Sprog:engelsk
Udgivet: 2018
Fag:
Online adgang:https://doi.org/10.1080/00268976.2017.1392628
Format: Electronisk Book Chapter
KOHA link:https://koha.lib.tpu.ru/cgi-bin/koha/opac-detail.pl?biblionumber=667039

MARC

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200 1 |a High resolution FTIR spectroscopy of fluoroform 12CHF3 and critical analysis of the infrared spectrum from 25 to 1500 cm−1  |f S. Albert, E. S. Bekhtereva, I. B. Bolotova [et al.] 
203 |a Text  |c electronic 
300 |a Title screen 
320 |a [References: 92 tit.] 
330 |a We report high-resolution ( 0.001 cm−1) Fourier Transform Infrared spectra of fluoroform (CHF3) including the pure rotational (far infrared or THz) range (28-65 cm−1), the ν3 fundamental ( = 700.099 cm−1), as well as the associated “hot' band 2ν3 − ν3 ( = 699.295 cm−1) and the 'atmospheric window' range 1100-1250 cm−1 containing the strongly coupled polyad of the levels ν2, ν5 and ν3 + ν6, at room temperature and at 120 K using the collisional cooling cell coupled to our Bruker IFS 125 HR prototype (ZP2001) spectrometer and Bruker IFS 125 HR ETH-SLS prototype at the Swiss Light Source providing intense synchrotron radiation. The pure rotational spectra provide new information about the vibrational ground state of CHF3, which is useful for further analysis of excited vibrational states. The ν3 fundamental band is re-investigated together with the corresponding 'hot' band 2ν3 − ν3 leading to an extension of the existing line lists up to 4430 transitions with = 66 for ν3 and 1040 transitions with = 43 for 2ν3 − ν3. About 6000 transitions were assigned to rovibrational levels in the polyad ν2/ν5/ν3 + ν6 with = 63 for ν2 ( = 1141.457 cm−1), = 63 for ν5 ( = 1157.335 cm−1) and = 59 for ν3 + ν6 ( = 1208.771 cm−1)( = in each case). The resonance interactions between the ν2, ν5 and ν3 + ν6 states have been taken into account providing an accurate set of effective hamiltonian parameters, which reproduce the experimental results with an accuracy close to the experimental uncertainties (with a root mean square deviation drms = 0.00025 cm−1). The analysis is further extended to the ν4 fundamental ( = 1377.847 cm−1) interacting with 2ν3 ( = 1399.394 cm−1). The results are discussed in relation to the importance of understanding the spectra of CHF3 as a greenhouse gas and as part of our large effort to measure and understand the complete spectrum of CHF3 from the far-infrared to the near-infrared as a prototype for intramolecular quantum dynamics and rovibrational energy redistribution. 
461 |t Molecular Physics 
463 |t Vol. 116, iss. 9  |v [P. 1091-1107]  |d 2018 
610 1 |a электронный ресурс 
610 1 |a труды учёных ТПУ 
610 1 |a CHF3 
610 1 |a fluoroform 
610 1 |a high-resolution infrared spectroscopy 
610 1 |a greenhouse gas absorption 
610 1 |a intramolecular quantum dynamics 
610 1 |a FTI 
610 1 |a RTHz 
610 1 |a инфракрасная спектроскопия 
610 1 |a поглощение 
610 1 |a парниковые газы 
610 1 |a квантовая динамика 
701 1 |a Albert  |b S.  |g Sieghard 
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 Bolotova  |b I. B. 
701 1 |a Hollenstein  |b Hans  |g H. A. 
701 1 |a Quack  |b M.  |g Martin 
701 1 |a Ulenekov (Ulenikov)  |b O. N.  |c physicist  |c Professor of Tomsk Polytechnic University, Doctor of physical and mathematical sciences  |f 1949-  |g Oleg Nikolaevich  |3 (RuTPU)RU\TPU\pers\34331  |9 17837 
712 0 2 |a Национальный исследовательский Томский политехнический университет  |b Исследовательская школа физики высокоэнергетических процессов  |c (2017- )  |3 (RuTPU)RU\TPU\col\23551 
801 2 |a RU  |b 63413507  |c 20220217  |g RCR 
856 4 |u https://doi.org/10.1080/00268976.2017.1392628 
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