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Title:SUBMILLIMETER WAVE SPECTROSCOPY FOR ISM: IMINES WITH INTERNAL ROTATION
Author(s):Margulès, L.
Contributor(s):Guillemin, J.-C. ; McGuire, Brett A.; Remijan, Anthony ; Dorovskaya, Olga ; Ilyushin, V. ; Motiyenko, R. A.
Subject(s):Mini-symposium: Astrochemistry and Astrobiology in the age of ALMA
Abstract:The aldimines are important to understand amino acids formation process as they appear in reaction scheme of Strecker-type synthesis. It seems reasonable to propose syntheses in the solid phase but the formation process is not clearly established. The number of imines and amines detected in the interstellar medium is limited, mainly due to lack of spectroscopic data. We present here the studies of ethanimine (CH$_{3}$CHNH) and methylimino-acetonitrile (CH$_{3}$N=CHCN). Both of them have has two isomers E and Z with E one being the most stable. These molecules represent a particular case where a quite high (570 and 714 cm$^{-1}$ respectively) internal rotation barrier is combined with relatively a high $\rho$ value (close to 0.3) making analysis of the spectra rather delicate. The fits were performed using a version of RAM36 code\footnote{Ilyushin, V.V. et al;{\em J. Mol. Spectrosc.}~{\bf259}, (2010) 26} which includes the treatment of the nuclear quadrupole hyperfine structure. Ethanimine was detected already in ISM\footnote{Loomis, R. A.; {\em et al.} {\em ApJ. Lett.}~{\bf765},(2013) L9}, but the spectrosocpic analyses were limited to low K$_{a}$ values\footnote{Lovas, F. J.; {\em et al.} {\em J. Chem. Phys.}~{\bf72}, (1980) 4964}$^{,}$\footnote{Melli A.; {\em et al.} {\em ApJ}~{\bf855}, (2018) 123}. In the current study we significantly extend the rotational quantum number coverage for this molecule.\\ The spectroscopic results for both molecules and searches of methylimino-acetonitrile in ISM will be presented.\\ \em{This work was supported by the CNES and the Action sur Projets de l'INSU, PCMI.}
Issue Date:2019-06-18
Publisher:International Symposium on Molecular Spectroscopy
Genre:Conference Paper / Presentation
Type:Text
Language:English
URI:http://hdl.handle.net/2142/104237
DOI:10.15278/isms.2019.TG05
Rights Information:Copyright 2019 L. Margulès
Date Available in IDEALS:2019-07-15
2020-01-25


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