2012
DOI: 10.1051/0004-6361/201218949
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Aminoacetonitrile characterization in astrophysical-like conditions

Abstract: Context. Aminoacetonitrile (AAN) has been detected in 2008 in the hot core SgrB2. This molecule is of particular interest because it is a central molecule in the Strecker synthesis of amino acids. This molecule can be formed from methanimine (CH 2 NH), ammonia (NH 3 ) and hydrogen cyanide (HCN) in astrophysical icy conditions. Nevertheless, few studies exist about its infrared (IR) identification or its astrophysical characterization. Aims. We present in this study a characterization of the pure solid AAN and … Show more

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Cited by 11 publications
(12 citation statements)
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“…The large uncertainty on this value most likely derives from the assumptions made in the calculations: that the absorption strengths of the CN − and HCN CN stretching mode absorptions, and the HCN bending mode absorption do not change with environment. As has been previously demonstrated by Borget et al (2012), the CN stretch in nitriles is very sensitive to environment, with the absorption strength of CN in aminoacetonitrile changing by a factor of two between the pure molecule and a mixture of aminoacetonitrile and H 2 O (1:3). Thus we conclude that, while we can accurately determine the absorption strength of CN − at low to intermediate temperatures in a pure salt, it is not possible from these data to reliably deconvolve HCN and CN − contributions to the CN stretching mode absorption at 2100 cm −1 .…”
Section: Determination Of the Cn − Ion Band Strengthmentioning
confidence: 57%
“…The large uncertainty on this value most likely derives from the assumptions made in the calculations: that the absorption strengths of the CN − and HCN CN stretching mode absorptions, and the HCN bending mode absorption do not change with environment. As has been previously demonstrated by Borget et al (2012), the CN stretch in nitriles is very sensitive to environment, with the absorption strength of CN in aminoacetonitrile changing by a factor of two between the pure molecule and a mixture of aminoacetonitrile and H 2 O (1:3). Thus we conclude that, while we can accurately determine the absorption strength of CN − at low to intermediate temperatures in a pure salt, it is not possible from these data to reliably deconvolve HCN and CN − contributions to the CN stretching mode absorption at 2100 cm −1 .…”
Section: Determination Of the Cn − Ion Band Strengthmentioning
confidence: 57%
“…[32] When the imine is the minor reactant with the salt, we observed the thermal formation of the aminoacetonitrile (NH 2 CH 2 CN) from 135 K. Aminoacetonitrile was detected in 2008 [33] and was characterized in ISM conditions. [34] Aminoacetonitrile is a glycine precursor through the Strecker's synthesis. We demonstrated that this step of this synthesis could be carried out in ISM conditions.…”
Section: Imines Reactivity In Interstellar Medium Icesmentioning
confidence: 99%
“…Aminoacetonitrile (AAN) is a small organic compound that contains an amino group (NH 2 ) at one end and nitrile group (CN) at the other. The discovery of AAN in the constellation Sagittarius B2 (Sgr B2), in 2008, is a significant event in astrochemistry, as it plays the central role in the Strecker amino acid synthesis mechanism . Amino acids are the building blocks of proteins and, therefore, the key ingredients for the origin of life.…”
Section: Introductionmentioning
confidence: 99%
“…Once the detection of glycine is confirmed in ISM, it may throw new light on the debate regarding the origin of life in early earth. Another important molecule, in the present context, is Hydrogen Cyanide (HCN) as it plays a major role in the synthesis of AAN . In fact, AAN can be formed from methanimine (CH 2 NH) and hydrogen cyanide (HCN) in astrophysical icy conditions .…”
Section: Introductionmentioning
confidence: 99%