scholarly journals Differential adsorption of complex organic molecules isomers at interstellar ice surfaces

2011 ◽  
Vol 532 ◽  
pp. A12 ◽  
Author(s):  
M. Lattelais ◽  
M. Bertin ◽  
H. Mokrane ◽  
C. Romanzin ◽  
X. Michaut ◽  
...  
2012 ◽  
Vol 58 ◽  
pp. 349-352
Author(s):  
M. Bertin ◽  
X. Michaut ◽  
M. Lattelais ◽  
H. Mokrane ◽  
F. Pauzat ◽  
...  

2021 ◽  
Author(s):  
Héctor Carrascosa ◽  
Cristóbal González Díaz ◽  
Guillermo M. Muñoz Caro ◽  
Pedro C. Gómez ◽  
María Luz Sanz

<p>Hexamethylentetramine has drawn a lot of attention due to its potential to produce prebiotic species. This work aims to gain a better understanding in the chemical processes concerning methylamine under astrophysically relevant conditions. In particular, this work deeps into the formation of N-heterocycles in interstellar ice analogs exposed to UV radiation, which may lead to the formation of prebiotic species.</p> <p>Experimental simulations of interstellar ice analogs were carried out in ISAC. ISAC is an ultra-high vacuum chamber equipped with a cryostat, where gas and vapour species are frozen forming ice samples. Infrared and ultraviolet spectroscopy were used to monitor the solid phase, and quadrupole mass spectrometry served to measure the composition of the gas phase. The variety of species detected after UV irradiation of ices containing  methylamine revealed the presence of 12 species which have been already detected in the ISM, being 4 of them typically classified as complex organic molecules: formamide (HCONH<sub>2</sub>), methyl cyanide (CH<sub>3</sub>CN), CH<sub>3</sub>NH and CH<sub>3</sub>CHNH. Warming up of the irradiated CH<sub>3</sub>NH<sub>2</sub>-bearing ice samples lead to the formation of trimethylentriamine (TMT), a N-heterocycle precursor of HMT, and the subsequent synthesis of HMT at temperatures above 230 K.</p>


2020 ◽  
Vol 501 (1) ◽  
pp. 1202-1214
Author(s):  
Diego N de Jesus ◽  
Jean M B A da Silva ◽  
Tatiane N Tejero ◽  
Gladson de Souza Machado ◽  
Neubi F Xavier ◽  
...  

ABSTRACT Complex organic molecules from extraterrestrial source are expected to have contributed to the Early Earth chemistry. Methylamine (CH3NH2)has already been observed in the interstellar medium (ISM) and is generally related to the formation of glycine, although the latter has not been identified in the ISM yet. In this work, a chemical model for CH3NH2 was investigated, comprising twenty-eight reactions and including reactions involving NH3 and HOOC, aiming to understand the main routes for formation and decomposition of methylamine and also to infer about the chemical behaviour of glycine in the ISM. Calculations were performed at the CCSD(T)/aug-cc-pVTZ//M06-2X/aug-cc-pVTZ level and rate coefficients were calculated adopting the canonical variational transition state theory (CVTST), in the temperature range 100 to 4000 K, including tunnelling effects. Starting from HCN, the preferred pathway for methylamine formation is through consecutive hydrogenation steps, forming CH2N, CH2NH, and CH2NH2 intermediates. Considering the decomposition, dissociation into CH3 and NH2 is the most favourable step. NH3 and HCN are common compounds in interstellar ice analogues and react producing NH2 and CH2N through NH2NCH2 and H2NCH2N intermediates. The latter is proposed here and spectroscopic data for any future experimental investigation are given. Finally, an extension to the ISM glycine chemistry is explored and routes to its formation, from the simplest compounds found in interstellar ices, are proposed.


2019 ◽  
Vol 15 (S350) ◽  
pp. 417-419
Author(s):  
Rafael Martín-Doménech ◽  
Karin I. Öberg ◽  
Mahesh Rajappan

AbstractComplex organic molecules (COMs) may have played a role in the formation of life in the early Earth (Herbst & van Dishoeck (2009)). Here we present the formation of NH2CHO and CH3CHO upon vacuum-ultraviolet (VUV) irradiation of CO:NH3 and CO:CH4 ice mixtures, simulating the UV processing of interstellar ices in the interior of dense clouds. We have found that the conversion from ${\rm{N}}{{\rm{H}}_{\dot 2}}$ radicals to NH2CHO is 4–15 times higer than that from ${\rm{N}}{{\rm{H}}_{\dot 3}}$ to CH3CHO, probably due to the competing formation of larger hydrocarbons in the latter case.


2018 ◽  
Vol 614 ◽  
pp. A107 ◽  
Author(s):  
P. Ghesquière ◽  
A. Ivlev ◽  
J. A. Noble ◽  
P. Theulé

Context. The synthesis of interstellar complex organic molecules in ice involves several types of reactions between molecules and/or radicals that are usually considered to be diffusion controlled. Aims. We aim to understand the coupling between diffusion and reactivity in the interstellar ice mantle using a model binary reaction in the diffusion-limited regime. Methods. We performed isothermal kinetic laboratory experiments on interstellar ice analogs at low temperatures, using the NH3:CO2:H2O model system where reactants NH3 and CO2 have a low reaction barrier and are diluted in a water-dominated ice. Results. We found that in the diffusion-limited regime, the reaction kinetics is not determined by the intrinsic bulk diffusivity of reactants. Instead, reactions are driven by structural changes evolving in amorphous water ice, such as pore collapse and crystallization. Diffusion of reactants in this case likely occurs along the surface of (tiny) cracks generated by the structural changes. Conclusions. The reactivity driven by the structural changes breaks the conventional picture of reactant molecules/radicals diffusing in a bulk water ice. This phenomenon is expected to lead to a dramatic increase in production rates of interstellar complex organic molecules in star-forming regions.


2015 ◽  
Vol 809 (2) ◽  
pp. L18 ◽  
Author(s):  
V. Vinogradoff ◽  
F. Duvernay ◽  
N. Fray ◽  
M. Bouilloud ◽  
T. Chiavassa ◽  
...  

1997 ◽  
Vol 161 ◽  
pp. 23-47 ◽  
Author(s):  
Louis J. Allamandola ◽  
Max P. Bernstein ◽  
Scott A. Sandford

AbstractInfrared observations, combined with realistic laboratory simulations, have revolutionized our understanding of interstellar ice and dust, the building blocks of comets. Since comets are thought to be a major source of the volatiles on the primative earth, their organic inventory is of central importance to questions concerning the origin of life. Ices in molecular clouds contain the very simple molecules H2O, CH3OH, CO, CO2, CH4, H2, and probably some NH3and H2CO, as well as more complex species including nitriles, ketones, and esters. The evidence for these, as well as carbonrich materials such as polycyclic aromatic hydrocarbons (PAHs), microdiamonds, and amorphous carbon is briefly reviewed. This is followed by a detailed summary of interstellar/precometary ice photochemical evolution based on laboratory studies of realistic polar ice analogs. Ultraviolet photolysis of these ices produces H2, H2CO, CO2, CO, CH4, HCO, and the moderately complex organic molecules: CH3CH2OH (ethanol), HC(= O)NH2(formamide), CH3C(= O)NH2(acetamide), R-CN (nitriles), and hexamethylenetetramine (HMT, C6H12N4), as well as more complex species including polyoxymethylene and related species (POMs), amides, and ketones. The ready formation of these organic species from simple starting mixtures, the ice chemistry that ensues when these ices are mildly warmed, plus the observation that the more complex refractory photoproducts show lipid-like behavior and readily self organize into droplets upon exposure to liquid water suggest that comets may have played an important role in the origin of life.


2020 ◽  
Author(s):  
Sukdev Bag ◽  
Sadhan Jana ◽  
Sukumar Pradhan ◽  
Suman Bhowmick ◽  
Nupur Goswami ◽  
...  

<p>Despite the widespread applications of C–H functionalization, controlling site selectivity remains a significant challenge. Covalently attached directing group (DG) served as an ancillary ligand to ensure proximal <i>ortho</i>-, distal <i>meta</i>- and <i>para</i>-C-H functionalization over the last two decades. These covalently linked DGs necessitate two extra steps for a single C–H functionalization: introduction of DG prior to C–H activation and removal of DG post-functionalization. We introduce here a transient directing group for distal C(<i>sp<sup>2</sup></i>)-H functionalization <i>via</i> reversible imine formation. By overruling facile proximal C-H bond activation by imine-<i>N</i> atom, a suitably designed pyrimidine-based transient directing group (TDG) successfully delivered selective distal C-C bond formation. Application of this transient directing group strategy for streamlining the synthesis of complex organic molecules without any necessary pre-functionalization at the distal position has been explored.</p>


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