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The purine nucleobases adenine and guanine are complex organic molecules that are essential for life. Despite their ubiquitous presence on Earth, purines have yet to be detected in observations of astronomical environments. This work therefore proposes to study the infrared spectra of purines linked to terrestrial biochemical processes under conditions analogous to those found in the interstellar medium. The infrared spectra of adenine and guanine, both in neat form and embedded within an ice made of H2O:NH3:CH4:CO:CH3OH (10:1:1:1:1), were analysed with the aim of determining which bands attributable to adenine and/or guanine can be observed in the infrared spectrum of an astrophysical ice analogue rich in other volatile species known to be abundant in dense molecular clouds. The spectrum of adenine and guanine mixed together was also analysed. This study has identified three purine nucleobase infrared absorption bands that do not overlap with bands attributable to the volatiles that are ubiquitous in the dense interstellar medium. Therefore, these three bands, which are located at 1255, 940, and 878 cm-1, are proposed as an infrared spectral signature for adenine, guanine, or a mixture of these molecules in astrophysical ices. All three bands have integrated molar absorptivity values (ψ) greater than 4 km mol-1, meaning that they should be readily observable in astronomical targets. Therefore, if these three bands were to be observed together in the same target, then it is possible to propose the presence of a purine molecule (i.e., adenine or guanine) there.
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As of early 2022, only six species bearing an N-O bond have been detected toward cold molecular clouds and regions of star formation. It is not clear yet if the small number of N-O bond species found in the interstellar medium so far stems from physical and technological limitations of astronomical detection techniques, or whether in fact molecules that bear an N-O bond are for some reason rare in these objects of the interstellar medium. Astronomical N-O bearing molecules are important because they are part of astrochemical models which propose that they are precursors of hydroxylamine (NH2OH), a species linked to the formation of prebiotic amino acids in space. The aim of this study is the better understanding of the open question of the interstellar synthesis of N-O bearing species. We have analyzed by infrared spectroscopy an astrophysically relevant polar ice mixture of N2O:H2O processed by 90 MeV 136Xe23+ ions, which can mimic the physicochemical processes triggered by cosmic rays in water-covered interstellar ice grains. The results show the formation of N2O3 and of H2O2, but no HN-O species of any kind were detected. Such findings are discussed in light of recent studies from our group and from the literature.
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Peróxido de Hidrógeno , Iones , Espectrofotometría Infrarroja/métodosRESUMEN
The surface mineralogy of dwarf planet Ceres is rich in ammonium (NH4+) bearing phyllosilicates. However, the origin and formation mechanisms of ammoniated phyllosilicates on Ceres's surface are still elusive. Here we report on laboratory simulation experiments under astrophysical conditions mimicking Ceres' physical and chemical environments with the goal to better understand the source of ammoniated minerals on Ceres' surface. We observe that thermally driven proton exchange reactions between phyllosilicates and ammonia (NH3) could trigger at low temperature leading to the genesis of ammoniated-minerals. Our study revealed the thermal (300 K) and radiation stability of ammoniated-phyllosilicates over a timescale of at least some 500 million years. The present experimental investigations corroborate the possibility that Ceres formed at a location where ammonia ices on the surface would have been stable. However, the possibility of Ceres' origin near to its current location by accreting ammonia-rich material cannot be excluded.
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We present the first formation of the previously elusive phosphine imide (HN[double bond, length as m-dash]PH3) along with its phosphinous amide (H2N-PH2) isomer via exposure of phosphine (PH3) and ammonia (NH3) ices to ionizing radiation. Our approach may be extended to prepare, separate, and detect highly reactive compounds such as intermediates of Wittig reactions.
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Although the chemistry of phosphorus and nitrogen has fascinated chemists for more than 350 years, the Hückel aromatic cyclotriphosphazene (P3N3, 2) molecule-a key molecular building block in phosphorus chemistry-has remained elusive. Here, we report a facile, versatile pathway producing cyclotriphosphazene and its Dewar benzene-type isomer (P3N3, 5) in ammonia-phosphine ices at 5 K exposed to ionizing radiation. Both isomers were detected in the gas phase upon sublimation via photoionization reflectron time-of-flight mass spectrometry and discriminated via isomer-selective photochemistry. Our findings provide a fundamental framework to explore the preparation of inorganic, isovalent species of benzene (C6H6) by formally replacing the CâH moieties alternatingly through phosphorus and nitrogen atoms, thus advancing our perception of the chemical bonding of phosphorus systems.
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For decades, the source of phosphorus incorporated into Earth's first organisms has remained a fundamental, unsolved puzzle. Although contemporary biomolecules incorporate P(+V) in their phosphate moieties, the limited bioavailability of phosphates led to the proposal that more soluble P(+III) compounds served as the initial source of phosphorus. Here, we report via laboratory simulation experiments that the three simplest alkylphosphonic acids, soluble organic phosphorus P(+III) compounds, can be efficiently generated in interstellar, phosphine-doped ices through interaction with galactic cosmic rays. This discovery opens a previously overlooked avenue into the formation of key molecules of astrobiological significance and untangles basic mechanisms of a facile synthesis of phosphorus-containing organics in extraterrestrial ices, which can be incorporated into comets and asteroids before their delivery and detection on Earth such as in the Murchison meteorite.
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With nearly 200 molecules detected in interstellar and circumstellar environments, the identification of the biologically relevant α-keto carboxylic acid, glyoxylic acid (HCOCOOH), is still elusive. Herein, the formation of glyoxylic acid via cosmic-ray driven, non-equilibrium chemistry in polar interstellar ices of carbon monoxide (CO) and water (H2 O) at 5â K via barrierless recombination of formyl (HCO) and hydroxycarbonyl radicals (HOCO) is reported. In temperature-programmed desorption experiments, the subliming neutral molecules were selectively photoionized and identified based on the ionization energy and distinct mass-to-charge ratios in combination with isotopically labeled experiments exploiting reflectron time-of-flight mass spectrometry. These studies unravel a key reaction path to glyoxylic acid, an organic molecule formed in interstellar ices before subliming in star-forming regions like SgrB2(N), thus providing a critical entry point to prebiotic organic synthesis.
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Phosphorus signifies an essential element in molecular biology, yet given the limited solubility of phosphates on early Earth, alternative sources like meteoritic phosphides have been proposed to incorporate phosphorus into biomolecules under prebiotic terrestrial conditions. Here, we report on a previously overlooked source of prebiotic phosphorus from interstellar phosphine (PH3) that produces key phosphorus oxoacids-phosphoric acid (H3PO4), phosphonic acid (H3PO3), and pyrophosphoric acid (H4P2O7)-in interstellar analog ices exposed to ionizing radiation at temperatures as low as 5 K. Since the processed material of molecular clouds eventually enters circumstellar disks and is partially incorporated into planetesimals like proto Earth, an understanding of the facile synthesis of oxoacids is essential to untangle the origin of water-soluble prebiotic phosphorus compounds and how they might have been incorporated into organisms not only on Earth, but potentially in our universe as well.
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Complex organic molecules are ubiquitous in star- and planet-forming regions as well as on comets such as on 67P/Churyumov-Gerasimenko, but their origins have remained largely unexplained until now. Here, we report the first laboratory detection of distinct C3 H8 O (propanol, methyl ethyl ether) and C4 H8 O (n-butanal, i-butanal) isomers formed within interstellar analog ices through interaction with ionizing radiation. This study reveals that complex organics with propyl (C3 H7 ) and butyl (C4 H9 ) groups can be synthesized easily in deep space and may act as key evolutionary tracers of a cosmic ray driven non-equilibrium chemistry in low temperature interstellar ices at 10â K. These processes are of vital importance in initiating a chain of chemical reactions leading to complex organics-some of which are responsible for the flavors of chocolate-not only in the interstellar medium, but also on comet 67P/Churyumov-Gerasimenko.
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1-Propanol/síntesis química , 2-Propanol/síntesis química , Aldehídos/síntesis química , Monóxido de Carbono/química , Monóxido de Carbono/efectos de la radiación , Cationes , Medio Ambiente Extraterrestre , Isomerismo , Espectrometría de Masas , Metano/química , Metano/efectos de la radiación , Radiación IonizanteRESUMEN
Thin films of ammonium perchlorate (NH4ClO4) were exposed to energetic electrons at 5.5 K to explore the radiolytic decomposition mechanisms. The effects of radiolysis were monitored on line and in situ via Fourier transform infrared spectroscopy (FTIR) in the condensed phase along with electron impact ionization quadrupole mass spectrometry (EI-QMS) and single-photon photoionization reflectron time-of-flight mass spectrometry (PI-ReTOF-MS) during the temperature-programmed desorption (TPD) phase to probe the subliming molecules. Three classes of molecules were observed: (i) nitrogen bearing species [ammonia (NH3), hydroxylamine (NH2OH), molecular nitrogen (N2), nitrogen dioxide (NO2)], (ii) chlorine carrying molecules [chlorine monoxide (ClO), chlorine dioxide (ClO2), dichlorine trioxide (Cl2O3)], and (iii) molecular oxygen (O2). Decay profiles of the reactants along with the growth profiles of the products as derived from the infrared data were fit kinetically to obtain a reaction mechanism with the initial steps involving a proton loss from the ammonium ion (NH4+) yielding ammonia (NH3) and the decomposition of perchlorate ion (ClO4-) forming chlorate ion (ClO3-) plus atomic oxygen. The latter oxidized ammonia to hydroxylamine and ultimately to nitrogen dioxide. Molecular oxygen and nitrogen were found to be formed via recombination of atomic oxygen and multistep radiolysis of ammonia, respectively.
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Extrasolar Earth and super-Earth planets orbiting within the habitable zone of M dwarf host stars may play a significant role in the discovery of habitable environments beyond Earth. Spectroscopic characterization of these exoplanets with respect to habitability requires the determination of habitability parameters with respect to remote sensing. The habitable zone of dwarf stars is located in close proximity to the host star, such that exoplanets orbiting within this zone will likely be tidally locked. On terrestrial planets with an icy shell, this may produce a liquid water ocean at the substellar point, one particular "Eyeball Earth" state. In this research proposal, HABEBEE: exploring the HABitability of Eyeball-Exo-Earths, we define the parameters necessary to achieve a stable icy Eyeball Earth capable of supporting life. Astronomical and geochemical research will define parameters needed to simulate potentially habitable environments on an icy Eyeball Earth planet. Biological requirements will be based on detailed studies of microbial communities within Earth analog environments. Using the interdisciplinary results of both the physical and biological teams, we will set up a simulation chamber to expose a cold- and UV-tolerant microbial community to the theoretically derived Eyeball Earth climate states, simulating the composition, atmosphere, physical parameters, and stellar irradiation. Combining the results of both studies will enable us to derive observable parameters as well as target decision guidance and feasibility analysis for upcoming astronomical platforms.