Thermal Synthesis of Carbamic Acid and Its Dimer in Interstellar Ices: A Reservoir of Interstellar Amino Acids

被引:11
作者
Marks, Joshua H. [1 ,2 ]
Wang, Jia [1 ,2 ]
Sun, Bing-Jian [3 ]
McAnally, Mason [1 ,2 ]
Turner, Andrew M. [1 ,2 ]
Chang, Agnes H. -H. [3 ]
Kaiser, Ralf I. [1 ,2 ]
机构
[1] Univ Hawaii Manoa, W M Keck Res Lab Astrochem, Honolulu, HI 96822 USA
[2] Univ Hawaii Manoa, Dept Chem, Honolulu, HI 96822 USA
[3] Natl Dong Hwa Univ, Dept Chem, Hualien 974, Taiwan
基金
美国国家科学基金会;
关键词
VACUUM-ULTRAVIOLET PHOTOIONIZATION; CARBON-DIOXIDE; MOLECULAR-STRUCTURE; AMMONIUM CARBAMATE; ORGANIC-MOLECULES; VUV SPECTROSCOPY; MID-IR; NH3; IRRADIATION; ASSIMILATION;
D O I
10.1021/acscentsci.3c01108
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Reactions in interstellar ices are shown to be capable of producing key prebiotic molecules without energetic radiation that are necessary for the origins of life. When present in interstellar ices, carbamic acid (H2NCOOH) can serve as a condensed-phase source of the molecular building blocks for more complex proteinogenic amino acids. Here, Fourier transform infrared spectroscopy during heating of analogue interstellar ices composed of carbon dioxide and ammonia identifies the lower limit for thermal synthesis to be 62 +/- 3 K for carbamic acid and 39 +/- 4 K for its salt ammonium carbamate ([H2NCOO-][NH4+]). While solvation increases the rates of formation and decomposition of carbamic acid in ice, the absence of solvent effects after sublimation results in a significant barrier to dissociation and a stable gas-phase molecule. Photoionization reflectron time-of-flight mass spectrometry permits an unprecedented degree of sensitivity toward gaseous carbamic acid and demonstrates sublimation of carbamic acid from decomposition of ammonium carbamate and again at higher temperatures from carbamic acid dimers. Since the dimer is observed at temperatures up to 290 K, similar to the environment of a protoplanetary disk, this dimer is a promising reservoir of amino acids during the formation of stars and planets.
引用
收藏
页码:2241 / 2250
页数:10
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