Mechanistical study on the formation of hydroxyacetone (CH3COCH2OH), methyl acetate (CH3COOCH3), and 3-hydroxypropanal (HCOCH2CH2OH) along with their enol tautomers (prop-1-ene-1,2-diol (CH3C(OH)CHOH), prop-2-ene-1,2-diol (CH2C(OH)CH2OH), 1-methoxyethen-1-ol (CH3OC(OH)CH2) and prop-1-ene-1,3-diol (HOCH2CHCHOH)) in interstellar ice analogs

被引:10
|
作者
Wang, Jia [1 ,2 ]
Marks, Joshua H. [1 ,2 ]
Turner, Andrew M. [1 ,2 ]
Nikolayev, Anatoliy A. [3 ,4 ]
Azyazov, Valeriy [3 ]
Mebel, Alexander M. [5 ]
Kaiser, Ralf, I [1 ,2 ]
机构
[1] Univ Hawaii Manoa, WM Keck Res Lab Astrochem, Honolulu, HI 96822 USA
[2] Univ Hawaii Manoa, Dept Chem, Honolulu, HI 96822 USA
[3] Lebedev Phys Inst, Samara 443011, Russia
[4] Samara Natl Res Univ, Samara 443086, Russia
[5] Florida Int Univ, Dept Chem & Biochem, Miami, FL 33199 USA
基金
美国国家科学基金会;
关键词
VACUUM-ULTRAVIOLET PHOTOIONIZATION; COMPLEX ORGANIC-MOLECULES; AMINO-ACIDS; IONIZING-RADIATION; ETHYLENE-OXIDE; UV-IRRADIATION; VINYL ALCOHOL; METHANOL; GAS; ACETALDEHYDE;
D O I
10.1039/d2cp03543j
中图分类号
O64 [物理化学(理论化学)、化学物理学];
学科分类号
070304 ; 081704 ;
摘要
We unravel, for the very first time, the formation pathways of hydroxyacetone (CH3COCH2OH), methyl acetate (CH3COOCH3), and 3-hydroxypropanal (HCOCH2CH2OH), as well as their enol tautomers within mixed ices of methanol (CH3OH) and acetaldehyde (CH3CHO) analogous to interstellar ices in the ISM exposed to ionizing radiation at ultralow temperatures of 5 K. Exploiting photoionization reflectron time-of-flight mass spectrometry (PI-ReToF-MS) and isotopically labeled ices, the reaction products were selectively photoionized allowing for isomer discrimination during the temperature-programmed desorption phase. Based on the distinct mass-to-charge ratios and ionization energies of the identified species, we reveal the formation pathways of hydroxyacetone (CH3COCH2OH), methyl acetate (CH3COOCH3), and 3-hydroxypropanal (HCOCH2CH2OH) via radical-radical recombination reactions and of their enol tautomers (prop-1-ene-1,2-diol (CH3C(OH)CHOH), prop-2-ene-1,2-diol (CH2C(OH)CH2OH), 1-methoxyethen-1-ol (CH3OC(OH)CH2) and prop-1-ene-1,3-diol (HOCH2CHCHOH)) via keto-enol tautomerization. To the best of our knowledge, 1-methoxyethen-1-ol (CH3OC(OH)CH2) and prop-1-ene-1,3-diol (HOCH2CHCHOH) are experimentally identified for the first time. Our findings help to constrain the formation mechanism of hydroxyacetone and methyl acetate detected within star-forming regions and suggest that the hitherto astronomically unobserved isomer 3-hydroxypropanal and its enol tautomers represent promising candidates for future astronomical searches. These enol tautomers may contribute to the molecular synthesis of biologically relevant molecules in deep space due to their nucleophilic character and high reactivity.
引用
收藏
页码:936 / 953
页数:19
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