化学
光解
光化学
从头算
光离子化
自然发生
化学反应
共价键
分子
化学物理
计算化学
卡宾
从头算量子化学方法
反应机理
烷基
反应中间体
构造形成
光谱学
化学键
非共价相互作用
协同反应
腈
物理化学
异氰
加成反应
量子化学
过渡状态
作者
Y W Li,Jiao Gao,Jiwen Guan,Jiao He,Min Xie,Yongjun Hu
摘要
The abiotic formation of prebiotic molecules with peptide or peptide-like bonds in the cold gaseous interstellar medium (ISM) and (exo)planetary atmospheric environments remains a critical unsolved question for elucidating cosmic chemical evolution and the origin of life. To explore the potential formation pathway, we combined vacuum ultraviolet–infrared (VUV-IR) photodissociation spectroscopy with ab initio quantum chemical calculations to investigate the ion–molecule reactions of three unsaturated nitriles (acrylonitrile, AN; 3-butenenitrile, 3BN; and 4-pentenenitrile, 4PN) with water under 118 nm photoionization. Experimental spectra reveal that the reaction products show a pronounced dependence on the alkyl chain length of the nitrile precursors. When short-chain AN reacts with water, it exclusively forms a kinetically trapped imine-alcohol cation (H + –N≡C–R–OH). In contrast, longer-chain 3BN and 4PN undergo efficient barrierless cyclization upon reaction with water, forming stable five- or six-membered cyclic cations with peptide-like bonds, respectively. The conclusions were supported by theoretical calculations of reaction pathways, which further reveal that all these reactions initially proceed via a mechanism analogous to Michael addition under basic conditions. These findings provide direct evidence for an ionization-induced intracluster covalent bond formation (ICBF) pathway to prebiotic peptide-like bonds under astrochemically relevant conditions, highlighting the critical role of molecular structure in governing its reaction selectivity.
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