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Molecular structure, vibrational spectra and photochemistry of 2-methyl-2 h -tetrazol-5-amine in solid argon

机译:固体氩气中2-甲基-2h-四唑-5-胺的分子结构,振动光谱和光化学

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摘要

In this work, the molecular structure, infrared spectrum and UV photochemistry of 2-methyl-2H-tetrazol-5-amine (2MTA) isolated in solid argon (10 K) were investigated. The experimental studies were supported byextensive DFT(B3LYP)/6-311++G(d,p) calculations. The infrared spectrum of matrix-isolated 2MTA was fully assigned and correlated with structural properties. Taking into consideration the observed frequency of the NH2 wagging mode, it is suggested that, in the matrixes, the amine group becomes slightly more planar than in the gas phase, due to matrix-packing effects. In situ UV irradiation (ì > 235 nm) of the matrixisolated 2MTA monomer is shown to induce three main primary photochemical processes: (1) tautomerization to mesoionic 3-methyl-1H-tetrazol-3-ium-5-aminide; (2) nitrogen elimination, with production of 1-methyl-1H-diazirene-3-amine; (3) ring cleavage leading to production of methyl azide and cyanamide. Following the primary photoproducts, secondary reactions were observed, leading to spectroscopic observation of methylenimine and isocyanidric acid.
机译:在这项工作中,研究了在固体氩气(10 K)中分离的2-甲基-2H-四唑-5-胺(2MTA)的分子结构,红外光谱和紫外光化学。 DFT(B3LYP)/ 6-311 ++ G(d,p)的广泛计算为实验研究提供了支持。完全分配了基质分离的2MTA的红外光谱,并将其与结构特性相关联。考虑到观察到的NH2摆动模式的频率,建议在基体中,由于基体的堆积效应,胺基的平面性比气相中的平面性略高。基质分离的2MTA单体的原位UV辐射(> 235 nm)已显示出诱导了三个主要的主要光化学过程:(1)互变异构化为中离子的3-甲基-1H-四唑-3-氨基-5-胺化物; (2)脱氮,生成1-甲基-1H-二氮杂-3-胺。 (3)环断裂导致叠氮化物和氰胺的产生。在初级光产物之后,观察到次级反应,从而导致对亚甲基亚胺和异氰基酸的光谱观察。

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