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Molecular Structure, Vibrational Spectra, Quantum Chemical Calculations and Photochemistry of Picolinamide and Isonicotinamide Isolated in Cryogenic Inert Matrixes and in the Neat Low-Temperature Solid Phases

机译:低温惰性基质和整洁的低温固相中分离的吡啶啉和异烟酰胺的分子结构,振动光谱,量子化学计算和光化学

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摘要

Picolinamide (PA) and isonicotinamide (INA), two structural isomers of pyridinecarboxamide, have been investigated by matrix isolation and low-temperature solid-state infrared spectroscopy, combined with UV (λ > 235 nm) photoexcitation and density functional theory and ab initio (MP2) theoretical studies. In consonance with the theoretical data, both PA and INA were found to exist in a single conformation in cryogenic rare gas matrixes. Comparison between the experimental spectra of the matrix-isolated compounds with those theoretically predicted allowed for full assignment of the experimental spectra. In situ UV (λ > 235 nm) irradiation of the matrixes showed that only PA reacts, with production of isocyanic acid and pyridine, the first photoproduct further reacting to yield CO + NH and cyanic acid. The different photochemical behavior of the two compounds was explained taking into consideration their different structures. The infrared spectra of (i) the low-temperature glassy state resulting from fast deposition of vapors of the compounds onto a substrate cooled to 10 K, (ii) the crystal resulting from the annealed amorphous film of the compound, and (iii) the room-temperature crystals (α-phase) of the studied compounds were also obtained, fully assigned and correlated with intermolecular interactions present in the condensed phases, in particular H-bond interactions, showing that these latter are stronger in INA than in PA.
机译:通过基质分离和低温固态红外光谱,结合紫外光(λ> 235 nm)的光激发和密度泛函理论以及从头算(Ab initio),研究了吡啶甲酰胺的两种结构异构体-吡啶甲酰胺(PA)和异烟酰胺(INA)。 MP2)理论研究。与理论数据相一致,在低温稀有气体基质中,PA和INA均以单一构型存在。将基质分离的化合物的实验光谱与理论上预测的光谱进行比较,可以完全分配实验光谱。基质的原位UV(λ> 235 nm)辐照表明,只有PA反应生成异氰酸和吡啶,第一个光产物进一步反应生成CO + NH和氰酸。考虑到它们的不同结构,解释了这两种化合物的不同光化学行为。 (i)化合物的蒸气快速沉积到冷却至10 K的基材上而形成的低温玻璃态的红外光谱,(ii)化合物的非晶态膜退火后产生的晶体,以及(iii)还获得了所研究化合物的室温晶体(α相),该晶体完全分配并与缩合相中存在的分子间相互作用(尤其是氢键相互作用)相关,这表明它们在INA中比在PA中更强。

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