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首页> 外文期刊>Journal of Molecular Structure >The analytical characterization of a depside in a living species: Spectroscopic and theoretical analysis of lecanoric acid extracted from Parmotrema tinctorum Del. Ex Nyl. lichen
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The analytical characterization of a depside in a living species: Spectroscopic and theoretical analysis of lecanoric acid extracted from Parmotrema tinctorum Del. Ex Nyl. lichen

机译:活体物种中的尿苷的分析特性:从Parmotrema tinctorum Del。Ex Nyl提取的柠檬酸的光谱学和理论分析。地衣

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FT-Raman spectroscopy has been used for the analytical characterization of the Parmotrema tinctorum Del. Ex Nyl. lichen. Lecanoric acid, the major lichen chemical present in the total mass, has been extracted from the lichen, purified and characterized by Raman spectroscopy supported by means of theoretical DFT calculations. The calculations indicate that the aromatic ring A of the lecanoric acid structure is kept in the molecular plane by a strong hydrogen bond between the ortho-hydroxyl group of ring A and the ester group; this hydrogen bond is shorter in the C1 isomer form, which is the main feature responsible for the Gibbs free energy difference (-2.96 kcal/mol) favouring the C1 isomer. In spite of the similarity of possible conformers and although many of the predicted Raman bands are found to be common for both forms, there is one Raman transition very characteristic of structure C2, centred at 1815 cm(-1), assigned to the stretching of the C=O group of the ester moiety (v(C=O, ester)). For the isomer C1 this transition was predicted at 1729 cm(-1), with a lower frequency ascribed to the stronger hydrogen bond present in the latter conformation. In the experimental spectrum two strong bands are found at 1654 and 1638 cm-1 (shoulder) attributed to the C=O stretching mode. The analysis of the normal modes for the corresponding transitions calculated at 1742 and 1729 cm-1 allowed the assignment to be made to v(C=O) from the carboxylic acid and ester moiety, respectively. Most of the other Raman bands were also assigned by comparison with the theoretical model. The Raman spectrum obtained directly from the A tinctorum lichen shows a remarkable similarity with the isolated lecanoric acid spectrum, as well as the presence of bands at 1529 and 1156 cm(-1) which are characteristic of a carotenoid species. The results confirm the potential of Raman spectroscopy for taxonomic characterization of lichen species.
机译:FT-拉曼光谱已用于Parmotrema tinctorum Del。Ex Nyl的分析表征。地衣。总质量中存在的主要地衣化学物质柠檬酸已从地衣中提取,纯化并通过拉曼光谱法进行了表征,并通过理论DFT计算得到了支持。计算表明,柠檬酸的结构的芳环A通过环A的邻羟基与酯基之间的强氢键而保持在分子平面内。该氢键以C1异构体形式较短,这是导致Gibbs自由能差(-2.96 kcal / mol)的主要特征,有利于C1异构体。尽管可能的构象异构体相似,并且尽管发现许多预测的拉曼谱带对于这两种形式都是相同的,但还是存在一个拉曼跃迁,其特征是结构C2,以1815 cm(-1)为中心,被指定用于拉伸酯部分的C = O基团(v(C = O,酯))。对于异构体C1,此转变预计在1729 cm(-1)处发生,较低的频率归因于后者构象中存在的较强氢键。在实验光谱中,在1654和1638 cm-1(肩部)发现了两个强带,这归因于C = O拉伸模式。对在1742和1729 cm-1处计算出的相应跃迁的正态模态的分析,使得可以分别从羧酸和酯部分分配v(C = O)。通过与理论模型比较,还分配了其他大多数拉曼波段。直接从丁香地衣获得的拉曼光谱显示了与孤立的lecanoric酸光谱的显着相似性,以及在1529和1156 cm(-1)处的条带,这些条带是类胡萝卜素物种的特征。结果证实了拉曼光谱法在地衣种类分类学表征中的潜力。

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