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13C NMR spectroscopic studies of the behaviors of carbonyl compounds in various solutions
Tetrahedron Letters ( IF 1.8 ) Pub Date : 2017-10-27 , DOI: 10.1016/j.tetlet.2017.10.071
Yoshikazu Hiraga , Saori Chaki , Satomi Niwayama

13C NMR spectroscopic studies were performed for carbonyl compounds having a hydroxyl group, a carboalkoxy group, an acetoxy group, or a carboxyl group in various solvents with different polarities for observation of their behaviors of 13C NMR chemical shifts of carbonyl carbons in solutions. It was found that the chemical shifts of the carbonyl carbons in 13C NMR have good correlation with the empirical parameter for solvent polarities, ETN, depending on the structures. Inter- or intramolecular hydrogen bonding and dipolar-dipolar interactions appear to play a key role in this observation.



中文翻译:

13 C NMR光谱研究各种溶液中羰基化合物的行为

在具有不同极性的各种溶剂中,对具有羟基,碳烷氧基,乙酰氧基或羧基的羰基化合物进行13 C NMR光谱研究,以观察其在溶液中的羰基碳的13 C NMR化学位移行为。发现在13 C NMR中羰基碳的化学位移与溶剂极性的经验参数E T N取决于结构,具有很好的相关性。分子间或分子内氢键和偶极-偶极相互作用似乎在这一观察中起关键作用。

更新日期:2017-10-27
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