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Acta Chimica Sinica ›› 1966, Vol. 32 ›› Issue (1): 18-25. Previous Articles Next Articles
陈庆云, 蒋锡夔, 陈秉启, 梁梦兰
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CHEN Ching-Yun, JIANG Hsi-Kwei, CHEN Bing-Qi, LIANG Meng-Lan
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Perfluoro-t-butyl iodide (Ⅰ) was synthesized by the application of the method of Krespan.It was found that this method can be extended by the use of bromine in place of iodine for the synthesis of the corresponding bromide (Ⅱ).The first step in the reactions of the iodide (Ⅰ) with diethyl amine and ethanolic potassium hydroxide is shown to involve an SN2-like attack on the iodine atom by the nucleophile.The products of the above reactions were identical with those from the reactions between perfluoro-isobutene and the corresponding nucleophiles.Ultraviolet solvent shifts,δ(H-B),were determined for CF3)3CI,(CF3)2CFI,and CF3CF2CF2I.The δ(H-B) values provide evidence for an electron-withdrawing inductive order for perfluoro alkyl groups such as:(CF3)3C->(CF3)2CF->CF3CF2->CF3-.Arguments for the above order and against the generally accepted views are presented.
CHEN Ching-Yun, JIANG Hsi-Kwei, CHEN Bing-Qi, LIANG Meng-Lan. CHEMISTRY OF THE PERFLUORO AND POLYFLUORO ORGANIC COMPOUNDS——PERFLUORO-t-BUTYL IODIDE AND THE INDUCTIVE ORDER OF PERFLUOROALKYL GROUPS[J]. Acta Chimica Sinica, 1966, 32(1): 18-25.
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