ON THE ELECTOCHEMICAL FLUORINATION OF AMINOETHERS TO GIVE PERFLUOROAMINOETHERS: POSSIBLE CANDIDATES FOR BLOOD SUBSTITUTES

DOI: 10.1016/S0022-1139(00)80346-2

Source and publish data:

Journal of Fluorine Chemistry p. 317 - 331 (1991)

Update date:2022-08-05

Topics:

Authors:

Dimitrov, A.

Radeck, W.

Ruediger, St.

Platonov, V.E.

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Article abstract of DOI:10.1016/S0022-1139(00)80346-2

Aminoethers, (R=C6H5, C6F5, C2H5), C6F5OC2H4N(CH2)5, were electrofluorinated in anhydrous hydrogen fluoride, the corresponding saturated perfluoroaminoethers being the largest individual substances in each case.One of them, F-<4-(2-cyclohexyloxy

Full text of DOI:10.1016/S0022-1139(00)80346-2

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