1865 Jrnl. Chem. Soc. XVIII. 308A combustion made of the pure acid gave numbers leading to the formula of iodoxybenzoic acid C7H5IO3.
1889 Ibid. LVI. 1150The authors are inclined to regard it as an iodoxydiiodobenzene, C6H3I2·OI.
1893 Ibid. LXIV. i. 506Iodoxybenzene, C6H5IO2, when treated with hydrochloric acid in aqueous solution, is converted into iodosobenzene hydrochloride.
1905 Jrnl. Soc. Chem. Industry 31 Jan. 104/1 (heading)Iodoxy compound (p-iodoxyphenol ester): and process of making same.
1935 Jrnl. Chem. Soc. 1669The present summary of several of our investigations, dealing particularly with the iodoxy-group IO2.
1950 N. V. Sidgwick Chem. Elements II. 1251The iodoxy-compounds hold their oxygen more firmly than the iodoso, and they are not such strong oxidizing agents.
1968 R. O. C. Norman Princ. Org. Synthesis xvi. 535Iodoxybenzene may be obtained in over 90% yield by steam-distilling iodosobenzene to remove the iodobenzene formed by the disproportionation.
iodoxy-
combining form
Etymology: International Scientific Vocabulary iod- + oxy-
: containing the univalent radical −IO2 of iodic acid, especially replacing hydrogen
< iodoxybenzoic acid C6H4(IO2)COOH >
< iodoxybenzoic acid C6H4(IO2)COOH >