91407-89-5Relevant academic research and scientific papers
Heteroleptic μ-nitrido diiron complex supported by phthalocyanine and octapropylporphyrazine ligands: Formation of oxo species and their reactivity with fluorinated compounds
Colomban, Cédric,Kudrik, Evgeny V.,Sorokin, Alexander B.
, p. 345 - 353 (2017)
The synthesis and reactivity of N-bridged diiron macrocyclic complexes have been a topic of increasing interest in recent years since the observation of particular catalytic properties of these complexes. Herein, we report a preparation of a novel heteroleptic μ-nitrido diiron complex with unsubstituted phthalocyanine and octapropylporphyrazine macrocycles. This complex reacts with m-chloroperbenzoic acid to form high-valent diiron oxo species showing strong oxidizing properties. The formation and structure of the transient oxo species was investigated by cryospray collision induced dissociation MS/MS technique. Analysis of fragmentation pattern showed that the attachment of oxo moiety occurred at either iron phthalocyanine or at iron porphyrazine site with slight preference for the phthalocyanine iron site. The catalytic properties of the heteroleptic μ-nitrido diiron complex were evaluated in the oxidative transformation of hexafluorobenzene and perfluoro(allylbenzene).
AROMATIC FLUORINE DERIVATIVES. XCVIII. HEPTAFLUOROPHENYLACETIC ACID. PRODUCTION AND SOME PROPERTIES
Bardin, V. V.,Furin, G. G.,Yakobson, G. G.
, p. 514 - 519 (2007/10/02)
A mixture of C6F5CHFCN and C6F5CF2CN is formed by the action of perchloryl fluoride on pentafluorophenylacetonirile in the presence of cesium fluoride.Hydrolysis of the second product gave the previously unknown heptafluorophenylacetic acid.This acid was also synthesized by the oxidation of perfluoroallylbenzene with potassium permanganate.The chloride, fluoride, amide, and methyl ester of heptafluorophenylacetic acid were obtained.
