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Coordination chemistry of anticrowns: Complexation of cyclic trimeric perfluoro-o-phenylenemercury with nitro compounds by I.A. Tikhonova; K.I. Tugashov; F.M. Dolgushin; A.A. Yakovenko; P.V. Petrovskii; G.G. Furin; A.P. Zaraisky; V.B. Shur is a Chemistry article available to read on EtoBox.

What is Coordination chemistry of anticrowns: Complexation of cyclic trimeric perfluoro-o-phenylenemercury with nitro compounds about?

Cyclic trimeric perfluoro-o-phenylenemercury (o-C 6 F 4 Hg) 3 ( ) is capable of reacting with nitromethane to give complex {[(o-C 6 F 4 Hg) 3 ](CH 3 NO 2 )} ( ) containing one molecule of the nitro compound per one macrocycle molecule. In this complex, the nitromethane ligand is bound to 1 by its both oxygen atoms, one of which is simultaneously coordinated to all three Hg centres of the macrocycle while the other interacts with a single Hg centre. The complex of similar composition, {[(o-C 6 F 4 Hg) 3 ](C 6 H 5 NO 2 )} (3), is produced in the interaction of 1 with nitrobenzene. In this complex too, the both oxygen atoms of the nitro group are involved in the bonding to the macrocycle. A distinctive feature of 3 is that here one oxygen atom of the coordinated nitro derivative is bound by only two Hg centres of 1 whereas the other interacts again with a single Hg site. The reaction of 1 with 5-nitroacenaphthene affords a 1:1 complex, {[(o-C 6 F 4 Hg) 3 ](C 12 H 9 NO 2 )} (4), having a polydecker sandwich structure in the crystal. Unlike in 3, the aromatic rings of the nitroarene units in 4 are disposed virtually in parallel to the macrocycles. The nitro compound in 4 behaves again a

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Author
I.A. Tikhonova; K.I. Tugashov; F.M. Dolgushin; A.A. Yakovenko; P.V. Petrovskii; G.G. Furin; A.P. Zaraisky; V.B. Shur
Publisher
Elsevier Science; Elsevier ; Elsevier BV (ISSN 0022-328X)
Published
2007
Language
EN
Field
Chemistry (Physical Sciences)

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