13709-61-0Relevant articles and documents
Crystal Structures of Photochemically Prepared (Xe2F11)2(MF6) (M = Sn, Pb) and (XeF5)4(Sn5F24) Containing Six- and Seven-Coordinated Tin(IV)
Mazej, Zoran,Goreshnik, Evgeny
, p. 1265 - 1272 (2019)
Single crystals of [Xe2F11]2[SnF6], [Xe2F11]2[PbF6], and [XeF5]4[Sn5F24] were grown from saturated aHF solutions upon crystallizations. The crystal structures of isotypic [Xe2F11]2[SnF6] and [Xe2F11]2[PbF6] consist of [Xe2F11]+ cations and [MF6]2– anions (M = Sn, Pb) that interact by means of fluorine bridge contacts. The single crystal structure determination of [XeF5]4[Sn5F24] reveals that it is built of two-dimensional ([Sn5F24]4–)∞ grids and [XeF5]+ cations located between them. The 2D grids have a wave-like conformation. The ([Sn5F24]4–)∞ layer contains, both, six- and seven-coordinated Sn(IV) interconnected by bridging fluorine atoms. The coordination of Sn(IV) by seven fluorine atoms is unprecedented. Attempts to synthesize and grow single crystals of the [XeF5][MF5] (M = Zr, Hf, Ni, Pd) compounds failed.
Templeton, D. H.,Zalkin, A.,Forrester, J. D.,Williamson, S. M.
, p. 242 - 242 (1963)
Largest perfluorometallate [Ti10F45]5- oligomer and polymeric ([Ti3F13]-)∞ and ([TiF5]-)∞ anions prepared as [XeF5]+ salts
Mazej, Zoran,Goreshnik, Evgeny A.
, p. 7320 - 7325 (2016/09/12)
Reactions between XeF2, TiF4 and UV-irradiated elemental F2 in anhydrous HF yielded XeF5TiF5 (XeF6·TiF4), [XeF5]5[Ti10F45] (XeF6·2TiF4), and [XeF5][Ti3F13] (XeF6·3TiF4) upon crystallization. [XeF5]5[Ti10F45] crystallizes in two crystal modifications at low (α-phase, 150 K) and ambient (β-phase, 296 K) temperatures. The crystal structure determination of [XeF5]5[Ti10F45] reveals the largest known discrete decameric [Ti10F45]5- anion built from ten TiF6 octahedra, sharing vertices, in the shape of a double-star. [XeF5]+ cations are completely ordered in the α-phase, while one of three crystallographically unique [XeF5]+ cations is two-fold disordered in the β-phase. The anionic part of [XeF5][Ti3F13] is built from tetrameric Ti4F20 and octameric Ti8F36 units sharing vertices and alternatively linked into ([Ti3F13]-)∞ columns. The charge balance is maintained by [XeF5]+ cations which form secondary Xe?F contacts with fluorine atoms of ([Ti3F13]-)∞ groups. The main structural feature of XeF5TiF5 is an infinite chain of distorted TiF6 octahedra joined by cis vertices.
Infrared spectroscopic observation of the radical XeF3 generated in solid argon
Misochko, Eugenii Ya,Akimov, Alexander V.,Belov, Vasilii A.,Tyurin, Daniil A.
, p. 8723 - 8728 (2009/12/08)
Xenon trifluoride radicals were generated by the solid-state chemical reaction of mobile fluorine atoms with XeF2 molecules isolated in a solid argon matrix. On the basis of spectroscopic and kinetic FTIR measurements and performed quantum chem