Anionic Complexes of the Perfluorinated Three-Mercury Anticrown (o,o'-C6F4C6F4Hg)3. Dependence of the Anion Coordination Type on Counter-Cation in Case of Chloride and Bromide Anions

被引:0
作者
Gribanyov, Dmitry A. [1 ]
Tugashov, Kirill, I [1 ]
Dolgushin, Fedor M. [2 ]
Peregudov, Alexander S. [1 ]
Kabaeva, Nina M. [1 ]
Tikhonova, Irina A. [1 ]
Shur, Vladimir B. [1 ]
机构
[1] Russian Acad Sci, AN Nesmeyanov Inst Organoelement Cpds, Vavilov St 28, Moscow 119991, Russia
[2] Russian Acad Sci, NS Kurnakov Inst Gen & Inorgan Chem, Leninskii Ave 31, Moscow 119071, Russia
来源
CHEMISTRYSELECT | 2022年 / 7卷 / 18期
关键词
Complexes; Halides; Mercury anticrowns; NMR spectroscopy; X-ray diffraction; ORTHO-PHENYLENEMERCURY; NONCOVALENT INTERACTIONS; LEWIS-ACIDS; O-XYLENE; CHEMISTRY; (O-C6F4HG)(3); RADII; ACETONITRILE; DISCRETE;
D O I
10.1002/slct.202200445
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The interaction of the macrocycle (o,o '-C6F4C6F4Hg)(3) (1) containing three mercury centres with arylphosphonium salts ([Ph4P]Cl or [Ph4P]Br) yields halide complexes, [Ph4P]{[(o,o '-C6F4C6F4Hg)(3)](eta(1):eta(1)-X)} (X=Cl, Br) having infinite polymer chain structure in the crystal. In both adducts, the halide anion is situated outside of the cavity of the three-mercury anticrown 1 and bridged by two mercury centres of neighbouring anticrown moieties. At the same time, when mercuracycle 1 interacts with tetraalkylammonium salts ([(Bu4N)-Bu-n]Cl or [(Bu4N)-Bu-n]Br), then the discrete 1 : 1 complexes [(Bu4N)-Bu-n]{[(o,o '-C6F4C6F4Hg)(3)](eta(3)-X)} (X=Cl, Br) of completely different structure are formed. In these halide complexes the anion is located inside the cavity of macrocycle 1 and coordinates the three mercury atoms symmetrically. The synthesized halide complexes [(Bu4N)-Bu-n]{[(o,o '-C6F4C6F4Hg)(3)](eta(3)-X)} (X=Cl, Br) are the first example of complexes of the macrocycle 1 where it behaves as anticrown.
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页数:6
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