decachlorocyclopentasilanes coordinated by pairs of chloride anions, with different cations, but the same solvent molecules

decachlorocyclopentasilanes coordinated by pairs of chloride anions, with different cations, but the same solvent molecules

;Maximilian Moxter;Julian Teichmann;Hans-Wolfram Lerner;Michael Bolte;Matthias Wagner
Disability and rehabilitation 2017 Vol. 73 pp. 1903-1907
140
moxter2017actadecachlorocyclopentasilanes

Abstract

We have determined the crystal structures of two decachlorocyclopentasilanes, namely bis(tetra-n-butylammonium) dichloride decachlorocyclopentasilane dichloromethane disolvate, 2C16H36N+·2Cl−·Si5Cl10·2CH2Cl2, (I), and bis(tetraethylammonium) dichloride decachlorocyclopentasilane dichloromethane disolvate, 2C8H20N+·2Cl−·Si5Cl10·2CH2Cl2, (II), both of which crystallize with discrete cations, anions, and solvent molecules. In (I), the complete decachlorocyclopentasilane ring is generated by a crystallographic twofold rotation axis. In (II), one cation is located on a general position and the other two are disordered about centres of inversion. These are the first structures featuring the structural motif of a five-membered cyclopentasilane ring coordinated from both sides by a chloride ion. The extended structures of (I) and (II) feature numerous C—H...Cl interactions. In (II), the N atoms are located on centres of inversion and as a result, the ethylene chains are disordered over equally occupied orientations.

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