THE FIRST SIH22-PICOLINE)SILICON DICHLORIDE-TETRAKIS(CHLOROFORM), [H2SI(3PIC)(4)]CL-2-CENTER-DOT-4 CHCL3 - FORMATION, CHEMICAL-EQUILIBRIA, AND STRUCTURAL INVESTIGATION BY NMR-SPECTROSCOPY AND SINGLE-CRYSTAL X-RAY-DIFFRACTION( COMPLEX, DIHYDRIDOTETRAKIS(3)

Citation
H. Fleischer et al., THE FIRST SIH22-PICOLINE)SILICON DICHLORIDE-TETRAKIS(CHLOROFORM), [H2SI(3PIC)(4)]CL-2-CENTER-DOT-4 CHCL3 - FORMATION, CHEMICAL-EQUILIBRIA, AND STRUCTURAL INVESTIGATION BY NMR-SPECTROSCOPY AND SINGLE-CRYSTAL X-RAY-DIFFRACTION( COMPLEX, DIHYDRIDOTETRAKIS(3), Chemische Berichte, 129(7), 1996, pp. 765-771
Citations number
35
Categorie Soggetti
Chemistry
Journal title
ISSN journal
00092940
Volume
129
Issue
7
Year of publication
1996
Pages
765 - 771
Database
ISI
SICI code
0009-2940(1996)129:7<765:TFSD[>2.0.ZU;2-Q
Abstract
Bis(dichlorosilyl) amine reacts in chloroform solution with 2-picoline to give H3SiCl, H2SiCl2, and HSiCl3, whereas with 3-picoline the two hypervalent silicon compounds H2SiCl2-(3pic)(2) and [H2Si(3pic)(4)]Cl- 2 . 4 CHCl3 containing hexacoordinated Si atoms are formed. These comp lexes are in a chemical equilibrium with each other in chloroform solu tion, from which crystals of [H2Si(3pic)(4)]Cl-2 . 4 CHCl3 could be is olated. The crystal structure of the latter was determined by single-c rystal X-ray diffraction. The complex can be regarded as an ''contact ion trio'' of [H2Si(3pic)(4)](2+) and two Cl- ions. The N-->Si bond le ngths, r(Si-N) = 196.9(3) and 197.5(3) pm, are similar to those found in neutral hexacoordinated Si complexes. The data obtained from a (HH) -H-1-H-1 ROESY experiment suggest that dissolution has no significant impact on the molecular structure of [H2Si(3pic)(4)]Cl-2 . 4 CHCl3.