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Crystal Structure Analysis and NMR Spectra of N-(Pentafluorobenzoyl)-4-dimethylaminopyridinium Hexachloroantimonate(V)

Sandro Hollenstein ; Laboratorium für Organische Chemie der Eidgenössischen Technischen Hochschule Zürich, ETH-Zentrum, Universitatstrasse 16, CH-8092 Zürich, Switzerland
Christian Lohse ; Laboratorium für Organische Chemie der Eidgenössischen Technischen Hochschule Zürich, ETH-Zentrum, Universitatstrasse 16, CH-8092 Zürich, Switzerland
Thomas Laube ; Laboratorium für Organische Chemie der Eidgenössischen Technischen Hochschule Zürich, ETH-Zentrum, Universitatstrasse 16, CH-8092 Zürich, Switzerland

Sažetak

The crystal structure analysis of N-(pentafluorobenzoyl)-4-dimethyl- aminopyridinium hexachloroantimonate(V) (space group: PI, measurement at -80 °C; high-order refinement; R = 0.035, Pw = 0.035 with all data) shows, that the carbonyl group and the dimethylaminopyridine (DMAP) fragment have a practically coplanar arrangement, while the pentafluorophenyl group is twisted b yea. 69° out of that plane. The resulting CO-DMAP-TT-interaction allows a charge delocalization towards the dimethylamino group, i.e. the cation may be best described as an iminium ion. The crystal packing reveals cation-anion interactions only in the formal iminium fragment. The carbonyl-C atom, which is attacked by a nucleophile in the course of an acylation reaction, has two intramolecular and one intermolecular van der Waals contacts to fluorine atoms. The structure is also interpreted in terms of a beginning dissociation into an acyl cation and DMAP. The 'H, 13C and 19F NMR spectra are compared with those of related molecules.

Ključne riječi

Hrčak ID:

137130

URI

https://hrcak.srce.hr/137130

Datum izdavanja:

15.10.1992.

Posjeta: 961 *