Hydrogen bonding of two 1-(phi-ammonioalkyl)-2-acyl-cyclopentadienides in the solid state

Authors
Citation
A. Muller et G. Maas, Hydrogen bonding of two 1-(phi-ammonioalkyl)-2-acyl-cyclopentadienides in the solid state, Z NATURFO B, 55(6), 2000, pp. 541-545
Citations number
20
Categorie Soggetti
Chemistry
Journal title
ZEITSCHRIFT FUR NATURFORSCHUNG SECTION B-A JOURNAL OF CHEMICAL SCIENCES
ISSN journal
09320776 → ACNP
Volume
55
Issue
6
Year of publication
2000
Pages
541 - 545
Database
ISI
SICI code
0932-0776(200006)55:6<541:HBOT1I>2.0.ZU;2-B
Abstract
The solid-state structures of a 1-(phi-ammoniopropyl)-2-(2-thienylcarbonyl) -cyclopentadienide (2) and a 1-(phi-ammoniopentyl)-2-(4-methoxybenzoyl)-cyc lopentadienide (3) have been determined. Both betaines self-assemble by NH ... O hydrogen bonds, but the motifs are different. In the ammoniopropyl ca se, both intramolecular and intermolecular hydrogen bonds of this type exis t, the latter bond being responsible for the formation of infinite chains. In the ammoniopentyl case, intermolecular hydrogen bonds build up a two-dim ensional network which contains centrosymmetric dimers held together by NH ... O=C-aryl hydrogen bonds.