TY - JOUR
T1 - Synthesis, characterization and thermal properties of new aromatic quaternary ammonium bromides
T2 - Precursors for ionic liquids and complexation studies
AU - Busi, Sara
AU - Lahtinen, Manu
AU - Ropponen, Jarmo
AU - Valkonen, Jussi
AU - Rissanen, Kari
N1 - Funding Information:
We thank Mr. Reijo Kauppinen and Prof. Erkki Kolehmainen for measuring the NMR spectra and Ms. Elina Hautakangas and Ms. Ritva Watia for measuring the elemental analysis data. K.R. gratefully acknowledges the financial support by the National Technology Agency (TEKES, proj. no. 40004/01) and S.B. correspondingly the Faculty of Mathematics and Science of University of Jyväskylä.
PY - 2004/10
Y1 - 2004/10
N2 - Series of new aromatic R 2R′ 2N +Br - (R=benzyl, 4-methylbenzyl, 2-phenylethyl, 3-phenylpropyl; R′=ethyl, methyl, isopropyl) or RR′ 2NH +Br --type (R=benzyl, R′=isopropyl) quaternary ammonium bromides were prepared by using novel synthetic route in which a formamide (N,N-diethylformamide, N,N-dimethylformamide, N,N-diisopropylformamide) is treated with aralkyl halide in presence of a weak base. The compounds were characterized by 1H-NMR and 13C-NMR spectroscopy and mass spectrometry. Structures of the crystalline compounds were determined by X-ray single crystal diffraction, and in addition the powder diffraction method was used to study the structural similarities between the single crystal and microcrystalline bulk material. Three of the compounds crystallized in monoclinic, two in orthorhombic and one in triclinic crystal system, showing ion pairs, which are interconnected by weak hydrogen bonds and weak π-π interactions between the phenyl rings. Three of the compounds appeared as viscous oil or waxes. Finally, TG/DTA and DSC methods were used to analyze thermal properties of the prepared compounds. The lowest melting points were obtained for diethyldi-(2-phenylethyl)ammonium bromide (122.2°C) and for diethyldi-(3-phenylpropyl)-ammonium bromide (109.1°C). In general, decomposition of the compounds started at 170-190°C without identifiable cleavages, thus liquid ranges of 30-70°C were observed for some of the compounds. The ion-pair ordering and hydrogen bonding of dimethyldi-(2-phenylethyl)ammonium bromide.
AB - Series of new aromatic R 2R′ 2N +Br - (R=benzyl, 4-methylbenzyl, 2-phenylethyl, 3-phenylpropyl; R′=ethyl, methyl, isopropyl) or RR′ 2NH +Br --type (R=benzyl, R′=isopropyl) quaternary ammonium bromides were prepared by using novel synthetic route in which a formamide (N,N-diethylformamide, N,N-dimethylformamide, N,N-diisopropylformamide) is treated with aralkyl halide in presence of a weak base. The compounds were characterized by 1H-NMR and 13C-NMR spectroscopy and mass spectrometry. Structures of the crystalline compounds were determined by X-ray single crystal diffraction, and in addition the powder diffraction method was used to study the structural similarities between the single crystal and microcrystalline bulk material. Three of the compounds crystallized in monoclinic, two in orthorhombic and one in triclinic crystal system, showing ion pairs, which are interconnected by weak hydrogen bonds and weak π-π interactions between the phenyl rings. Three of the compounds appeared as viscous oil or waxes. Finally, TG/DTA and DSC methods were used to analyze thermal properties of the prepared compounds. The lowest melting points were obtained for diethyldi-(2-phenylethyl)ammonium bromide (122.2°C) and for diethyldi-(3-phenylpropyl)-ammonium bromide (109.1°C). In general, decomposition of the compounds started at 170-190°C without identifiable cleavages, thus liquid ranges of 30-70°C were observed for some of the compounds. The ion-pair ordering and hydrogen bonding of dimethyldi-(2-phenylethyl)ammonium bromide.
KW - Ionic liquid
KW - Quaternary ammonium bromide
KW - Thermal analysis
KW - Weak interactions
KW - X-ray powder diffraction
KW - X-ray single crystal diffraction
UR - http://www.scopus.com/inward/record.url?scp=7244231534&partnerID=8YFLogxK
U2 - 10.1016/j.jssc.2004.06.046
DO - 10.1016/j.jssc.2004.06.046
M3 - Article
AN - SCOPUS:7244231534
SN - 0022-4596
VL - 177
SP - 3757
EP - 3767
JO - Journal of Solid State Chemistry
JF - Journal of Solid State Chemistry
IS - 10
ER -