Four short chain members of the copper(II) n-alkanoate series Cu(Cn)(2), from propanoate to hexanoate, have been synthesized, purified and characterized by means of optical microscopy, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), FTIR and Raman spectroscopy. The TGA study shows that decomposition starts on heating above 420 - 470K ( depending on the sample) in a nitrogen atmosphere. In addition, thermal decomposition was investigated by DSC using special high pressure pans and endo- and excthermic processes were found which have not been reported previously. All but one of the compounds melt to a liquid crystal phase, which decomposes before the clearing point. The exception is the propanoate homologue, which decomposes directly from the solid state. Despite this problem of sample decomposition, the identification by optical microscopy of the tetragonal ( butanoate) and hexagonal ( pentanoate and hexanoate) discotic columnar phases was, for first time, possible by the addition of small amounts of the corresponding acid to the samples. These results are in agreement with the X-ray diffraction study performed using swelled mixtures of these salts with hydrocarbon solvents. Two solid - solid transitions, not previously reported in the literature, were found for the butanoate homologue at 395.9 and 422.9K with DeltaH = 8.27 and 1.37 kJ mol(-1), respectively. The solid and liquid crystalline phases were investigated using variable temperature FTIR spectroscopy.

Short chain copper(II) n-alkanoate liquid crystals

FERLONI, PAOLO
2004-01-01

Abstract

Four short chain members of the copper(II) n-alkanoate series Cu(Cn)(2), from propanoate to hexanoate, have been synthesized, purified and characterized by means of optical microscopy, thermogravimetric analysis (TGA), differential scanning calorimetry (DSC), FTIR and Raman spectroscopy. The TGA study shows that decomposition starts on heating above 420 - 470K ( depending on the sample) in a nitrogen atmosphere. In addition, thermal decomposition was investigated by DSC using special high pressure pans and endo- and excthermic processes were found which have not been reported previously. All but one of the compounds melt to a liquid crystal phase, which decomposes before the clearing point. The exception is the propanoate homologue, which decomposes directly from the solid state. Despite this problem of sample decomposition, the identification by optical microscopy of the tetragonal ( butanoate) and hexagonal ( pentanoate and hexanoate) discotic columnar phases was, for first time, possible by the addition of small amounts of the corresponding acid to the samples. These results are in agreement with the X-ray diffraction study performed using swelled mixtures of these salts with hydrocarbon solvents. Two solid - solid transitions, not previously reported in the literature, were found for the butanoate homologue at 395.9 and 422.9K with DeltaH = 8.27 and 1.37 kJ mol(-1), respectively. The solid and liquid crystalline phases were investigated using variable temperature FTIR spectroscopy.
2004
The Physical Chemistry/Chemical Physics category includes resources on photochemistry, solid state chemistry, kinetics, catalysis, quantum chemistry, surface chemistry, electro-chemistry, chemical thermodynamics, thermo-physics, colloids, fullerenes and zeolites. Resources dealing with (liquid) crystals and crystallography are also included in this category. This category also includes resources on atomic, molecular and chemical physics, which concerns the structure of atoms and molecules, atomic and molecular interactions with radiation, magnetic resonance and relaxation, Mossbauer effect, and atomic and molecular collision processes and interactions.
Sì, ma tipo non specificato
Inglese
Internazionale
STAMPA
31
1
1
14
Copper propanoate; copper butanoate; copper pentanoate
5
info:eu-repo/semantics/article
262
Cheda, J. A. R.; Garcia, M. V.; Redondo, M. I.; Gargani, S; Ferloni, Paolo
1 Contributo su Rivista::1.1 Articolo in rivista
none
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/107554
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