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 Chemistry category includes resources that are general in nature and cover a broad spectrum of topics in the chemical sciences. Resources specifically covering analytical chemistry, inorganic and nuclear chemistry, organic chemistry, physical chemistry, and polymer science will be placed in those particular categories. Miscellaneous and applied chemistry resources may be placed in this category when not appropriate for specific subfields in chemistry.
Sì, ma tipo non specificato
Inglese
Internazionale
STAMPA
31
1
1
14
Tematica Ex SIR: Studi su materiali polimerici per sensoristica e optoelettronica (Classif. Ex SIR:Articoli su riviste ISI )
5
info:eu-repo/semantics/article
262
Ferloni, Paolo; Cheda, J. A. R.; Garcia, M. V.; Redondo, M. I.; Gargani, S.
1 Contributo su Rivista::1.1 Articolo in rivista
none
File in questo prodotto:
Non ci sono file associati a questo prodotto.

I documenti in IRIS sono protetti da copyright e tutti i diritti sono riservati, salvo diversa indicazione.

Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11571/16580
Citazioni
  • ???jsp.display-item.citation.pmc??? ND
  • Scopus ND
  • ???jsp.display-item.citation.isi??? ND
social impact