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Título

(S)-Isoleucine and (R)-2-octanol as chiral precursors of new chiral liquid crystalline thiadiazoles: synthesis, mesomorphic and ferroelectric properties

AutorParra, M. L.; Vergara, Jorge CSIC ORCID; Hidalgo, P.; Barberá, Joaquín CSIC ORCID; Sierra, Teresa CSIC ORCID
Palabras claveCrystallography
Inorganic Chemistry
Materials Chemistry
Materials Science
Physical Chemistry
Polymer Science
Fecha de publicaciónjun-2006
EditorTaylor & Francis
CitaciónLiquid Crystals 33(6): 739-745 (2006)
ResumenNew chiral Schiff bases with a 1,3,4-thiadiazole unit in the rigid core were synthesized (SB1-SB4). These compounds contain a chiral chain derived from (S)-isoleucine and (R)-2-octanol. Their liquid crystalline properties were studied by polarizing optical microscopy, differential scanning calorimetry and X-ray diffraction. Thereby it was found that most of the new compounds exhibit a chiral Smectic C phase. A study of the ferroelectric properties is described.
Descripción7 pages.
Versión del editorhttp://dx.doi.org/10.1080/02678290600722866
URIhttp://hdl.handle.net/10261/19828
DOI10.1080/02678290600722866
ISSN0267-8292
E-ISSN1366-5855
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