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Inne
Esters of 4-nitrocinnamic acids and 4-halogene-4'-hydroxyazobenzenes : synthesis, mesogenic and optical studies.
Autorzy
Rok wydania
2019
Czasopismo
Numer woluminu
92
Strony
217-228
DOI
10.1080/01411594.2018.1563790
Kolekcja
Język
Angielski
Typ publikacji
Artykuł
Six new compounds were synthesized that have no alkyl chains in their structure: 4-nitrocinnonates of 4-hydroxyazobenzene, 4-nitro-4’-hydroxyazobenzene, 4-fluoro-4’-hydroxyazobenzene, 4-chloro-4’-hydroxyazobenzene, 4-bromo-4’-hydroxyazobenzene and 4-iodo-4’-hydroxyazobenzene. Using the polarizing microscopy and differential scanning calorimetry, enthalpies and temperatures of phase transitions were determined. All investigated compounds have an enantiotropic nematic phase. These compounds proved to be extremely thermally stable. Thermal decomposition was observed in temperatures above 300°C. Investigated compounds contain two different chromophore groups (i.e. azo and ethene moieties), which influenced the complex trans–cis isomerization processes of both groups (three time-separated processes were observed). It was shown that the presence of the ethene group significantly shifts the π-π* band towards higher energies. The substituent polarity in the azo group also affected the energy of this absorption band. A weak luminescence effect was observed in the 4-nitrocinnonates of 4-hydroxyazobenzene compound.
Słowa kluczowe
Azobenzenes, nematic, DSC calorymetry, Polarizing microscopy, trans-cis izomerization, luminescence
Adres publiczny
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