Preparation and characterization of new aliphatic-tailed five- and six-membered azomethine-diimides

Bijak, K; Filapek, M; Wiacek, M; Janeczek, H; Grucela, M; Smolarek, K; Mackowski, S; Schab-Balcerzak, Ewa

HERO ID

3575432

Reference Type

Journal Article

Year

2016

Language

English

HERO ID 3575432
In Press No
Year 2016
Title Preparation and characterization of new aliphatic-tailed five- and six-membered azomethine-diimides
Authors Bijak, K; Filapek, M; Wiacek, M; Janeczek, H; Grucela, M; Smolarek, K; Mackowski, S; Schab-Balcerzak, Ewa
Journal Materials Chemistry and Physics
Volume 171
Page Numbers 97-108
Abstract New azomethine-phthalic (AzPhDIs) and azomethine-naphthalene (AzNDIs) diimides were synthesized in condensation reaction of diamines containing phthalic or naphthalene diimide core and two aldehydes: 4-(4,4,5,5,6,6,7,7,8,8,9,9,10,10,11,11,11-heptadecafluoroundecyloxy)benzaldehyde and 4-octadecyloxybenzaldehyde. The phase behavior of azomethine-diimides was examined by differential scanning calorymetry (DSC) and polarized optical microscopy (POM). AzPhDIs exhibited liquid crystalline properties in wide temperature range, whereas AzNDIs were not liquid crystalline. Thermal stability was investigated by thermogravimetric analysis (TGA). Azomethine-diimides exhibited high decomposition temperatures in the range between 360 and 401 degrees C. Optical properties were studied by UV-vis and photoluminescence (PL) measurements. Azomethine-diimides emitted blue light in NMP solution and blends with PMMA. The investigated compounds were electrochemically active and underwent reversible reduction and irreversible oxidation processes as evidenced by cyclic voltammetry (CV). Azomethine-diimides exhibited LUMO and HOMO levels in the range of -3.87 to -4.2 eV and -5.56 to -6.02 eV, respectively. (C) 2015 Elsevier B.V. All rights reserved.
Doi 10.1016/j.matchemphys.2015.12.005
Wosid WOS:000384703500016
Url <Go to ISI>://WOS:000384703500016
Is Certified Translation No
Dupe Override No
Is Public Yes
Language Text English
Keyword Organic compounds; Chemical synthesis; Photoemission; Differential scanning calorimetry (DSC); Electrochemical techniques