Synthesis of novel multifunctional carbazole-based molecules and their thermal, electrochemical and optical properties

被引:10
作者
Altinolcek, Nuray [1 ]
Battal, Ahmet [2 ,3 ]
Tavasli, Mustafa [1 ]
Peveler, William J. [3 ]
Yu, Holly A. [3 ]
Skabara, Peter J. [3 ]
机构
[1] Uludag Univ, Fac Sci Art, Dept Chem, TR-16059 Bursa, Turkey
[2] Mus Alparslan Univ, Fac Educ, Dept Elementary Sch Educ, TR-49100 Mus, Turkey
[3] Univ Glasgow, Sch Chem, WestCHEM, Joseph Black Bldg, Glasgow G12 8QQ, Lanark, Scotland
基金
英国工程与自然科学研究理事会;
关键词
carbazole; electrochemistry; fluorescence; formyl group; solvatochromism; LIGHT-EMITTING-DIODES; SELECTIVE DETECTION; IRIDIUM COMPLEXES; FLUORESCENT SENSOR; SOLVENT POLARITY; HOST MATERIALS; DEEP RED; BLUE; EFFICIENCY; FLUORIDE;
D O I
10.3762/bjoc.16.93
中图分类号
O62 [有机化学];
学科分类号
070303 ; 081704 ;
摘要
Two novel carbazole-based compounds 7a and 7b were synthesised as potential candidates for application in organic electronics. The materials were fully characterised by NMR spectroscopy, mass spectrometry, FTIR, thermogravimetric analysis, differential scanning calorimetry, cyclic voltammetry, and absorption and emission spectroscopy. Compounds 7a and 7b, both of which were amorphous solids, were stable up to 291 degrees C and 307 degrees C, respectively. Compounds 7a and 7b show three distinctive absorption bands: high and mid energy bands due to locally excited (LE) transitions and low energy bands due to intramolecular charge transfer (ICT) transitions. In dichloromethane solutions compounds 7a and 7b gave emission maxima at 561 nm and 482 nm with quantum efficiencies of 5.4% and 97.4% +/- 10%, respectively. At positive potential, compounds 7a and 7b gave two different oxidation peaks, respectively: quasi-reversible at 0.55 V and 0.71 V, and reversible at 0.84 V and 0.99 V. At negative potentials, compounds 7a and 7b only exhibited an irreversible reduction peak at -1.86 V and -1.93 V, respectively.
引用
收藏
页码:1066 / 1074
页数:9
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