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化驗
97%
形狀
powder
mp
228-233
SMILES 字串
CC(C)(C)c1ccc2[nH]c3ccc(cc3c2c1)C(C)(C)C
InChI
1S/C20H25N/c1-19(2,3)13-7-9-17-15(11-13)16-12-14(20(4,5)6)8-10-18(16)21-17/h7-12,21H,1-6H3
InChI 密鑰
OYFFSPILVQLRQA-UHFFFAOYSA-N
一般說明
3,6-Di-tert-butylcarbazole is a carbazole based material with hole transporting characteristics. The 3,6-Di-tert-butyl component of the carbazole results in an increase in the glass transition temperature (Tg) of the compound. It can be used in combination with another carbazole to form novel electroluminescent materials.
應用
3,6-Di-tert-butylcarbazole is mainly used as a monomeric precursor in the syntheses of new carbazole based materials which consist of ethynylphenyl. These materials include 9-(4-bromophenyl)-3,6-di-tert-butylcarbazol and 2-(4-(2-(4-(3,6-di-tert-butyl-9H-carbazol-9-yl)phenyl)ethynyl)benzylidene)malononitrile (PBM) which can be further be used in organic light emitting diodes (OLEDs) and optical switching devices.
訊號詞
Warning
危險分類
Acute Tox. 4 Oral - Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
標靶器官
Respiratory system
儲存類別代碼
11 - Combustible Solids
水污染物質分類(WGK)
WGK 3
閃點(°F)
Not applicable
閃點(°C)
Not applicable
其他客户在看
Carbazole based hole transporting materials for solid state dye sensitizer solar cells: role of the methoxy groups.
Polymer International, 63(8), 1387-1393 (2014)
Solvent dependant optical switching in carbazole-based fluorescent nanoparticles.
Langmuir, 25(4), 2402-2406 (2009)
Synthesis and photophysical properties of carbazole-based blue light-emitting dendrimers.
The Journal of Organic Chemistry, 72(13), 4727-4732 (2007)
Bis (carbazolyl) derivatives of pyrene and tetrahydropyrene: synthesis, structures, optical properties, electrochemistry, and electroluminescence.
Journal of Material Chemistry C, 1(8), 1638-1650 (2013)
Physical chemistry chemical physics : PCCP, 18(45), 31330-31336 (2016-11-09)
Bis(phenylsulfone) was developed as a strong electron acceptor of thermally activated delayed fluorescent emitters. The connection of two electron withdrawing phenylsulfone moieties through meta-position of phenyl produced the bis(phenylsulfone) acceptor and the strong electron acceptor strength of bis(phenylsulfone) enabled preparation
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