303006-90-8Relevant articles and documents
Effective Synthesis of Ladder-type Oligo(p-aniline)s and Poly(p-aniline)s via Intramolecular SNAr Reaction
Wang, Hui,Zhao, Hongchi,Chen, Shuang,Bai, Libin,Su, Zhiyi,Wu, Yonggang
, p. 2217 - 2221 (2021)
Symmetric ladder-type oligo(p-aniline)s and poly(p-aniline)s were successfully synthesized by an intramolecular ring closure in a highly efficient SNAr reaction from oligo(p-phenylene)s and poly(p-phenylene)s with fluorine (F) and secondary amine (NH) groups. Unlike Cadogan ring closure, the newly designed cyclization reaction will not produce a mixture of symmetric and nonsymmetric structures. Moreover, the introduction of the F atom does not hinder Suzuki polymerization. The result indicates that preparing regular oligomers and polymers with a nitrogen bridge is possible.
Nitrogen-containing heterocyclic compound and use thereof
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Paragraph 0128-0129, (2021/11/02)
[Problem] to provide a nitrogen-containing heterocyclic compound which emits technology and its use. [Solution] a nitrogen-containing heterocyclic compounds, wherein: (1) a compound represented Cz a-L-a Ar [formula (1) in, the Cz, (2) the formula:(In the
A containing different conjugate bridge of the binuclear platinum (II) complex near-infrared phosphorescence material synthesis and application of (by machine translation)
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Paragraph 0056; 0059; 0060, (2017/12/27)
The invention discloses a conjugate bridge containing different of the binuclear platinum (II) complex near-infrared phosphorescent material and its in the organic electroluminescent diode in the application. Such a binuclear platinum complex near-infrare