554458-97-8Relevant academic research and scientific papers
A simple strategy for constructing PET fluorescent probe and its application in hypochlorite detection
Zhang, Xiaowen,Zhang, Fei,Yang, Binsheng,Liu, Bin
, (2021/05/03)
It is great meaningful to develop a fast and efficient method for detecting hypochlorite (ClO?) owing to its importance in the immune system. In this work, we proposed a strategy to construct fluorescent probes for ClO? based on photoinduced electron transfer (PET) mechanism. According to the strategy, we developed four fluorescent probes named TPA-NO2, TPA-2NO2, TPB-NO2 and TPB-2NO2, and studied their detecting performances for hypochlorite. Among them, TPB-NO2 displayed the most obvious fluorescence changes towards ClO? with a rapid response (2 was successfully used to detect ClO? in living cells and zebrafish. These results demonstrated the feasibility of our strategy and provided a guidance for developing more excellent probes in the future.
Silicon phthalocyanine substituted by trianilino fluoro aryl benzyl ether dendritic ligand and preparing method and application thereof
-
Paragraph 0020; 0022, (2019/01/08)
The invention discloses silicon phthalocyanine substituted by a trianilino fluoro aryl benzyl ether dendritic ligand and a preparing method and application thereof. Firstly, 4'-(diphenylamino)-[1,1'-biphenyl]-4-carboxylic acid is synthesized from 4-bromotriphenylamine and phenylboronic acid, and is then subjected to condensation with hexafluorobisphenol A or bisphenol A respectively to prepare 4-(diphenylamino)-1-biphenylcarboxylic acid-1-carbobenzoxy-1,1,1,3,3,3-hexafluoropropyl phenol and 4-(diphenylamino)-1-biphenylcarboxylic acid-1-carbobenzoxy propyl phenol; and finally, the 4-(diphenylamino)-1-biphenylcarboxylic acid-1-carbobenzoxy-1,1,1,3,3,3-hexafluoropropyl phenol and the 4-(diphenylamino)-1-biphenylcarboxylic acid-1-carbobenzoxy propyl phenol react separately with silicon phthalocyanine dichloride to synthesize bis-(4-(diphenylamino)-1-biphenylcarboxylic acid-1-carbobenzoxy-4-(1,1,1,3,3,3-hexafluoropropyl-4-phenoxy) axially substituted silicon phthalocyanine and bis-(4-(diphenylamino)-1-biphenylcarboxylic acid-1-carbobenzoxypropylphenoxy) axially substituted silicon phthalocyanine. The products can be used as fluorescence imaging agents and photodynamic therapy photosensitizers.
Synthesis of triphenylamine-modified arylates and ketones via suzuki coupling reactions
Wang, Jian,Yang, Chang-Jian,Peng, Hua-Nan,Deng, Yang-Sheng,Gao, Xi-Cun
, p. 832 - 840 (2011/04/22)
A series of triphenylamine-mdified arylates and ketones were synthesized via Pd-catalyzed Suzuki coupling reaction of triphenylamine boronic acid with aryl bromide. The triphenylamine boronic acid was synthesized by iodization of 4-bromoaniline, Ullmann reaction of 1-bromo-4-iodobenzene with diphenylamine, and boronic acidification of 4-bromotriphenylamine.
Structurally simple dipolar organic dyes featuring 1,3-cyclohexadiene conjugated unit for dye-sensitized solar cells
Chen, Kuan-Fu,Hsu, Ying-Chan,Wu, Qiongyou,Yen, Ming-Chang P.,Sun, Shih-Sheng
supporting information; experimental part, p. 377 - 380 (2009/08/15)
(Chemical Equation Presented) A series of structurally simple dipolar light-harvesting organic dyes featuring 1,3-cyclohexadiene in the aromatic π framework for dye-sensitized solar cells has been synthesized and characterized. The highest conversion effi
