120360-52-3Relevant academic research and scientific papers
Organic ligand BDPO, rhodamine B for detecting the metal organic framework compound and its preparation method and application (by machine translation)
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Paragraph 0037; 0038; 0039, (2017/01/02)
The present invention discloses an organic ligand BDPO, rhodamine B for detecting the metal organic framework compound and its preparation and application, the preparation method is as follows: in water, nitric acid and the presence of organic solvent, the illinium salt with the formula (I) organic ligand of the structure shown in the coordinate BDPO reaction of the compound in order to make metal-organic framework. Through this method and machine biligand BDPO of the prepared metal organic framework of the rhodamine B compound has the advantages of high efficiency, the sensitivity of the detection, (by machine translation)
A luminescent 2D coordination polymer for selective sensing of nitrobenzene
Wang, Guan-Yao,Yang, Le-Le,Li, Yue,Song, Han,Ruan, Wen-Juan,Chang, Ze,Bu, Xian-He
supporting information, p. 12865 - 12868 (2013/09/12)
A luminescent two-dimensional (2D) coordination polymer is demonstrated to be a selective sensing material for the straightforward detection of nitrobenzene via a redox fluorescence quenching mechanism.
Synthesis of analogues of Congo red and evaluation of their anti-prion activity
Sellarajah, Shane,Lekishvili, Tamuna,Bowring, Claire,Thompsett, Andrew R.,Rudyk, Helene,Birkett, Christopher R.,Brown, David R.,Gilbert, Ian H.
, p. 5515 - 5534 (2007/10/03)
No cure as of yet exists for any of the transmissible spongiform encephalopathies. In this paper, we describe the synthesis of analogues of Congo red and evaluation against a cellular model of infection, the SMB (scrapie mouse brain) persistently infected cell line, for their ability to inhibit the infectivity of the abnormal form of prion protein (PrP-res). The compounds have also been tested for their ability to inhibit the polymerization of PrP C by PrP-res. A number of analogues showed inhibition of PrP-res infectivity at nanomolar concentrations. Several analogues show promise; the most active compound, 2a, inhibits the formation of PrP-res in SMB cells with an EC50 of 25-50 nM.
