599-61-1Relevant articles and documents
Systematic study of synthesizing various heteroatom-substituted rhodamines from diaryl ether analogues
Deng, Fei,Huang, Chunfang,Huang, Wei,Liu, Limin,Qiao, Qinglong,Xu, Zhaochao
, (2020/06/09)
The dye rhodamine, as the most popular scaffold to construct fluorescent labels and probes, has been explored extensively on its structure-fluorescence relationships. Particularly, the replacement of the oxygen atom in the 10th position with heteroatoms obtained various new rhodamines with improved photophysical properties, such as brightness, photostability, red-shifted emission and fluorogenicity. However, the applications of heteroatom-substituted rhodamines have been hindered by difficult synthetic routes. Herein, we explored the condensation strategy of diaryl ether analogues and o-tolualdehyde to synthesize various heteroatom-substituted rhodamines. We found that the electron property and steric effect in the rhodamine 10th position determined the synthetic yield. It's concluded that this condensation method was more suitable for the synthesis of heteroatom-substituted rhodamines with small or electron-donating groups like rhodamine, S-rhodamine and Si-rhodamine. We hope these results will benefit the design and synthesis of heteroatom-substituted rhodamines.
Catalytic hydrogenation of sulfur-containing nitrobenzene over Pd/C catalysts: In situ sulfidation of Pd/C for the preparation of PdxSy catalysts
Zhang, Qunfeng,Xu, Wei,Li, Xiaonian,Jiang, Dahao,Xiang, Yizhi,Wang, Jianguo,Cen, Jie,Romano, Stephen,Ni, Jun
, p. 17 - 21 (2015/09/28)
The preparation of supported palladium sulfides catalysts has attracted much attention due to their good sulfur-resistant properties in the hydrogenation of sulfur-containing compounds. In this work, we unambiguously demonstrated that Pd/C catalyst could be in situ sulfided by organic sulfur-containing reactant molecules and the sulfidation was highly dependent on temperature. The in situ sulfidation of Pd/C catalyst was composed of a reaction of Pd with the sulfur derived from the cleavage of C-S bond of sulfur-containing reactant molecules, followed by a transformation to PdxSy at high temperatures (around 120 °C). The sulfided Pd/C catalyst could be used for at least 18 recycles without a significant loss in its activity during the hydrogenation of sulfur-containing nitrobenzene at 180 °C with 3 MPa H2, which could be attributed to the stable presence of Pd4S and Pd16S7.
Fluorimetric and prototropic studies on the inclusion complexation of 3,3′-diaminodiphenylsulphone with β-cyclodextrin and its unusual behavior
Enoch, Muthu Vijayan,Rajamohan, Rajaram,Swaminathan, Meenakshisundaram
body text, p. 473 - 477 (2010/12/19)
The photophysical and photoprototropic properties of 3,3′- diaminodiphenylsulphone (3DADPS) in aqueous β-cyclodextrin (β-CDx) solution have been investigated using absorption and fluorescence spectral techniques. β-CDx forms 1:1 inclusion complex with 3DA
