42241-95-2Relevant academic research and scientific papers
A highly sensitive fluorescent chemosensor for simultaneous determination of Ag(I), Hg(II), and Cu(II) ions: Design, synthesis, characterization and application
Hien, Nguyen Khoa,Bao, Nguyen Chi,Ai Nhung, Nguyen Thi,Trung, Nguyen Tien,Nam, Pham Cam,Duong, Tran,Kim, Jong Seung,Quang, Duong Tuan
, p. 89 - 96 (2015)
A fluorescent chemosensor based on dimethylaminocinnamaldehyde-aminothiourea (DA) has been designed, synthesized, and applied with a combined theoretical and experimental study. The synthetic path, optimized molecular structure and characteristics of DA were carried out using the calculations at the B3LYP/LanL2DZ level of theory. The experimental investigations have a good agreement with the theoretical results. DA can be used as a chemosensor for simultaneous quantification of silver, copper, and mercury ions in aqueous solution at the ppb level. The stable geometric structures of the complexes between DA and Ag+, Hg2+, Cu2+ with stoichiometry of 1:1, 2:1, and 2:1, have been found and investigated for electronic properties and fluorescence quenching phenomena by using Atoms in Molecules (AIM) and Natural Bond Orbitals (NBO) analyses.
A new fluorescent chemosensor for Hg2+ in aqueous solution
Quang, Duong Tuan,Hop, Nguyen Van,Luyen, Nguyen Dinh,Thu, Ha Phuong,Oanh, Doan Yen,Hien, Nguyen Khoa,Hieu, Nguyen Van,Lee, Min Hee,Kim, Jong Seung
, p. 222 - 225 (2013)
We prepared an aminothiourea-derived Schiff base (DA) as a fluorescent chemosensor for Hg2+ ions. Addition of 1 equiv of Hg2+ ions to the aqueous solution of DA gave rise to an obvious fluorescence enhancement and the subsequent addition of more Hg2+ induced gradual fluorescence quenching. Other competing ions, including Pb2+, Cd 2+, Cr3+, Zn2+, Fe2+, Co 3+, Ni2+, Ca2+, Mg2+, K+ and Na+, did not induce any distinct fluorescence changes, indicating that DA can selectively detect Hg2+ ions in aqueous solution. Copyright
Structure-activity relationship study of thiosemicarbazones on an African trypanosome: Trypanosoma brucei brucei
Fatondji, Houssou Raymond,Kpoviessi, Salome,Gbaguidi, Fernand,Bero, Joanne,Hannaert, Veronique,Quetin-Leclercq, Joelle,Poupaert, Jacques,Moudachirou, Mansourou,Accrombessi, Georges Coffi
, p. 2151 - 2162 (2013/07/26)
To explore the structure-activity relationships of thiosemicarbazones on African trypanosome: Trypanosoma brucei brucei, a series of thirty-five thiosemicarbazones (1-35) have been synthesized and characterized by their 1H NMR, 13C NMR, and FT-IR spectra. All compounds were tested for trypanocidal activity using the method "Lilit alamar blue". The comparison of trypanocidal power of thiosemicarbazones was performed considering their structures. This study that was done using acetophenone thiosemicarbazone (1) as basic model, showed that: (a) the presence of lipophilic substituents in para position on benzene ring, (b) substitution of benzene ring and (c) substitution of hydrogen of thioamide function by a phenyl, strongly influence trypanocidal activity. The various modifications to basic structure (1) allowed the synthesis of 1-(4-chlorophenyl) ethylidene-4-phenyl- thiosemicarbazide (34). With a trypanocidal activity of 3.97 μM, this compound is the most active of the series.
