16363-79-4Relevant academic research and scientific papers
Synthesis, crystal structure, characterisation, and antifungal activity of 3-thiophene aldehyde semicarbazone (3STCH), 2,3-thiophene dicarboxaldehyde bis(semicarbazone) (2,3BSTCH2) and their nickel (II) complexes
Alomar, Kusai,Gaumet, Vincent,Allain, Magali,Bouet, Gilles,Landreau, Anne
, p. 36 - 43 (2012)
The reaction of nickel (II) chloride and bromide with 3-thiophene aldehyde semicarbazone (3STCH) and 2,3-thiophene dicarboxaldehyde bis(semicarbazone) (2,3BSTCH2) leads to the formation of a series of new complexes: [NiCl2(3STCH)2], [NiBr2(3STCH)2], [NiCl(2,3BSTCH2)(H2O)]Cl, and [NiBr(2,3BSTCH 2)(H2O)]Br respectively. The crystal structures of the two ligands 3STCH, 2,3BSTCH2 and of the complex [NiBr(2,3BSTCH 2)(H2O)]Br have been determined by X-ray diffraction methods. For all these complexes, the central ion is coordinated through the oxygen atom of the carbonyle and the azomethine nitrogen atom of the semicarbazone. The antifungal activity of the complexes and their corresponding ligands was evaluated against some strains of respectively, Candida albicans, Candida glabrata and Aspergillus fumigatus. The complexes with 3STCH and 2,3BSTCH2 revealed interesting CMI80 values specifically against C. glabrata. Cytotoxicity assay was also carried out in vitro on MRC5 cells.
Reaction of anhydrous zinc chloride with 2,3-thiophenedicarbaldehyde bis(semicarbazone) (2,3BSTCH2) and bis(thiosemicarbazone) (2,3BTSTCH2): Crystal structure of {[C6H5N2S]+[ZnCl3(C6H4N2S)]-} complex
Alomar, Kusa?,Allain, Magali,Richomme, Pascal,Bouet, Gilles
, p. 1591 - 1597 (2015)
The reaction of anhydrous zinc chloride with 2,3-thiophenedicarbaldehyde bis(semicarbazone) or 2,3-bis(thiosemicarbazone) leads to the formation of compound {[C6H5N2S]+[ZnCl3(C6H4N2S)]-}, where C6H4N2S is thieno[2,3-d]pyridazine, via an elimination-cyclisation reaction of the semicarbazone or the thiosemicarbazone moiety. Crystal structures of thieno[2,3-d]pyridazine and {[C6H5N2S]+[ZnCl3(C6H4N2S)]-} are described. 2015 Institute of Chemistry, Slovak Academy of Sciences
