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首页> 外文期刊>Phosphorus, Sulfur, and Silicon and the Related Elements >Synthesis, Characterization, and Antitumor Activity of Some Metal Complexes with Schiff Bases Derived from 9-Fluorenone as a Polycyclic Aromatic Compound
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Synthesis, Characterization, and Antitumor Activity of Some Metal Complexes with Schiff Bases Derived from 9-Fluorenone as a Polycyclic Aromatic Compound

机译:一些以9-氟酮为多环芳族化合物的席夫碱金属配合物的合成,表征和抗肿瘤活性

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摘要

New bidendate Schiff base ligands HL~1 [(9H-fluorene-9-ylidene)thiosemicarbazide], HL~2 [(9H-fluorene-9-ylidene)semicarbazide] and L3~ [N~1,N~2di(9H-fluorene-9-ylidene)ethan-1,2-diamine] derived from the condensation of thiosemicarbazide, semicarbazide, and ethylenediamine with 9-fluorenone as polycyclic aromatic compound (PAC). Ag(I), Cu(II), VO(IV), La(III), and Zn(II) of the ligands HL~1, HL~2, and L~3 have been prepared and characterized by conductance and magnetic measurements, and electronic, infrared, and 1H NMR spectral data. Tetrahedral structures are suggested for Ag (I) with HL~1, HL~2, and L~3, whereas Cu(II)-HL~1 and VO(IV)-HL~2 have octahedral and square-planar structures, respectively. The Erlich antitumor activity in vivo (E. A. A.) have been studied and showed that the free ligands L~3, HL~2, and its VO(IV)-HL~2 complex are the most active in the inhibition of cell viability, whereas the ligands HL~1, La(III) -L~3, and Cu(II)-HL~1 are the least active ones.
机译:新的双齿席夫碱配体HL〜1 [(9H-芴-9-亚基)硫代氨基脲],HL〜2 [(9H-芴-9-亚基)亚氨基脲]和L3〜[N〜1,N〜2di(9H-芴-9-亚丙基)1,2-二胺],它是由硫代氨基脲,氨基脲和乙二胺与9-芴酮作为多环芳族化合物(PAC)缩合而得。制备了配体HL〜1,HL〜2和L〜3的Ag(I),Cu(II),VO(IV),La(III)和Zn(II)并通过电导和磁测量进行了表征,电子,红外和1H NMR光谱数据。对于具有HL〜1,HL〜2和L〜3的Ag(I),建议采用四面体结构,而Cu(II)-HL〜1和VO(IV)-HL〜2分别具有八面体和方平面结构。研究了体内Erlich抗肿瘤活性(EAA),结果表明,游离配体L〜3,HL〜2及其VO(IV)-HL〜2复合物在抑制细胞活力方面最活跃,而配体HL-1,La(III)-L-3和Cu(II)-HL-1是活性最低的配体。

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