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Spectral investigations on the binding of DNA-CTMA complex with Tetrameric Copper Phthalocyanines

机译:用四聚铜酞菁与四聚铜酞菁结合的光谱研究

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The binding of DNA-CTMA (Deoxyribonucleic acid-cetyltrimethylammonium) complex with two tetrameric Copper Phthalocyanine (CuPc) systems, substituted with carboxylic acid (CuPc-COOH) and derivatized further as an imidazolium salt (CuPc-COOR), was investigated in dimethylsulfoxide (DMSO) solutions using UV/Visible Spectroscopy. Absorbance changes at 685 mn (Q band of the CuPc) were monitored as a function of DNA-CTMA added to the dye solution and stock concentrations of DNA-CTMA in DMSO were varied to facilitate observation of the full binding process. Our findings indicated that while binding with DNA-CTMA was more well-defined in the case of CuPc-COOH, the binding profile of the CuPc-COOR showed initial growth followed by decay in its Q-band absorbance which was indicative of a more complex binding mechanism involving the dye and DNA-CTMA. Preliminary findings from photophysical studies involving the CuPc tetramers and DNA-CTMA are also discussed in this paper.
机译:DNA-CTMA(脱氧核糖核酸 - 甲基三硫铵)复合物与两种四聚铜酞菁(CUPC)系统的结合,被羧酸(CUPC-COOH)取代并进一步作为咪唑鎓盐(CUPC-COOR)的衍生化,在二甲基磺酰甲醚( DMSO)使用紫外/可见光谱溶液。 监测685mn(Q带)的吸光度变化作为添加到染料溶液中的DNA-CTMA的函数,并改变DMSO中DNA-CTMA的储备浓度,以便于观察完整结合过程。 我们的发现表明,在CupC-CoOH的情况下与DNA-CTMA的结合更良好地定义,Cupc-CoOR的结合轮廓显示出初始生长,然后在其Q型吸光度下衰减,其表示更复杂 涉及染料和DNA-CTMA的结合机制。 本文还讨论了涉及CupC四聚体和DNA-CTMA的光物理研究的初步发现。

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