化学
吡啶
阳离子聚合
离子液体
卟啉
位阻效应
离子键合
溶剂化
结晶学
DNA
无机化学
光化学
立体化学
高分子化学
离子
药物化学
有机化学
催化作用
生物化学
作者
Kaoru Nobuoka,Kensuke Sumi,Eri Kitagawa,K. Sato,Ayumi Nakamura,Satoshi Kitaoka
标识
DOI:10.1142/s1088424623500487
摘要
We studied the interaction of water-soluble cationic metalloporphyrins, [Formula: see text]Py and TMPyP, with the DNA double helix in ionic liquid solutions using CD and absorption spectra. The dispersibility of their porphyrin complexes was improved by electrostatic interactions of the anions of the ionic liquid. In the case of Cu(II) and Zn(II) complexes, the [Formula: see text]Py complexes with pyridinium cations attached to the meso-phenyl groups via methylene groups intercalated into the DNA double helix, while the compact TMPyP complexes with pyridinium cations at the meso-position could not interact with DNA. Thus, it was suggested that the solvation behavior by ionic liquids depends on the structure of the porphyrin and also affects its interaction with DNA. Neither Mn(III) complexes with axial ligands could interact with DNA, regardless of the presence of the ionic liquids, due to their steric hindrance.
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