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Aggregation of an anionic porphyrin with chiral metal complexes and the competitive binding influences of a surfactant and a polyelectrolyte

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Aggregation of an anionic porphyrin with chiral metal complexes and the competitive binding influences of a surfactant and a polyelectrolyte.pdf (1.268Mb)
Date
2011-04-13
Author
Wang, Jian(Chinese Acad Sci, Grad Univ, Coll Chem & Chem Engn)
Liu, Chengyong
Ding, Dongdong
Zeng, Lixi(Chinese Acad Sci, Grad Univ, Coll Chem & Chem Engn)
Cao, Qian(Chinese Acad Sci, Grad Univ, Coll Chem & Chem Engn)
Zhang, Hui
章慧
Zhao, Hong( Chinese Acad Sci, Grad Univ, Coll Chem & Chem Engn)
Li, Xiangjun( Chinese Acad Sci, Grad Univ, Coll Chem & Chem Engn)
Xiang, Kaixiang( Huaihua Med Coll)
He, Yujian( Chinese Acad Sci, Grad Univ, Coll Chem & Chem Engn)
Wang, Guangwei( Hunan Normal Univ, Coll Med)
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  • 化学化工-已发表论文 [14235]
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Abstract
The non-covalent interactions of chiral metal complexes with the achiral 5,10,15,20-tetrakis (4-sulonatophenyl) porphyrin (H(4)TTPS(2-)) have been investigated by UV-vis and circular dichroism (CD) spectra. The results show that under acidic environments, only the chiral complex cations ([CoBr(NH(3))(en)(2)](+), [Co(en)(3)](3+), [Ru(phen)(3)](2+)) could interact with H(4)TTPS(2-) to form chiral aggregates, accompanied with the metal-centered chirality information transferred to the formed J-aggregates. However, the chiral complex anion ([Co(edta)](-)) does not cause the self-assembly process. The competitive binding interactions between an achiral water-soluble cationic surfactant (N-hexadecyltrimethyl ammonium chloride, CTAC) and a cationic polyelectrolyte (polyallylamine, PAA) with the chiral metal complex H(4)TTPS(2-) J-aggregates, respectively, were also investigated. It was found that chiral-symmetry-breaking phenomena occur in the cationic surfactant induced event. In the case of a cationic polyelectrolyte, it could change the conformational flexibility of the H(4)TTPS(2-) aggregates. These results may lead us to understand the possible mechanism of the supramolecular self-assembly process by the non-covalent interactions.
Citation
NEW JOURNAL OF CHEMISTRY,2011,35(7):1424-1432
URI
http://dx.doi.org/doi:10.1039/c1nj20193j
WOS:000292161900011
https://dspace.xmu.edu.cn/handle/2288/11961

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