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- W2063001086 abstract "The self-assembly and induced supramolecular chirality of a dianionic meso-tetraphenylsulfonato porphyrin (TPPS) on the optically active polylysine has been investigated. Our research has confirmed that in the presence of poly(l-lysine) (PLL) or poly(d-lysine) (PDL), TPPS could form both H and J aggregates and the exciton type Cotton effect was induced in the corresponding absorption bands of H and J-aggregates. We have further revealed that the induced chirality of the H-band always followed the chirality of PLL or PDL, while the sign of the exciton couplet in the J-band could be the same as or opposite to that of the H-band depending on the mixing sequence and the ratio of PLL or PDL to TPPS (P/T ratio). At a P/T ratio less than 4, both the J and H aggregates showed the same symbolic CD signal. At a P/T ratio larger than 4, the opposite sign of the exciton couplet was observed for H and J-bands when TPPS was added into PLL, while the same sign was obtained when PLL was added into TPPS. Interestingly, the J-band with the same sign as that of the H-band can be inverted into the opposite sign under heating. A mechanism relating to the dynamic and thermodynamic formation of the chiral aggregates in the presence of PLL or PDL was proposed." @default.
- W2063001086 created "2016-06-24" @default.
- W2063001086 creator A5058453644 @default.
- W2063001086 creator A5066716873 @default.
- W2063001086 date "2009-09-25" @default.
- W2063001086 modified "2023-09-24" @default.
- W2063001086 title "Supramolecular Chirality and Chiral Inversion of Tetraphenylsulfonato Porphyrin Assemblies on Optically Active Polylysine" @default.
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- W2063001086 doi "https://doi.org/10.1021/jp902870f" @default.
- W2063001086 hasPubMedId "https://pubmed.ncbi.nlm.nih.gov/19827847" @default.
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