Journal
SOFT MATTER
Volume 13, Issue 17, Pages 3072-3075Publisher
ROYAL SOC CHEMISTRY
DOI: 10.1039/c7sm00414a
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Funding
- National Natural Science Foundation of China [21573132]
- Postdoctoral Science Foundation of China [2016M592174]
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Through the formation of dynamic covalent bonds, we succeeded, for the first time, in achieving a reversible chiral transfer from amino acids to perylene bisimide aggregates in aqueous solutions. Two opposite helical aggregations are induced with L-phenylalanine and L-tyrosine, respectively. It is possible that the change in configurations of phenyl groups in amino acids leads to the chiral inversion of BAPBI arrangements.
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