4.8 Article

CPL on/off control of an assembled system by water soluble macrocyclic chiral sources with planar chirality

期刊

CHEMICAL SCIENCE
卷 13, 期 20, 页码 5846-5853

出版社

ROYAL SOC CHEMISTRY
DOI: 10.1039/d2sc00952h

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资金

  1. JSPS KAKENHI [JP15H00990, JP17H05148, JP18H04510, JP20H04670, JP19H00909, JP21K14612, JP20K22528, JP21K14611]
  2. JST CREST [JPMJCR18R3]
  3. Nanotechnology Platform Program of the Ministry of Education, Culture, Sports, Science and Technology (MEXT)
  4. MEXT World Premier International Research Center Initiative (WPI), Japan

向作者/读者索取更多资源

A water-soluble cationic pillar[5]arene with stereogenic carbons was found to exhibit planar chiral properties and transmit chiral information, resulting in circularly polarized luminescence. The chirality transfer process and resulting CPL were highly sensitive to the feed ratio of the chiral pillar[5]arene.
Herein, we report the synthesis and planar chiral properties of a pair of water-soluble cationic pillar[5]arenes with stereogenic carbons. Interestingly, although units of the molecules were rotatable, only one planar chiral diastereomer existed in water in both cases. As a new type of chiral source, these molecules transmitted chiral information from the planar chiral cavities to the assembly of a water-soluble extended pi-conjugated compound, affording circularly polarized luminescence (CPL). The chirality transfer process and resulting CPL were extremely sensitive to the feed ratio of the chiral pillar[5]arenes owing to the combined action of their planar chirality, bulkiness, and strong binding properties. When a limited amount of chiral source was added, further assembly of the extended pi-conjugated compound into helical fibers with CPL was triggered. Unexpectedly, larger amounts of chiral source destroyed the helical fiber assemblies, resulting in elimination of the chirality and CPL properties from the assembled structures.

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