期刊
BULLETIN OF THE CHEMICAL SOCIETY OF JAPAN
卷 95, 期 4, 页码 621-627出版社
CHEMICAL SOC JAPAN
DOI: 10.1246/bcsj.20210452
关键词
Cavitand; Supramolecular polymer; Chiral polymer
资金
- JSPS KAKENHI Grant [JP21H04685, 20K15335, JP20K21196, JP21H0549, JP 18J13703]
- Natural Science Center for Basic Research Development [JP 18J13703]
- Grants-in-Aid for Scientific Research [20K15335] Funding Source: KAKEN
Chiral supramolecular polymers were successfully constructed through the host-guest complexation of an octaphosphonate biscavitand and a chiral diammonium guest. The complexation was found to be enthalpy-and entropy-favored with high binding constants. Various experimental techniques confirmed the occurrence of supramolecular polymerization, most likely through a ring-chain mechanism. Atomic force microscopy visualized the cyclic oligomers and supramolecular polymer chains. Circular dichroism was observed, indicating the formation of chirally twisted supramolecular polymers.
Chiral supramolecular polymers were constructed through the host-guest complexation of an octaphosphonate biscavitand and a chiral diammonium guest. Isothermal titration calorimetry determined that host-guest complexation was enthalpy-and entropy-favored with high binding constants. Diffusion-ordered NMR spectroscopy and viscometry of the host-guest solution revealed that supramolecular polymerization occurred, which most likely followed a ring-chain mechanism. The cyclic oligomers and the supramolecular polymer chains were visualized by atomic force microscopy. Circular dichroism was observed when the octaphosphonate biscavitand and the chiral diammonium guest were mixed, which suggested that chirally twisted supramolecular polymers were formed.
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