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Supramolecular copolymerization of hydrophobic and hydrophilic monomers in liquid crystalline media.


ABSTRACT: In the case of covalent polymers, immiscible polymers can be integrated by covalently linking them together, but such a strategy is not possible in supramolecular polymers. Here we report the supramolecular copolymerization of two porphyrin-based monomers, C10P2H and TEGPCu with side chains bearing cyanobiphenyl (CB) groups at the ends of hydrophobic alkyl or hydrophilic tetraethylene glycol chains, respectively. These monomers undergo self-sorting supramolecular polymerization in highly diluted solutions ([monomer] = 3.4 × 10-9 mol% (2.0 × 10-8 mol L-1)) in nonpolar media due to the incompatibility of the side chains. Surprisingly, these monomers undergo supramolecular copolymerization under high concentration conditions ([monomer] = 7.7 mol%) in the medium of 4-cyano-4'-pentyloxybiphenyl (5OCB) to form a columnar liquid crystalline phase under thermodynamic conditions, where the individual columns are composed of supramolecular block copolymers. The combination of CB ends of both monomers and the 5OCB medium is essential for the two monomers to form an integrated structure in a condensed system without phase separation.

SUBMITTER: Morishita D 

PROVIDER: S-EPMC10935670 | biostudies-literature | 2024 Mar

REPOSITORIES: biostudies-literature

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Supramolecular copolymerization of hydrophobic and hydrophilic monomers in liquid crystalline media.

Morishita Daiki D   Itoh Yoshimitsu Y   Furukawa Ko K   Arai Noriyoshi N   Zhang Xu-Jie XJ   Aida Takuzo T  

Chemical science 20240205 11


In the case of covalent polymers, immiscible polymers can be integrated by covalently linking them together, but such a strategy is not possible in supramolecular polymers. Here we report the supramolecular copolymerization of two porphyrin-based monomers, <sup>C10</sup>P<sub>2H</sub> and <sup>TEG</sup>P<sub>Cu</sub> with side chains bearing cyanobiphenyl (CB) groups at the ends of hydrophobic alkyl or hydrophilic tetraethylene glycol chains, respectively. These monomers undergo self-sorting sup  ...[more]

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