Transforming a C (3)-Symmetrical Liquid Crystal to a π-Gelator by Alkoxy Chain Variation

通过烷氧基链变化将C(3)对称液晶转化为π-凝胶剂

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Abstract

Rational understanding of the structural features involving different noncovalent interactions is necessary to design a liquid crystal (LC) or an organogelator. Herein, we report the effect of the number and positions of alkoxy chains on the self-assembly induced physical properties of a few π-conjugated molecules. For this purpose, we designed and synthesized three C (3)-symmetrical molecules based on oligo(p-phenylenevinylene), C (3) OPV1-3. The self-assembly properties of these molecules are studied in the solid and solution states. All of the three molecules follow the isodesmic self-assembly pathway. Upon cooling from isotropic melt, C (3) OPV1 having nine alkoxy chains (-OC(12)H(25)) formed a columnar phase with two-dimensional rectangular lattice and retained the LC phase even at room temperature. Interestingly, when one of the -OC(12)H(25) groups from each of the end benzene rings is knocked out, the resultant molecule, C (3) OPV2 lost the LC property, however, transformed as a gelator in toluene and n-decane. Surprisingly, when the -OC(12)H(25) group from the middle position is removed, the resultant molecule C (3) OPV3 failed to form either the LC or the gel phases.

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