Journal
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
Volume 135, Issue 39, Pages 14797-14805Publisher
AMER CHEMICAL SOC
DOI: 10.1021/ja4071333
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Funding
- MEXT [23685032]
- Ritsumeikan R-GIRO project
- JSPS
- Grants-in-Aid for Scientific Research [12J09598, 24108740, 23685032, 13J00831] Funding Source: KAKEN
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Oriented salts from planar charged species were prepared by combining positively and negatively charged receptor anion complexes with similar geometries using dicationic and electronically neutral pi-conjugated receptors. Phenylene- or pyrimidine-bridged bis(imidazolium) dicationic anion receptors formed monocationic receptor-Cl- complexes that were accompanied by a free Cl-. This free Cl- was subsequently captured by pyrrole-based neutral anion receptors to form negatively charged receptor-Cl- complexes. The ion pair of the resulting positively and negatively charged planar receptor-Cl- complexes could produce a supramolecular octane gel, adopting a lamellar self organized structure in its xerogel state. On the other hand, the solid-state ion pairs had hexagonal columnar mesophases, which formed via alternate stacking of the positively and negatively charged planar receptor-Cl- complexes. By use of the flash-photolysis time-resolved microwave conductivity technique, the one-dimensional charge-carrier transporting property, with a mobility of 0.05 cm(2) V-1 s(-1), was determined for the newly prepared solid-state ion pairs.
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