Abstract
We report on the effect of placement of nucleobase units, thymine or N6-(4-methoxybenzoyl)-adenine onto the ends of the mesogenic and fluorescent core: bis-4-alkoxy-substituted bis(phenylethynyl)-benzene (AA and BB type monomers). While the addition of these bulky polar groups significantly reduces the range of liquid crystalline behavior, mixing two complementary nucleobase-containing monomer units together yields stable thermotropic liquid crystalline phases. Here, we focus on the effect of non-stoichiometric mixing of AA + BB monomers. Hydrogen bonding is shown to play an important role in the formation of these LC phases consistent with the formation of oligomeric or polymeric hydrogen bonding aggregates. Differential scanning calorimetry (DSC) and polarizing optical microscopy (POM) have been used in our studies, revealed greater stability of LC phase formation for the 1:1 mixture.
Original language | English |
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Title of host publication | Liquid Crystal Materials, Devices, and Applications XI |
Volume | 6135 |
DOIs | |
Publication status | Published - 2006 |
Externally published | Yes |
Event | Liquid Crystal Materials, Devices, and Applications XI - San Jose, CA, United States Duration: 2006 Jan 21 → 2006 Jan 25 |
Other
Other | Liquid Crystal Materials, Devices, and Applications XI |
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Country/Territory | United States |
City | San Jose, CA |
Period | 06/1/21 → 06/1/25 |
Keywords
- Hydrogen Bonds
- Liquid Crystal
- Nucleobases
- Polymers
- Supramolecular Chemistry
ASJC Scopus subject areas
- Electrical and Electronic Engineering
- Condensed Matter Physics