Supergelation via Purely Aromatic π-π Driven Self-Assembly of Pseudodiscotic Oxadiazole Mesogens

被引:49
|
作者
Sivadas, Aneesh P. [1 ,2 ]
Kumar, N. S. Saleesh [1 ,2 ]
Prabhu, Deepak D. [1 ,2 ]
Varghese, Shinto [1 ,2 ]
Prasad, S. Krishna [3 ]
Rao, D. S. Shankar [3 ]
Das, Suresh [1 ,2 ]
机构
[1] NIIST, Chem Sci & Technol Div, Photosci & Photon Sect, Trivandrum 695019, Kerala, India
[2] CSIR, Network Inst Solar Energy, Trivandrum 695019, Kerala, India
[3] Ctr Soft Matter Res, Bangalore 560013, Karnataka, India
关键词
SUPRAMOLECULAR GELS; PHOTOPHYSICS; AGGREGATION; ORGANOGELS; EMISSION; GELATORS; STATES; DYE;
D O I
10.1021/ja500607d
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
A series of highly luminescent oxadiazole-based stilbene molecules (OXD4, OXD8, OXD10, and OXD12) exhibiting interesting enantiotropic liquid crystalline and gelation properties have been synthesized and characterized. The molecules possessing longer alkyl substituents, OXD10 and OXD12, possess a pseudodisc shape and are capable of behaving as supergelators in nonpolar solvents, forming self-standing gels with very high thermal and mechanical stability. Notably the self-assembly of these molecules, which do not possess any hydrogen-bonding motifs normally observed in most reported supergelators, is driven purely by pi-stacking interactions of the constituent molecules. The d-spacing ratios estimated from XRD analysis of OXD derivatives possessing longer alkyl chains show that the molecules are arranged in a columnar fashion in the mesogens and the self-assembled nanofibers formed in the gelation process.
引用
收藏
页码:5416 / 5423
页数:8
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