| Article ID | Journal | Published Year | Pages | File Type |
|---|---|---|---|---|
| 5218136 | Tetrahedron | 2013 | 7 Pages |
Abstract
J-AT nucleoside-based organogelators 1a and 1b were designed and synthesized. They were endowed with unparalleled superiority to natural nucleobase analogues 2-6 to gelate aromatic solvents due to their excellent self-assembly properties. The J-AT nucleoside-based organogelators showed a specific self-complementary base pair recognition characteristic. The gel stabilities of 1a and 1b were drastically influenced by adenine analogue 2, hardly affected by thymine analogue 3, uracil analogue 4, cytosine analogue 5, and mildly interrupted by guanine analogue 6.
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Physical Sciences and Engineering
Chemistry
Organic Chemistry
Authors
Shiliang He, Hang Zhao, Xiurong Guo, Guang Xin, Baozhan Huang, Limei Ma, Xinglong Zhou, Rui Zhang, Dan Du, Xiaohua Wu, Zhihua Xing, Wen Huang, Qianming Chen, Yang He,