Author/Authors :
Shiliang He، نويسنده , , Hang Zhao، نويسنده , , Xiurong Guo، نويسنده , , Guang Xin، نويسنده , , Baozhan Huang، نويسنده , , Limei Ma، نويسنده , , Xinglong Zhou، نويسنده , , Rui Zhang، نويسنده , , Dan Du، نويسنده , , Xiaohua Wu، نويسنده , , Zhihua Xing، نويسنده , , Wen Huang، نويسنده , , Qianming Chen، نويسنده , , Yang He، نويسنده ,
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.
Keywords :
5-d]pyrimidine , modified nucleosides , Supramolecular gelators , Base pair recognition
