134856-57-8Relevant articles and documents
Symmetrically backfolded molecules emulating the self-similar features of a Sierpinski triangle
Hu, Jie-Ying,Sun, Yan-Qiong,Xiao, Ran,Cheng, Shengxian,He, Jun,Zeller, Matthias,Wong, Wai-Yeung,Xu, Zhengtao
, p. 6032 - 6037 (2019/06/24)
We synthesized self-similar molecules (G3 and G2; based on phenylalkynyl backbones) with symmetrically backfolded shapes inspired by the famous fractal of a Sierpinski triangle. Unlike the more traditional, starburst dendrimers, the centripetal-shaped Sierpinski molecules feature side branches symmetrically bent away from the growth direction of the main branch, thus contrasting the natural-tree shape. Molecule G3 exhibits three distinct levels of the structural hierarchy comprising the primary, secondary and tertiary branches, while the smaller G2 contains only features of the 1st and 2nd orders. In spite of the much larger conjugated backbone of G3, its solution UV-vis absorption and fluorescence exhibit no red shift relative to G2. In a test of nitrobenzene sensing, a thin film of G3 deposited from THF was more sensitively quenched in fluorescence than the smaller G2.
Rapid solution and solid phase synthesis of monodisperse oligo[(1,4-phenyleneethynylene)-alt-(2,5-thiopheneethynylene)]s
Li, Guorong,Wang, Xianhong,Li, Ji,Zhao, Xiaojiang,Wang, Fosong
, p. 2576 - 2582 (2007/10/03)
Monodisperse oligo[(1,4-phenyleneethynylene)-alt-(2,5-thiopheneethynylene)] s, new candidates for molecular wires, were rapidly synthesized via an iterative divergent/convergent doubling strategy in solution as well as on Merrifield's resin.
Synthesis of monodisperse oligo[(1,4-phenyleneethynylene)-alt-(2,5- thiopheneethynylene)]s
Li, Guorong,Wang, Xianhong,Li, Ji,Zhao, Xiaojiang,Wang, Fosong
, p. 115 - 119 (2007/10/03)
The synthesis of monodisperse oligo[(1,4-phenyleneethynylene)-alt-(2,5- thioph-eneethynylene)]s using an iterative divergent/convergent doubling strategy based on Sonogashira coupling reaction was presented.