Elbert Sven M, Rominger Frank, Mastalerz Michael
Organisch-Chemisches Institut, Ruprecht-Karls-Universität Heidelberg, Im Neuenheimer Feld 270, 69120 Heidelberg (Germany).
Chemistry. 2014 Dec 8;20(50):16707-20. doi: 10.1002/chem.201404829. Epub 2014 Oct 21.
The development of a synthetic approach to a C3v -symmetric tris-salicylaldehyde based on triptycene is presented. The tris-salicylaldehyde is a versatile precursor for porous molecular materials, as demonstrated in the [4+4] condensation reaction with a triptycene triamine to form a molecular shape-persistent porous cube. The amorphous material of the molecular porous cube shows a very high surface area of 1014 m(2) g(-1) (BET model) and a high uptake of CO2 (18.2 wt % at 273 K and 1 bar). Furthermore, during the multistep synthesis of the tris-salicylaldehyde precursor, a relatively rare (twofold) addition of the aryne to the anthracene in the 1,4- and 1,4,5,8-positions have been found during a Diels-Alder reaction, as proven by X-ray structure analysis.
本文介绍了一种基于三蝶烯的C3v对称三水杨醛的合成方法。三水杨醛是多孔分子材料的通用前体,如在与三蝶烯三胺的[4+4]缩合反应中形成分子形状持久的多孔立方体所示。分子多孔立方体的无定形材料显示出非常高的表面积1014 m² g⁻¹(BET模型)和对CO₂的高吸附量(在273 K和1 bar下为18.2 wt%)。此外,在三水杨醛前体的多步合成过程中,通过X射线结构分析证明,在狄尔斯-阿尔德反应中,发现了相对罕见的(双重)芳炔在蒽的1,4-和1,4,5,8-位的加成。