Synthesis of a Rigid C3v-Symmetric Tris-salicylaldehyde as a Precursor for a Highly Porous Molecular Cube

被引:84
作者
Elbert, Sven M. [1 ]
Rominger, Frank [1 ]
Mastalerz, Michael [1 ]
机构
[1] Heidelberg Univ, Inst Organ Chem, D-69120 Heidelberg, Germany
关键词
cage compounds; carbon dioxide capture; cycloaddition; microporous materials; Schiff bases; METAL-ORGANIC FRAMEWORK; DYNAMIC COVALENT CHEMISTRY; DIELS-ALDER REACTIONS; HIGH SURFACE-AREAS; CAGE COMPOUNDS; CARBON-DIOXIDE; GAS-SORPTION; INTRINSIC MICROPOROSITY; LARGE CAVITIES; CO2; CAPTURE;
D O I
10.1002/chem.201404829
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The development of a synthetic approach to a C-3v-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.
引用
收藏
页码:16707 / 16720
页数:14
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