| Literature DB >> 26464045 |
Qing Ji1, Ha T M Le1, Xiqu Wang1, Yu-Sheng Chen2, Tatyana Makarenko1, Allan J Jacobson1, Ognjen Š Miljanić3.
Abstract
Cyanide-catalyzed benzoin condensation of terephthaldehyde produces a cyclic tetramer, which we propose to name cyclotetrabenzoin. Cyclotetrabenzoin is a square-shaped macrocycle ornamented with four α-hydroxyketone functionalities pointing away from the central cavity, the dimensions of which are 6.9×6.9 Å. In the solid state, these functional groups extensively hydrogen bond, resulting in a microporous three-dimensional organic framework with one-dimensional nanotube channels. This material exhibits permanent-albeit low-porosity, with a Langmuir surface area of 52 m(2) g(-1) . Cyclotetrabenzoin's easy and inexpensive synthesis and purification may inspire the creation of other shape-persistent macrocycles and porous molecular crystals by benzoin condensation.Entities:
Keywords: adsorption; benzoin condensation; dynamic combinatorial chemistry; macrocycles; shape-persistent macrocycles
Year: 2015 PMID: 26464045 DOI: 10.1002/chem.201503851
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236