Taylor, Rupert G. D., Bezzu, C. Grazia, Carta, Mariolino, Msayib, Kadhum J., Walker, Jonathan, Short, Rhys, Kariuki, Benson ORCID: https://orcid.org/0000-0002-8658-3897 and McKeown, Neil B. 2016. The synthesis of organic molecules of intrinsic microporosity designed to frustrate efficient molecular packing. Chemistry - A European Journal 22 (7) , pp. 2466-2472. 10.1002/chem.201504212 |
Preview |
PDF
- Published Version
Available under License Creative Commons Attribution. Download (1MB) | Preview |
Abstract
Efficient reactions between fluorine-functionalised biphenyl and terphenyl derivatives with catechol-functionalised terminal groups provide a route to large, discrete organic molecules of intrinsic microporosity (OMIMs) that provide porous solids solely by their inefficient packing. By altering the size and substituent bulk of the terminal groups, a number of soluble compounds with apparent BET surface areas in excess of 600 m2 g−1 are produced. The efficiency of OMIM structural units for generating microporosity is in the order: propellane>triptycene>hexaphenylbenzene>spirobifluorene>naphthyl=phenyl. The introduction of bulky hydrocarbon substituents significantly enhances microporosity by further reducing packing efficiency. These results are consistent with findings from previously reported packing simulation studies. The introduction of methyl groups at the bridgehead position of triptycene units reduces intrinsic microporosity. This is presumably due to their internal position within the OMIM structure so that they occupy space, but unlike peripheral substituents they do not contribute to the generation of free volume by inefficient packing.
Item Type: | Article |
---|---|
Date Type: | Publication |
Status: | Published |
Schools: | Chemistry |
Subjects: | Q Science > QD Chemistry |
Publisher: | Wiley-Blackwell |
ISSN: | 0947-6539 |
Date of First Compliant Deposit: | 30 March 2016 |
Last Modified: | 05 May 2023 04:38 |
URI: | https://orca.cardiff.ac.uk/id/eprint/87825 |
Citation Data
Cited 45 times in Scopus. View in Scopus. Powered By Scopus® Data
Actions (repository staff only)
Edit Item |