The Synthesis of Organic Molecules of Intrinsic Microporosity Designed to Frustrate Efficient Molecular Packing. Issue 7 (11th January 2016)
- Record Type:
- Journal Article
- Title:
- The Synthesis of Organic Molecules of Intrinsic Microporosity Designed to Frustrate Efficient Molecular Packing. Issue 7 (11th January 2016)
- Main Title:
- The Synthesis of Organic Molecules of Intrinsic Microporosity Designed to Frustrate Efficient Molecular Packing
- Authors:
- Taylor, Rupert G. D.
Bezzu, C. Grazia
Carta, Mariolino
Msayib, Kadhum J.
Walker, Jonathan
Short, Rhys
Kariuki, Benson M.
McKeown, Neil B. - Abstract:
- 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 m 2 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. Abstract : Poor packing, packed porosity : Organic molecules of intrinsic microporosity (OMIMs) are large, discrete molecules that provide porous solids solely by their inefficient packing. By altering the number, size, and bulk of the terminal groups, a number of OMIMs with apparent BET surface areas in excess of 600 mAbstract: 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 m 2 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. Abstract : Poor packing, packed porosity : Organic molecules of intrinsic microporosity (OMIMs) are large, discrete molecules that provide porous solids solely by their inefficient packing. By altering the number, size, and bulk of the terminal groups, a number of OMIMs with apparent BET surface areas in excess of 600 m 2 g −1 are produced. … (more)
- Is Part Of:
- Chemistry. Volume 22:Issue 7(2016)
- Journal:
- Chemistry
- Issue:
- Volume 22:Issue 7(2016)
- Issue Display:
- Volume 22, Issue 7 (2016)
- Year:
- 2016
- Volume:
- 22
- Issue:
- 7
- Issue Sort Value:
- 2016-0022-0007-0000
- Page Start:
- 2466
- Page End:
- 2472
- Publication Date:
- 2016-01-11
- Subjects:
- adsorption -- aromatic nucleophilic substitution -- microporous materials -- molecular packing -- triptycene
Chemistry -- Periodicals
540 - Journal URLs:
- http://onlinelibrary.wiley.com/journal/10.1002/(ISSN)1521-3765 ↗
http://onlinelibrary.wiley.com/ ↗ - DOI:
- 10.1002/chem.201504212 ↗
- Languages:
- English
- ISSNs:
- 0947-6539
- Deposit Type:
- Legaldeposit
- View Content:
- Available online (eLD content is only available in our Reading Rooms) ↗
- Physical Locations:
- British Library DSC - 3168.860500
British Library DSC - BLDSS-3PM
British Library STI - ELD Digital store - Ingest File:
- 9171.xml