Please use this identifier to cite or link to this item:
https://doi.org/10.1021/ol201361f
DC Field | Value | |
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dc.title | Planar macrocyclic fluoropentamers as supramolecular organogelators | |
dc.contributor.author | Ren, C. | |
dc.contributor.author | Xu, S. | |
dc.contributor.author | Xu, J. | |
dc.contributor.author | Chen, H. | |
dc.contributor.author | Zeng, H. | |
dc.date.accessioned | 2014-06-23T05:46:48Z | |
dc.date.available | 2014-06-23T05:46:48Z | |
dc.date.issued | 2011-08-05 | |
dc.identifier.citation | Ren, C., Xu, S., Xu, J., Chen, H., Zeng, H. (2011-08-05). Planar macrocyclic fluoropentamers as supramolecular organogelators. Organic Letters 13 (15) : 3840-3843. ScholarBank@NUS Repository. https://doi.org/10.1021/ol201361f | |
dc.identifier.issn | 15237060 | |
dc.identifier.uri | http://scholarbank.nus.edu.sg/handle/10635/76765 | |
dc.description.abstract | Despite their great diversities, 2D-shaped macrocycles that can serve as the organogelators have been surprisingly rare; two planar macrocyclic fluoropentamers designed by us were highly able to gelate organic solvents, largely derived from their strong tendency to form 1D stacked fibrillar structures stabilized by both interplanar H-bonds and π-π stacking forces. © 2011 American Chemical Society. | |
dc.description.uri | http://libproxy1.nus.edu.sg/login?url=http://dx.doi.org/10.1021/ol201361f | |
dc.source | Scopus | |
dc.type | Article | |
dc.contributor.department | CHEMISTRY | |
dc.description.doi | 10.1021/ol201361f | |
dc.description.sourcetitle | Organic Letters | |
dc.description.volume | 13 | |
dc.description.issue | 15 | |
dc.description.page | 3840-3843 | |
dc.identifier.isiut | 000293252800019 | |
Appears in Collections: | Staff Publications |
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