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- Publisher Website: 10.1002/cplu.201100075
- Scopus: eid_2-s2.0-84860257284
- WOS: WOS:000301446500001
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Article: Mechanically interlocked molecules assembled by π-π Recognition
Title | Mechanically interlocked molecules assembled by π-π Recognition |
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Authors | |
Keywords | π-π interactions Catenanes Donor-acceptor systems Mechanically interlocked molecules Rotaxanes |
Issue Date | 2012 |
Citation | ChemPlusChem, 2012, v. 77, n. 3, p. 159-185 How to Cite? |
Abstract | The beauty and utility of interlocked architectures have been making their way relentlessly into chemistry in the form of mechanically interlocked molecules (MIMs) for almost half a century now. Few would challenge the assertion that the emergence of template-directed synthetic protocols has aided and abetted the facile and efficient construction of MIMs compared with the statistical approaches employed while the field was still in its infancy. To date, a panoply of MIMs has been created in the wake of emerging recognition motifs and the template-directed synthetic protocols they have forged. Among these motifs, those dependent on π-π stacking in the form of donor-acceptor interactions have played an important role in the increasingly rapid development of the field. The few integrated systems that have so far emerged based on this class of MIMs demonstrate their ability to act as active components in many potential applications. This review focuses on the progress which has been accomplished during the past decade involving MIMs comprising aromatic π-π stacking interactions. While progress has been remarkable, opportunities still abound for MIMs assembled by π-π recognition. © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. |
Persistent Identifier | http://hdl.handle.net/10722/332974 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Barin, Gokhan | - |
dc.contributor.author | Coskun, Ali | - |
dc.contributor.author | Fouda, Moustafa M.G. | - |
dc.contributor.author | Stoddart, J. Fraser | - |
dc.date.accessioned | 2023-10-06T05:15:46Z | - |
dc.date.available | 2023-10-06T05:15:46Z | - |
dc.date.issued | 2012 | - |
dc.identifier.citation | ChemPlusChem, 2012, v. 77, n. 3, p. 159-185 | - |
dc.identifier.uri | http://hdl.handle.net/10722/332974 | - |
dc.description.abstract | The beauty and utility of interlocked architectures have been making their way relentlessly into chemistry in the form of mechanically interlocked molecules (MIMs) for almost half a century now. Few would challenge the assertion that the emergence of template-directed synthetic protocols has aided and abetted the facile and efficient construction of MIMs compared with the statistical approaches employed while the field was still in its infancy. To date, a panoply of MIMs has been created in the wake of emerging recognition motifs and the template-directed synthetic protocols they have forged. Among these motifs, those dependent on π-π stacking in the form of donor-acceptor interactions have played an important role in the increasingly rapid development of the field. The few integrated systems that have so far emerged based on this class of MIMs demonstrate their ability to act as active components in many potential applications. This review focuses on the progress which has been accomplished during the past decade involving MIMs comprising aromatic π-π stacking interactions. While progress has been remarkable, opportunities still abound for MIMs assembled by π-π recognition. © 2012 Wiley-VCH Verlag GmbH & Co. KGaA, Weinheim. | - |
dc.language | eng | - |
dc.relation.ispartof | ChemPlusChem | - |
dc.subject | π-π interactions | - |
dc.subject | Catenanes | - |
dc.subject | Donor-acceptor systems | - |
dc.subject | Mechanically interlocked molecules | - |
dc.subject | Rotaxanes | - |
dc.title | Mechanically interlocked molecules assembled by π-π Recognition | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1002/cplu.201100075 | - |
dc.identifier.scopus | eid_2-s2.0-84860257284 | - |
dc.identifier.volume | 77 | - |
dc.identifier.issue | 3 | - |
dc.identifier.spage | 159 | - |
dc.identifier.epage | 185 | - |
dc.identifier.eissn | 2192-6506 | - |
dc.identifier.isi | WOS:000301446500001 | - |