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Article: Molecular spur gears comprising triptycene rotators and bibenzimidazole-based stators

TitleMolecular spur gears comprising triptycene rotators and bibenzimidazole-based stators
Authors
Issue Date2012
Citation
Journal of the American Chemical Society, 2012, v. 134, n. 3, p. 1528-1535 How to Cite?
AbstractDynamic gearing of molecular spur gears, the most common type of mechanical gear, is elucidated. Molecular design and conformational analysis show that derivatives of 4,4-bis(triptycen-9-ylethynyl)bibenzimidazole represent suitable constructs to investigate gearing behavior of collateral triptycene (Tp) groups. To test this design, DFT calculations (B97-D/Def2-TZVP) were employed and the results suggest that these molecules undergo geared rotation preferentially to gear slippage. Synthesis of derivatives was carried out, providing a series of molecular spur gears, including the first desymmetrized spur gear molecules, which were subsequently subjected to stereochemical analysis. © 2012 American Chemical Society.
Persistent Identifierhttp://hdl.handle.net/10722/341120
ISSN
2023 Impact Factor: 14.4
2023 SCImago Journal Rankings: 5.489
ISI Accession Number ID

 

DC FieldValueLanguage
dc.contributor.authorFrantz, Derik K.-
dc.contributor.authorLinden, Anthony-
dc.contributor.authorBaldridge, Kim K.-
dc.contributor.authorSiegel, Jay S.-
dc.date.accessioned2024-03-13T08:40:18Z-
dc.date.available2024-03-13T08:40:18Z-
dc.date.issued2012-
dc.identifier.citationJournal of the American Chemical Society, 2012, v. 134, n. 3, p. 1528-1535-
dc.identifier.issn0002-7863-
dc.identifier.urihttp://hdl.handle.net/10722/341120-
dc.description.abstractDynamic gearing of molecular spur gears, the most common type of mechanical gear, is elucidated. Molecular design and conformational analysis show that derivatives of 4,4-bis(triptycen-9-ylethynyl)bibenzimidazole represent suitable constructs to investigate gearing behavior of collateral triptycene (Tp) groups. To test this design, DFT calculations (B97-D/Def2-TZVP) were employed and the results suggest that these molecules undergo geared rotation preferentially to gear slippage. Synthesis of derivatives was carried out, providing a series of molecular spur gears, including the first desymmetrized spur gear molecules, which were subsequently subjected to stereochemical analysis. © 2012 American Chemical Society.-
dc.languageeng-
dc.relation.ispartofJournal of the American Chemical Society-
dc.titleMolecular spur gears comprising triptycene rotators and bibenzimidazole-based stators-
dc.typeArticle-
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1021/ja2063346-
dc.identifier.scopuseid_2-s2.0-84856289978-
dc.identifier.volume134-
dc.identifier.issue3-
dc.identifier.spage1528-
dc.identifier.epage1535-
dc.identifier.eissn1520-5126-
dc.identifier.isiWOS:000301084400035-

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