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- Publisher Website: 10.1021/ja2063346
- Scopus: eid_2-s2.0-84856289978
- WOS: WOS:000301084400035
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Article: Molecular spur gears comprising triptycene rotators and bibenzimidazole-based stators
Title | Molecular spur gears comprising triptycene rotators and bibenzimidazole-based stators |
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Authors | |
Issue Date | 2012 |
Citation | Journal of the American Chemical Society, 2012, v. 134, n. 3, p. 1528-1535 How to Cite? |
Abstract | Dynamic 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 Identifier | http://hdl.handle.net/10722/341120 |
ISSN | 2023 Impact Factor: 14.4 2023 SCImago Journal Rankings: 5.489 |
ISI Accession Number ID |
DC Field | Value | Language |
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dc.contributor.author | Frantz, Derik K. | - |
dc.contributor.author | Linden, Anthony | - |
dc.contributor.author | Baldridge, Kim K. | - |
dc.contributor.author | Siegel, Jay S. | - |
dc.date.accessioned | 2024-03-13T08:40:18Z | - |
dc.date.available | 2024-03-13T08:40:18Z | - |
dc.date.issued | 2012 | - |
dc.identifier.citation | Journal of the American Chemical Society, 2012, v. 134, n. 3, p. 1528-1535 | - |
dc.identifier.issn | 0002-7863 | - |
dc.identifier.uri | http://hdl.handle.net/10722/341120 | - |
dc.description.abstract | Dynamic 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.language | eng | - |
dc.relation.ispartof | Journal of the American Chemical Society | - |
dc.title | Molecular spur gears comprising triptycene rotators and bibenzimidazole-based stators | - |
dc.type | Article | - |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1021/ja2063346 | - |
dc.identifier.scopus | eid_2-s2.0-84856289978 | - |
dc.identifier.volume | 134 | - |
dc.identifier.issue | 3 | - |
dc.identifier.spage | 1528 | - |
dc.identifier.epage | 1535 | - |
dc.identifier.eissn | 1520-5126 | - |
dc.identifier.isi | WOS:000301084400035 | - |