完整後設資料紀錄
DC 欄位 | 值 | 語言 |
---|---|---|
dc.contributor.author | Tsai, Chia-Chen | en_US |
dc.contributor.author | Ho, I-Ting | en_US |
dc.contributor.author | Chu, Jean-Ho | en_US |
dc.contributor.author | Shen, Li-Ching | en_US |
dc.contributor.author | Huang, Shou-Ling | en_US |
dc.contributor.author | Chung, Wen-Sheng | en_US |
dc.date.accessioned | 2014-12-08T15:21:51Z | - |
dc.date.available | 2014-12-08T15:21:51Z | - |
dc.date.issued | 2012-03-02 | en_US |
dc.identifier.issn | 0022-3263 | en_US |
dc.identifier.uri | http://dx.doi.org/10.1021/jo2024784 | en_US |
dc.identifier.uri | http://hdl.handle.net/11536/15559 | - |
dc.description.abstract | An efficient synthetic pathway for the synthesis of biscalix[4]arenes 5-10 using 1,3-dipolar cycloaddition reactions is reported. Biscalix[4]arene 10 is capable of forming a complex with methyl viologen because of favorable cation-pi interactions and a proper cavity size to accommodate the guest. Moreover, biscalix[4]arenes 8a and 8b were found to be atropisomers at room temperature. These two conformers were unable to exchange at room temperature because of the restricted rotation of the C-9-C-11 or C-10-C-12 bonds of the beta-amino-alpha,beta-unsaturated ketones of anthracene. | en_US |
dc.language.iso | en_US | en_US |
dc.title | Synthesis of 9,10-Bis-ketoenaminoanthryl and 9,10-Bisi-isoxazolylanthryl Linked Biscalix[4]arenes: Atropisomers and Molecular Recognitions | en_US |
dc.type | Article | en_US |
dc.identifier.doi | 10.1021/jo2024784 | en_US |
dc.identifier.journal | JOURNAL OF ORGANIC CHEMISTRY | en_US |
dc.citation.volume | 77 | en_US |
dc.citation.issue | 5 | en_US |
dc.citation.spage | 2254 | en_US |
dc.citation.epage | 2262 | en_US |
dc.contributor.department | 應用化學系 | zh_TW |
dc.contributor.department | Department of Applied Chemistry | en_US |
dc.identifier.wosnumber | WOS:000300915900018 | - |
dc.citation.woscount | 7 | - |
顯示於類別: | 期刊論文 |