Files in this item
Comparison of N-(3,4,5-trimethoxybenzylidene)naphthalen-1-amine and its reduction product N-(3,4,5-trimethoxybenzyl)naphthalen-1-amine
Item metadata
dc.contributor.author | Garay, A. | |
dc.contributor.author | Abonía, R. | |
dc.contributor.author | Cobo, J. | |
dc.contributor.author | Glidewell, C. | |
dc.date.accessioned | 2014-08-27T10:01:05Z | |
dc.date.available | 2014-08-27T10:01:05Z | |
dc.date.issued | 2014-02-01 | |
dc.identifier.citation | Garay , A , Abonía , R , Cobo , J & Glidewell , C 2014 , ' Comparison of N-(3,4,5-trimethoxybenzylidene)naphthalen-1-amine and its reduction product N-(3,4,5-trimethoxybenzyl)naphthalen-1-amine ' , Acta Crystallographica Section C: Crystal Structure Communications , vol. 70 , no. 2 , pp. 210-215 . https://doi.org/10.1107/S2053229613034839 | en |
dc.identifier.issn | 0108-2701 | |
dc.identifier.other | PURE: 143706978 | |
dc.identifier.other | PURE UUID: b39acd87-6806-4b4e-aaa2-f75e61f2e485 | |
dc.identifier.other | Scopus: 84905511399 | |
dc.identifier.other | WOS: 000332218000021 | |
dc.identifier.uri | https://hdl.handle.net/10023/5247 | |
dc.description | The authors thank the Centro de Instrumentación Científico-Técnica of the Universidad de Jaén and the staff for the data collection. AG and RA thank COLCIENCIAS and the Universidad del Valle for financial support. JC thanks the Consejería de Innovación, Ciencia y Empresa (Junta de Andalucía, Spain) and the Universidad de Jaén for financial support. | en |
dc.description.abstract | The molecules in (E)-N-(3,4,5-trimethoxybenzylidene)naphthalen-1-amine, C20H21NO3, (I), and its reduction product N-(3,4,5-trimethoxybenzyl)naphthalen-1-amine, C20H19NO3, (II), are both conformationally chiral, but (I) crystallizes in a centrosymmetric space group, while (II) crystallizes with just one conformational enantiomer in each crystal. A combination of two C - H⋯O hydrogen bonds links the molecules of (I) into sheets containing a single type of R66(44) ring, and these sheets are linked into a continuous three-dimensional array by a single π-π stacking interaction. The molecules of (II) are linked into complex sheets by a combination of N - H⋯O, C - H⋯O and C - H⋯π(arene) hydrogen bonds. | |
dc.format.extent | 6 | |
dc.language.iso | eng | |
dc.relation.ispartof | Acta Crystallographica Section C: Crystal Structure Communications | en |
dc.rights | © International Union of Crystallography 2014 | en |
dc.subject | Crystal structure | en |
dc.subject | Supramolecular structure | en |
dc.subject | Hydrogen bonding | en |
dc.subject | QD Chemistry | en |
dc.subject.lcc | QD | en |
dc.title | Comparison of N-(3,4,5-trimethoxybenzylidene)naphthalen-1-amine and its reduction product N-(3,4,5-trimethoxybenzyl)naphthalen-1-amine | en |
dc.type | Journal article | en |
dc.description.version | Publisher PDF | en |
dc.contributor.institution | University of St Andrews. School of Chemistry | en |
dc.identifier.doi | https://doi.org/10.1107/S2053229613034839 | |
dc.description.status | Peer reviewed | en |
dc.identifier.url | http://www.scopus.com/inward/record.url?eid=2-s2.0-84905511399&partnerID=8YFLogxK | en |
dc.identifier.url | http://scripts.iucr.org/cgi-bin/sendsup?sf3215 | en |
This item appears in the following Collection(s)
Items in the St Andrews Research Repository are protected by copyright, with all rights reserved, unless otherwise indicated.