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dc.contributor.authorLahtinen, Manu
dc.contributor.authorNättinen, Kalle
dc.contributor.authorNummelin, Sami
dc.date.accessioned2016-02-01T06:32:14Z
dc.date.available2016-02-01T06:32:14Z
dc.date.issued2013
dc.identifier.citationLahtinen, M., Nättinen, K., & Nummelin, S. (2013). Methyl 3',4',5'-trimethoxybiphenyl-4-carboxylate. <i>Acta Crystallographica Section E : Structure Reports Online</i>, <i>69</i>(3), o383. <a href="https://doi.org/10.1107/S1600536813004133" target="_blank">https://doi.org/10.1107/S1600536813004133</a>
dc.identifier.otherCONVID_22356190
dc.identifier.otherTUTKAID_55947
dc.identifier.urihttps://jyx.jyu.fi/handle/123456789/48550
dc.description.abstractIn the title compound, C17H18O5, the dihedral angle between the benzene rings is 31.23 (16). In the crystal, the molecules are packed in an antiparallel fashion in layers along the a axis. In each layer, very weak C—HO hydrogen bonds occur between the methoxy and methyl ester groups. Weak C— H interactions between the 40 - and 50 -methoxy groups and neighbouring benzene rings [methoxy-C–ring centroid distances = 4.075 and 3.486 A˚ , respectively] connect the layers.
dc.language.isoeng
dc.publisherInternational Union of Crystallography
dc.relation.ispartofseriesActa Crystallographica Section E : Structure Reports Online
dc.relation.urihttp://scripts.iucr.org/cgi-bin/paper?S1600536813004133
dc.subject.otherröntgendiffraktio
dc.subject.otherkiderakenne
dc.subject.otherdendrimeeriprekursori
dc.subject.otherX-ray diffraction
dc.subject.othercrystal structure
dc.subject.otherdendrimer precursor
dc.titleMethyl 3',4',5'-trimethoxybiphenyl-4-carboxylate
dc.typearticle
dc.identifier.urnURN:NBN:fi:jyu-201601291343
dc.contributor.laitosKemian laitosfi
dc.contributor.laitosDepartment of Chemistryen
dc.contributor.oppiaineEpäorgaaninen ja analyyttinen kemiafi
dc.contributor.oppiaineInorganic and Analytical Chemistryen
dc.type.urihttp://purl.org/eprint/type/JournalArticle
dc.date.updated2016-01-29T13:15:31Z
dc.type.coarhttp://purl.org/coar/resource_type/c_2df8fbb1
dc.description.reviewstatuspeerReviewed
dc.format.pagerangeo383
dc.relation.issn1600-5368
dc.relation.numberinseries3
dc.relation.volume69
dc.type.versionpublishedVersion
dc.rights.copyright© the Authors, 2013. This is an open access article publised by ICUr.
dc.rights.accesslevelopenAccessfi
dc.relation.doi10.1107/S1600536813004133
dc.type.okmA1


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