2,3-Diphenylmaleimide 1-methylpyrrolidin-2-one monosolvate
| dc.contributor.author | Bulatov, Evgeny | |
| dc.contributor.author | Boyarskaya, Dina | |
| dc.contributor.author | Chulkova, Tatiana | |
| dc.contributor.author | Haukka, Matti | |
| dc.date.accessioned | 2016-02-09T07:01:50Z | |
| dc.date.available | 2016-02-09T07:01:50Z | |
| dc.date.issued | 2014 | |
| dc.identifier.citation | Bulatov, E., Boyarskaya, D., Chulkova, T., & Haukka, M. (2014). 2,3-Diphenylmaleimide 1-methylpyrrolidin-2-one monosolvate. <i>Acta Crystallographica Section E : Structure Reports Online</i>, <i>70</i>(3), o260. <a href="https://doi.org/10.1107/S1600536814002372" target="_blank">https://doi.org/10.1107/S1600536814002372</a> | |
| dc.identifier.other | CONVID_25525279 | |
| dc.identifier.other | TUTKAID_69055 | |
| dc.identifier.uri | https://jyx.jyu.fi/handle/123456789/48685 | |
| dc.description.abstract | In the title compound, C16H11NO2C5H9NO, the dihedral angles between the maleimide and phenyl rings are 34.7 (2) and 64.8 (2). In the crystal, the 2,3-diphenylmaleimide and 1- methylpyrrolidin-2-one molecules form centrosymmetrical dimers via pairs of strong N—HO hydrogen bonds and – stacking interactions between the two neighboring maleimide rings [centroid–centroid distance = 3.495 (2) A˚ ]. The dimers are further linked by weak C—HO and C— H hydrogen bonds into a three-dimensional framework. | |
| dc.language.iso | eng | |
| dc.publisher | Wiley-Blackwell Publishing, Inc. | |
| dc.relation.ispartofseries | Acta Crystallographica Section E : Structure Reports Online | |
| dc.subject.other | kristallografia | |
| dc.subject.other | chrystallography | |
| dc.title | 2,3-Diphenylmaleimide 1-methylpyrrolidin-2-one monosolvate | |
| dc.type | article | |
| dc.identifier.urn | URN:NBN:fi:jyu-201602041444 | |
| dc.contributor.laitos | Kemian laitos | fi |
| dc.contributor.laitos | Department of Chemistry | en |
| dc.contributor.oppiaine | Epäorgaaninen ja analyyttinen kemia | fi |
| dc.contributor.oppiaine | Inorganic and Analytical Chemistry | en |
| dc.type.uri | http://purl.org/eprint/type/JournalArticle | |
| dc.date.updated | 2016-02-04T10:15:22Z | |
| dc.type.coar | http://purl.org/coar/resource_type/c_2df8fbb1 | |
| dc.description.reviewstatus | peerReviewed | |
| dc.format.pagerange | o260 | |
| dc.relation.issn | 1600-5368 | |
| dc.relation.numberinseries | 3 | |
| dc.relation.volume | 70 | |
| dc.type.version | publishedVersion | |
| dc.rights.copyright | © the Authors. This is an open-access article distributed under the terms of the Creative Commons Attribution (CC-BY) Licence. | |
| dc.rights.accesslevel | openAccess | fi |
| dc.rights.url | http://creativecommons.org/licenses/by/2.0/uk/legalcode | |
| dc.relation.doi | 10.1107/S1600536814002372 | |
| dc.type.okm | A1 |
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