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Article: Efficient solvent-controlled crystallization of pure polymorphs of 1-nitro-4-(4-nitrophenylmethylthio)benzene

TitleEfficient solvent-controlled crystallization of pure polymorphs of 1-nitro-4-(4-nitrophenylmethylthio)benzene
Authors
Issue Date20-Jun-2014
PublisherRoyal Society of Chemistry
Citation
CrystEngComm, 2014, v. 16, n. 38, p. 8960-8968 How to Cite?
Abstract

Four pure polymorphs (I-IV) and a monohydrate of 1-nitro-4-(4-nitrophenylmethylthio)benzene (abbreviated as NNB) were readily obtained in bulk quantities through a solvent-control strategy. A total of 15 common solvents were used to explore the crystallization behaviour of NNB. Forms II and IV and the monohydrate exhibit solvent-dependent polymorphic selectivity. Form I can be preferentially crystallized from solvents with high dielectric constants, while III is obtainable from solvents with low dielectric constants. All of the forms were characterized via single-crystal X-ray determination, and the rationalization of structural features is discussed. Phase behaviours of the polymorphs were observed through differential scanning calorimetry (DSC) and powder X-ray diffraction. This study may contribute to the strategic discovery and development of a desirable polymorph of any organic drug substance via solvent control.


Persistent Identifierhttp://hdl.handle.net/10722/367048
ISSN
2023 Impact Factor: 2.6
2023 SCImago Journal Rankings: 0.535

 

DC FieldValueLanguage
dc.contributor.authorWan, C.Q.-
dc.contributor.authorLi, A.M.-
dc.contributor.authorAl-Thabaiti, S.A.-
dc.contributor.authorEl-Mosslamy, E.S.H.-
dc.contributor.authorMak, T.C.W.-
dc.date.accessioned2025-12-02T00:35:24Z-
dc.date.available2025-12-02T00:35:24Z-
dc.date.issued2014-06-20-
dc.identifier.citationCrystEngComm, 2014, v. 16, n. 38, p. 8960-8968-
dc.identifier.issn1466-8033-
dc.identifier.urihttp://hdl.handle.net/10722/367048-
dc.description.abstract<p>Four pure polymorphs (I-IV) and a monohydrate of 1-nitro-4-(4-nitrophenylmethylthio)benzene (abbreviated as NNB) were readily obtained in bulk quantities through a solvent-control strategy. A total of 15 common solvents were used to explore the crystallization behaviour of NNB. Forms II and IV and the monohydrate exhibit solvent-dependent polymorphic selectivity. Form I can be preferentially crystallized from solvents with high dielectric constants, while III is obtainable from solvents with low dielectric constants. All of the forms were characterized via single-crystal X-ray determination, and the rationalization of structural features is discussed. Phase behaviours of the polymorphs were observed through differential scanning calorimetry (DSC) and powder X-ray diffraction. This study may contribute to the strategic discovery and development of a desirable polymorph of any organic drug substance via solvent control.<br></p>-
dc.languageeng-
dc.publisherRoyal Society of Chemistry-
dc.relation.ispartofCrystEngComm-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleEfficient solvent-controlled crystallization of pure polymorphs of 1-nitro-4-(4-nitrophenylmethylthio)benzene-
dc.typeArticle-
dc.identifier.doi10.1039/c4ce00753k-
dc.identifier.scopuseid_2-s2.0-84907153081-
dc.identifier.volume16-
dc.identifier.issue38-
dc.identifier.spage8960-
dc.identifier.epage8968-
dc.identifier.eissn1466-8033-
dc.identifier.issnl1466-8033-

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