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GrzybowskiBartosz Andrzej

Grzybowski, Bartosz A.
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dc.citation.endPage 79 -
dc.citation.number 7797 -
dc.citation.startPage 73 -
dc.citation.title NATURE -
dc.citation.volume 579 -
dc.contributor.author Sun, Jian-Ke -
dc.contributor.author Sobolev, Yaroslav I. -
dc.contributor.author Zhang, Weiyi -
dc.contributor.author Zhuang, Qiang -
dc.contributor.author Grzybowski, Bartosz A. -
dc.date.accessioned 2023-12-21T17:46:29Z -
dc.date.available 2023-12-21T17:46:29Z -
dc.date.created 2020-07-16 -
dc.date.issued 2020-03 -
dc.description.abstract The ability to grow properly sized and good quality crystals is one of the cornerstones of single-crystal diffraction, is advantageous in many industrial-scale chemical processes(1-3), and is important for obtaining institutional approvals of new drugs for which high-quality crystallographic data are required(4-7). Typically, single crystals suitable for such processes and analyses are grown for hours to days during which any mechanical disturbances-believed to be detrimental to the process-are carefully avoided. In particular, stirring and shear flows are known to cause secondary nucleation, which decreases the final size of the crystals (though shear can also increase their quantity(8-14)). Here we demonstrate that in the presence of polymers (preferably, polyionic liquids), crystals of various types grow in common solvents, at constant temperature, much bigger and much faster when stirred, rather than kept still. This conclusion is based on the study of approximately 20 diverse organic molecules, inorganic salts, metal-organic complexes, and even some proteins. On typical timescales of a few to tens of minutes, these molecules grow into regularly faceted crystals that are always larger (with longest linear dimension about 16 times larger) than those obtained in control experiments of the same duration but without stirring or without polymers. We attribute this enhancement to two synergistic effects. First, under shear, the polymers and their aggregates disentangle, compete for solvent molecules and thus effectively 'salt out' (that is, induce precipitation by decreasing solubility of) the crystallizing species. Second, the local shear rate is dependent on particle size, ultimately promoting the growth of larger crystals (but not via surface-energy effects as in classical Ostwald ripening). This closed-system, constant-temperature crystallization driven by shear could be a valuable addition to the repertoire of crystal growth techniques, enabling accelerated growth of crystals required by the materials and pharmaceutical industries. -
dc.identifier.bibliographicCitation NATURE, v.579, no.7797, pp.73 - 79 -
dc.identifier.doi 10.1038/s41586-020-2042-1 -
dc.identifier.issn 0028-0836 -
dc.identifier.scopusid 2-s2.0-85081042399 -
dc.identifier.uri https://scholarworks.unist.ac.kr/handle/201301/49532 -
dc.identifier.url https://www.nature.com/articles/s41586-020-2042-1 -
dc.identifier.wosid 000543777700001 -
dc.language 영어 -
dc.publisher NATURE PUBLISHING GROUP -
dc.title Enhancing crystal growth using polyelectrolyte solutions and shear flow -
dc.type Article -
dc.description.isOpenAccess FALSE -
dc.relation.journalWebOfScienceCategory Multidisciplinary Sciences -
dc.relation.journalResearchArea Science & Technology - Other Topics -
dc.type.docType Article -
dc.description.journalRegisteredClass scie -
dc.description.journalRegisteredClass scopus -
dc.subject.keywordPlus SECONDARY NUCLEATION -
dc.subject.keywordPlus POLYMER-SOLUTIONS -
dc.subject.keywordPlus FLUID SHEAR -
dc.subject.keywordPlus CRYSTALLIZATION -

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