模板诱导的新型正交 9,10-二苯基蒽多晶型结晶

IF 3.2 2区 化学 Q2 CHEMISTRY, MULTIDISCIPLINARY
Alina A. Sonina, Darya S. Cheshkina, Maxim S. Kazantsev
{"title":"模板诱导的新型正交 9,10-二苯基蒽多晶型结晶","authors":"Alina A. Sonina, Darya S. Cheshkina, Maxim S. Kazantsev","doi":"10.1021/acs.cgd.4c00744","DOIUrl":null,"url":null,"abstract":"Polymorphism in organic semiconductor materials has attracted great interest due to the potential for tuning both structure and optoelectronic properties for next-generation optoelectronic devices. Therefore, developing methods to control the solution crystallization process is important for improving the kinetics of crystal nucleation and obtaining the desired functional systems. Template-induced crystallization is an intriguing crystallization control approach that enables heterogeneous nucleation of the solute on template surfaces, either intentionally introduced into the system or naturally occurring during crystallization. Here, we studied template-induced crystallization of the organic luminophore 9,10-diphenylanthracene (DPA) on the following crystals used as substrates: pyrene, perylene, anthracene, and rubrene. Crystallization of DPA in the presence of pyrene and perylene resulted in the formation of their cocrystals, whereas crystallization with anthracene and triclinic rubrene crystals had no effect on DPA polymorphism. We found that, in the presence of orthorhombic rubrene used as a template, a novel orthorhombic DPA polymorph (δ-DPA) crystallized. δ-DPA has herringbone packing similar to that of the used template. δ-DPA crystals demonstrated blue emission with a photoluminescence quantum yield of 52% and needlelike morphology. The results obtained could be used for crystallization control and engineering of high-performance conjugated crystalline materials.","PeriodicalId":34,"journal":{"name":"Crystal Growth & Design","volume":null,"pages":null},"PeriodicalIF":3.2000,"publicationDate":"2024-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Template-Induced Crystallization of Novel Orthorhombic 9,10-Diphenylanthracene Polymorph\",\"authors\":\"Alina A. Sonina, Darya S. Cheshkina, Maxim S. Kazantsev\",\"doi\":\"10.1021/acs.cgd.4c00744\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Polymorphism in organic semiconductor materials has attracted great interest due to the potential for tuning both structure and optoelectronic properties for next-generation optoelectronic devices. Therefore, developing methods to control the solution crystallization process is important for improving the kinetics of crystal nucleation and obtaining the desired functional systems. Template-induced crystallization is an intriguing crystallization control approach that enables heterogeneous nucleation of the solute on template surfaces, either intentionally introduced into the system or naturally occurring during crystallization. Here, we studied template-induced crystallization of the organic luminophore 9,10-diphenylanthracene (DPA) on the following crystals used as substrates: pyrene, perylene, anthracene, and rubrene. Crystallization of DPA in the presence of pyrene and perylene resulted in the formation of their cocrystals, whereas crystallization with anthracene and triclinic rubrene crystals had no effect on DPA polymorphism. We found that, in the presence of orthorhombic rubrene used as a template, a novel orthorhombic DPA polymorph (δ-DPA) crystallized. δ-DPA has herringbone packing similar to that of the used template. δ-DPA crystals demonstrated blue emission with a photoluminescence quantum yield of 52% and needlelike morphology. The results obtained could be used for crystallization control and engineering of high-performance conjugated crystalline materials.\",\"PeriodicalId\":34,\"journal\":{\"name\":\"Crystal Growth & Design\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.2000,\"publicationDate\":\"2024-09-17\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Crystal Growth & Design\",\"FirstCategoryId\":\"92\",\"ListUrlMain\":\"https://doi.org/10.1021/acs.cgd.4c00744\",\"RegionNum\":2,\"RegionCategory\":\"化学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"CHEMISTRY, MULTIDISCIPLINARY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Crystal Growth & Design","FirstCategoryId":"92","ListUrlMain":"https://doi.org/10.1021/acs.cgd.4c00744","RegionNum":2,"RegionCategory":"化学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"CHEMISTRY, MULTIDISCIPLINARY","Score":null,"Total":0}
引用次数: 0

摘要

有机半导体材料中的多晶体现象引起了人们的极大兴趣,因为它具有调整下一代光电设备的结构和光电特性的潜力。因此,开发控制溶液结晶过程的方法对于改善晶体成核动力学和获得所需的功能系统非常重要。模板诱导结晶是一种有趣的结晶控制方法,它能使溶质在模板表面发生异质成核,这些模板可以是有意引入系统的,也可以是在结晶过程中自然形成的。在这里,我们研究了有机发光体 9,10-二苯基蒽(DPA)在以下晶体上的模板诱导结晶:芘、珀烯、蒽和红芘。在有芘和过烯时,DPA 的结晶会形成它们的共晶体,而与蒽和三菱红宝石晶体的结晶对 DPA 的多态性没有影响。我们发现,在以正交红芘为模板的情况下,会结晶出一种新的正交 DPA 多晶体(δ-DPA)。δ-DPA具有与所用模板相似的人字形堆积。δ-DPA 晶体发出蓝色光,其光致发光量子产率为 52%,并呈现针状形态。所获得的结果可用于结晶控制和高性能共轭晶体材料的工程设计。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Template-Induced Crystallization of Novel Orthorhombic 9,10-Diphenylanthracene Polymorph

Template-Induced Crystallization of Novel Orthorhombic 9,10-Diphenylanthracene Polymorph
Polymorphism in organic semiconductor materials has attracted great interest due to the potential for tuning both structure and optoelectronic properties for next-generation optoelectronic devices. Therefore, developing methods to control the solution crystallization process is important for improving the kinetics of crystal nucleation and obtaining the desired functional systems. Template-induced crystallization is an intriguing crystallization control approach that enables heterogeneous nucleation of the solute on template surfaces, either intentionally introduced into the system or naturally occurring during crystallization. Here, we studied template-induced crystallization of the organic luminophore 9,10-diphenylanthracene (DPA) on the following crystals used as substrates: pyrene, perylene, anthracene, and rubrene. Crystallization of DPA in the presence of pyrene and perylene resulted in the formation of their cocrystals, whereas crystallization with anthracene and triclinic rubrene crystals had no effect on DPA polymorphism. We found that, in the presence of orthorhombic rubrene used as a template, a novel orthorhombic DPA polymorph (δ-DPA) crystallized. δ-DPA has herringbone packing similar to that of the used template. δ-DPA crystals demonstrated blue emission with a photoluminescence quantum yield of 52% and needlelike morphology. The results obtained could be used for crystallization control and engineering of high-performance conjugated crystalline materials.
求助全文
通过发布文献求助,成功后即可免费获取论文全文。 去求助
来源期刊
Crystal Growth & Design
Crystal Growth & Design 化学-材料科学:综合
CiteScore
6.30
自引率
10.50%
发文量
650
审稿时长
1.9 months
期刊介绍: The aim of Crystal Growth & Design is to stimulate crossfertilization of knowledge among scientists and engineers working in the fields of crystal growth, crystal engineering, and the industrial application of crystalline materials. Crystal Growth & Design publishes theoretical and experimental studies of the physical, chemical, and biological phenomena and processes related to the design, growth, and application of crystalline materials. Synergistic approaches originating from different disciplines and technologies and integrating the fields of crystal growth, crystal engineering, intermolecular interactions, and industrial application are encouraged.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术官方微信