N-Iodosaccharin-pyridine co-crystal system under pressure: experimental evidence of reversible twinning.

Vishnu Vijayakumar-Syamala, E. Aubert, M. Deutsch, E. Wenger, Arun Dhaka, M. Fourmigué, M. Nespolo, Enrique Espinosa
{"title":"N-Iodosaccharin-pyridine co-crystal system under pressure: experimental evidence of reversible twinning.","authors":"Vishnu Vijayakumar-Syamala, E. Aubert, M. Deutsch, E. Wenger, Arun Dhaka, M. Fourmigué, M. Nespolo, Enrique Espinosa","doi":"10.1107/s2052520622002542","DOIUrl":null,"url":null,"abstract":"This work presents a single-crystal X-ray diffraction study of an organic co-crystal composed of N-iodosaccharin and pyridine (NISac·py) under hydrostatic pressure ranging from 0.00 (5) GPa to 4.5 (2) GPa. NISac·py crystallizes in the monoclinic system (space group B21/e). The unconventional setting of the space group is adopted (the conventional setting is P21/c, No. 14) to emphasise the strongly pseudo-orthorhombic symmetry of the lattice, with a β angle very close to 90°. The crystal structure contains one molecule each of N-iodosaccharin (NISac) and pyridine (py) in the asymmetric unit (Z' = 1), linked via an Nsac...I...N'py halogen-bonding motif. A gradual modification of this motif is observed under pressure as a result of changes in the crystalline environment. Mechanical twinning is observed under compression and the sample splits into two domains, spanning an unequal volume that is mapped by a twofold rotation about the [100] direction of the B21/e unit cell. The twinning is particularly significant at high pressure, being reversible when the pressure is released. The structure of the twinned sample reveals the continuity of a substantial substructure across the composition plane. The presence of this common substructure in the two orientations of the twinned individuals can be interpreted as a structural reason for the formation of the twin and is the first observed example in a molecular crystal. These results indicate that the anisotropy of intermolecular interactions in the crystal structure results in an anisotropic strain generated upon the action of hydrostatic compression. Periodic density functional theory calculations were carried out by considering an isotropic external pressure, the results showing good agreement with the experimental findings. The bulk modulus of the crystal was obtained from the equations of state, being 7 (1) GPa for experimental data and 6.8 (5) GPa for theoretical data.","PeriodicalId":7080,"journal":{"name":"Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials","volume":"14 1","pages":"436-449"},"PeriodicalIF":0.0000,"publicationDate":"2022-04-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Crystallographica Section B Structural Science, Crystal Engineering and Materials","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1107/s2052520622002542","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

This work presents a single-crystal X-ray diffraction study of an organic co-crystal composed of N-iodosaccharin and pyridine (NISac·py) under hydrostatic pressure ranging from 0.00 (5) GPa to 4.5 (2) GPa. NISac·py crystallizes in the monoclinic system (space group B21/e). The unconventional setting of the space group is adopted (the conventional setting is P21/c, No. 14) to emphasise the strongly pseudo-orthorhombic symmetry of the lattice, with a β angle very close to 90°. The crystal structure contains one molecule each of N-iodosaccharin (NISac) and pyridine (py) in the asymmetric unit (Z' = 1), linked via an Nsac...I...N'py halogen-bonding motif. A gradual modification of this motif is observed under pressure as a result of changes in the crystalline environment. Mechanical twinning is observed under compression and the sample splits into two domains, spanning an unequal volume that is mapped by a twofold rotation about the [100] direction of the B21/e unit cell. The twinning is particularly significant at high pressure, being reversible when the pressure is released. The structure of the twinned sample reveals the continuity of a substantial substructure across the composition plane. The presence of this common substructure in the two orientations of the twinned individuals can be interpreted as a structural reason for the formation of the twin and is the first observed example in a molecular crystal. These results indicate that the anisotropy of intermolecular interactions in the crystal structure results in an anisotropic strain generated upon the action of hydrostatic compression. Periodic density functional theory calculations were carried out by considering an isotropic external pressure, the results showing good agreement with the experimental findings. The bulk modulus of the crystal was obtained from the equations of state, being 7 (1) GPa for experimental data and 6.8 (5) GPa for theoretical data.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
压力下n-碘糖精-吡啶共晶体系:可逆孪晶的实验证据。
本文在0.00 (5)GPa到4.5 (2)GPa的静水压力下,对n -碘糖精和吡啶组成的有机共晶(NISac·py)进行了单晶x射线衍射研究。NISac·py在单斜晶系中结晶(空间群B21/e)。采用非常规的空间群设置(常规设置为P21/c, No. 14)来强调晶格的强拟正交对称性,其β角非常接近90°。该晶体结构在不对称单元(Z′= 1)中包含n -碘糖精(NISac)和吡啶(py)各一个分子,通过Nsac连接。N'py卤素键基序。由于晶体环境的变化,在压力下观察到这种基序的逐渐改变。在压缩下观察到机械孪晶,样品分裂成两个区域,跨越一个不相等的体积,该体积是通过围绕B21/e单元胞的[100]方向的两次旋转来映射的。这种孪生在高压下特别显著,当压力被释放时是可逆的。孪晶样品的结构揭示了跨组合物平面的实质性子结构的连续性。在双胞胎个体的两个取向中存在这种共同的亚结构可以解释为双胞胎形成的结构原因,并且是在分子晶体中首次观察到的例子。这些结果表明,晶体结构中分子间相互作用的各向异性导致静水压缩作用下产生各向异性应变。在考虑各向同性外压的情况下,进行了周期密度泛函理论计算,结果与实验结果吻合较好。由状态方程得到晶体的体积模量,实验数据为7 (1)GPa,理论数据为6.8 (5)GPa。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
Chalcogen Chemistry: Fundamentals and Applications. Edited by Vito Lippolis, Claudio Santi, Eder J. Lenardão and Antonio L. Braga. Royal Society of Chemistry, 2023. Hardcover, pp. 728. Price EUR 156.00. ISBN 978-1-83916-422-4 Synthesis and structure of high-purity BaCe0.25Mn0.75O3: an improved material for thermochemical water splitting Preparation and crystallographic characterization of 1H-tetrazole/NaClO4 energetic cocrystal Evolution of intermolecular contacts with temperature and pressure in bromoethane and iodoethane – a comparative study Design of a series of cocrystals featuring isoniazid modified with diacetone alcohol
×
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
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 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 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1