Crystal structures and Hirshfeld surface analyses of di-phenyl-methyl 2-(3,5-di-meth-oxy-phen-yl)acetate and di-phenyl-methyl 2-(3,4,5-tri-meth-oxy-phen-yl)acetate.
{"title":"Crystal structures and Hirshfeld surface analyses of di-phenyl-methyl 2-(3,5-di-meth-oxy-phen-yl)acetate and di-phenyl-methyl 2-(3,4,5-tri-meth-oxy-phen-yl)acetate.","authors":"Manivel Kavitha, Chandiran Jayakodi, Ganesan Meenambigai, Sekar Janarthanan, Srinivasan Pazhamalai, Sivashanmugam Selvanayagam","doi":"10.1107/S2056989025004943","DOIUrl":null,"url":null,"abstract":"<p><p>The title compounds, C<sub>23</sub>H<sub>22</sub>O<sub>4</sub>, (I), and C<sub>24</sub>H<sub>24</sub>O<sub>5</sub>, (II), differ in the presence of a meth-oxy group instead of a hydrogen atom between two meth-oxy groups attached to the phenyl ring of the phenyl acetate moiety, which affects not only the symmetry and number of formula units [triclinic, <i>P</i>1, <i>Z</i> = 2 for (I); monoclinic, <i>P</i>2<sub>1</sub>/<i>n</i>, <i>Z</i> = 4 for (II)], but also the mol-ecular conformations. An overlay of the two mol-ecular structures reveals a large root-mean-square-deviation of 2.4 Å. Intra and inter-molecular C-H⋯O hydrogen bonds are responsible for the consolidation of the mol-ecular conformations and the crystal packing of both structures. Their inter-molecular inter-actions were qu-anti-fied and analysed using Hirshfeld surface analysis, revealing that H⋯H inter-actions contribute most to the crystal packing.</p>","PeriodicalId":7367,"journal":{"name":"Acta Crystallographica Section E: Crystallographic Communications","volume":"81 Pt 7","pages":"618-622"},"PeriodicalIF":0.5000,"publicationDate":"2025-06-12","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12230619/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Crystallographica Section E: Crystallographic Communications","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1107/S2056989025004943","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/7/1 0:00:00","PubModel":"eCollection","JCR":"Q4","JCRName":"CRYSTALLOGRAPHY","Score":null,"Total":0}
引用次数: 0
Abstract
The title compounds, C23H22O4, (I), and C24H24O5, (II), differ in the presence of a meth-oxy group instead of a hydrogen atom between two meth-oxy groups attached to the phenyl ring of the phenyl acetate moiety, which affects not only the symmetry and number of formula units [triclinic, P1, Z = 2 for (I); monoclinic, P21/n, Z = 4 for (II)], but also the mol-ecular conformations. An overlay of the two mol-ecular structures reveals a large root-mean-square-deviation of 2.4 Å. Intra and inter-molecular C-H⋯O hydrogen bonds are responsible for the consolidation of the mol-ecular conformations and the crystal packing of both structures. Their inter-molecular inter-actions were qu-anti-fied and analysed using Hirshfeld surface analysis, revealing that H⋯H inter-actions contribute most to the crystal packing.
期刊介绍:
Acta Crystallographica Section E: Crystallographic Communications is the IUCr''s open-access structural communications journal. It provides a fast, simple and easily accessible publication mechanism for crystal structure determinations of inorganic, metal-organic and organic compounds. The electronic submission, validation, refereeing and publication facilities of the journal ensure rapid and high-quality publication of fully validated structures. The primary article category is Research Communications; these are peer-reviewed articles describing one or more structure determinations with appropriate discussion of the science.