Dhandayutham Saravanan , C. Ponraj , Themmila Khamrang , Madhukar Hemamalini , G. Jerald Maria Antony , W. T. A. Harrison (Editor)
{"title":"2-(10-溴-蒽-9-基)-N-苯基-苯胺。","authors":"Dhandayutham Saravanan , C. Ponraj , Themmila Khamrang , Madhukar Hemamalini , G. Jerald Maria Antony , W. T. A. Harrison (Editor)","doi":"10.1107/S2414314624004759","DOIUrl":null,"url":null,"abstract":"<div><p>The N—H group of the title compound does not form a hydrogen bond due to steric hindrance.</p></div><div><p>In the title compound, C<sub>26</sub>H<sub>18</sub>BrN, the central benzene ring makes dihedral angles with its adjacent anthracene ring system and pendant benzene ring of 87.49 (13) and 62.01 (17)°, respectively. The N—H moiety is sterically blocked from forming a hydrogen bond, but weak C—H⋯π interactions occur in the extended structure. <span><figure><span><img><ol><li><span>Download : <span>Download high-res image (239KB)</span></span></li><li><span>Download : <span>Download full-size image</span></span></li></ol></span></figure></span> </p></div>","PeriodicalId":94324,"journal":{"name":"IUCrData","volume":"9 5","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2024-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11151289/pdf/","citationCount":"0","resultStr":"{\"title\":\"2-(10-Bromoanthracen-9-yl)-N-phenylaniline\",\"authors\":\"Dhandayutham Saravanan , C. Ponraj , Themmila Khamrang , Madhukar Hemamalini , G. Jerald Maria Antony , W. T. A. Harrison (Editor)\",\"doi\":\"10.1107/S2414314624004759\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><p>The N—H group of the title compound does not form a hydrogen bond due to steric hindrance.</p></div><div><p>In the title compound, C<sub>26</sub>H<sub>18</sub>BrN, the central benzene ring makes dihedral angles with its adjacent anthracene ring system and pendant benzene ring of 87.49 (13) and 62.01 (17)°, respectively. The N—H moiety is sterically blocked from forming a hydrogen bond, but weak C—H⋯π interactions occur in the extended structure. <span><figure><span><img><ol><li><span>Download : <span>Download high-res image (239KB)</span></span></li><li><span>Download : <span>Download full-size image</span></span></li></ol></span></figure></span> </p></div>\",\"PeriodicalId\":94324,\"journal\":{\"name\":\"IUCrData\",\"volume\":\"9 5\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2024-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11151289/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"IUCrData\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2414314624000452\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"IUCrData","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2414314624000452","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The N—H group of the title compound does not form a hydrogen bond due to steric hindrance.
In the title compound, C26H18BrN, the central benzene ring makes dihedral angles with its adjacent anthracene ring system and pendant benzene ring of 87.49 (13) and 62.01 (17)°, respectively. The N—H moiety is sterically blocked from forming a hydrogen bond, but weak C—H⋯π interactions occur in the extended structure.