Toshiki Sakami , Hikaru Watanabe , Takuma Sato , Yasuhiro Okuda , Kan Wakamatsu , Haruo Akashi , Akihiro Orita
{"title":"5,10-二-(苯基磺基)四氢二苯五烯的合成及晶体结构。","authors":"Toshiki Sakami , Hikaru Watanabe , Takuma Sato , Yasuhiro Okuda , Kan Wakamatsu , Haruo Akashi , Akihiro Orita","doi":"10.1107/S205698902500060X","DOIUrl":null,"url":null,"abstract":"<div><div>The structure of a curved 6–5–5–6 fused-ring system, with two benzene rings attached at both termini and a pair of phenylsulfonyl groups bonded to the two five-membered rings, is described.</div></div><div><div>5,10-Bis(phenylsulfonyl)tetrahydrodibenzopentalene, C<sub>28</sub>H<sub>22</sub>O<sub>4</sub>S<sub>2</sub>, <strong>1</strong>, was successfully synthesized <em>via</em> the photocatalyst-promoted hydrogenative transannulation of disulfonylcyclooctatetraene, <strong>2</strong>, using perylene as the photocatalyst in the presence of (<em>i</em>-Pr)<sub>2</sub>NEt under UV-light irradiation (398 nm, 30 W). In this reaction, the cyclooctatetraene moiety of <strong>2</strong> underwent hydrogenative transannulation, yielding <strong>1</strong>. Single-crystal X-ray analysis revealed that both enantiomers of <strong>1</strong> are arranged alternately along the <em>a</em> axis of the unit cell. The structure features a wide V-shaped motif consisting of 6–5–5–6 fused rings, with a dihedral angle of approximately 97.2° between the planes of the terminal phenylene rings. Additionally, a pair of phenylsulfonyl groups were observed at the <em>exo</em> positions relative to the V-shaped array.</div></div>","PeriodicalId":7367,"journal":{"name":"Acta Crystallographica Section E: Crystallographic Communications","volume":"81 2","pages":"Pages 172-176"},"PeriodicalIF":0.6000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11799786/pdf/","citationCount":"0","resultStr":"{\"title\":\"Synthesis and crystal structure of 5,10-bis(phenylsulfonyl)tetrahydrodibenzopentalene\",\"authors\":\"Toshiki Sakami , Hikaru Watanabe , Takuma Sato , Yasuhiro Okuda , Kan Wakamatsu , Haruo Akashi , Akihiro Orita\",\"doi\":\"10.1107/S205698902500060X\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><div>The structure of a curved 6–5–5–6 fused-ring system, with two benzene rings attached at both termini and a pair of phenylsulfonyl groups bonded to the two five-membered rings, is described.</div></div><div><div>5,10-Bis(phenylsulfonyl)tetrahydrodibenzopentalene, C<sub>28</sub>H<sub>22</sub>O<sub>4</sub>S<sub>2</sub>, <strong>1</strong>, was successfully synthesized <em>via</em> the photocatalyst-promoted hydrogenative transannulation of disulfonylcyclooctatetraene, <strong>2</strong>, using perylene as the photocatalyst in the presence of (<em>i</em>-Pr)<sub>2</sub>NEt under UV-light irradiation (398 nm, 30 W). In this reaction, the cyclooctatetraene moiety of <strong>2</strong> underwent hydrogenative transannulation, yielding <strong>1</strong>. Single-crystal X-ray analysis revealed that both enantiomers of <strong>1</strong> are arranged alternately along the <em>a</em> axis of the unit cell. The structure features a wide V-shaped motif consisting of 6–5–5–6 fused rings, with a dihedral angle of approximately 97.2° between the planes of the terminal phenylene rings. Additionally, a pair of phenylsulfonyl groups were observed at the <em>exo</em> positions relative to the V-shaped array.</div></div>\",\"PeriodicalId\":7367,\"journal\":{\"name\":\"Acta Crystallographica Section E: Crystallographic Communications\",\"volume\":\"81 2\",\"pages\":\"Pages 172-176\"},\"PeriodicalIF\":0.6000,\"publicationDate\":\"2025-02-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11799786/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Acta Crystallographica Section E: Crystallographic Communications\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://www.sciencedirect.com/org/science/article/pii/S2056989025000313\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"CRYSTALLOGRAPHY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Acta Crystallographica Section E: Crystallographic Communications","FirstCategoryId":"1085","ListUrlMain":"https://www.sciencedirect.com/org/science/article/pii/S2056989025000313","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"CRYSTALLOGRAPHY","Score":null,"Total":0}
Synthesis and crystal structure of 5,10-bis(phenylsulfonyl)tetrahydrodibenzopentalene
The structure of a curved 6–5–5–6 fused-ring system, with two benzene rings attached at both termini and a pair of phenylsulfonyl groups bonded to the two five-membered rings, is described.
5,10-Bis(phenylsulfonyl)tetrahydrodibenzopentalene, C28H22O4S2, 1, was successfully synthesized via the photocatalyst-promoted hydrogenative transannulation of disulfonylcyclooctatetraene, 2, using perylene as the photocatalyst in the presence of (i-Pr)2NEt under UV-light irradiation (398 nm, 30 W). In this reaction, the cyclooctatetraene moiety of 2 underwent hydrogenative transannulation, yielding 1. Single-crystal X-ray analysis revealed that both enantiomers of 1 are arranged alternately along the a axis of the unit cell. The structure features a wide V-shaped motif consisting of 6–5–5–6 fused rings, with a dihedral angle of approximately 97.2° between the planes of the terminal phenylene rings. Additionally, a pair of phenylsulfonyl groups were observed at the exo positions relative to the V-shaped array.
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.