<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>81(Pt 2)</volume><submitter>Sakami T</submitter><pubmed_abstract>5,10-Bis(phenyl-sulfon-yl)tetra-hydro-dibenzo-penta-lene, C&lt;sub>28&lt;/sub>H&lt;sub>22&lt;/sub>O&lt;sub>4&lt;/sub>S&lt;sub>2&lt;/sub>, &lt;b>1&lt;/b>, was suc-cessfully synthesized &lt;i>via&lt;/i> the photocatalyst-promoted hy-dro-genative transannulation of di-sulfonyl-cyclo-octa-tetra-ene, &lt;b>2&lt;/b>, using perylene as the photocatalyst in the presence of (&lt;i>i&lt;/i>-Pr)&lt;sub>2&lt;/sub>NEt under UV-light irradiation (398 nm, 30 W). In this reaction, the cyclo-octa-tetra-ene moiety of &lt;b>2&lt;/b> underwent hy-dro-genative transannulation, yielding &lt;b>1&lt;/b>. Single-crystal X-ray analysis revealed that both enanti-omers of &lt;b>1&lt;/b> are arranged alternately along the &lt;i>a&lt;/i> 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 phenyl-ene rings. Additionally, a pair of phenyl-sulfonyl groups were observed at the &lt;i>exo&lt;/i> positions relative to the V-shaped array.</pubmed_abstract><journal>Acta crystallographica. Section E, Crystallographic communications</journal><pagination>172-176</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC11799786</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Synthesis and crystal structure of 5,10-bis-(phenyl-sulfon-yl)tetra-hydro-dibenzo-penta-lene.</pubmed_title><pmcid>PMC11799786</pmcid><pubmed_authors>Sato T</pubmed_authors><pubmed_authors>Wakamatsu K</pubmed_authors><pubmed_authors>Orita A</pubmed_authors><pubmed_authors>Watanabe H</pubmed_authors><pubmed_authors>Akashi H</pubmed_authors><pubmed_authors>Sakami T</pubmed_authors><pubmed_authors>Okuda Y</pubmed_authors></additional><is_claimable>false</is_claimable><name>Synthesis and crystal structure of 5,10-bis-(phenyl-sulfon-yl)tetra-hydro-dibenzo-penta-lene.</name><description>5,10-Bis(phenyl-sulfon-yl)tetra-hydro-dibenzo-penta-lene, C&lt;sub>28&lt;/sub>H&lt;sub>22&lt;/sub>O&lt;sub>4&lt;/sub>S&lt;sub>2&lt;/sub>, &lt;b>1&lt;/b>, was suc-cessfully synthesized &lt;i>via&lt;/i> the photocatalyst-promoted hy-dro-genative transannulation of di-sulfonyl-cyclo-octa-tetra-ene, &lt;b>2&lt;/b>, using perylene as the photocatalyst in the presence of (&lt;i>i&lt;/i>-Pr)&lt;sub>2&lt;/sub>NEt under UV-light irradiation (398 nm, 30 W). In this reaction, the cyclo-octa-tetra-ene moiety of &lt;b>2&lt;/b> underwent hy-dro-genative transannulation, yielding &lt;b>1&lt;/b>. Single-crystal X-ray analysis revealed that both enanti-omers of &lt;b>1&lt;/b> are arranged alternately along the &lt;i>a&lt;/i> 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 phenyl-ene rings. Additionally, a pair of phenyl-sulfonyl groups were observed at the &lt;i>exo&lt;/i> positions relative to the V-shaped array.</description><dates><release>2025-01-01T00:00:00Z</release><publication>2025 Feb</publication><modification>2025-04-26T01:36:42.434Z</modification><creation>2025-04-26T01:36:42.434Z</creation></dates><accession>S-EPMC11799786</accession><cross_references><pubmed>39927386</pubmed><doi>10.1107/S205698902500060X</doi></cross_references></HashMap>