Synthesis, structure and π-expansion of tris(4,5-dehydro-2,3:6,7-dibenzotropone)

The polycyclic skeleton of tris(4,5-dehydro-2,3:6,7-dibenzotropone) is a key structural fragment in carbon schwarzites, a theoretical form of negatively curved carbon allotrope. This report presents a new synthesis of this compound using a Ni-mediated Yamamoto coupling reaction and structural analys...

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Veröffentlicht in:Beilstein journal of organic chemistry 2025-01, Vol.21 (1), p.1-7
Hauptverfasser: Xiong, Yongming, Ma, Xue Lin, Su, Shilong, Miao, Qian
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Sprache:eng
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Zusammenfassung:The polycyclic skeleton of tris(4,5-dehydro-2,3:6,7-dibenzotropone) is a key structural fragment in carbon schwarzites, a theoretical form of negatively curved carbon allotrope. This report presents a new synthesis of this compound using a Ni-mediated Yamamoto coupling reaction and structural analysis of it with X-ray crystallography. Interestingly, it is observed that tris(4,5-dehydro-2,3:6,7-dibenzotropone) crystallized from its solution in hexane resulting in colorless and yellow crystal polymorphs, where it adopts conformations of approximate and symmetry, respectively. Furthermore, expanding its π-skeleton through the Barton-Kellogg and Scholl reactions led to the successful synthesis of a curved polycyclic arene containing three heptagons and two pentagons.
ISSN:1860-5397
1860-5397
DOI:10.3762/bjoc.21.1