Bulletin of the Chemical Society of Japan
Online ISSN : 1348-0634
Print ISSN : 0009-2673
ISSN-L : 0009-2673
Structures, Dynamic Behavior, and Spectroscopic Properties of 1,8-Anthrylene–Ethenylene Cyclic Dimers and Their Substituent Effects
Masataka InoueTetsuo IwanagaShinji Toyota
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JOURNAL RESTRICTED ACCESS Advance online publication

Article ID: 20150245


Cyclic compounds consisting of two 1,8-anthrylene units and two ethenylene linkers were studied as π-conjugated compounds. Three derivatives having substituents (H, Me, and Ph) at the linker moieties were synthesized by Suzuki-Miyaura coupling of the corresponding diethenylanthracene boronic esters with 1,8-diiodo-10-mesitylanthracene. The X-ray analysis and DFT calculations revealed that all the compounds had nonplanar cyclic frameworks where the two ethenylene linkers were syn to the anthracene units. Exchanges between the two syn forms were observed from the line shape changes in the 1H NMR signals of the mesityl group. Their barriers increased in the order of H, Ph, and Me compounds from 34 to 70 kJ/mol. The effects of substituents on the molecular structure, dynamic behavior, and electronic properties are discussed.

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