@article{oai:soar-ir.repo.nii.ac.jp:00019881,
 author = {Shoji, Taku and Shimomura, Erika and Maruyama, Mitsuhisa and Ito, Shunji and Okujima, Tetsuo and Morita, Noboru},
 issue = {5},
 journal = {EUROPEAN JOURNAL OF ORGANIC CHEMISTRY},
 month = {Feb},
 note = {Ene-diyne systems possessing 1- and 2-azulenyl groups at the periphery were prepared by palladium-catalyzed cross-coupling reaction of 1- and 2-ethynylazulenes with 9-di-bromomethylene-9H-fluorene and 9,10-bis(dibromomethylene)-9,10-dihydroanthracene or 2-iodoazulene with 9,10-bis(diethynylmethylene)-9,10-dihydroanthracene under Sonogashira-Hagihara conditions. The redox behavior of the ene-diyne compounds was examined by cyclic voltammetry (CV) and differential pulse voltammetry (DPV). Moreover, a significant color change of the ene-diyne derivatives was observed with visible spectroscopy under electrochemical reduction conditions., Article, EUROPEAN JOURNAL OF ORGANIC CHEMISTRY. 2013(5):957-964 (2013)},
 pages = {957--964},
 title = {Synthesis, Properties and Redox Behavior of Ene-Diyne Scaffolds Bearing 1- and 2-Azulenyl Groups at the Periphery},
 volume = {2013},
 year = {2013}
}