ESR studies of nitrogen-centered free radicals 35. Reaction of a thioaminyl diradical with 7,7,8,8-tetracyanoquinodimethane(TCNQ). The formation of a cyclophane compound.

スポンサーリンク

概要

• 論文の詳細を見る

• The reactions of thioaminyl mono- (MONOR) and diradicals (DIR) with 7,7,8,8-tetracyanoquinodimethane (TCNQ) have been investigated. The reactions of TCNQ with MONOR gave 1:2 adducts of TCNQ and MONOR in 85–88% yields, while the reaction with DIR afforded either a cyclophane compound (77%), or an alternating polymer of TCNQ and DIR (59 wt%), dependent on the structures of DIR.

• 公益社団法人 日本化学会の論文

著者

• Ohana Tsuguyori

  Department of Applied Chemistry, Faculty of Engineering, Osaka City University

関連論文

• ESR studies of nitrogen-centered free radicals 35. Reaction of a thioaminyl diradical with 7,7,8,8-tetracyanoquinodimethane(TCNQ). The formation of a cyclophane compound.

スポンサーリンク