849466-20-2Relevant articles and documents
Delayed fluorescence behaviors of aminopyridine oligomers: Azacalix[n](2,6)pyridines (n = 3 and 4) and their linear analog
Uchida, Natsuko,Sato, Tohru,Kuwabara, Junpei,Nishimura, Yoshinobu,Kanbara, Takaki
, p. 459 - 461 (2014)
Aminopyridine oligomers exhibited long-lived emission at 77 K, which could be assigned to the delayed fluorescence. The macrocyclic structure predominantly dictated the emission behaviors. Their emission behaviors were elucidated from timedependent densit
Preparation of N-(p-tolyl)azacalix[n](2,6)pyridines constructed of various numbers of the recurring unit
Suzuki, Yutaka,Yanagi, Takanori,Kanbara, Takaki,Yamamoto, Takakazu
, p. 263 - 266 (2005)
Synthetic routes for N-(p-tolyl)-substituted azacalix[n](2,6)pyridines via Cu- and Pd-catalyzed aryl amination reactions have been elaborated, and the macrocycles constructed of various numbers (n = 3-8, and 10) of a N-(p-tolyl)aminopyridine recurring uni