1315337-47-3Relevant academic research and scientific papers
N -1- and N-2-anthryl succinimide derivatives: C-N bond rotational behaviors and fluorescence energy transfer
Chou, Teh-Chang,Wu, Ren-Tsung,Liao, Kung-Ching,Wang, Chun-Hung
, p. 6813 - 6818 (2011/10/18)
New rigid bicyclic N-anthrylsuccinimide 1a, 1b, 2a, and 2b were prepared. The Caryl-Nimide bond rotational barriers, intra/intermolecular arene-arene interactions, and photophysical properties were investigated. The rotational behaviors are more significantly controlled by the position of Caryl-Nimide connection than the sidewall framework. The fluorescence energy transfer (ΦET) in 1a and 1b was estimated to be 61% and 53%, respectively. The difference is attributed to the position of Caryl-Nimide connection, which directly influences the relative orientation of donor (naphthalene) and acceptor (anthracene).
