Synthesis 2004(16): 2743-2746  
DOI: 10.1055/s-2004-834859
SPECIALTOPIC
© Georg Thieme Verlag Stuttgart · New York

Synthesis and Properties of N-Arylcarbazolophane-Paracyclophane Combined with Carbazoles

Yosuke Nakamura, Takuzo Yamazaki, Yasuhiko Kakinoya, Hideyuki Shimizu, Jun Nishimura*
Department of Nano-Material Systems, Graduate School of Engineering, Gunma University, Kiryu, Gunma 376-8515, Japan
Fax: +81(277)301314; e-Mail: nisimura@chem.gunma-u.ac.jp;
Further Information

Publication History

Received 12 July 2004
Publication Date:
07 October 2004 (online)

Abstract

The intramolecular etherification of precursor tetrol 7 afforded N-arylcarbazolophane 5 as a single isomer. Carbazolophane 5 is considered to be a paracyclophane combined with a carbazole, and possesses excimer-like fluorescence properties with λmax = 423 nm.

8

The fluorescence excitation spectra were in good agreement with the corresponding absorption spectra in all cases.