Synthesis and Photochromism of Novel Chromene Derivatives Bearing a Monoazacrown Ether Moiety

✍ Scribed by Saleh A. Ahmed; Mutsuo Tanaka; Hisanori Ando; Hitoshi Iwamoto; Keiichi Kimura

• Publisher: John Wiley and Sons
• Year: 2003
• Tongue: English
• Weight: 190 KB
• Volume: 2003
• Category: Article
• ISSN: 1434-193X
• DOI: 10.1002/ejoc.200300070

✦ Synopsis

Abstract

Crowned chromenes − four novel naphthopyrans (chromenes) bearing monoaza‐12‐crown‐4, ‐15‐crown‐5, ‐18‐crown‐6, and a noncyclic analogue at the 5‐position − were synthesized, and their photochromism in acetonitrile was examined in the presence of alkali and alkaline‐earth metal ions. Incorporation of crown ether units to chromene moieties facilitated to a great extent both the thermal isomerization and photoisomerization of the chromene moiety, reflecting the metal‐ion‐binding ability of the crown ether moiety. Comparison of the crowned chromenes with the corresponding crowned spirobenzopyrans reveals that photochromism of the crowned chromene reflects an interaction between the metal ion and the crown ether moiety that is stronger than that of the crowned spirobenzopyran, and shows only positive photochromism with significant red‐shifts in the UV/Vis absorption spectra, in contrast to the crowned spirobenzopyrans reported previously. (© Wiley‐VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2003)