Synthesis and spectrokinetic studies of a new family of photochromic 2H-chromenes (=2H-1-benzopyrans): Dimethyl 6-aryl-2,2-dimethyl-2H-chromene-7,8-dicarboxylates
A. Maggiani et al., Synthesis and spectrokinetic studies of a new family of photochromic 2H-chromenes (=2H-1-benzopyrans): Dimethyl 6-aryl-2,2-dimethyl-2H-chromene-7,8-dicarboxylates, HELV CHIM A, 83(3), 2000, pp. 650-657
A series of dimethyl 6-aryl-2,2dimethyl-2N-chromene-7,8-dicarboxylates were
synthesized, and the photochromic properties of this new family of dimethy
l-2H-chromenes were studied under continuous irradiation. The presence of t
he methoxycarbonyl groups was shown to stabilize the colored forms. This st
abilization depended on the solvent, and in two cases the formation of long
-lived opened forms was observed. Under irradiation with a mercury lamp, th
is family of 2H-chromenes showed a strong resistance: to photodegradation.