Abstract
A novel macrocyclic [Formula: see text]-skeleton 1 containing thiazole and thiophene rings was synthesized via MacDonald [3+1]-type condensation, and its optical properties were investigated. Two sulfur atoms were effective for the bathochromic shift of the ultraviolet-visible absorption bands in comparison with the traditional porphyrin and chlorin compounds. The characteristics of the absorption spectrum and the nucleus-independent chemical shift calculations show that the [Formula: see text]-skeleton 1 is the chlorin-type compound.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Paper version not known
Talk to us
Join us for a 30 min session where you can share your feedback and ask us any queries you have
Schedule a call
