Abstract
The triplet states of chlorophyll and its structural analogs, metalloporphyrins, provide for important photobiological reactions. These reactions are often accompanied by the formation of free radicals [ 1] capable of efficiently deactivating triplet states [2]. Such processes have been studied in detail for aromatic hydrocarbons [2-6]. Metalloporphyrins have virtually not been studied in such reactions.
Full Text 
Sign-in/Register to access full text options
Sign-in/Register to access full text options 
Published version (
Free)
Free) 
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
