Abstract
The technique of energy transfer has been used in an attempt to establish the photoreactive state of acridine in solution. It is shown that the lowest-lying triplet of acridine, the ππ* triplet, is not the reactive species and that the reaction originates, at least in part, through the nπ* triplet. In the course of this work, the transfer of triplet-state energy from biacetyl to acridine, phenazine, anthracene, 1,2-benzanthracene, pyrene, 1,2-benzpyrene and 3,4-benzpyrene has been studied by an intensity method.
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 callDisclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.
