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  4. A NEW REDUCTIVE ELECTROPHOTOCATALYSIS: NEW ARYL DIIMIDE CATALYST UNLOCKS CHALLENGING ARYL HALIDES FOR RADICAL COUPLING

A NEW REDUCTIVE ELECTROPHOTOCATALYSIS: NEW ARYL DIIMIDE CATALYST UNLOCKS CHALLENGING ARYL HALIDES FOR RADICAL COUPLING

File(s)
Fan_cornell_0058_11630.pdf (2.07 MB)
Permanent Link(s)
https://doi.org/10.7298/wgbq-4e09
https://hdl.handle.net/1813/113012
Collections
Cornell Theses and Dissertations
Author
Fan, Wenjie
Abstract

In this research, we described a new catalytic strategy that merges the power of light and electricity to obtain a super-reducing radical anion of NTCDA-TPAPA. The excited NTCDA-TPAPA radical anion with high reducing ability is supposed to activate aryl halide substrates with a very high reduction potential (Ered<-1.90V) under a mild condition. This electrophotocatalysis help to overcome the limitation of potential back electron transfer and ensure sustainability with little waste.

Description
46 pages
Date Issued
2022-12
Keywords
aryl halide
•
electrophotocatalysis
•
NTCDA-TPAPA
•
radical anion
Committee Chair
Milner, Phillip
Committee Member
Zax, David
Degree Discipline
Chemistry and Chemical Biology
Degree Name
M.S., Chemistry and Chemical Biology
Degree Level
Master of Science
Type
dissertation or thesis
Link(s) to Catalog Record
https://newcatalog.library.cornell.edu/catalog/15644049

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