While
the use of visible light to drive chemical reactivity is of high importance to
the development of environmentally benign chemical transformations, the
concomitant use of a stoichiometric electron donor or acceptor is often
required to steer the desired redox behavior of these systems. The low-cost and
ubiquity of tertiary amine bases has led to their widespread use as reductive
additives in photoredox catalysis. Early use of trialkylamines in this context
was focused on their role as reductive excited state quenchers of the
photocatalyst, which in turn provides a more highly reducing catalytic
intermediate.
Website: http://www.arjonline.org/physical-sciences/american-research-journal-of-chemistry/
Website: http://www.arjonline.org/physical-sciences/american-research-journal-of-chemistry/
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