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Role of the 3(n—π*) State in the Photoreduction of Acridine

Emile Vander Donckt, George Porter

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Abstract

Photosensitization of acridine reduction by benzophenone is shown to occur via the ketyl radical of benzophenone rather than by an energy-transfer mechanism. The principal evidence for participation of an upper triplet n—π* state of acridine in the photoreduction reaction is therefore discounted and the reaction probably occurs via the lowest excited singlet level.

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Photosensitization of acridine reduction by benzophenone is shown to occur via the ketyl radical of benzophenone rather than by an energy-transfer mechanism. The principal evidence for participation of an upper triplet n—π* state of acridine in the photoreduction reaction is therefore discounted and the reaction probably occurs via the lowest excited singlet level.

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Available abstract

Photosensitization of acridine reduction by benzophenone is shown to occur via the ketyl radical of benzophenone rather than by an energy-transfer mechanism. The principal evidence for participation of an upper triplet n—π* state of acridine in the photoreduction reaction is therefore discounted and the reaction probably occurs via the lowest excited singlet level.

Key concepts: Benzophenone, Acridine, Photochemistry, Chemistry, Singlet state, Excited state, Triplet state, Ketyl

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