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Aliphatic alcohols photochemical reaction with

For the reactions described so far in this section, the ketone substrates have lowest excited states that are (n.ii ) in character aliphatic ketones may react by way of the singlet or the triplet state, and aryl ketones normally through the triplet because intersystem crossing is very efficient. The efficiency of photochemical hydrogen abstraction from compounds such as alcohols or ethers is very much lower if the ketone has a lowest (Ji,n triplet state, as does I - or 2-acetylnaphthalene (CmH-COMe). However, all aryl ketones, regardless of whether their lowest triplet state is fn,Jt l or (Jt.Ji ), react photochemically with amines to give photoreduction or photoaddition products. A different mechanism operates (4.38), that begins... [Pg.183]


See other pages where Aliphatic alcohols photochemical reaction with is mentioned: [Pg.266]    [Pg.117]    [Pg.183]    [Pg.236]    [Pg.154]    [Pg.155]    [Pg.164]    [Pg.472]    [Pg.880]    [Pg.330]    [Pg.159]    [Pg.282]    [Pg.53]    [Pg.117]    [Pg.154]    [Pg.155]    [Pg.69]    [Pg.585]   


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Alcohols photochemical reactions

Aliphatic alcohols

Aliphatics reactions with

Photochemical reaction with

Reaction with alcohols

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