Reaction benzophenone-4-maleimide

Thermally unstable azetidines may be obtained by irradiation of furan in the presence of oxazolinones or 3-ethoxyisoindolone by [7r2s+ .2s] cycloaddition (Scheme 90) (75JA7298). Benzophenone photosensitized [ 2S+W2S] cycloaddition of furan to dimethylmaleic anhydride yields an adduct (34%). This reaction has been extended to 2,5-dimethylfuran and other maleic anhydrides and maleimides (76CA(84)120785). 

Dichloro- and dibromo-maleimide react with ethylene without the necessity for presence of benzophenone but reaction of dichloromaleic anhydride with ethylene gives only a 7% yield of the cycloadduct in absence of benzophenone whereas it is almost quantitative in its presence 63... 

The topological control of such polymerization reactions has been the subject of recent extensive reviews,52 and the same phenomenon in 2,5-distyrylpyrazine has been further discussed.53 The true photopolymerization process discussed here is typified by the u.v.-induced polymerization of AW -polymethylenebis-(maleimides) discussed above,51 and a complete study of the kinetics of the process is included in this series of papers. The conclusion is reached that the triplet state of the chromophore is the reactive species this can be quenched by the addition of ferrocene or 3,3,4,4-tetramethyl-l,2-diazetine 1,2-dioxide. The kinetics of a further example of true photopolymerization, the reductive photocopolymerization of diaryl ketones, have been compared with those of the photoreduction of the model compound benzophenone and found to be similar.53 The photoreductive poly-recombination of the diaryl ketones shown in Schemes 2 and 3 has been studied extensively.54... 

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