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Unsubstituted spiropyrans and spirooxazines

As for the multiplicity of the excited state from which the X isomer is generated, we have already mentioned that Krysanov and Alfimov8 proposed a mechanism in which the vibrationally excited triplet state of SPNo2 acts as the precursor to the cis-cisoid ring-opened photoproduct X. On the other hand, Kalisky et al.19 claimed that X is formed from SPNo2 in less than lOps. An excited singlet precursor SP is also postulated for the formation of X, with the [Pg.71]

From what has been so far reported, it would seem that the intermediacy of the cis-cisoid ring-opened nonplanar intermediate X is much better documented for nitrospiropyrans than for spiroazines, for which the matter is still controversial. No studies have so far been reported on the importance of the X isomer in the photodegradation mechanistic schemes. [Pg.72]

Only in the scheme of Malkin et al. does the X isomer seem to be involved in the formation of photodegradation products. [Pg.73]


See other pages where Unsubstituted spiropyrans and spirooxazines is mentioned: [Pg.70]   
See also in sourсe #XX -- [ Pg.70 ]




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Spirooxazines

Spiropyran

Spiropyrane

Spiropyrans

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