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Fulgides photochemical ring closure

Photochromic reactions of the heterocyclic fulgides are also in accordance with the Woodward-Hoffmann selection rules. The molecular structures have dramatic effects on the quantum yields of photoinduced ring-closure and ring-opening reactions of fulgides. The photochemical reactions of furyl fulgides are shown in Scheme 35 and the quantum yields are summarized in Table 4.29.44 45 104... [Pg.190]

The oxalylfulgides (129) have been prepared and studied. These photochromic yellow dyes undergo ring closure in the conventional manner. The quantum yields for the process and the solvent dependency results are shown below the struetures. " A double Stobbe condensation of 3,5-dimethoxybenzaldehyde with succinic anhydride affords the fulgide (130). This is photochemically reactive and undergoes cyclization to afford a pink cyclic form on irradiation at 366 nm. ... [Pg.46]


See other pages where Fulgides photochemical ring closure is mentioned: [Pg.722]    [Pg.722]    [Pg.218]    [Pg.693]    [Pg.180]    [Pg.224]    [Pg.183]    [Pg.232]   
See also in sourсe #XX -- [ Pg.722 ]

See also in sourсe #XX -- [ Pg.5 , Pg.722 ]

See also in sourсe #XX -- [ Pg.722 ]

See also in sourсe #XX -- [ Pg.5 , Pg.722 ]




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