Beilstein J. Org. Chem.2011,7, 1173–1181, doi:10.3762/bjoc.7.136
-component approach to heterocyclic derivatives of azulene is well suited for the development of functional chromophores with extended π-conjugation.
Selected resonance structures of azulene (1a) and structure of the sesquiterpene guaiazulene (1b).
Synthesis of ynones by glyoxylation–decarbonylative
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Graphical Abstract
Scheme 1:
Selected resonance structures of azulene (1a) and structure of the sesquiterpene guaiazulene (1b).
Beilstein J. Org. Chem.2010,6, 830–845, doi:10.3762/bjoc.6.92
monomer (Figure 4). The same coupling reaction of M-4 resulted in polymer P-22, its π-conjugation being interrupted at the N-lactam units. Consequently, the absorption and emission behaviour were not much different from the corresponding monomer, the band gaps of the two isomers being 2 and 2.3 eV
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Graphical Abstract
Figure 1:
Structure of 3,6-diphenyl-substituted 2,5-diketopyrrolo[3,4-c]pyrrole (DPP).