Search

Abstract: The synthesis and spectroscopic properties of a series of new organic electron donors derived from dibenzo[2,3:5,6]pyrrolizino-[1,7-bc]indolo[1,2,3-lm]carbazole are described. These compounds can be considered as planar hybrids of carbazole and p-phenylenediamine and possess high thermal stability. The electron donating properties and one- and two-photon spectroscopic features of methoxy derivatives are very sensitive to the number and positions of the methoxy groups. The X-ray structure of the 2,11-dimethoxy derivatives features slipped π-stacks and short interplanar distance between the molecules in the stacks similar to those found in the unsubstituted derivative. [Copyright &y& Elsevier]

Abstract: Synthesis and characterization of a series of new 2-unsubstituted 3-(2-benzylbenzoyl)quinolin-4(1H)-ones is described. In addition to their potential biological activity, these compounds exhibit photoreversible photochromic properties in anaerobic conditions. Using the 1 and 2D NMR techniques we demonstrated that the coloration occurred owing to the formation of fluorescent 5a,6-dihydrobenzo[b]acridin-(5H)-ones. The photoreaction is stereoselective and the S,R-isomers are the major products (83%) whereas the S,S-isomers are the minor (6%). In addition, the irreversible formation of two oxidation products, 3-(2-benzoylbenzoyl)quinolin-4(1H)-ones, and acridin-12(5H)-one derivatives was observed in the presence of air. [ABSTRACT FROM AUTHOR]