The oligosquaraines 1−5, with stilbenoid scaffolds, were prepared by multistep syntheses in which the final steps consisted of condensation reactions between the semisquaric acid 21 and multiple resorcinols 12b−15b and 17b. The target compounds exhibit intense (ϵ > 250000 L·mol−1·cm−1) and sharp absorption bands with maxima between 687 to 778 nm, depending on the conjugation in the stilbenoid scaffold. Comparison with the monosquaraine 6 as a model compound reveals intramolecular interactions between different donor−acceptor−donor moieties, which give rise to increased absorption intensities.
No takes yet. Share an insight, caveat, or question.
Gerold et al. (2001) studied this question.
Synapse has enriched 3 closely related papers on similar clinical questions. Consider them for comparative context: