Chiral exciton coupling of merocyanine dyes within a well defined hydrogen-bonded assembly

Multichromophoric hydrogen-bonded assemblies 1(3)⋅(BAR)(6) are studied that bear a remarkably close resemblance to commelinin, a naturally occurring assembly responsible for an intense blue color of flowers. The incorporated chromophores exhibit a hypsochromic shift in the UV/visible (Vis) absorption maximum (Δ λ(max) = 14 nm) compared with the free chromophores. In addition, the chiroptical properties of incorporated chromophores can be rationally controlled by changing the supramolecular chirality of the assembly. These properties have been used to study the stability of this type of assembly with UV and CD spectroscopy at concentrations far below the NMR sensitivity threshold (10(−4) M). The determined C(50%) values of 2–3 μM in benzene show the extremely high stability of these hydrogen-bonded assemblies.