We synthesized a series of biomimetic self-assembling phthalocyanines equipped with carbonyl groups as recognition motifs, a central zinc atom and diverse solubilizing alkyl chains mimicking for the first time with these robust pigments the natural chlorosomal bacteriochlorophylls. Upon self-assembly a very broad and red-shifted Q-band absorption extending to over 900 nm is put into evidence.

A highly selective recognition of fluoride was achieved through the design of a small hemicryptophane cage (3) presenting a southern tris-urea hosting moiety. The resulting host−guest complex has been characterized by electrospray ionization-highresolution mass spectrometry, 1 H and 19 F NMR, and X-ray diffraction techniques. In particular, X-ray diffraction analysis of [3•F − ] reveals that the encapsulation of one fluoride, within 3, occurs through NH•••F − H-bonding with the six NH residues of the tris-urea ligand. An association constant of 1200 M −1 was extracted from 1 H NMR titration experiments, indicating that efficient fluoride binding also occurs in solution. Finally, in sharp contrast with previously reported urea-based hemicryptophane hosts, the small preorganized cavity found in 3 allows for an exclusive selectivity for fluoride over other competing halides.