Low molecular-mass gelators with diyne functional groups and their unpolymerized and polymerized gel assemblies

A series of low molecular-mass organogelators (LMOGs) with conjugated diyne units, R-CdropC-CdropC-R', has been synthesized from 10,12-pentacosadiynoic acid. R is a long alkyl chain and R' is a short or long alkyl chain containing an amide or ester group. The gelation efficiencies of these LMOGs and the parent acid (as assessed by the variety of liquids gelled, the amount of gelator needed for gelation, and the temporal and thermal stabilities of the gels) differ widely according to the nature of the substituents. Am LMOG with an amide substituent is much more efficient than the corresponding molecule with an ester group, and LMOGs with longer R' chains are more efficient than those with shorter ones. V hen irradiated, some gel networks polymerize. In most cases, the polymerized aggregates phase-separate microscopically, but maintain the gel structure macroscopically. These gels are irreversibly photo- and thermo-chromic, and the thermal stabilities of some of the colored polymerized organogel networks are similar to those of the monomeric assemblies. The molecular packing of the LMOGs as neat powders and in gels before and after polymerization has been examined by X-ray diffraction techniques. This and analyses of IR, UV, and CD (in the case of a chiral diyne LMOG) data allow the nature of the aggregate assemblies before and after irradiation to be assessed. These monomeric organogels and their treatment with light and heat afford an approach to the synthesis of microheterogeneous polymerized networks from relatively simple molecules.