posted on 2006-04-26, 00:00authored byRui Xu, Volker Gramlich, Holger Frauenrath
The symmetric diacetylenes, 2,4-hexadiynylene dibenzoate 4 and 2,4-hexadiynylene bis(pentafluorobenzoate) 5, as well as the unsymmetric 6-(pentafluorobenzoyloxy)hexa-2,4-diynyl benzoate
6 were prepared and investigated with respect to their reactivity toward topochemical polymerization in the
crystalline state. The 1:1 cocrystal 4·5 was successfully polymerized to the corresponding poly(diacetylene)
copolymer 7, as evidenced by solid-state 13C NMR and Raman spectroscopy, as well as single-crystal
structure analysis of the monomer−polymer cocrystal. Thus, perfluorophenyl−phenyl interactions were
utilized as complementary supramolecular synthons in the cocrystallization of two different diacetylene
monomers and their unprecedented conversion into a strictly alternating diacetylene copolymer.