114464-05-0Relevant articles and documents
Synthesis of a series of symmetrically disubstituted diacetylenes with polychlorophenyl rings as side groups and linear polyether chains as spacers
Hernandez,Galan,Rovira,Veciana
, p. 1164 - 1169 (2007/10/02)
Aryl disubstituted diacetylenes with spacers of different lengths (CH2O, CH2OCH2CH2O, and CH2OCH2CH2CH2O) have been synthesized. Smaller homologues of the series were readily obtained by nucleophilic substitutions on 2,4-hexadiynylene bis(p-toluenesulfonate). However higher homologues could not be prepared by this method from the corresponding extended bistosylates due to their low reactivities. The observed decrease of reactivity with phenoxides of such extended bistosylates is ascribed to folded conformations adopted by these derivatives. Consequently, the synthesis of higher members of the series was carried out by a multistep procedure involving appropriately functionalized monoacetylenes.
NEW ARYLETHER SUBSTITUTED DIACETYLENES AS MONOMERS FOR SOLID STATE POLYMERIZATIONS. STABLE FREE RADICALS AS SIDE GROUPS.
Veciana, Jaume,Galan, Angels,Riaza, Joan,Armet, Olga,Molins, Elies,et al.
, p. 289 - 300 (2007/10/02)
Some diacetylenes (DA's) of general structure R-CC-CC-R' (R identical to or different from R') polymerize in the solid state to give fully conjugated eneyne polymer chains.Although several types of side groups have been extensively examined, there a
