Polyfluorenylacetylene for near-infrared laser protection: polymer synthesis, optical limiting mechanism and relationship between molecular structure and properties. Issue 85 (22nd November 2017) - Zhao, Gang
Abstract : The incorporation of styryl/stilbene–fluorene into polyacetylenes not only endowed the polymers with novel near-infrared optical limiting properties based on a two-photon absorption mechanism but good solubility and high thermal stability. Abstract : A series of functional polyacetylenes bearing the fluorene moiety with different conjugated lengths and terminal substituents, poly[2-ethynyl-7-(4-nitrostyryl)-9, 9-dioctyl-9 H -fluorene] (P1 ), poly[2-ethynyl-7-(4-(4-nitrostyryl)styryl)-9, 9-dioctyl-9 H -fluorene] (P2 ), poly[2-ethynyl-7-(4-(4-methoxystyryl)styryl)-9, 9-dioctyl-9 H -fluorene] (P3 ), poly[2-ethynyl-7-(4-(4-methylstyryl)styryl)-9, 9-dioctyl-9 H -fluorene] (P4 ), and poly[2-ethynyl-7-(4-(4-methylstyryl)styryl)-9, 9-didodecyl-9 H -fluorene] (P5 ), were designed and prepared using [Rh(nbd)Cl]2 as the catalyst. Their structures and properties were characterized and evaluated by FTIR, NMR, UV, FL, GPC and TGA analyses. The optical limiting properties were investigated using 450 fs laser pulses at 780 nm. These results show that the incorporation of styryl/stilbene functionalized polyfluorenylacetylenes has endowed resultant polyacetylenes with novel near-infrared laser protection properties and enhanced thermal stability. The optical limiting mechanism for laser protection was studied. It was found that the optical limiting properties mainly originated from two-photon absorption (TPA) of molecules in the resulting polyacetylenes. Additionally, it was also found that the functionalized polyacetylene with a longer fluorene-based conjugated chromophore and a stronger terminal electron acceptor group exhibits better optical limiting properties because of the larger π-electron delocalization and dipolar effect.