Abstract:In this paper results are presented on two different acrylic monomers 1 and 2 that have been converted by relatively fast UV curing (90 min) at modest temperatures (ca. 60-70 °C) into highly stable nonlinear optic (NLO) materials in which loadings of NLO molecules up to 50 w/w % can be achieved. Although the azobenzene derivatives such as NLO chromophores 1 and 2 exhibit partial degradation during UV-initiated radical polymerization, the highly cross-linked formulations showed very stable second harmonic gener… Show more
“…For photocrosslinkable polymers, there is a great advantage because these polymers can be directly patterned by shining UV light through a mask for making channel waveguides and other integrated optical devices. Photocrosslinking for second harmonic generation (SHG) has been achieved via either a [2 + 2] cycloaddition of cinnamates,6–8 a radical polymerization or [2 + 2] cycloaddition of (meth)acrylate,9–11 a photoactivated reaction of benzophenone with butenyl side groups,12, 13 or a photocleavage of azides to nitrenes 14…”
ABSTRACT:Two photocrosslinkable NLO polymers of poly(glycidyl methacrylate) substituted with 4-nitro-4Ј-hydroxyl stilbene (PGMAS) and acryloyl-functionalized epoxybased polymer (PENAA) carrying 4-nitroaniline moieties were synthesized and characterized. By using the sulfonium salt cationic photoinitiator BDS ⅐ 2PF 6 which can induce cationic or/and radical polymerization, the photocrosslinking of PGMAS and the interpenetrating polymer network (IPN) formed by the photocrosslinking of PGMAS and PENAA simultaneously were reported. The poled and photocrosslinked polymer films and IPN films exhibit relatively stable second-order nonlinear optical activity. The influence of stilbene isomerization in PGMAS films with different crosslink densities on the SHG stability was also investigated.
“…For photocrosslinkable polymers, there is a great advantage because these polymers can be directly patterned by shining UV light through a mask for making channel waveguides and other integrated optical devices. Photocrosslinking for second harmonic generation (SHG) has been achieved via either a [2 + 2] cycloaddition of cinnamates,6–8 a radical polymerization or [2 + 2] cycloaddition of (meth)acrylate,9–11 a photoactivated reaction of benzophenone with butenyl side groups,12, 13 or a photocleavage of azides to nitrenes 14…”
ABSTRACT:Two photocrosslinkable NLO polymers of poly(glycidyl methacrylate) substituted with 4-nitro-4Ј-hydroxyl stilbene (PGMAS) and acryloyl-functionalized epoxybased polymer (PENAA) carrying 4-nitroaniline moieties were synthesized and characterized. By using the sulfonium salt cationic photoinitiator BDS ⅐ 2PF 6 which can induce cationic or/and radical polymerization, the photocrosslinking of PGMAS and the interpenetrating polymer network (IPN) formed by the photocrosslinking of PGMAS and PENAA simultaneously were reported. The poled and photocrosslinked polymer films and IPN films exhibit relatively stable second-order nonlinear optical activity. The influence of stilbene isomerization in PGMAS films with different crosslink densities on the SHG stability was also investigated.
“…Two approaches to minimize the randomization have been proposed. One is to use a crosslinking method4, 5 and the other is to utilize high T g polymers such as polyimides 6–8. Polymers with NLO‐chromophores in the main chain9–11 or in the side chain12–14 were prepared and investigated.…”
“…To suppress this reorientation, rigid polymer backbones exhibiting high T g 's were synthesized. This can be achieved either in cross‐linked systems2–11 or with thermoplastics like polyimides12–17 or maleimide‐based polymers 18–28…”
Summary: Nonlinear optical (NLO) polymers with high glass transition temperatures were prepared by the functionalization of poly(ether sulfone)s with hydroxyalkyl chromophores via the Mitsunobu reaction. Glass transition temperatures obtained were in the range of 158–212 °C. Thin spin‐coated films of the polymers were corona‐poled and analyzed by second‐harmonic generation measurements; second‐order susceptibility values (d33) up to 181 pm · V−1 were obtained. Poled‐order stability measurements over a period of 1 600 h showed that the percentage of the remaining NLO‐response at 125 °C was 84–96% under nitrogen and 54–76% in air.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.