Synthesis of Organic/Inorganic Hybrid Quatrefoil-Shaped Star-Cyclic Polymer Containing a Polyhedral Oligomeric Silsesquioxane Core
2009; American Chemical Society; Volume: 42; Issue: 8 Linguagem: Inglês
10.1021/ma802585k
ISSN1520-5835
AutoresZhishen Ge, Di Wang, Yueming Zhou, Hewen Liu, Shiyong Liu,
Tópico(s)Synthesis and properties of polymers
ResumoWe report the synthesis of quatrefoil-shaped star-cyclic polystyrene, star-cyclic PS, containing a polyhedral oligomeric silsesquioxane (POSS) core via the combination of atom transfer radical polymerization (ATRP) and click chemistry techniques. The obtained star-cyclic PS represents a new chain topology in the category of nonlinear-shaped polymers. Using octa(3-chloropropyl) polyhedral oligomeric silsesquioxane, POSS-(Cl)8, as the starting material, its azidation and subsequent click reaction with a slight excess of propargyl 2-bromobutyrate afforded octafunctional initiator, POSS-(Br)8. 8-arm star-linear PS-N3 was obtained by the azidation of star-linear PS-Br, which was synthesized by the ATRP of styrene using POSS-(Br)8 as the initiator. Model reaction between α,ω-diazido-terminated PS (N3-PS-N3) and difunctional propargyl ether confirmed that bimolecular click cyclization reaction can effectively occur under highly dilute conditions. Next, intramolecular click ring closure of star-linear PS-N3 was conducted under highly dilute conditions, using propargyl ether as the difunctional linker and CuBr/PMDETA as the catalyst, affording quatrefoil-shaped star-cyclic PS. Gel permeation chromatography (GPC), 1H NMR, and FT-IR analysis confirmed the complete consumption of azide moieties in star-linear PS-N3 and that the coupling reaction proceeded via the intramolecular manner. Differential scanning calorimetry (DSC) results revealed that star-cyclic PS possesses higher glass transition temperature (Tg) than that of star-linear PS, possibly due to the ring topology of PS arms in the former.
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