Triblock copolymers composed of soft and semi-crystalline segments—synthesis and characterization of poly[(n-butyl acrylate)-block-(ε-caprolactone)-block-(L-lactide)]
Abstract:Poly(n-butyl acrylate) terminated with benzyl alcohol units (PnBA-MI) of varying molecular weights were synthesized by polymerizing n-butyl acrylate using substituted benzyl alcohol based initiators under atom transfer radical polymerization (ATRP) conditions. Between the ligands bipyridine and PMDETA, the latter ligand showed better control for the polymerization of n-BA. High molecular weight diblock copolymers of poly[(n-butyl acrylate)-block-(3-caprolactone)] were synthesized by ring opening polymerization… Show more
“…The Dual hydrophilic BCPs showed stepwise degradation in the thermogravimetric analysis (TGA). Stepwise degradation is normally observed for block copolymers which are composed of segments of contrasting thermal stability [39][40][41] as well as in those polymers where the loss of side chains precedes the backbone degradation. 33 The TGA behavior of the BCPs studied here is due to a combination of these two phenomena.…”
“…The Dual hydrophilic BCPs showed stepwise degradation in the thermogravimetric analysis (TGA). Stepwise degradation is normally observed for block copolymers which are composed of segments of contrasting thermal stability [39][40][41] as well as in those polymers where the loss of side chains precedes the backbone degradation. 33 The TGA behavior of the BCPs studied here is due to a combination of these two phenomena.…”
“…3,4 The ring-opening polymerization technique has been successfully used to synthesize copolymers of lactones such as glycolide, lactide (LA), b-butyrolactone, 3-caprolactone and 1,5-dioxepan-2-one. [5][6][7][8][9][10] The architecture of the copolymers was tailored to yield random, diblock, triblock, gra and star copolymers by controlling the sequence of addition and varying the initiator catalyst system. 11 There have been preliminary reports of the homopolymerization of d-valerolactone.…”
A d,l-lactide–δ-valerolactone–d,l-lactide triblock copolymer, synthesized by sequential ring-opening polymerization, showed a nanolamellar morphology and was fabricated into microspheres for drug delivery.
Novel, predominantly alternating poly(ether ester)s, poly(butylene-3/4-hydroxy benzoate)s (PBHB)s were synthesized by the hydrogenation of the corresponding unsaturated polymers obtained by forming ether and ester linkages under one pot conditions. The ether substitution caused a reduction in glass transition temperature, T g . The melting transition was also lowered by more than 100°C compared to poly(butylene terephthalate) as studied by the differential scanning calorimetry (DSC). Crystallization was observed during heating as well as cooling in the DSC studies. Wide angle X-ray diffraction (WAXRD) analysis also indicated that PB-4-HB was semicrystalline in nature. The thermal stability of hydrogenated polymer was better than that of the unsaturated polymer.
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