This study utilizes different types of bisphenol monomers instead of bisphenol-A to synthesize phenol terminated polydimethylsiloxane-polycarbonate block copolymers. The copolymers were synthesized by interfacial phosgenation of β£, -phenol-organofunctional polydimethylsiloxane oligomer with various
Bisphenol-A polycarbonate/polydimethylsiloxane multiblock copolymers. I. Synthesis and characterization
β Scribed by Chen-Chi M. Ma; Jen-Tau Gu; Lih-Haur Shauh; Jen-Chang Yang; Wen-Chen Fang
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 228 KB
- Volume
- 66
- Category
- Article
- ISSN
- 0021-8995
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β¦ Synopsis
Aminopropyl-terminated polydimethylsiloxane (PDMS)-bisphenol-A polycarbonate block copolymers were synthesized by interfacial phosgenation reaction of 2,2-bis(4-hydroxyphenyl) propane (BPA) and aminopropyl-terminated PDMS. A new synthetic procedure shows better conversion yield of PDMS oligomer. IR, 1 H, 13 C, and 29 Si nuclear magnetic resonance spectra were used to identify the exact chemical structures of the PDMS-PC block copolymers. The conversions of PDMS of these copolymers were Γ 90% and independent of the PDMS content. The intrinsic viscosities, IV, [ h] studied were in the range between 0.23 and 2.25 dL/g in dichloromethane at 25ΠC with different reaction conditions. The intrinsic viscosity and the glass transition temperature decreased with increasing PDMS content at the same reaction temperature, while the melting flow indices increase with increasing PDMS content. Transparent and colorless films, which showed good oxygen-to-nitrogen permselectivity, could be cast from dichloromethane.
π SIMILAR VOLUMES
Polycarbonate-polydimethylsiloxane (PDMS) copolymers were synthesized by interfacial phosgenation of 2,2-bis(4-hydroxyphenyl)propane (bisphenol-A) with different types of PDMS oligomers including a,v-amino-organofunctional polydimethylsiloxane (AT-PDMS oligomer), a,v-hydroxy-organofunctional polydim
An o,oΠ-methylene-bridged bisphenol A (BPA) dimer 2 was synthesized by a one-step reaction between formalin and excess BPA in the presence of a cation exchange resin in a polar aprotic solvent. Novel oligomeric polycyclic structures were synthesized by the reaction of reactive difunctional halides,
Randomly branched bisphenol A polycarbonates (PCs) were prepared by interfacial polymerization methods to explore the limits of gel-free compositions available by the adjustment of various composition and process variables. A molecular weight distribution (MWD) model was devised to predict the MWD,
Novel poly(oxyethylene)/poly(caprolactone) POE/PCL copolymers were synthesized by step growth polymerization of poly(e-caprolactone) diols and poly(ethylene glycol) diacids using dicyclohexylcarbodiimide as coupling agent. The reaction was performed at room temperature and yielded multiblock copolym
## Abstract A new copolymer with short alternating conjugated and nonconjugated blocks, derived from bisphenol A (BPAEt~2~βPPV) containing separated phenylenevinylene (PV) units has been synthesized by Wittig condensation. The copolymer is fully soluble in common organic solvents and has a numberβa