Synthesis, characterization and UV curing kinetics of hyperbranched polysiloxysilanes from A2 and CB2 type monomers
✍ Scribed by Sheng-Jie Wang; Xiao-Dong Fan; Jie Kong; Jian-Ren Lu
- Book ID
- 104087882
- Publisher
- Elsevier Science
- Year
- 2009
- Tongue
- English
- Weight
- 419 KB
- Volume
- 50
- Category
- Article
- ISSN
- 0032-3861
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✦ Synopsis
A 2 and CB 2 type monomers UV curing kinetics a b s t r a c t A controllable approach to synthesize UV curable hyperbranched polysiloxysilanes from A 2 (1,1,3,3-tetramethyldisiloxane) and CB 2 type monomers (methyl(vinyl)silanediylbis(oxy)bis(ethane-2,1-diyl) diacrylate and methyl(vinyl) silanediylbis(oxy)bis(ethane-2,1-diyl)bis(2-methylacrylate)) was developed in the presented paper. The polymerization was monitored using FTIR, where a two-step polyaddition mode was observed. Vinyl silane group preferentially reacted with hydride silane, resulting in the formation of AB 2 type intermediates containing one hydride silane and two acrylate (or methacrylate) groups, at the same time, there may be low quantity of B 4 type intermediates. The intermediates further polymerized to form hyperbranched polymers. The UV curing kinetics of the hyperbranched polymers, especially the effects of atmosphere, content of photoinitiator and light intensity on UV curing behavior were studied in detail. The results indicated that the hyperbranched polymers could be cured rapidly under UV irradiation. The curing rates increased with the enhancement of light intensity, and the inhibition effect of oxygen could be restrained by increasing light intensity.
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## Abstract A new trifluoromethyl‐activated trifluoro monomer was successfully prepared by Pd‐initiated coupling of 1,3,5‐tribromobenzene with 4‐fluoro‐3‐trifluoromethylphenylboronic acid. 1,3,5‐Tris(4‐fluoro‐3‐trifluoromethylphenyl)benzene (**B**~**3**~) leads to several hyperbranched poly(arylene