Three carbazole-containing methacrylic monomers, 2-(N-carbazolyl)ethyl methacrylate(CzEMA), 6-(N-carbazolyl)hexyl methacrylate(CzHMA), and 11-(N-carbazolyl)undecyl methacrylate (CzUMA), and their saturated model compounds, 2-(Ncarbazolyl)ethyl isobutyrate, 6-(N-carbazolyl)hexyl isobutyrate, and 11-(
Synthesis and characterization of two new cyclobutyl and aryl hydroxyethyl methacrylate monomers and their polymers
✍ Scribed by Mehmet Coşkun; Kadir Demirelli; Ibrahim Erol; Misir Ahmetzade
- Publisher
- John Wiley and Sons
- Year
- 1997
- Tongue
- English
- Weight
- 170 KB
- Volume
- 35
- Category
- Article
- ISSN
- 0887-624X
No coin nor oath required. For personal study only.
✦ Synopsis
Two new hydroxyethyl methacrylates having aryl and cyclobutane rings were synthesized by addition to 1-(epoxyethyl)-3-aryl-3-methylcyclobutane to methacrylic acid. The monomers prepared are 2-(3-methyl-3-phenylcyclobutyl)-2-hydroxyethyl methacrylate (PCHEMA) and 2-(3-methyl-3-mesitylcyclobutyl)-2-hydroxyethyl methacrylate (MCHEMA). Both monomers were polymerized at 60ЊC in 1,4-dioxane solution using benzoyl peroxide as initiator. Poly(PCHEMA) and poly(MCHEMA) and their monomers were characterized by FT-IR and 1 H-and 13 C-NMR techniques. Weight average molecular weights of the polymers were determined for poly(PCHEMA) poly(MCHEMA) by gel permation chromatography. Thermal stabilities of the polymers were essentially the same. Glass transition temperatures for poly(PCHEMA) and poly(MCHEMA) were determined as 105 and 137ЊC, respectively. No changes of the polymers by irradiation with UV light at 254 nm were observed.
📜 SIMILAR VOLUMES
Several aromatic dicyanate monomers have been synthesized bearing paralinked strong electron withdrawing groups, such as phenylphosphine oxide, sulfone, and carbonyl. These groups increased the reactivity of the cyanate functional groups and eliminated the need for curing catalysts. However, an unde
Some copolymers of 2-(3-phenyl-3-methylcyclobutyl)-2-hydroxyethyl methacrylate (PCHEMA) with acrylonitrile (AN) have been prepared in the presence of 2,2'-azobisisobutyronitrile in 1,4-dioxane solvent at 60 °C. The copolymers have been characterized by infrared, 1 H and 13 C NMR techniques. The perc
A limitation in the use of hydrophilic poly(2hydroxyethyl methacrylate) (PHEMA) sponges as implantable devices is their inherently poor mechanical strength. This precludes proper surgical manipulation, especially in the eye where the size of the implant is usually small. In this study a new method w