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Acryloylic groups

In the 3-(5 -nitro-2 -furyl)acryloyl group XV, activity was poor when Z was pyrazoline, alkyl or carbethoxyalkyl.°l °2 en Z was 2-imidazoline. Staph, activity was lost without change in Coli activity relative to the sin5>le amide J z = VJhen bromine is present (z = CHpBr or NF—CH=... [Pg.117]

A tricyclic, Cj-symmetrical polyoxa diol auxiliary can be used to attach acryloyl groups to form chiral dienophiles (6). ... [Pg.90]

From the 1940 s to the 1960 s, the acryloyl group was induced directly to the hydroxyl group of monosaccharide protected by isopropylidene or benzylidene such as methyl 2,3-di-O-acryloyl 4,6-benzylidene glucoside 1 (//), l,2 3,4-di-0-isopropylidene- 6-O-acryloyl a-D-galactopyranose 2, 6-0-... [Pg.383]

This full IPN combines the network of an NLO active epoxy-based polymer and the network of an NLO active phenoxy-silicon polymer. l The epoxy-based NLO network is prepared from the epoxy prepolymer (BPAZO) based on the diglycidyl ether of bisphenol A and 4-(4 -nitrophenylazo)aniline functionalized with crosslinkable acryloyl groups. The second NLO network of a phenoxy-silicon polymer is based on an alkoxysilane dye (ASD) of (3-glycidoxypropyl)trimethoxysilane and 4(4 -nitrophenylazo)aniline, and the multifunctional phenoxyl molecule 1,1,1- tris(4-hydroxyphenyl)ethane (THPE).22 Figure 4 shows the chemical structures of BPAZO, ASD, and THPE. Each network can be formed... [Pg.232]

Fujioka-kobayashi, M., Ota, M.S., Shimoda, A., Nakahama, K., Akiyoshi, K., Miyamoto, Y, Iseki, S., 2012. Cholesteryl group and acryloyl group-bearing pullulan nanogel to dehver BMP2 and FGF18 for bone tissue engineering. Biomaterials 33, 7613-7620. [Pg.103]

Heterobifunctional PEG with acryloyl and isocyanate end groups Determination of acryloyl groups [149]... [Pg.415]

Variously substituted oxazoline monomers, 2-ethyl, 2-n-pro-pyl, and 2-vinyl oxazoline monomers for HA, were newly prepared and polymerized with HAase catalysis. The reactions proceeded with total control of regioselectivity and stereochemistry, to afford the corresponding HA and Ch derivatives (unnatural polysaccharides) possessing N-propionyl, N-butyryl, and N-acryloyl group in every hexosamine unit (Scheme 40). Similarly, Ch derivatives were also achieved. The resulting N-acryloyl HA and Ch are functional polymers having a reactive vinyl group. [Pg.414]

Hyperbranched polymers (HBP) with a sulfonic acid (SA) group (HBP-SA), with an acryloyl (Ac) group (HBP-Ac), and with both sulfonic acid and acryloyl groups (HBP-SA-Ac)... [Pg.525]

See other pages where Acryloylic groups is mentioned: [Pg.427]    [Pg.141]    [Pg.80]    [Pg.187]    [Pg.88]    [Pg.485]    [Pg.8]    [Pg.303]    [Pg.233]    [Pg.233]    [Pg.77]    [Pg.266]    [Pg.149]    [Pg.825]    [Pg.215]    [Pg.532]    [Pg.37]    [Pg.79]    [Pg.166]    [Pg.166]    [Pg.346]    [Pg.348]    [Pg.352]    [Pg.45]    [Pg.119]    [Pg.199]    [Pg.200]    [Pg.181]    [Pg.199]    [Pg.200]    [Pg.135]    [Pg.95]    [Pg.527]    [Pg.527]    [Pg.527]    [Pg.531]    [Pg.532]    [Pg.539]    [Pg.543]    [Pg.547]   
See also in sourсe #XX -- [ Pg.5 ]



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Acryloyl

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