ライフサイエンスコーパス: butyl acrylate

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1 k copolymers of polyacrylonitrile and poly(n-butyl acrylate).

2 ous 2-substituted 4-chloroquinolines to tert-butyl acrylate.

3 d nanoparticles containing properly balanced butyl acrylate and acrylamide monomers render essentiall

4 xample, in reaction with highly unreactive n-butyl acrylate and using only 2 equiv of MDFA, a yield o

5 -poly(methyl methacrylate), PEO-Au-poly(tert-butyl acrylate) and hydrophilic PEO-Au-poly(acrylic acid

6 lyferrocenyldimethylsilane, PtBA = poly(tert-butyl acrylate), and PDMS = polydimethylsiloxane) were c

7 lycol) methyl ether acrylate (PEGA480), tert-butyl acrylate, and methyl methacrylate, as well as styr

8 Postgrafting hydrolysis of poly(tert-butyl acrylate) arms imparts amphiphilicity to the brush

9 Radical G* reacts with butyl acrylate at a rate of 1.2 +/- 0.1 x 10(8) and 3.2

10 le polymer chains (polystyrene and poly(tert-butyl acrylate)) attached to a functional stemlike segme

11 ne-N3, poly(n-butyl acrylate)-N3, and poly(n-butyl acrylate)-b-polystyrene-N3.

12 transfer radical polymerization (ATRP) of n-butyl acrylate (BA) and a dimethacrylate-based cross-lin

13 reactions, similar to results observed for n-butyl acrylate (BA) polymerization under conventional eA

14 2-hydroxyethyl acrylate), yielding poly(tert-butyl acrylate)-block-poly(2-acryloyloxyethyl cobaltocen

15 quently attached to side chains of poly(tert-butyl acrylate)-block-poly(2-hydroxyethyl acrylate), yie

16 A poly(n-butyl acrylate)-block-poly(tert-butyl acrylate) diblock

17 e allows synthesis of 100 nm thick poly(tert-butyl acrylate) brushes from initiator-modified Au surfa

18 A poly(n-butyl acrylate)-block-poly(tert-butyl acrylate) diblock copolymer was synthesized with a

19 Using a monomer such as butyl acrylate for the emulsion's oil phase, elastomeric

20 ic properties were synthesized by grafting n-butyl acrylate from the PE macroinitiators via ATRP.

21 The butyl acrylate group was found to be a useful redox labe

22 monomer 2, by condensation of TRIS with tert-butyl acrylate, is reported.

23 VP = poly(2-vinylpyridine), PtBA = poly(tert-butyl acrylate), M = micelle segment].

24 ition-fragmentation chain-transfer agent and butyl acrylate monomers.

25 glycol)-N3 (PEO-N3), polystyrene-N3, poly(n-butyl acrylate)-N3, and poly(n-butyl acrylate)-b-polysty

26 polymerized at seven comonomer ratios with n-butyl acrylate (NBA), methyl methacrylate (MMA), and sty

27 (PAN), and a sacrificial block, i.e., poly(n-butyl acrylate) (PBA).

28 verall shape and spacing, whereas the poly(n-butyl acrylate) phase was sacrificed.

29 MMs containing polylactide (PLA) and poly(n-butyl acrylate) (PnBA) side chains at similar MWs.

30 e O (SO) reagent onto a self-adhesive poly(n-butyl acrylate) [poly(nBA)] microspheres matrix, which w

31 UPy) end-functionalized polystyrene-b-poly(n-butyl acrylate) (PS-b-PBA) AB diblock copolymers have be

32 " nanoparticles by growth of mixed poly(tert-butyl acrylate) (PtBA)/polystyrene (PS) brushes from sil

33 e separation of well-defined mixed poly(tert-butyl acrylate) (PtBA)/polystyrene (PS) brushes on silic

34 Grafting times of 30 and 60 s for AMPS and butyl acrylate, respectively, enabled the preparation of

35 ology was developed for direct attachment of butyl acrylate to 5-iodoracil, 5-iodocytosine, 7-iodo-7-

36 However, tert-butyl acrylates were sufficiently stable to couple with

37 sium ionophore III, and grafted AU-1 in poly(butyl acrylate) were the ionophores used in the bulk opt

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