ライフサイエンスコーパス: butyl acrylate

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

2 etween two different type 1 alkenes and tert-butyl acrylate.

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

4 epared through radical copolymerization of n-butyl acrylate, 4-acryloyloxy benzophenone (ABP) photo-c

5 ons of alpha-lipoic acid (up to 10 mol %), n-butyl acrylate, a surfactant, and a costabilizer generat

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

7 by copolymerizing traditional PSA monomers, butyl acrylate and acrylic acid, with mussel-inspired ly

8 iple polymers comprising different ratios of butyl acrylate and methyl methacrylate were prepared wit

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

10 ethyl-3-oxidopyrazinium with methyl and tert-butyl acrylate and with methyl crotonate afforded a 3,8-

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

12 show that MBBs with randomly grafted poly(n-butyl acrylate) and pH-responsive poly(2-(N,N-diethylami

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

14 acrylics (methyl acrylate, ethyl acrylate, n-butyl acrylate, and methyl methacrylate) in broad molecu

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

16 ting substrates, such as methyl, ethyl, tert-butyl acrylates, and substituted styrenes with 2-iodo-N,

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

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

19 can initiate the radical polymerization of n-butyl acrylate at ambient temperature.

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

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

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

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

24 lment released toxic vinyl chloride (VC) and butyl acrylate (BA), which entered the watershed.

25 2-hydroxyethyl acrylate), yielding poly(tert-butyl acrylate)-block-poly(2-acryloyloxyethyl cobaltocen

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

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

28 ino)ethyl methacrylate) (PDMAEMA) and poly(n-butyl acrylate-block-methyl methacrylate) (PBA-b-PMMA).

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

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

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

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

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

34 yl acrylate), poly(ethyl acrylate), and poly(butyl acrylate) is described.

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

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

37 (M(n) 135 kg mol(-1)) methyl methacrylate-n-butyl acrylate-methyl methacrylate triblock copolymer wi

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

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

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

41 es show that primarily alternating styrene/n-butyl acrylate [p(Sty/nBA)] copolymers self-heal without

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

43 ith poly(methyl methacrylate) (PMMA), poly(n-butyl acrylate) (PBMA), poly(2-dimethylamino)ethyl metha

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

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

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

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

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

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

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

51 he solubility of dithiolane derivatives in n-butyl acrylate, resulting in copolymers that degrade to

52 large scales (4 L), yielding 600 g of poly(n-butyl acrylate-stat-alpha-lipoic acid) latexes that degr

53 of lignin-based syringyl methacrylate and n-butyl acrylate, through di-initiation and compounded seq

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

55 gen bonding sites was incorporated into poly(butyl acrylate) to create a reprocessable and recyclable

56 ATRP of n-butyl acrylate using only 10-25 part per million loading

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

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

59 rization of commodity materials, styrene and butyl acrylate, which makes it inexpensive and opens the