ライフサイエンスコーパス: polybutadiene

1 g the backbone of cis-polynorbornene and cis-polybutadiene.

2 d in the polynorbornene scaffold relative to polybutadiene.

3 lever with greater mechanical advantage than polybutadiene.

4 slate these learnings to leverage commercial polybutadiene and acrylonitrile butadiene styrene (ABS)

5 Epoxidized polybutadiene and epoxidized polynorbornene were subject

6 such as poly(dimethylsiloxane), hydrogenated polybutadiene, and ethylene phthalate.

7 approach, and a mixture of polyisobutylene, polybutadiene, and polystyrene has been confirmed in the

8 The distinct selectivity differences between polybutadiene- and carbon-coated zirconia as well as the

9 fferent chromatographic selectivities (e.g., polybutadiene- and carbon-coated zirconia) are serially

10 ocyclopropane (gDCC) copolymers derived from polybutadiene are subjected to ultrasonication, the gDCC

11 hes to repurpose unsaturated polymers (e.g., polybutadiene) are scarce.

12 sules formed from a commercial polystyrene-b-polybutadiene-b-polystyrene triblock polymer.

13 mentation kinetics of micelles formed by 1,2-polybutadiene-block-poly(ethylene oxide) (PB-PEO) copoly

14 ly bound to a cross-linked polystyrene-block-polybutadiene-block-polystyrene (SBS) polymer have been

15 Polybutadiene-coated zirconia (PBD-ZrO2) is very useful

16 ombination of an octadecylsilane (ODS) and a polybutadiene-coated zirconia (PBD-ZrO2) phase was used

17 on octadecyl silane-bonded silica (ODS) and polybutadiene-coated zirconia (PBD-ZrO2) phases.

18 to other phases, especially with respect to polybutadiene-coated zirconia (PBD-ZrO2).

19 This material has been compared to polybutadiene-coated zirconia, octadecyl- and phenyl-bon

20 The polybutadiene contributes to the reversed-phase interact

21 Among these materials, the hydrogenated polybutadiene-Cp analog can be thermally depolymerized (

22 ed polyepichlorohydrin, polyisobutylene, and polybutadiene gratings, respectively, were found to be 8

23 tegy to upcycle waste polyalkenamers such as polybutadiene into new, performance-advantaged materials

24 ers surface-modified with grafted epoxidized polybutadiene layers enabled the direct detection of cru

25 tathesis catalyst, a chemically cross-linked polybutadiene network becomes malleable at room temperat

26 gle-step method to selectively add amines to polybutadienes, offering an efficient strategy to access

27 In this work, we propose a method to upcycle polybutadiene, one of the most widely used commercial ru

28 Polybutadiene (PB) and polyisoprene (PI), the two most c

29 and hemi- and post-metallocenes, in cis-1,4-polybutadiene (PB) degradation reveals, for the first ti

30 methacrylate) (PMMA), polystyrene (PS), and polybutadiene (PB) molecular weights were determined by

31 ion Ru metathesis catalyst into cross-linked polybutadiene (PBD) network, the material self-heals eff

32 on a reversed-phase material made by coating polybutadiene (PBD) on porous zirconia.

33 using a trithiocarbonate-capped hydrogenated polybutadiene (PhBD) steric stabilizer block in n-dodeca

34 er membrane protein F (OmpF), in short-chain polybutadiene-poly(ethylene oxide) (PB-PEO) membranes.

35 e both 28 wt% (PBD13) and 70 wt% (PBD50) 1,2-polybutadiene polymers.

36 Oxidation of the surface of cross-linked 1,4-polybutadiene provided a hydrophilic substrate that reco

37 n of challenging internal alkenes of the 1,4-polybutadiene unit was observed.

38 cis-substituted gem-difluorocyclopropanated polybutadiene using the extensional forces generated by

39 Primary amine-functionalized polybutadiene was also prepared, demonstrating that a br

40 Polybutadiene was functionalized with dibromocyclopropan

41 When epoxidized polybutadiene was sonicated, there was no observable sma

42 The vinyl groups of 1,2-polybutadiene were aminated with ease, and unexpectedly

43 ehavior of a single chain of cyclopropanated polybutadiene, which is governed by rapid isomerization

44 By treating polybutadiene with a difluorocarbene source, we embedded

45 generate an optical response and to degrade polybutadiene with embedded HF-cleavable silyl ethers (1

46 carbon-based analogues, polycyclooctene and polybutadiene, with stretching constants that agree well