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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.
5 The distinct selectivity differences between polybutadiene- and carbon-coated zirconia as well as the
6 fferent chromatographic selectivities (e.g., polybutadiene- and carbon-coated zirconia) are serially
7 ocyclopropane (gDCC) copolymers derived from polybutadiene are subjected to ultrasonication, the gDCC
8 ly bound to a cross-linked polystyrene-block-polybutadiene-block-polystyrene (SBS) polymer have been
10 ombination of an octadecylsilane (ODS) and a polybutadiene-coated zirconia (PBD-ZrO2) phase was used
15 ed polyepichlorohydrin, polyisobutylene, and polybutadiene gratings, respectively, were found to be 8
16 ers surface-modified with grafted epoxidized polybutadiene layers enabled the direct detection of cru
17 tathesis catalyst, a chemically cross-linked polybutadiene network becomes malleable at room temperat
18 ion Ru metathesis catalyst into cross-linked polybutadiene (PBD) network, the material self-heals eff
20 er membrane protein F (OmpF), in short-chain polybutadiene-poly(ethylene oxide) (PB-PEO) membranes.
21 Oxidation of the surface of cross-linked 1,4-polybutadiene provided a hydrophilic substrate that reco
22 cis-substituted gem-difluorocyclopropanated polybutadiene using the extensional forces generated by
25 ehavior of a single chain of cyclopropanated polybutadiene, which is governed by rapid isomerization
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