ライフサイエンスコーパス: copolymerization

1 relationships for stereoselective homo- and copolymerization.

2 ic acid is controlled by the degree of graft copolymerization.

3 period prior to reaching the maximum rate of copolymerization.

4 te Ti catalyst is the active species for the copolymerization.

5 (i.e., ionic or radical) cannot explain this copolymerization.

6 ates chain growth and precludes propylene/VC copolymerization.

7 s can be substituted for Zn and still effect copolymerization.

8 (2)]PdMe(THF), is active for CO and ethylene copolymerization.

9 ty) for carbon dioxide and cyclohexene oxide copolymerization.

10 r mass distributions, and the possibility of copolymerization.

11 ns of the well-established field of covalent copolymerization.

12 s which may not be accessible through direct copolymerization.

13 zenium cations were selected to initiate the copolymerization.

14 d for sufficient control over supramolecular copolymerizations.

15 the polymerization behavior of BisGMA/TEGDMA copolymerizations.

16 ating Ru center toward different monomers in copolymerizations.

17 ion and possible side reactions; a dinuclear copolymerization active site is implicated.

18 zation, polar solvents are found to increase copolymerization activities and coproduce atactic polyst

19 The copolymerization activity and polyketone molecular weigh

20 the copolymerization behavior including the copolymerization activity, copolymer sequence distributi

21 zing chelating diphosphines (e.g., CO/alkene copolymerization and alkene hydroformylation) are consid

22 Further, we propose a mechanism for the copolymerization and analyze the copolymer structure in

23 membranes (AEMs), which were synthesized by copolymerization and cross-linking of a norbornene monom

24 chemical properties of polymer scaffold via copolymerization and electrospinning techniques.

25 lenCo(III)X-catalyzed styrene oxide SO/CO(2) copolymerization and ring-opening polymerization of lact

26 t system leads to similar reaction rates for copolymerization and ROP and therefore to a terpolymer w

27 fully synthesized via NCA-based ring-opening copolymerization and their composition was confirmed by

28 evel (elemental doping) and molecular level (copolymerization), and (3) modification of g-C3N4 with w

29 s microtubule plus-ends by a preassociation, copolymerization, and regulated release mechanism.

30 further demonstrated the versatility of this copolymerization approach by synthesizing AB graft diblo

31 Herein, we demonstrated a simple ternary copolymerization approach to develop a terpolymer donor

32 The latter two monomers are used in a copolymerization approach with BTA-Glc, BTA-Man, or ethy

33 ions of these results for olefin/vinyl ether copolymerization are discussed.

34 cessful examples of ethylene + polar monomer copolymerization are rare, especially without Lewis acid

35 ions (MWD approximately 1.1), indicating the copolymerizations are living.

36 The copolymerizations are well controlled and produce hydrox

37 red by a standard statistical description of copolymerization, are found to have a negligible influen

38 of functionalized monomers in Ziegler-Natta copolymerizations, are presented.

39 ts in remarkable activity enhancement of the copolymerization as well as improved stereoselectivity a

40 The BisGMA/TEGDMA copolymerization behaved similarly to other dimethacryla

41 substituent R and the bridge E influence the copolymerization behavior including the copolymerization

42 lid-state structures, solution dynamics, and copolymerization behavior with CO(2) and cyclohexene oxi

43 can be synthesized by a palladium catalyzed copolymerization between 9,10-dibromoanthracene and a va

44 The results indicate that copolymerization between a strong electron donor and wea

45 We focus on the supramolecular copolymerization between two derivatives of benzene-1,3,

46 Here, the supramolecular copolymerization between two slightly structurally diffe

47 ace the general principles of supramolecular copolymerization by analyzing them through the lens of t

48 rs that govern the rROP mechanism; (iii) the copolymerization by conventional or controlled/living ra

49 component sequence controlled supramolecular copolymerization by manipulating thermodynamic and kinet

50 Similarly, efficient one-pot diblock copolymerization by sequential addition of ethylene glyc

51 ning polymerization (ROP) of BBL and CHO/CO2 copolymerization by the presence of CO2 in the reaction

52 versatile high temperature ethylene-1-octene copolymerization capabilities of this catalyst class, an

53 udy, polymerization kinetics, stereocontrol, copolymerization characteristics, and the properties of

54 Under ethylene/octene copolymerization conditions, a plurality of new catalyst

55 ue; this finding is seemingly independent of copolymerization conversion or reaction parameters.

56 study, determined that there is, however, no copolymerization detectable (i.e., that the synthesis an

57 tches between anhydride/epoxide ring-opening copolymerization, epoxide ring-opening polymerization an

58 lymerization conditions, rate studies on the copolymerization exhibit no dependence in [CO(2)], a fir

59 in which chain transfer agents are added to copolymerization experiments indicate that rapid chain t

60 osphate time-courses from polymerization and copolymerization experiments of ATP- and ADP-actin are s

61 Initiation of the copolymerization favors insertion of DIB over propylene;

62 + B1 and Ti1 + B1-mediated ethylene-styrene copolymerizations follow second-order Markovian statisti

63 sible addition-fragmentation chain transfer) copolymerization, followed by chain extension.

64 n-growth mechanism, similar to that of chain copolymerization for covalent block copolymers.

65 ering the bandgap (Eg), donor-acceptor (D-A) copolymerization for narrowing Eg and 2-dimensional conj

66 stry of the monomer and catalyst used in the copolymerization has dramatic effects on catalytic activ

67 Significant increases in the rate of copolymerization have been achieved with turnover freque

68 at modification of the proposed biosensor by copolymerization have provided to give perfect response

69 , to date, regioselective processes for this copolymerization have remained relatively unexplored.

70 ene + amino olefin [AO; H2 C=CH(CH2 )n NR2 ] copolymerizations in the absence of a Lewis-acidic maski

71 ent for epoxide and carbon dioxide/anhydride copolymerizations; in contrast, so far pure heterodinucl

72 Stoichiometric reactions of the copolymerization initiation steps show that zinc alkoxid

73 iffusion of two monomers and their oxidative copolymerization inside a solid-state gel electrolyte is

74 ched covalently to the solid support through copolymerization into acrylamide beads.

75 Carbon dioxide/epoxide copolymerization is an efficient way to add value to was

76 Carbon dioxide and epoxide copolymerization is an industrially relevant means to va

77 monitoring of the reactions, a mechanism of copolymerization is proposed where the neutral cocatalys

78 Although this copolymerization is well-studied using light microscopic

79 In fact, the statistical copolymerizations lead to faster incorporation of the 2-

80 ure of the nanoparticles allowed for further copolymerization leading to multiresponsive nanostructur

81 nts also indicate that known noncoordination copolymerization mechanisms (i.e., ionic or radical) can

82 rent state of the field of epoxide/anhydride copolymerization mediated by discrete catalysts and the

83 The polymer is synthesized by template copolymerization methods and consists of a porous methac

84 ants were determined according to a terminal copolymerization model.

85 clic vinyl ethers, a controlled chain-growth copolymerization occurs that exhibits high degrees of al

86 were performed on the perfectly alternating copolymerization of 1-butene oxide and carbic anhydride

87 r hydrophobicity as a monolith prepared from copolymerization of 2-acrylamido-2-methyl-1-propanesulfo

88 The organocatalytic anionic ring-opening copolymerization of 2-alkyl-2-oxo-1,3,2-dioxaphospholane

89 Herein, we demonstrate that the statistical copolymerization of 2-oxazines with 2-oxazolines can lea

90 ustness of the method was highlighted in the copolymerization of a 256-membered ANNNN library compris

91 ial) derived from zinc-mediated coordination copolymerization of a dicarboxylic and tricarboxylic aci

92 n of hydrogel hydrophobicity from either the copolymerization of a hydrolyzable lactone ring or the h

93 The copolymerization of a modified UiO-66-NH(2) MOF with a g

94 Via solvothermal copolymerization of a monomeric ionic liquid and divinyl

95 ts (i.e., macroinitiators for a miniemulsion copolymerization of a monovinyl monomer and divinyl cros

96 nthesized semicrystalline polyesters via the copolymerization of a range of epoxide/anhydride monomer

97 to alkaline anion exchange membranes via the copolymerization of a tetraalkylammonium-functionalized

98 highly active, regioselective system for the copolymerization of a variety of terminal epoxides and c

99 thesized via inverse emulsion (water-in-oil) copolymerization of acrylamide and a low percentage (app

100 olecular polymer networks through an in situ copolymerization of acrylamide and functional monomers,

101 density that can be tailored by ring-opening copolymerization of alpha-propargyl-delta-valerolactone

102 t, modification of the proposed biosensor by copolymerization of amine functionalized monomer, which

103 temperature (LCST) were created through the copolymerization of an aminooxy-bearing methacrylamide w

104 One-pot copolymerization of an omega-norbornenyl macromonomer an

105 ant obstacles to insertion polymerization or copolymerization of AN using L(2)PdR+ catalysts are the

106 r chains, which are prepared via statistical copolymerization of anionic 2-(phosphonooxy)ethyl methac

107 We further demonstrate that block copolymerization of betaMdeltaVL and lactide leads to a

108 le surface chemistries is easily achieved by copolymerization of butyl methacrylate with ethylene dim

109 The reaction kinetics of the copolymerization of carbon dioxide and cyclohexene oxide

110 The ring-opening copolymerization of carbon dioxide and propene oxide is

111 nd regioslective copolymers derived from the copolymerization of carbonyl sulfide (COS) and epoxides

112 of the temperature-controlled supramolecular copolymerization of chiral and achiral biphenyl tetracar

113 sition, whereas 40 bar CO2 affords exclusive copolymerization of CHO/CO2.

114 sing the salen cobalt(III) complex catalyzed copolymerization of CO(2) and a derivatized oxirane.

115 anation of the role of the cocatalyst in the copolymerization of CO2 and cyclohexene oxide catalyzed

116 Here, we show that copolymerization of collagen I with polyacrylamide produ

117 oly(propylene succinate) synthesized via the copolymerization of cyclic anhydrides and epoxides.

118 out compromising their crystallinity via the copolymerization of cyclic lactones with propargyl 3-met

119 highly active dimagnesium catalysts for the copolymerization of cyclohexene oxide and carbon dioxide

120 The mechanism of the copolymerization of cyclohexene oxide and carbon dioxide

121 Furthermore, copolymerization of cyclopentene oxide (CPO) and CO2 was

122 ith pendant functionalities via ring-opening copolymerization of delta-valerolactone with alpha-allyl

123 Copolymerization of DPP with DPP yields a copolymer with

124 to -12) have been synthesized as crystals by copolymerization of either Zn(II) (ZIF-1 to -4, -6 to -8

125 sable polymeric materials through the direct copolymerization of elemental sulfur with vinylic monome

126 istence of activated NMII monomers in cells, copolymerization of endogenous NMIIA and NMIIB molecules

127 EG (mf-PEG) and PPO structures accessible by copolymerization of EO or PO with functional epoxide com

128 highly active catalysts for the alternating copolymerization of epoxides and CO2.

129 ains excellent activity for the ring-opening copolymerization of epoxides and cyclic anhydrides at lo

130 lyesters synthesized through the alternating copolymerization of epoxides and cyclic anhydrides compo

131 s in catalysis have enabled the ring-opening copolymerization of epoxides and cyclic anhydrides to af

132 ing polymerizations, such as the alternating copolymerization of epoxides and cyclic anhydrides.

133 sized for the first time through the anionic copolymerization of epoxides with CO2, under metal-free

134 m catalysts for the ring-opening alternating copolymerization of epoxides with cyclic anhydrides.

135 polymerization of lactones and ring-opening copolymerization of epoxides/anhydrides.

136 A detailed mechanistic investigation of the copolymerization of ethylene and methyl acrylate (MA) by

137 The copolymerization of ethylene and propylene with bridged

138 time commercially relevant catalysts for the copolymerization of ethylene and styrene have been ident

139 es the homopolymerization of styrene and the copolymerization of ethylene and styrenic comonomers med

140 formation of polyethylene from ethylene, and copolymerization of ethylene with 1-octene.

141 Direct coordinative copolymerization of ethylene with functionalized co-mono

142 In principal, the direct copolymerization of ethylene with polar comonomers shoul

143 or the first time successfully controlled by copolymerization of ethylene with polar olefins using a

144 report the cooperative supramolecular block copolymerization of fluorescent monomers in solution und

145 Heparan sulfate formation occurs by the copolymerization of glucuronic acid (GlcA) and N-acetylg

146 Simultaneous copolymerization of green fluorescing dCTP and dUTP nucl

147 e reactivity is broad in scope, enabling the copolymerization of highly functionalized aromatic and a

148 coatings via ultraviolet (UV) photoinitiated copolymerization of ionic liquid (IL) monomers on a fuse

149 We show here that copolymerization of kinetically trapped states of one PB

150 lymers were synthesized via enzyme-catalyzed copolymerization of lactone with dialkyl diester and ami

151 phasis is on homopolymerization, but related copolymerization of less activated monomers is mentioned

152 ing mesochlorin e6 (Mce6) was synthesized by copolymerization of MA-Fab', HPMA, and MA-GFLG-Mce6.

153 rotaxanes via ring-opening olefin metathesis copolymerization of macrocycles and metalated [2]catenan

154 The ring-opening copolymerization of maleic anhydride and propylene oxide

155 We report the ring-opening copolymerization of maleic anhydride with a variety of e

156 The pCQ polymers were synthesized by copolymerization of methacryloylated hydroxy-CQ (HCQ) an

157 ica capillaries in a single step by a simple copolymerization of mixtures of O-[2-(methacryloyloxy)et

158 conditions, this catalyst also mediates the copolymerization of MMA + styrene (1:19 ratio) at 50 deg

159 The copolymerization of monocationic and dicationic IL cross

160 The statistical copolymerization of MTEGE with ethylene oxide results in

161 lung abnormalities of Tsk/+ mice are due to copolymerization of mutant and wild-type molecules into

162 witterionic monolith was prepared by thermal copolymerization of N,N-dimethyl-N-methacryloxyethyl-N-(

163 We show that copolymerization of NMIIA and NMIIB followed by their di

164 The metal catalyst-mediated copolymerization of non-polar olefins with polar comonom

165 (BDI)Zn-1 also enables controlled copolymerization of OCAs and lactide, facilitating the s

166 ylammonium silanolate-initiated ring-opening copolymerization of octamethylcyclotetrasiloxane (D(4))

167 hylene carbonate and 107.6 kJ x mol (-1) for copolymerization of oxetane and carbon dioxide supports

168 re prepared with comb-like structure by RAFT copolymerization of peptide macromonomers with N-(2-hydr

169 polar functional groups and the block/graft copolymerization of PHAs with hydrophilic components in

170 resonance spectroscopy of products from the copolymerization of piceatannol and monolignols confirms

171 r the past 20 years has greatly advanced the copolymerization of polar vinyl monomers and olefins.

172 Alkyne-containing beads prepared by direct copolymerization of propargyl acrylate with ethylene dim

173 active catalysts for the living, alternating copolymerization of propylene oxide (PO) and CO(2), yiel

174 Just add water: The copolymerization of propylene oxide and CO2 catalyzed by

175 The alternating copolymerization of propylene oxide with terpene-based c

176 ilaments similar to the structures formed by copolymerization of purified Y53A-actin and wild-type ac

177 arbonate)s are obtained via the ring-opening copolymerization of rac-/(R)-benzyl glycidate with CO2 u

178 rbonate)s were obtained via the ring-opening copolymerization of rac-/(R)-benzyl glycidyl ether with

179 f 620 turnovers per hour is achieved for the copolymerization of rac-PO and CO(2), yielding iso-enric

180 Copolymerization of racemic alpha-olefins with ethylene

181 ne backbone linkages can be synthesized from copolymerization of readily accessible aryl dibromides a

182 composite hydrogel particles are prepared by copolymerization of sodium acrylate and N-isopropylacryl

183 ca capillaries, by thermally induced in situ copolymerization of styrene and divinylbenzene.

184 lymers were prepared by a controlled radical copolymerization of styrene with designer boron or phosp

185 sors were synthesized by sequence-controlled copolymerization of styrene with N-substituted maleimide

186 MS(2) data provided conclusive evidence that copolymerization of styrene/DMSS mixtures leads to chain

187 One was prepared from the copolymerization of sulfoethyl methacrylate and poly(eth

188 n vesicle-templated nanocapsules prepared by copolymerization of tert-butyl methacrylate, butyl metha

189 The copolymerization of the chiral binaphthyl monomer with t

190 The copolymerization of the eight membered monomers with 6-m

191 It was prepared by copolymerization of the PEG-trypsin-aprotinin complex du

192 One-pot copolymerization of the two monomers to give block copol

193 Surprisingly, to date, the statistical copolymerization of these two cyclic imino ether monomer

194 s-ends, an observation inconsistent with the copolymerization of this complex with tubulin for plus-e

195 ion side reactions at high conversion in the copolymerization of tricyclic anhydrides with excess pro

196 Additionally, copolymerization of Tsk fibrillin 1 with wild-type fibri

197 contrast, when microtubules are generated by copolymerization of tubulin and tau, a distinct populati

198 ss reminiscent of a living covalent gradient copolymerization of two different monomers.

199 We introduce the hybrid copolymerization of two disparate monomer classes (vinyl

200 gies used thus far have relied on the random copolymerization of two electronically distinct molecula

201 Keratin filaments arise from the copolymerization of type I and II sequences, and form a

202 to metal-catalyzed insertion polymerization/copolymerization of VC.

203 The copolymerizations of CHO (1.98 M in toluene) and 300 psi

204 Copolymerizations of cyclohexene oxide (CHO) and CO2 wit

205 Copolymerizations of ethylene with alpha-olefins such as

206 Copolymerizations of ethylene with vinyltrialkoxysilanes

207 Copolymerizations of ethylene with vinyltrialkoxysilanes

208 hydrophobicity of the polymer through random copolymerizations of modular norbornene derivatives, hig

209 alyst is also highly active and selective in copolymerizations of other epoxides with carbon dioxide.

210 Most notably, stereoselective copolymerizations of rac-8DL(Me) with rac-8DL(R) (R=Et,

211 complex architectures were achieved through copolymerizations of selected diluents with a poly(d,l-l

212 ertive stereoregular homopolymerizations and copolymerizations of styrene and methyl methacrylate (MM

213 gest that the coexpression, and probably the copolymerization, of the abundant ACT7 with the other ac

214 Conventional one gallon batch reactor copolymerizations performed using selected amide-ether h

215 nt strategies, including surface coating and copolymerization/physical blending, necessitate compromi

216 For ethylene-styrene copolymerization, polar solvents are found to increase c

217 tant/HbS hybrid was found to be 6.2, and the copolymerization probability for the triple mutant/HbS h

218 Relative to HbS, the copolymerization probability of the quadruple mutant/HbS

219 c cycles is proposed wherein the alternating copolymerization proceeds via intermediates that have ca

220 echanistic differences in the supramolecular copolymerization process is investigated as a function o

221 and assay workflow, we introduce a one-step copolymerization process that creates protein-decorated

222 opic probing during the supramolecular block copolymerization process to unravel a nucleation-growth

223 nd different species start to coexist in the copolymerization process.

224 ment in homogenous olefin polymerization and copolymerization processes.

225 )B(C(6)F(5))(2) (BN(2)) in ethylene + olefin copolymerization processes.

226 of d(0) metal-catalyzed polar olefin monomer copolymerization processes.

227 Multicomponent supramolecular copolymerization promises to construct complex nanostruc

228 ts comparable to those produced using Stille copolymerization protocols.

229 OMP mechanism, monomer design, and homo- and copolymerization rate trends offer a general strategy fo

230 CTAs in reversible-deactivation ring-opening copolymerizations (RD-ROCOP), yet the predominant binary

231 able a mechanism to be proposed for both the copolymerization reaction and possible side reactions; a

232 In these latter cases the copolymerization reaction exhibits ideal kinetic behavio

233 The working mechanistic model for the copolymerization reaction involves first aziridine inser

234 nd infrared spectroscopy, a mechanism of the copolymerization reaction is proposed.

235 mably is true for the initiation step of the copolymerization reaction, the rate of carbonate chain g

236 Conducting copolymerization reactions in the presence of both monom

237 polymerizations and developing one-pot block copolymerization reactions in which the dispersities of

238 ene oxide and exo-2,3-epoxynorbornane toward copolymerization reactions with carbon dioxide, in the p

239 Both homopolymerization and copolymerization results argue that substantial cooperat

240 lines of evidence from both homo- and block copolymerization results have demonstrated living charac

241 al conjugate addition steps to explain these copolymerization results.

242 erization (ROP) of lactones and ring-opening copolymerization (ROCOP) of epoxides, anhydrides, and CO

243 re introduced as comonomers for ring-opening copolymerization (ROCOP) with epoxides.

244 Cyclopolymerization and ethylene/propylene copolymerization strategies are employed to support this

245 We adopted a photoinduced post-synthetic copolymerization strategy to realize a membranous ratiom

246 ated in this work is a simple random ternary copolymerization strategy to synthesize a series of poly

247 Results from propylene copolymerizations suggested that chain end control arisi

248 The advantages of such a copolymerization system are manifold: (i) no need for mu

249 ucidates the thermodynamic parameters of the copolymerization, the distributions of the various speci

250 Controlled copolymerization therefore expands the parameter space f

251 In ethylene copolymerization, Ti(2) + BN(2) enchains approximately 2

252 In ethylene copolymerization, Ti2 + B1 enchains 15.4% more styrene (

253 onomers and mediates efficient homo or block copolymerization to generate hydrophilic polymers with c

254 end of the salenCo(III)X-catalyzed SO/CO(2) copolymerization to in situ generate hydroxyl groups at

255 e at or above the critical concentration for copolymerization to occur, indicating that FtsZ is nucle

256 In catalytic copolymerization, undesired chain transfer after incorpo

257 4%) in comparison with EBICGCTi2Me4-mediated copolymerizations (up to 32%).

258 re consistently higher for CGCTiMe2-mediated copolymerizations (up to 54%) in comparison with EBICGCT

259 lity is further exemplified by in situ block copolymerization upon sequential monomer addition for th

260 pon the kinetic analysis of ethylene-styrene copolymerization using constrained geometry catalyst (et

261 activated and non-activated alkenes prevents copolymerization using established polymer synthesis tec

262 um i.d. capillaries by one-step UV-initiated copolymerization using methanol and ethyl ether as porog

263 rtin-Hammett kinetic behavior as observed in copolymerization using the normal Brookhart type of Pd(I

264 nusually high incorporations of acrylates in copolymerization using this catalyst prompted us to cond

265 CH(2) =CH(CH(2) )(x) N(n) Pr(2) , x=2, 3, 6) copolymerizations using the activated precatalysts rac-[

266 extensions to full conversion or multiblock copolymerization via iterative monomer addition after fu

267 The copolymerization was found to proceed in a nonexpected w

268 ne and acrylonitrile, both cycloaddition and copolymerization were observed experimentally; these tre

269 duct a full mechanistic study on ethylene/MA copolymerization, which indicates a dramatic departure f

270 Polymerization of EDOT-PdBPI and copolymerization with 4-amino-N-(2,5-di(thiophene-2-yl)-

271 is monomer enables a room temperature Suzuki copolymerization with a diketopyrrolopyrrole comonomer t

272 which can be controlled by cross-linking and copolymerization with acrylamide, which also improves th

273 crylic-functionalized glass surfaces through copolymerization with acrylic monomer.

274 containing the C terminus were competent for copolymerization with capsid subunits into procapsid she

275 ucing biocompatible polymers via alternating copolymerization with carbon dioxide.

276 The rac-PO/CO(2) copolymerization with catalyst rac-(salcy)CoBr yields sy

277 long-chain polyamides by thiol-ene addition copolymerization with diamide diene monomers.

278 conductors are synthesized by end-capping or copolymerization with dithienothiophen-2-yl units.

279 Copolymerization with ethyl acrylate is also possible.

280 s, we generate two types of DHT monomers for copolymerization with high cooperativity and low dispers

281 Copolymerization with Mal3 favors 13 protofilament micro

282 nsoluble product, [NH(2)-BH(2)](n) (8d), but copolymerization with MeNH(2).BH(3) gave soluble random

283 Ethylene/propylene copolymerization with metallocenes having heterotopic ac

284 methacrylamide) nanogels were synthesized by copolymerization with N,O-(dimethacryloyl) hydroxylamine

285 Structural integrity is provided by copolymerization with tetraethoxysilane, which produces

286 s by phalloidin and improved greatly through copolymerization with the wild-type actin.

287 Copolymerization with thiophene afforded a polymer with

288 Copolymerization with thiophene resulted in a semicrysta

289 olymerization incompetent, the impact of its copolymerization with unlabeled actin on filament struct

290 a 75-microm-i.d. capillary by photoinitiated copolymerization with water, methanol, and ethyl ether a

291 Both defects are attenuated by copolymerization with WT.

292 ve for ethylene + CH(2) =CH(CH(2) )(n) NR(2) copolymerizations with activities up to 3400 Kg copolyme

293 nalized (AA-type) monomers in Suzuki-Miyaura copolymerizations with dibromo-heteroarenes (BB-type mon

294 FI(2)-Ni(2)-catalyzed copolymerizations with ethylene + methylacrylate or meth

295 FI(2)-Ni(2)-mediated copolymerizations with ethylene + polar-functionalized n

296 Copolymerizations with ethylene revealed that the polyme

297 or the behavior of VA and VA(f) in attempted copolymerizations with ethylene.

298 monomers, RAFT-mediated radical ring-opening copolymerizations with traditional vinyl monomers such a

299 complex exhibits exceptional selectivity for copolymerization without transesterification or epimeriz

300 found to be incompetent for ethylene-styrene copolymerization, yielding only mixtures of polyethylene