✦ LIBER ✦

Relative reactivities of the cis and trans crotonic compounds in anionic polymerization

✍ Scribed by Kobuke, Yoshiaki ;Furukawa, Junji ;Fueno, Takayuki

Publisher: Wiley (John Wiley & Sons)
Year: 1967
Tongue: English
Weight: 181 KB
Volume: 5
Category: Article
ISSN: 0449-296X
DOI: 10.1002/pol.1967.150051020

No coin nor oath required. For personal study only.

📜 SIMILAR VOLUMES

Determination of the relative reactiviti

Determination of the relative reactivities of cis and trans isomers of β-bromostyrene towards polystyryllithium by Raman spectroscopy

✍ H.G.M Edwards; A.F Johnson; M.T O'Brien; S.A Dobrowski 📂 Article 📅 2004 🏛 Elsevier Science 🌐 English ⚖ 156 KB

Cis—trans-isomerization of active centre

Cis—trans-isomerization of active centres and the role of associates in stereoregulation in anionic-coordination polymerization of dienes

✍ S.I. Beilin; B.A. Dolgoplosk; E.I. Tinyakova 📂 Article 📅 1975 🏛 Elsevier Science 🌐 English ⚖ 144 KB

Reactivities of cis- and trans-buten-2-y

Reactivities of cis- and trans-buten-2-yl free radicals in presence of D2S. I. Relative values of rate constants

✍ C. Richard; R. Martin 📂 Article 📅 1985 🏛 John Wiley and Sons 🌐 English ⚖ 248 KB

Cisand trans-buten-2-yl free radicals are shown to react with D2S in metathetical steps: Relative formation rates of monodeuteriated butenes in D2S -2 -C,Hs mixtures were measured at low extent of reaction in the experimental range: 20-200 torr 2 -C4Hs, 0-41-torr D2S and 717-817 K. In these pressur

Anionic polymerization initiated by the

Anionic polymerization initiated by the lamellar compounds of LiC12: 2. Thermodynamics and the propagation mechanisms in 1,4 Cis and 1.4 Trans of isoprene, -H-n.m.r. study

✍ E. Loria; J. Gole; J.P. Pascault; Q.T. Pham; I.B. Rashkov 📂 Article 📅 1981 🏛 Elsevier Science 🌐 English ⚖ 575 KB

Cyclic oligomers in the cationic polymer

Cyclic oligomers in the cationic polymerization of cis- and trans-2,3-dimethylthiirane

✍ Wilfried M. Van Craeynest; Eric J. Goethals 📂 Article 📅 1976 🏛 Elsevier Science 🌐 English ⚖ 452 KB

Under the influence of triethyloxonium tetrafluoroborate in methylene chloride, cis-and trans-2,3-dimethylthiirane are transformed to their corresponding polymers almost instantaneously (at temperatures between 0 and 20 °) but within a few hours these polymers completely degrade to form a mixture of

The reactivity of atoms and groups in or

The reactivity of atoms and groups in organic compounds. VIII: The relative reactivities of the hydroxyl groups in certain alcohols

✍ James F. Norris 📂 Article 📅 2010 🏛 Elsevier Science 🌐 English ⚖ 252 KB