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Head-to-head polymers: 34. Head-to-head poly(1-vinylnaphthalene)

✍ Scribed by Masato Nanasawa; Liping Hu; Otto Vogl


Publisher
Elsevier Science
Year
1987
Tongue
English
Weight
492 KB
Volume
28
Category
Article
ISSN
0032-3861

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📜 SIMILAR VOLUMES


Head-to-head polymers
✍ Otto Vogl 📂 Article 📅 2000 🏛 John Wiley and Sons 🌐 English ⚖ 154 KB 👁 1 views
Head-to-head polymers 27: Thermal degrad
✍ M. Malanga; F. Xi; O. Vogl 📂 Article 📅 1983 🏛 Society for Plastic Engineers 🌐 English ⚖ 256 KB

## Abstract Head‐to‐head polyisobutylene degrades at a maximum rate at 320°C, a temperature about 65°C lower than head‐to‐tail polyisobutylene. Under our conditions, head‐to‐tail (the regular polyisobutylene) degrades (as do many other disubstituted vinyl monomers) to a high yield of the monomer is

Head-to-head polymers—II. Dilute solutio
✍ S. Arichi; M.Y. Pedram; J.M.G. Cowie 📂 Article 📅 1979 🏛 Elsevier Science 🌐 English ⚖ 423 KB

The behaviour in dilute solution of head-to-head (H-HI polypropylenes, covering the range M,, = 0.22 to 4.19 × 104, has been studied in cyclohexane as solvent at 303 K. The data could be represented by two distinct Mark-Houwink equations describing the low and the high molecular weight regions. The

Head to head polymers—38. An improved sy
✍ Enikö Földes; Gyorgy Deak; Ferenc Tüdös; Otto Vogl 📂 Article 📅 1993 🏛 Elsevier Science 🌐 English ⚖ 665 KB

A greatly improved and very reliable synthesis of head to head polystyrene (HHPS) was worked out. HHPS was prepared in a sequence of four steps starting with a reductive photodimerization of acetophenone. The resultant 2,3-diphenyl-2,3-butanediol was dehydrated in vacuum to 2,3-diphenyl-1,3butadiene