𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Synthesis of poly(dihalophenylene oxide)s by solid-state thermal decomposition of manganese phenolate complexes with ethylenediamine ligand

✍ Scribed by Mehlika Pulat; Oya Şanli


Publisher
John Wiley and Sons
Year
1996
Tongue
English
Weight
352 KB
Volume
197
Category
Article
ISSN
1022-1352

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

The synthesis of poly(dihalophenylene oxide)s by solid‐state thermal decomposition of manganese phenolate complexes with ethylenediamine ligand was achieved. The complexes were characterized by infrared (IR) spectroscopy and C, H, N elemental analysis. The dependence of the yield of polymers on temperature and decomposition time of the manganese complexes with 2,4,6‐trichlorophenol, 2,4,6‐tribromophenol and 2,6‐dibromo‐4‐chlorophenol was investigated. The polymers obtained were characterized by ^1^H NMR, IR spectroscopy and differential scanning calorimetry and found to be branched. 1,2‐Catenation is favoured over 1,4‐addition in 2,4,6‐tribromophenoxide and 2,6‐dibromo‐4‐chlorophenoxide derived polymers, however, polymers synthesized from trichlorophenolate display a selectivity in favour of 1,2‐catenation.


📜 SIMILAR VOLUMES


Synthesis and characterization of poly(d
✍ Pulat, Mehlika; Çalíşkan, Gülsüm 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 205 KB 👁 2 views

The characterization of poly(dihalophenylene oxide)s synthesized by solid-state thermal decomposition of manganese phenolate complexes with tetramethylethylenediamine (TMEN) ligand is reported. The complexes prepared with 2,4,6-trichlorophenol (TCP) and 2,4,6-tribromophenol (TBP) have been character

Synthesis of poly(dihalophenylene oxide)
✍ Oya Şanli; Mehlika Pulat; Duygu Kisakürek 📂 Article 📅 1995 🏛 Elsevier Science 🌐 English ⚖ 378 KB

## In this study the synthesis of poly(dihalophenylene oxides) by the solid state thermal decomposition of a bis (4-chloro-2,6-dibromo phenoxo) ethylenediamine copper (II) complex was achieved. Yields, structures and intrinsic viscosities of the polymers were compared with those of electroinitiate