𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Sodium Hydride/Trialkylaluminum Complexes for the Controlled Anionic Polymerization of Styrene at High Temperature

✍ Scribed by Stéphane Carlotti; Stephane Menoret; Philippe Desbois; Norbert Nissner; Volker Warzelhan; Alain Deffieux


Publisher
John Wiley and Sons
Year
2006
Tongue
English
Weight
128 KB
Volume
27
Category
Article
ISSN
1022-1336

No coin nor oath required. For personal study only.

✦ Synopsis


Abstract

Summary: A new generation of anionic initiators (butyllithium free), based on trialkylaluminum and a readily available alkali metal hydride, has been developed for the control of styrene polymerization at high temperature. Triisobutylaluminum and sodium hydride form heterocomplexes that are efficient for the initiation of styrene polymerization at 100 °C in toluene or in bulk. To be active under such conditions, these systems require the presence of an excess of metal hydride with respect to AlR~3~ ([Al]/[Na] < 1). PS chains are specifically initiated by the hydrides coming from NaH, and molar masses are controlled in the range 0.8 < [Al]/[Na] < 1. Fast exchange between dormant 1:1 and active 1:2 complexes (Al:Na), and ligand rearrangements within the 1:2 complex, can explain the observed results.

Initiation of styrene with i‐Bu~3~Al/NaH systems.

magnified imageInitiation of styrene with i‐Bu~3~Al/NaH systems.


📜 SIMILAR VOLUMES


Towards the control of the reactivity in
✍ Philippe Desbois; Michel Fontanille; Alain Deffieux; Volker Warzelhan; Stephan L 📂 Article 📅 1999 🏛 John Wiley and Sons 🌐 English ⚖ 105 KB 👁 3 views

The influence of n,s-dibutylmagnesium on the kinetics of styrene polymerization initiated by sbutyllithium was investigated in cyclohexane at 50 8C. The presence of n,s-dibutylmagnesium, in molar ratios ranging from 0 to 20 with respect to polystyryllithium, leads to a drastic and continuous reducti