Picture of mobile phone running fintech app

Fintech: Open Access research exploring new frontiers in financial technology

Strathprints makes available Open Access scholarly outputs by the Department of Accounting & Finance at Strathclyde. Particular research specialisms include financial risk management and investment strategies.

The Department also hosts the Centre for Financial Regulation and Innovation (CeFRI), demonstrating research expertise in fintech and capital markets. It also aims to provide a strategic link between academia, policy-makers, regulators and other financial industry participants.

Explore all Strathclyde Open Access research...

Lithium amides as initiators of anionic polymerisation of methyl methacrylate

Couper, S A and Mulvey, Robert and Sherrington, D C (1998) Lithium amides as initiators of anionic polymerisation of methyl methacrylate. European Polymer Journal, 34 (12). pp. 1877-1887. ISSN 0014-3057

Full text not available in this repository. Request a copy from the Strathclyde author


Reaction of (BuLi)-Li-n with isopropylcyclohexylamine and 2,6-dimethylpiperidine allows isolation of the corresponding lithium amides. Both of these are effective initiators of polymerisation of methyl methacrylate (MMA). A more convenient procedure however is to generate the lithium amides in situ and six secondary amines have been used in this way. Polymerisations in THF at -78 degrees C, both with and without added TMEDA Lewis base, yield polymer quantitatively with a high degree of syndiotacticity. (M) over bar(n) values, however, are somewhat larger than expected for clean living systems and likewise molecular weight distributions are rather broad. Similar reactions at 25 degrees C give much lower yields of polymer, somewhat reduced syndiotacticity and similar molecular weight effects. Using diisopropylaminolithium as the initiator in toluene solution at -78 degrees C yields highly isotactic polymer essentially quantitatively. Again the (M) over bar(n) and molecular weight distributions are higher than ideal. Adding trace levels of TMEDA to this polymerisation switches the microstructure of the polymer to high levels of syndiotacticity, but the initiator efficiency is reduced at the same time resulting in a very high (M) over bar(n), and a broad molecular weight distribution. Addition of varying levels of LiOBut to the polymerisation in toluene retains the isotactic selectivity of the propagation and improves the initiator efficiency significantly. The results are discussed in the light of current understanding of anionic vinyl polymerisations. (C) 1998 Elsevier Science Ltd. All rights reserved.