Abstract
Dienes can undergo olefin metathesis reactions of two types: (i) intermolecular, and (ii) intramolecular. Intramolecular metathesis (RCM) reactions occur with great readiness henever the product is a 6-membered ring. They are also often favoured for the production of 5-, 7-, and 8-membered rings, depending on the nature, number and location of any substituents. Intermolecular metathesis reactions lead eventually to high polymers and proceed very cleanly when initiated by metal carbene complexes; these are known as ADMET (acyclic diene metathesis) polymerizations (Figure 1). This class of polymerization reactions has been well established and comprehensively studied by Wagener and his group [1–6]. ADMET polymerization has been also a convenient route to linear polymers containing inorganic elements and functional groups for the preparation of new materials [7].
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Derelİ, O., Düz, B., İmamoğlu, Y. (2003). Acyclic Diene Metathesis (ADMET) Polymerization by Electrochemically Generated Tungsten-Based Active Catalyst System: Optimization of Reaction Conditions. In: Imamoglu, Y., Bencze, L. (eds) Novel Metathesis Chemistry: Well-Defined Initiator Systems for Specialty Chemical Synthesis, Tailored Polymers and Advanced Material Applications. NATO Science Series, vol 122. Springer, Dordrecht. https://doi.org/10.1007/978-94-010-0066-6_20
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DOI: https://doi.org/10.1007/978-94-010-0066-6_20
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