H2020Individual fellowship2017–2019

POLY-WITTIG · Tuning mechanical properties of elastomers with stereocontrolled π-bonds using Wittig chemistry

Horizon 2020 — Marie Skłodowska-Curie Actions

Duration
2017-06-26 → 2019-06-25
EU contribution
€195,455
Participants
2
Scheme
MSCA-IF-EF-ST

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Results in brief

Tuning mechanical properties of elastomers with stereocontrolled π-bonds using Wittig chemistry

"Rubbers (also referred to as elastomers) are hugely important and widely used in many industries (such as automotive or medical) as a result of their ability to be deformed yet return to their original size and shape upon removal of stress. Owing to these properties and their wide-ranging applicability, a significant body of research has been, and continues to be directed towards the discovery of new materials (or polymers) with specific properties for a wide array of application areas. However, many of our commercially useful elastomers are thermosets (meaning the polymer chains are irreversibly cross-linked together and can't be reprocessed) which limits their reusability and thus contributes to the growing environmental concerns associated with non-recyclable and non-degradable materials. In contrast, thermoplastic elastomers (TPEs) are a special class of materials that display elastic behaviour but are not cross-linked (meaning we can remould them into different shapes after use) and they have the potential to be recycled. However, TPEs are more challenging and expensive to produce than traditional rubbers, thus making TPEs suitable for only specialty applications. Thus, there exists a need to develop more environmentally friendly (reusable) elastomers that are easy to make and inexpensive to produce. The main objective of this action was to mimic the properties of the specialty elastomers (TPEs) in a material that had a more simple chemical composition and was thus easier to produce. We sought to borrow concepts learned from ""natural"" elastomers in order to achieve this. In particular, the strength and stretchability of natural elastomers, e.g. those coming from Rubber or Gutta Percha Trees, are known to change depending upon the orientation of chemical bonds in the polymer. However, this strategy has not been used to change properties of synthetic (produced in the lab) elastomers despite the obvious potential advantages. This is primarily because of the inherent challenges associated with controlling the orientation of the chemcial bonds in polymers i.e. nature is much better at this than we are as chemists. However, in this action, we used a straightforward method to make our polymers that also provided us with control over the orientation of the chemical bonds; this allowed us to change our material properties on demand. More importantly, these materials were elastic but they were not thermosets which meant that we could recycle them into whatever form we would like multiple times over. This would be analogous to taking a car tire and remoulding it into a shoe after its usefulness as a tire was exhausted. "

Data: CORDIS, © European Union

Project objective

Elastomer materials (or rubbers) are hugely important and widely used as a result of their ability to be deformed yet return to their original size and shape upon removal of stress. Owing to these properties and their wide-ranging applicability, a significant body of research has been, and continues to be directed towards the discovery of new materials with specific properties for a wide array of application areas. The properties of elastomers are dependent on a number of factors such as chain length, topology, tacticity, pendant functionality, or cross-linking density. Specifically, the mechanical characteristics of natural elastomers, e.g., those based on polyisoprene, are known to be highly dependent upon the stereochemistry of the double bond in the isoprene unit. However, this concept is seldom exploited to modulate properties of synthetic elastomers despite the potential clear advantages to create materials in which the control over their mechanical properties can be decoupled from their functionality. This is primarily a consequence of the inherent challenges associated with metal-catalyzed stereocontrolled polymerisations. The POLY-WITTIG project proposes to utilize the highly practical Wittig reaction to modulate the stereochemistry of the π-bond in the elastomer backbone to inturn allow the modulation of materials properties to be controlled. Additionally, heteroatom-modified Wittig variants will be used to synthesize and analyze mechanical properties of elastomers with heteroatom–carbon π-bonds (e.g., N=C or P=C). Thus, the versatility of Wittig chemistry will provide the unprecedented opportunity to systematically study a library of isolobally substituted elastomers.

Original text from CORDIS.

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Data: CORDIS, © European Union