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Plant oils: The perfect renewable resource for polymer science?!

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TLDR
In this paper, the authors provide an overview of the present situation with special attention to the use of olefin metathesis and thiol-ene chemistry as synthetic methods and as polymerization techniques.
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This article is published in European Polymer Journal.The article was published on 2011-05-01 and is currently open access. It has received 551 citations till now.

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Vegetable oil-based polyols for sustainable polyurethanes

TL;DR: In this article, the authors summarized recent progress on preparing VO-based polyols and PUs, and indicated that VO based polyols can be eco-friendly families of industrially important polymers with a low environmental footprint.
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Polymeric triglyceride analogs prepared by enzyme-catalyzed condensation polymerization

TL;DR: In this paper, unique crosslinkable unsaturated polyesters were prepared by a one-pot lipase-catalyzed copolymerization of crude linoleic acid (LA), glycerol (G), and 1,18-cis-9-octanedecenedioic acid(oleic diacid, OD).
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Synthesis of levulinic acid–glycerol ketal–ester oligomers and structural characterization using NMR spectroscopy

TL;DR: In this article, the authors studied the average degree of oligomerization of renewable resources based monomers levulinic acid and glycerol using three different catalysts, Sb 2 O 3, p -toluenesulfonic acid, and 1-(1-propylsulfonic)-3-methylimidazolium chloride.
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The bio-based economy can serve as the springboard for camelina and crambe to quit the limbo

TL;DR: In this paper, the potentialities of two alternative oilseed crops for Europe, camelina (Camelina sativa ) and crambe (Crambe abyssinica ), identified as major candidates for the future European bio-based economy as testified by the recently funded EU Project (Horizon 2020) COSMOS (CARMOS) as Sources of Medium-chain Oils for Specialty oleochemicals).
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Renewable sulfur-containing thermoplastics via AB-type thiol-ene polyaddition

TL;DR: In this paper, an AB-type monomer derived from 10-undecenoic acid, which is a bio-sourced building block obtained from castor oil, was used for the synthesis of polymers with similar structures to existing bulk and engineering plastics such as polyethylene.
References
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Journal ArticleDOI

Thiol–Ene Click Chemistry

TL;DR: The radical-mediated thiol-ene reaction has all the desirable features of a click reaction, being highly efficient, simple to execute with no side products and proceeding rapidly to high yield.
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Recent developments in the chemistry of halogen-free flame retardant polymers

TL;DR: An overview of recent developments of the chemistry of halogen-free flame retardant polymers is presented in this article, along with their thermal stabilities and flame-retardant properties.
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Thiol-ene “click” reactions and recent applications in polymer and materials synthesis

TL;DR: In this paper, a review highlights examples of recent applications of both the radical-mediated and base/nucleophile-initiated thiol-ene reactions in polymer and materials synthesis.
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Plant oil renewable resources as green alternatives in polymer science

TL;DR: The synthesis of monomers as well as polymers from plant fats and oils has already found some industrial application and recent developments in this field offer promising new opportunities, as is shown within this contribution.
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Click Chemistry beyond Metal-Catalyzed Cycloaddition

TL;DR: This Minireview discusses the success and applicability of new, in particular metal-free, click reactions, which expand the opportunities for synthesizing small organic compounds as well as tailor-made macromolecules and bioconjugates.
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