Poetzsch R, Komber H, Stahl BC, Hawker CJ, Voit B (2013)
Publication Type: Journal article
Publication year: 2013
Book Volume: 34
Pages Range: 1772-1778
Journal Issue: 22
A powerful variation of traditional radical thiol-yne reaction with diphenylacetylene (DPA)-based starting materials leading to the quantitative and selective formation of the corresponding vinyl sulfides is reported. A variety of different thiols are shown to undergo reaction with DPA and the influence of their structure on reactivity is studied. The results obtained from the model reactions are then used to guide the efficient synthesis of hyperbranched poly(vinyl sulfide) (hb-PVS) systems by employing a dithiol and a trialkyne in an A
APA:
Poetzsch, R., Komber, H., Stahl, B.C., Hawker, C.J., & Voit, B. (2013). Radical thiol-yne chemistry on diphenylacetylene: Selective and quantitative addition enabling the synthesis of hyperbranched poly(vinyl sulfide)s. Macromolecular Rapid Communications, 34(22), 1772-1778. https://dx.doi.org/10.1002/marc.201300707
MLA:
Poetzsch, Robert, et al. "Radical thiol-yne chemistry on diphenylacetylene: Selective and quantitative addition enabling the synthesis of hyperbranched poly(vinyl sulfide)s." Macromolecular Rapid Communications 34.22 (2013): 1772-1778.
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