Superbase catalyzed regio-selective polyhydroalkoxylation of alkynes: a facile route towards functional poly(vinyl ether)s

The polyhydro X ations, such as polyhydro thiol ation and polyhydro amin ation, of alkynes have been well-established. However, the polyhydro alkoxyl ation is rarely reported. In this paper, the polyhydroalkoxylation of aromatic diynes was successfully developed in the presence of a superbase, phosp...

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Veröffentlicht in:Polymer chemistry 2017-05, Vol.8 (17), p.2713-2722
Hauptverfasser: Wang, Jia, Li, Baixue, Xin, Dehua, Hu, Rongrong, Zhao, Zujin, Qin, Anjun, Tang, Ben Zhong
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Sprache:eng
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Zusammenfassung:The polyhydro X ations, such as polyhydro thiol ation and polyhydro amin ation, of alkynes have been well-established. However, the polyhydro alkoxyl ation is rarely reported. In this paper, the polyhydroalkoxylation of aromatic diynes was successfully developed in the presence of a superbase, phosphazene base ( t -BuP 4 ). A series of soluble and regio-regular anti-Markovnikov additive poly(vinyl ether)s with high molecular weights ( M w up to 40 600) were obtained in high yields (up to 99%). All the polymers are thermally and morphologically stable. The tetraphenylethene (TPE)-containing P 1a2a , P 1a2b and P 1a2c showed unique aggregation-enhanced emission (AEE) characteristics, and their aggregates could be used for explosive detection with a superamplification quenching effect. The poly(vinyl ether)s are degradable under acidic conditions. Thus, this work not only established a new polymerization but also generated a series of functional polymeric materials that are potentially applicable in optoelectronic and biomedical fields.
ISSN:1759-9954
1759-9962
DOI:10.1039/C7PY00363C