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 |
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Format: | Artikel |
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. |
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ISSN: | 1759-9954 1759-9962 |
DOI: | 10.1039/C7PY00363C |