Improving the Charge Conductance of Elemental Sulfur
via Tandem Inverse Vulcanization and Electropolymerization
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Abstract
The synthesis of polymeric materials
using elemental sulfur (S<sub>8</sub>) as the chemical feedstock has
recently been developed using
a process termed inverse vulcanization. The preparation of chemically
stable sulfur copolymers was previously prepared by the inverse vulcanization
of S<sub>8</sub> and 1,3-diisopropenylbenzene (DIB); however, the
development of synthetic methods to introduce new chemical functionality
into this novel class of polymers remains an important challenge.
In this report the introduction of polythiophene segments into poly(sulfur-<i>random</i>-1,3-diisopropenylbenzene) is achieved by the inverse
vulcanization of S<sub>8</sub> with a styrenic functional 3,4-propylenedioxythiophene
(ProDOT-Sty) and DIB, followed by electropolymerization of ProDOT
side chains. This methodology demonstrates for the first time a facile
approach to introduce new functionality into sulfur and high sulfur
content polymers, while specifically enhancing the charge conductivity
of these intrinsically highly resistive materials