Photopolymerization of Thiol-Alkynes: Polysulfide Networks

Authors

Justin W. Chan, University of Southern Mississippi
Hui Zhou, University of Southern Mississippi
Charles E. Hoyle, University of Southern MississippiFollow
Andrew B. Lowe, University of Southern Mississippi

Document Type

Article

Publication Date

4-28-2009

Department

Polymers and High Performance Materials

Abstract

A series of photoinitiated reactions involving radical chain addition of dithiols across the triple bonds of dialkynes results in quantitative loss of all of the thiol and alkyne groups in 1:1 molar functional group neat mixtures. The reactions proceed rapidly to give uniform networks with relatively narrow differential scanning calorimetry (DSC) and dynamic mechanical analysis (DMA) glass transition ranges. The glass transitions of the network films are directly related to the network structure and range from below 0 degrees C to about 40 degrees C as determined by DMA. The thiol-alkyne based hydrocarbon networks with sulfide linking groups have refractive index values which extend as high as 1.66. There is a linear relationship between the density and the refractive index, both of which increase linearly with weight percent sulfur.

Publication Title

Chemistry of Materials

Volume

21

Issue

8

First Page

1579

Last Page

1585

Recommended Citation

Chan, J. W., Zhou, H., Hoyle, C. E., Lowe, A. B. (2009). Photopolymerization of Thiol-Alkynes: Polysulfide Networks. Chemistry of Materials, 21(8), 1579-1585.
Available at: https://aquila.usm.edu/fac_pubs/1179