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A. E. G. Valdez, R. A. Ortiz, M. G. M. and M. L. B. Duarte, “Effect of the Degree of Substitution of the Diallyl Sucrose on the Reactivity and Physical and Mecha- nical Properties of the Polymers Obtained by the Thiol- Ene Photopolymerization Mechanism,” Current Trends in Polymer Science, Vol. 13, 2009, pp. 25-36.

has been cited by the following article:

• TITLE: Synthesis of Novel Hexathiolated Squalene and Its Thiol-Ene Photopolymerization with Unsaturated Monomers

  AUTHORS: Ricardo Acosta Ortiz, Ena Adeligna Obregón Blandón, Ramiro Guerrero Santos

  KEYWORDS: Squalene; Thiol-Ene; Photopolymerization; Biomaterials; Kinetics

  JOURNAL NAME: Green and Sustainable Chemistry, Vol.2 No.2, May 11, 2012

  ABSTRACT: In this work is described the synthesis of a multifunctional thiolated squalene. Thiol-ene coupling reactions were employed to functionalize the six double bonds of squalene, using thiolacetic acid. Hydrolysis of the resulting thioacetates, rendered the corresponding hexathiolated squalene SQ6SH. This compound was further photopolymerized separately with triallyl cyanurate, pentaerythritol triacrylate and diethyleneglycol divinyl ether. Real Time FTIR kinetics revealed that homopolymerization of the ene monomers took place in addition to the thiol-ene photopolymerization. Flexible films were obtained when SQ6SH was photopolymerized in bulk with the above mentioned unsaturated monomers.