Zavada Scott R, Furgal Joseph C, Wood Nathan D, Scott Timothy F
Macromolecular Science and Engineering Program, University of Michigan, Ann Arbor, MI 48109-2136, USA.
Department of Chemical Engineering, University of Michigan, Ann Arbor, MI 48109-2136, USA.
J Polym Sci A Polym Chem. 2017 Apr 15;55(8):1373-1382. doi: 10.1002/pola.28507. Epub 2017 Feb 11.
A pyrrolopyrazine-thione derived from oltipraz, a compound that has been investigated as a chemopreventive agent, affords radicals in the presence of thiols and oxygen via a redox cycle, an attribute that suggests its suitability as an initiator for oxygen-mediated polymerization. Here, we explore the utilization of this pyrrolopyrazine-thione, generated in situ from a precursor, as an initiator for the radical-mediated thiol-ene polymerization. While the pyrrolopyrazine-thione was shown to be capable of generating radicals in the presence of atmospheric oxygen and thiol groups, the reaction extents achievable were lower than desired owing to the presence of unwanted side reactions that would quench radical production and, subsequently, suppress polymerization. Moreover, we found that complex interactions between the pyrrolopyrazine-thione, its precursor, oxygen, and thiol groups determine whether or not the quenching reaction dominates over those favorable to polymerization.
一种由奥替普拉衍生而来的吡咯并吡嗪硫酮,奥替普拉是一种已被研究用作化学预防剂的化合物,它在硫醇和氧气存在下通过氧化还原循环产生自由基,这一特性表明它适合作为氧介导聚合反应的引发剂。在此,我们探索将由前体原位生成的这种吡咯并吡嗪硫酮用作自由基介导的硫醇-烯聚合反应的引发剂。虽然已表明吡咯并吡嗪硫酮在大气氧和硫醇基团存在下能够产生自由基,但由于存在会淬灭自由基生成并随后抑制聚合反应的不良副反应,可实现的反应程度低于预期。此外,我们发现吡咯并吡嗪硫酮、其前体、氧气和硫醇基团之间的复杂相互作用决定了淬灭反应是否比有利于聚合的反应占主导地位。