Mitchell Sarah M, Niradha Sachinthani K A, Pulukkody Randinu, Pentzer Emily B
Department of Chemistry, Department of Materials Science and Engineering, Texas A&M University, College Station, Texas 77840, United States.
ACS Macro Lett. 2020 Jul 21;9(7):1046-1059. doi: 10.1021/acsmacrolett.0c00396. Epub 2020 Jul 7.
Polymer chemistry offers exciting opportunities to tailor the properties of soft materials through control of the composition of the polymers and their interaction with each other, additives, and surfaces. Ongoing advances in the synthesis of polymeric materials demonstrate the drive for materials with tailored properties for enhanced performance in the next generation of materials and devices. One class of small molecules that can serve as monomers in chain growth polymerization are cumulated double bonds of the general form X═Y═Z. The three most common classes of these molecules are isocyanates (N═C═O), allenes (C═C═C), and ketenes (C═C═O), each of which has been explored as monomers under a variety of conditions. The orthogonality of the two pi bonds of the cumulated double bonds (i.e., lack of conjugation) enables the formation of different polymer backbones from a single monomer, provided the regioreactivity is controlled. This Viewpoint outlines the use of these three cumulated double bonds as monomers, illustrating success and current limitations to established polymerization methods. We then provide an outlook to the future of cumulated double bonds as monomers for the generation of tailored polymer compositions.
高分子化学为通过控制聚合物的组成及其彼此之间、与添加剂和表面的相互作用来定制软材料的性能提供了令人兴奋的机会。聚合物材料合成方面的不断进展表明,人们渴望获得具有定制性能的材料,以在下一代材料和器件中实现更高的性能。一类可作为链式增长聚合单体的小分子是通式为X═Y═Z的累积双键。这些分子中最常见的三类是异氰酸酯(N═C═O)、丙二烯(C═C═C)和乙烯酮(C═C═O),每一类都已在各种条件下作为单体进行了探索。累积双键的两个π键的正交性(即缺乏共轭)使得能够从单一单体形成不同的聚合物主链,前提是区域反应性得到控制。本观点概述了将这三种累积双键用作单体的情况,阐述了现有聚合方法的成功之处和当前局限性。然后,我们展望了累积双键作为生成定制聚合物组合物的单体的未来。