Jordi Mark Anderson, Seery Thomas A P
Department of Chemistry and Polymer Program, University of Connecticut, Storrs, Connecticut 06269, USA.
J Am Chem Soc. 2005 Mar 30;127(12):4416-22. doi: 10.1021/ja044456i.
Nanoparticle hybrid materials consisting of a silica core surrounded by a poly(norbornene) brush have been prepared by ring opening metathesis polymerization (ROMP). A quantitative determination of each stage of composite formation has been accomplished, including a determination of the density of surface-bound functional groups, catalyst molecules, and polymer chains. This analysis has enabled the determination of the reaction efficiency between the catalyst and the surface-bound functional groups as well as the determination of the fraction of metal-mediating species that initiate a polymer chain. Control of the chain density was demonstrated by two methods: the use of controlled reaction times between the catalyst and the surface, and the variation of the surface functional group density. Polymer chain densities resulting from composites prepared with different tether structures will also be reported. The resulting brush densities were found to span a wide range, including those previously reported for polymer layers formed by adsorption, grafting of preformed polymer chains, and surface-initiated polymerization (SIP).
由聚降冰片烯刷包围的二氧化硅核组成的纳米粒子杂化材料已通过开环易位聚合(ROMP)制备。已经完成了复合材料形成各阶段的定量测定,包括表面结合官能团、催化剂分子和聚合物链密度的测定。该分析能够确定催化剂与表面结合官能团之间的反应效率,以及引发聚合物链的金属介导物种的比例。通过两种方法证明了对链密度的控制:使用催化剂与表面之间的受控反应时间,以及表面官能团密度的变化。还将报告由具有不同拴系结构制备的复合材料产生的聚合物链密度。发现所得的刷密度范围很广,包括先前报道的通过吸附、预形成聚合物链的接枝和表面引发聚合(SIP)形成的聚合物层的密度。