Rittner Till, Kim Jaeshin, Haben Aaron, Kautenburger Ralf, Janka Oliver, Kim Jungtae, Gallei Markus
Polymer Chemistry, Saarland University, Campus C4 2, 66123, Saarbrücken, Germany.
Inorganic Solid State Chemistry, Saarland University, Campus C4 1, 66123, Saarbrücken, Germany.
Chemistry. 2024 Oct 8;30(56):e202402338. doi: 10.1002/chem.202402338. Epub 2024 Sep 19.
Porous organic cobaltocenium-containing particles are scarce in literature but highly interesting for their electrochemical properties and reusability in, for example, catalysis or magnetic systems. In this work, we present a scalable one-pot strategy to introduce tailorable amounts of cobaltocenium on a porous substrate, adjusting the electrochemical switching capability. For this purpose, 3-(triethoxysilyl)propan-1-amine (APTES) and ethynyl cobaltocenium hexafluorophosphate is used as functionalization agents for in-situ catalyst-free hydroamination, followed by silane condensation at the particles' surface. Functionalized particles are characterized by attenuated total reflection infrared spectroscopy (ATR-IR), thermogravimetric analysis (TGA), laser scanning confocal microscopy (LSCM), scanning electron microscopy (SEM), energy dispersive X-ray spectroscopy (EDS), inductively coupled plasma mass spectrometry (ICP-MS), powder X-ray diffraction (PXRD) and cyclic voltammetry (CV) showing excellent control over the degree of functionalization, i. e., the added cobaltocenium reagents. The electrochemical stability and good addressability while preserving the porous structure are shown. By utilizing higher amounts of APTES, the overall cobaltocenium amount can be reduced in favor of additional amine groups, strongly affecting the electrochemical behavior, making this functionalization strategy a good platform for metallopolymer immobilization and tailored functionalization. Additionally, thermal treatment of the synthesized metallopolymer microparticles paves the way to magnetic properties with tailorable microporous architectures for end-of-life and upcycling aspects.
含多孔有机钴茂的颗粒在文献中较为稀少,但因其电化学性质以及在催化或磁性系统等方面的可重复使用性而备受关注。在这项工作中,我们提出了一种可扩展的一锅法策略,在多孔基底上引入可定制量的钴茂,以调节电化学开关能力。为此,使用3-(三乙氧基甲硅烷基)丙-1-胺(APTES)和乙炔基钴茂六氟磷酸盐作为原位无催化剂氢胺化的官能化剂,随后在颗粒表面进行硅烷缩合。通过衰减全反射红外光谱(ATR-IR)、热重分析(TGA)、激光扫描共聚焦显微镜(LSCM)、扫描电子显微镜(SEM)、能量色散X射线光谱(EDS)、电感耦合等离子体质谱(ICP-MS)、粉末X射线衍射(PXRD)和循环伏安法(CV)对功能化颗粒进行表征,结果表明对功能化程度,即添加的钴茂试剂具有出色的控制。展示了在保持多孔结构的同时具有的电化学稳定性和良好的可寻址性。通过使用更多量的APTES,可以减少钴茂的总量,有利于增加胺基,这对电化学行为有很大影响,使这种功能化策略成为金属聚合物固定化和定制功能化的良好平台。此外,对合成的金属聚合物微粒进行热处理,为具有可定制微孔结构的磁性性能在报废和升级循环方面铺平了道路。