Göbel Christoph, Hörner Gerald, Greiner Andreas, Schmalz Holger, Weber Birgit
Department of Chemistry, Inorganic Chemistry IV, Universität Bayreuth Universitätsstraße 30 95447 Bayreuth Germany
Department of Chemistry, Macromolecular Chemistry II, Keylab Synthesis and Molecular Characterization, Bavarian Polymer Institute, Universität Bayreuth Universitätsstraße 30 95447 Bayreuth Germany
Nanoscale Adv. 2020 Sep 8;2(10):4557-4565. doi: 10.1039/d0na00334d. eCollection 2020 Oct 13.
Nanoparticles of the 1D and 2D coordination polymers [Zn(OAc)(bipy)] and [Zn(TFA)(bppa)] were prepared, employing polystyrene--poly(4-vinylpyridine) diblock copolymers with different weight fractions of the 4-vinylpyridine (4VP) block and comparable overall molecular weights of ≈ 155 kg mol as template (SV-15 and SV-42 with 15 and 42 wt% 4VP, respectively). [Zn(OAc)(bipy)] nanoparticles were successfully synthesised within the 4VP core of SV-42 micelles, showing a core size of = 47 ± 5 nm and a hydrodynamic diameter of = 157 ± 46 nm, determined by transmission electron microscopy (TEM) and dynamic light scattering (DLS). The crystallinity of the composite is quite low, showing only low intensity reflexes in the powder X-ray diffraction (PXRD) pattern with the highest particle load. No indications for larger microcrystals were detected by scanning electron microscopy (SEM), proving the successful integration of the coordination polymer nanoparticles within the micellar cores. Nanocomposites of the 2D coordination network [Zn(TFA)(bppa)] were synthesised using both diblock copolymers. The particle core sizes (from TEM) and hydrodynamic diameters (from DLS) correlate with the 4VP fraction of the micelles, resulting in = 46 ± 6 nm for SV-42 and 15 ± 2 nm for SV-15 and = 340 ± 153 nm and 177 ± 57 nm, respectively. The successful synthesis was proven by PXRD and SEM images, confirming the absence of larger crystallites. Hence, it is possible to synthesise nanocomposites of Zn-based 1D and 2D coordination polymers by a direct approach utilizing diblock copolymer micelles as template.
制备了一维和二维配位聚合物[Zn(OAc)(bipy)]和[Zn(TFA)(bppa)]的纳米颗粒,采用具有不同4-乙烯基吡啶(4VP)嵌段重量分数且总分子量约为155 kg/mol的聚苯乙烯-聚(4-乙烯基吡啶)二嵌段共聚物作为模板(分别为含15 wt%和42 wt% 4VP的SV-15和SV-42)。[Zn(OAc)(bipy)]纳米颗粒在SV-42胶束的4VP核内成功合成,通过透射电子显微镜(TEM)和动态光散射(DLS)测定,其核尺寸为 = 47 ± 5 nm,流体动力学直径为 = 157 ± 46 nm。复合材料的结晶度相当低,在粉末X射线衍射(PXRD)图谱中,即使在颗粒负载量最高时也仅显示出低强度反射。扫描电子显微镜(SEM)未检测到较大微晶的迹象,证明配位聚合物纳米颗粒成功整合到胶束核内。使用这两种二嵌段共聚物合成了二维配位网络[Zn(TFA)(bppa)]的纳米复合材料。颗粒核尺寸(来自TEM)和流体动力学直径(来自DLS)与胶束的4VP分数相关,SV-42的分别为 = 46 ± 6 nm,SV-15的为15 ± 2 nm,流体动力学直径分别为340 ± 153 nm和177 ± 57 nm。PXRD和SEM图像证明了成功合成,确认不存在较大的微晶。因此,利用二嵌段共聚物胶束作为模板,通过直接方法可以合成锌基一维和二维配位聚合物的纳米复合材料。