The Joseph Priestly Building, School of Biological and Chemical Sciences, Queen Mary University of London, Mile End Road, London, E1 4NS, UK.
Inorg Chem. 2010 Apr 19;49(8):3789-800. doi: 10.1021/ic901939x.
In an effort to improve upon the recently reported cyclam based zinc sensor 1, the "click"-generated 1,8-disubstituted analogue 2 has been prepared. The ligand shows a 2-fold increase in its fluorescence emission compared to 1 exclusively in the presence of Zn(II) that is typical of switch-on PET fluorescent sensors. Single crystal X-ray diffraction of complexes of model ligand 10 reveals that the configuration adopted by the macrocyclic framework is extremely sensitive to the metal ion to which it coordinates. For Zn(II), Mg(II), and Li(I) the metal ions adopt an octahedral geometry with a trans III configuration of the cyclam ring. In contrast for Ni(II) the ligand adopts the rare cis V configuration, while for Cu(II) a clear preference for five-coordinate geometry is displayed with a trans I configuration of the macrocyclic ring being observed in two essentially isostructural compounds prepared via different routes. The ligand displays an increased selectivity for Zn(II) compared to 1 in the majority of cases with excellent selectivity upheld over Na(I), Mg(II), Ca(II), Mn(II), Ni(II), Co(II), and Fe(III). In contrast for Cu(II) and Hg(II) little improvement was observed for 2 compared to 1 and for Cd(II) the selectivity of the new ligand was inferior. In the light of these findings and the slower response times for ligand 2, our original "click"-generated cyclam sensor system 1 was employed in a proof of concept study to prepare a heterogeneous sol-gel based material which retains its PET response to Zn(II). The versatile nature of the sol-gel process importantly allows the simple preparation of a variety of nanostructured materials displaying high surface area-volume ratio using fabrication methods such as soft lithography, electrospinning, and nanopipetting.
为了改进最近报道的基于环脒的锌传感器 1,我们制备了“点击”生成的 1,8-二取代类似物 2。与仅在存在 Zn(II)时才会发生的典型开关型 PET 荧光传感器相比,该配体的荧光发射强度增加了 2 倍。模型配体 10 的配合物的单晶 X 射线衍射表明,大环骨架所采用的构型对与之配位的金属离子极为敏感。对于 Zn(II)、Mg(II)和 Li(I),金属离子采用八面体几何构型,环脒环呈反式 III 构型。相比之下,对于 Ni(II),配体采用罕见的顺式 V 构型,而对于 Cu(II),则表现出明显的五配位几何偏好,观察到两种基本上结构相同的化合物通过不同途径制备,大环环呈反式 I 构型。与 1 相比,该配体在大多数情况下对 Zn(II)表现出更高的选择性,对 Na(I)、Mg(II)、Ca(II)、Mn(II)、Ni(II)、Co(II)和 Fe(III)具有优异的选择性。相比之下,对于 Cu(II)和 Hg(II),与 1 相比,2 的选择性几乎没有改善,而对于 Cd(II),新配体的选择性较差。鉴于这些发现以及配体 2 的响应时间较慢,我们最初的“点击”生成的环脒传感器系统 1 被用于概念验证研究,以制备一种保留其对 Zn(II)的 PET 响应的异质溶胶-凝胶基材料。溶胶-凝胶过程的多功能性重要地允许使用各种制造方法(如软光刻、电纺丝和纳米移液)简单地制备具有高表面积-体积比的各种纳米结构材料。