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Synthesis of Ni-Based Metallo-Supramolecular Polymer with Bis-NNO-Tridentate Ligand for Electrochromic Devices

机译:电致变色器件的双-NNO-三叉形配体的镍基金属超分子聚合物的合成

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摘要

An imine-based bis-NNO-tridentate ligand (L1) was prepared by condensation of a salicylaldehyde derivative with 8-aminoquinoline. L1 formed a 1:1 complex with Ni(II) ions with a high coordination constant. A one-dimensional, Ni-based metallo-supramolecular polymer (polyNiL1) was synthesized via the 1:1 complexation of Li with Ni(II) ions in DMF at 60 degrees C. L1 and polyNiL1 were characterized by IR absorption spectroscopy. In the IR spectrum of polyNiL1, a shift of the C=N absorption peak based on the complexation was observed. In UV-vis spectroscopy of polyNiLl, a strong absorption appeared at 505 nm, which is attributed to the metal-to-ligand charge transfer (MLCT) band from Ni(II) ions to Li. In a cyclic voltammogram of polyNiL1 in a DMF solution, a reversible redox wave was observed at +0.58 V. PolyNiL1 in a film state exhibited electrochromism between reddish-orange and green color by applying -2.5 V and +2.5 V, respectively. The green color in the oxidation state comes from the ligand-to-ligand charge transfer (LLCT) of a radical cation between the phenyl ring and the quinoline ring in polyNiLl. Since the radical cation of Li was stabilized by a Ni(II) ion in the complex, this electrochromism showed good reversibility about 10 times under ambient conditions.
机译:通过使水杨醛衍生物与8-氨基喹啉缩合制备基于亚胺的双-NNO-三齿配体(L1)。 L1与具有高配位常数的Ni(II)离子形成1:1的络合物。通过在60°C下在DMF中将Li与Ni(II)离子进行1:1络合,合成了一维Ni基金属超分子聚合物(polyNiL1)。利用红外吸收光谱对L1和polyNiL1进行了表征。在聚NiL1的IR光谱中,观察到基于络合的C = N吸收峰的移动。在聚NiL1的UV-可见光谱中,在505nm处出现强吸收,这归因于从Ni(II)离子到Li的金属-配体电荷转移(MLCT)带。在DMF溶液中的polyNiL1的循环伏安图中,在+0.58 V处观察到可逆的氧化还原波。膜状态的PolyNiL1分别施加-2.5 V和+2.5 V,在橙红色和绿色之间表现出电致变色。处于氧化态的绿色来自聚NiL1中苯环和喹啉环之间的自由基阳离子的配体到配体的电荷转移(LLCT)。由于Li的自由基阳离子被配合物中的Ni(II)离子稳定,因此该电致变色在环境条件下显示出约10倍的良好可逆性。

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