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首页> 外文期刊>Journal of Photopolymer Science and Technology >Synthesis of Metallo-Supramolecular Polymers with Bis-NNN-Tridentate Ligand for Electrochromic Devices
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Synthesis of Metallo-Supramolecular Polymers with Bis-NNN-Tridentate Ligand for Electrochromic Devices

机译:电致变色器件的双-NNN-三齿配体的金属超分子聚合物的合成

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A bis-tridentate ligand with 2,6-bis(phenylamide)pyridine moieties (L1) was synthesized by amidation and Suzuki-Miyaura cross coupling reaction from chelidamic acid monohydrate. Novel metallo-supramolecular polymers containing iron(II), ruthenium(II), or nickel(II) ions (PolyFeL1, PolyRuL1 and PolyNiL1, respectively) were obtained as yellowish brown solid via complexation of L1 with the metal ions in the presence of a strong base. The polymers were characterized by IR, UV-vis-NIR absorption spectra, and cyclic voltammetry (CV). The IR spectra showed disappearance of NH stretching peak and shift of C=O stretching peak due to the complexation. The characteristic LMCT absorption appeared at 470 (Fe), 442 (Ru), or 367 (Ni) nm. The solution of the polymers showed a reversible redox wave attributed to the redox of metal ions. PolyFeL1 exhibited reversible electrochromism between orange and brown by applying + 3 V or 0 V.
机译:通过酰胺化和铃木-宫浦的交叉偶联反应,从一水合氯胺酸合成了具有2,6-双(苯酰胺)吡啶部分(L1)的双三齿配体。通过在金属离子存在下,L1与金属离子络合,获得了黄褐色固体状的新型金属超分子聚合物,该聚合物含有铁(II),钌(II)或镍(II)离子(分别为PolyFeL1,PolyRuL1和PolyNiL1)。强碱。通过IR,UV-vis-NIR吸收光谱和循环伏安法(CV)表征聚合物。红外光谱显示由于络合,NH伸展峰消失,C = O伸展峰移动。 LMCT的特征吸收出现在470(Fe),442(Ru)或367(Ni)nm。聚合物的溶液显示归因于金属离子的氧化还原的可逆氧化还原波。通过施加+ 3 V或0 V,PolyFeL1在橙色和棕色之间表现出可逆的电致变色现象。

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