首页> 外文期刊>Inorganica Chimica Acta >The first example of calix[4]pyrrole functionalized vic-dioxime ligand: Synthesis, characterization, spectroscopic studies and redox properties of the mononuclear transition metal complexes
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The first example of calix[4]pyrrole functionalized vic-dioxime ligand: Synthesis, characterization, spectroscopic studies and redox properties of the mononuclear transition metal complexes

机译:杯[4]吡咯官能化的vic-二肟配体的第一个例子:单核过渡金属配合物的合成,表征,光谱研究和氧化还原性质

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摘要

Novel calix[4]pyrrole bearing vic-dioxime ligand (LH_2) of the general formula, R_1R_2C_2N_2O _2H_2 (where, R_1 = C_6H_5- and R_2 = C_(39)H_(50)N_5-) has been synthesized by the reaction of anti-chlorophenylglyoxime with 3-aminophenylcalix[4]pyrrole at room temperature. The mononuclear Cu(II), Ni(II) and Co(II)complexes of this vic-dioxime ligand were prepared and their structures were confirmed by elemental analysis, FT-IR, TGA and magnetic susceptibility measurements; the HMBC, DEPT, ~1H and ~(13)C NMR spectra of the LH_2 ligand were also reported. The electrochemical property of the complexes was investigated in DMSO by cyclic voltammetry at 200 mV s~(-1) scan rate. The cyclic voltammetric measurements clearly indicated that Co(LH)_2·2H_2O complex differs from the Ni(LH)_2 and Cu(LH)_2 complexes upon the exhibition of quasi-reversible one-electron transfer reduction process in the negative region instead of an irreversible process.
机译:通过反式反应,合成了具有通式R_1R_2C_2N_2O_2H_2(其中R_1 = C_6H_5-和R_2 = C_(39)H_(50)N_5-)的带有新的杯二叠氮基cal [4]吡咯的化合物。 -氯苯基乙二肟与3-氨基苯基杯[4]吡咯在室温下。制备了这种vic-dioxime配体的单核Cu(II),Ni(II)和Co(II)配合物,并通过元素分析,FT-IR,TGA和磁化率测量确定了它们的结构。还报道了LH_2配体的HMBC,DEPT,〜1H和〜(13)C NMR光谱。在200mV s〜(-1)扫描速率下,通过循环伏安法研究了配合物在DMSO中的电化学性质。循环伏安法测量清楚地表明,在负区域出现准可逆的单电子转移还原过程时,Co(LH)_2·2H_2O络合物不同于Ni(LH)_2和Cu(LH)_2络合物。不可逆转的过程。

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