SINTESIS DAN TRANSISI ELEKTRONIK KOMPLEKS TEMBAGA (II)-KLOROFIL

I. H. Silalahi, Julan Julan, Muhammad Yusprianto, R. Rudiyansyah
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Abstract

The copper (II)-chlorophyll complex was prepared from the reaction between the chlorophyll isolated from cassava leaves and the metal ion precursor, CuSO4.5H2O in methanol under reflux for four hours. The FTIR spectra of the reaction product compared to the chlorophyll spectra show an indication of a complexation through metal coordination with the N atom from the phyrol ring replacing the magnesium (II) ion in chlorophyll.This assumption is drawn based on changes on FTIR spectra, i.e. vibration absorption originating from the CN and NH groups in the porphyrin ring and the appearance of the distinctive vibration band of nitrogen-metal bonds which is annotated as Cu-N groups at 599.88 cm-1. Another sign is the change in the OH and CO vibration bands which imply changes in aggregate properties that occur through inter-molecular interactions due to the introduction of copper (II) metal into the chlorophyll structure. The formation of copper (II)-chlorophyll compounds is also shown from the results of atomic absorption spectroscopy by recording copper metal in the product and reducing magnesium metal concentration. UV-vis spectra of chlorophyll in methanol show a characteristic band in the dark area (Soret band) at a maximum wavelength of 404 nm and the visible area (Q band) with the strongest intensity at 665 nm. These peaks appear to shift hypsochromically in the copper (II)-chlorophyll compound to 397 nm and 650 nm with higher absorptivity, indicating a change in the electronic transition of the chlorophyll after coordinating with the copper (II) ion. A new peak at 411 nm was also observed which is suggested to indicate that the copper (II) -chlorophyll complex is in an octahedral geometry in the aggregate coordinated via nitrogen atoms in the phyrol ring in place of the magnesium (II) ion.
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合成和过渡复杂的铜(II)-叶绿素
从木薯叶中分离的叶绿素与金属离子前体CuSO4.5H2O在甲醇中回流4小时,制备了铜(II)-叶绿素复合物。反应产物的红外光谱与叶绿素光谱的对比表明,反应产物通过金属配位发生了络合反应,来自phyrol环的N原子取代了叶绿素中的镁离子。这一假设是根据FTIR光谱的变化得出的,即卟啉环中CN和NH基团的振动吸收以及在599.88 cm-1处标记为Cu-N基团的氮金属键的独特振动带的出现。另一个标志是OH和CO振动带的变化,这意味着由于铜(II)金属引入叶绿素结构而通过分子间相互作用发生的聚集性质的变化。通过记录产物中的金属铜和降低金属镁的浓度,原子吸收光谱结果也显示了铜(II)-叶绿素化合物的形成。甲醇中叶绿素的紫外可见光谱在最大波长为404 nm的暗区(Soret波段)和665 nm的可见区(Q波段)中表现出最强的强度。在铜(II)-叶绿素化合物中,这些峰出现了低色移,达到397nm和650nm,具有较高的吸收率,表明叶绿素在与铜(II)离子配合后发生了电子跃迁的变化。在411 nm处还观察到一个新的峰,这表明铜(II) -叶绿素复合物在聚集体中呈八面体结构,通过氮原子代替镁(II)离子在phyrol环上配位。
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