Department of Organic Chemistry, University of Szeged, Dóm tér 8, Szeged, Hungary; Materials and Solution Structure Research Group, University of Szeged, Hungary.
Department of Physical Chemistry and Materials Science, University of Szeged, Rerrich B. tér 1, Szeged, Hungary; Materials and Solution Structure Research Group, University of Szeged, Hungary.
Spectrochim Acta A Mol Biomol Spectrosc. 2014 Mar 25;122:257-9. doi: 10.1016/j.saa.2013.11.082. Epub 2013 Nov 21.
One of the aims of our long-term research is the identification of metal ion-ligand coordination sites in bioinspired metal ion-C- or N-protected amino acid (histidine, tyrosine, cysteine or cystine) complexes immobilised on the surface of chloropropylated silica gel or Merrifield resin. In an attempt to reach this goal, structurally related, but much simpler complexes have been prepared and their metal ion-ligand vibrations were determined from their low-frequency IR spectra. The central ions were Mn(II), Co(II), Ni(II) or Cu(II) and the ligands (imidazole, isopropylamine, monosodium malonate) were chosen to possess only one-type of potential donor group. The low-frequency IR spectra were taken of the complexes for each ion-ligand combination and the typical metal ion-functional group vibration bands were selected and identified. The usefulness of the obtained assignments is demonstrated on exemplary immobilised metal ion-protected amino acid complexes.
我们长期研究的目的之一是确定生物模拟金属离子-C 或 N 保护氨基酸(组氨酸、酪氨酸、半胱氨酸或胱氨酸)配合物在氯丙基化硅胶或 Merrifield 树脂表面固定化后的金属离子-配体配位位点。为了达到这个目标,我们制备了结构相关但简单得多的配合物,并从它们的低频红外光谱中确定了它们的金属离子-配体振动。中心离子为 Mn(II)、Co(II)、Ni(II)或 Cu(II),配体(咪唑、异丙胺、丙二酸单钠盐)仅选择具有一种潜在供体基团的配体。为每个离子-配体组合的配合物拍摄了低频红外光谱,并选择和鉴定了典型的金属离子-功能基团振动带。所获得的分配结果在示例固定化金属离子保护氨基酸配合物上得到了验证。