卟啉嗪
化学
镍
卟啉
配体(生物化学)
金属
X射线光电子能谱
密度泛函理论
四吡咯
结晶学
结合能
光化学
计算化学
原子物理学
核磁共振
有机化学
受体
酶
物理
生物化学
作者
Maria Rachele Guascito,Giampaolo Ricciardi,Angela Rosa
标识
DOI:10.1142/s1088424617500328
摘要
An electronic structure analysis of two nickel(II) tetrapyrrole complexes bearing β-alkylthio substituents, NiOMTP and NiOETPz, has been carried out through a combination of high-resolution XPS experiments and DFT calculations. The Ni 2p XPS spectra show a 0.5 eV shift to higher energy of the Ni 2p[Formula: see text] and Ni 2p[Formula: see text] binding energies on going from the porphyrin to the porphyrazine complex. This shift, which is well-reproduced by relativistic spin-orbit ZORA calculations, is indicative of a depletion of electron density on the central metal. Such a depletion of electron density is related to the macrocycle-induced changes in the metal-ligand interactions. In the porphyrazine complex both the ligand to metal [Formula: see text] donation and the metal to ligand [Formula: see text]-back donation increase. The latter increases slightly more than the former, however, leading to a decrease of electron density on the central metal.
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