Spin-orbit coupling and zero-field splitting of the high-spin ferric enzyme-substrate complex: Protocatechuate 3,4-dioxygenase complexed with 3,4-dihydroxyphenylacetate
Year: 2012
Type: article
Abstract: We used density functional calculations to investigate the electronic origins of the magnetic properties of the high-spin ferric enzyme-substrate complex protocatechuate 3,4-dioxygenase (3,4-PCD). The calculated g-tensors show that ligand-to-metal charge transfer transitions are from the protocatechuate (PCA) and Tyr408 orbitals to the Fe dπ orbitals, which lead to x- and y-polarized transitions. These polarized transitions require a spin-orbit coupling (SOC) matrix element in the z-direction, L z (z = z′), resulting in a g z′ value of 2.0158, significantly deviating from 2.0023. A large zero-field splitting parameter value of +1.147 cm−1 is due to ΔS = −1 spin-orbit mixing with the quartet states for the sextet ground state, accounting for around 73% of the SOC contribution. The SOC matrix elements indicate that the high-spin d5 system Fe(III), 3,4-PCD-PCA is a weak spin-crossover compound with an SOC of 31.56 cm−1.
Source: Chinese Science Bulletin
Authors: LingLing Lü, YuanCheng Zhu, XiaoFang Wang, GuoFang Zuo, Feng Guo, SuRui Zhao, YongCheng Wang
Institutions: Tianshui Normal University, Northwest Normal University
Language: English
Subfield: Inorganic Chemistry
Field: Chemistry
Domain: Physical Sciences
Open Access status: hybrid
OpenAlex ID: W2051845003