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首页> 外文期刊>International Journal of Quantum Chemistry >Hybrid Density Functional Study of Ligand Coordination Effects on the Magnetic Couplings and the Dioxygen Binding of the Models of Hemocyanin
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Hybrid Density Functional Study of Ligand Coordination Effects on the Magnetic Couplings and the Dioxygen Binding of the Models of Hemocyanin

机译:配体配位效应对血蓝蛋白模型的磁耦合和双氧结合的混合密度泛函研究

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Ligand coordination effects on the magnetic interaction and the reversible dioxygen binding process for the models of hemocyanin have been investigated with hybrid density functional theory.Hemocyanin is an oxygen transport protein found in mollusks and arthropods.The active site of hemocyanin contains a pair of copper atoms,each of which is coordinated by three histidine residues.We utilized NH3(a),methylimidazole(b),and histidine(c)as the ligands of the models of hemocyanin,which coordinate to the binuclear copper core in the active site of oxygenated(1z)(z=a-c)and deoxygenated hemocyanin(2z).The difference of the ligand coordination in the magnetic couplings for the model of hemocyanin 1z complexed with peroxide(1z-O_2~(2-))shows that the substitution from histidine to methylimidazole group is not serious,but that the substitution from imidazole to NH3 is influential.In the dioxygen binding process,the ligands influence the binding energy and the shapes of potential energy surfaces of the models of hemocyanin 1z and 2z with dioxygen due to the strength of the mixing between the ground state and the charge transfer one.The active d_(xy)±d_(xy)orbitals of the copper core of 1b and 1c strongly interact with pi*_h and pi*_V orbitals of the dioxygen than those of 1a,leading to the larger binding energy of the model 1b(1c)with dioxygen.The orbital energies of the active orbitals for the synthetic model,[Cu(HB(3,5-iPr2-Pz)3)]2(HB(3,5-iPr2-Pz)3=hydrotris{3,5-diisopropyl-pyrazolyl}borate),imply that it irreversibly binds dioxygen because HB(3 5-iPr2-Pz)3 groups show stronger electron-release character and raise the orbital energies nearer that to pi* orbitals of O2.The effective bond-order,localized electron density,and information entropy for 1z with dioxygen were calculated in terms of occupation numbers of the natural orbitals of the broken-symmetry UB2LYP solution in order to elucidate the nature of the Cu2O2 bonding.These chemical indices indicate that the copper-oxygen bonds in He exhibit an intermediate covalent-bonding character(half bonding),which is the origin of an active control of oxygen transport:addition and dissociation of O2 in hemocyanin by the conformational changes.
机译:利用杂化密度泛函理论研究了配体配位对血蓝蛋白模型的电磁相互作用和可逆双氧结合过程的影响。血蓝蛋白是一种在软体动物和节肢动物中发现的氧转运蛋白。血蓝蛋白的活性位点包含一对铜原子,每个氨基酸都由三个组氨酸残基协调。我们使用NH3(a),甲基咪唑(b)和组氨酸(c)作为血蓝蛋白模型的配体,它们与含氧活性位点的双核铜核协调(1z)(z = ac)和脱氧的血蓝蛋白(2z)。血红蛋白1z与过氧化物(1z-O_2〜(2-))络合的模型在磁耦合中配体配位的差异表明,组氨酸被取代甲基咪唑基团并不严重,但是从咪唑到NH3的取代是有影响的。在双氧键合过程中,配体影响键合能和势能表面的形状由于基态和电荷转移之一之间的混合强度,血红素1z和2z具有双氧的模型的建立。1b和1c的铜芯的活动d_(xy)±d_(xy)轨道与pi * _h和pi * _V的双氧轨道比1a的轨道大,导致模型1b(1c)与双氧的结合能更大。合成模型的活动轨道的轨道能量[Cu(HB(3 ,5-iPr2-Pz)3)] 2(HB(3,5-iPr2-Pz)3 = hydrotris {3,5-diisopropyl-pyrazolyl} borate),暗示它不可逆地结合了双氧,因为HB(3 5-iPr2 -Pz)3基团显示出更强的电子释放特性,并将轨道能量提高到更接近O2的pi *轨道。根据氧的职业数计算了1z的有效键序,局部电子密度和信息熵。为了阐明Cu2O2键的性质,采用了对称的UB2LYP溶液的自然轨道,这些化学指标表明铜-氧He中的gen键表现出中间的共价键结合特性(半键结合),这是氧控制活性的起源:通过构象变化,血红素中O2的添加和解离。

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