Corsi Daniele M., Murthy Narasimha N., Young Victor G., Karlin aK and Kenneth D.
The Department of Chemistry, The Johns Hopkins University, Charles and 34th Streets, Baltimore, Maryland 21218, and The X-ray Crystallographic Laboratory, Department of Chemistry, The University of Minnesota, 207 Pleasant St. S.E., Minneapolis, Minnesota 55455.
Inorg Chem. 1999 Mar 8;38(5):848-858. doi: 10.1021/ic981091s.
A range of small molecules, such as cyanide, are known to bind and/or inhibit the active site of the heme-copper oxidase enzymes. As such, model studies are aimed at elucidating ligand binding modes and their subsequent impact on spectroscopic properties of derived complexes. We describe here the isolation and characterization of two compounds containing the Fe-CN-Cu moiety, (py)(F(8)-TPP)Fe(III)-CN-Cu(II)(TMPA) (5) and (F(8)-TPP)Fe(III)-(CN)(2)-{Cu(II)(TMPA)}(2) (6) [py = pyridine, TMPA = tris(2-pyridylmethyl)amine, and (F(8)-TPP) = tetrakis(2,6-difluorophenyl)porphyrinate(2-)]. Cu(II)(TMPA)(CH(3)CN)(2) and [(py)(F(8)-TPP)Fe(III)(CN)] (3) react to yield 5, while 6 is formed by combination of [Cu(II)(TMPA)(CN)]PF(6) (2-(PF(6))) and [(F(8)-TPP)Fe(III)(PF(6))] (4). Complex 2-(PF(6)) crystallizes in the orthorhombic space group Iba2 with a = 17.2269(5) Å, b = 17.3143(4) Å, and c = 14.4971(4) Å, Z = 8, complex (5-(Sb/P)F(6))(1.5)(ClO(4))(0.5) was obtained in the orthorhombic space group P222 with a = 17.9541(2) Å, b = 20.5359(1) Å, and c = 21.2023(2) Å, Z = 4, and 6-(PF(6))(3) crystallized in the monoclinic space group P2(1)/c with a = 15.318(4) Å, b = 33.921(2) Å, and c = 19.649(6) Å, beta = 109.69(2) degrees, and Z = 4. Compound 5 possesses a low-spin iron(III) center, bridged via cyanide to copper. The iron-cyanide vector deviates slightly from linearity (174.6(5) degrees ). The copper(II) ion is five-coordinated by the TMPA N-donor atoms and the cyanide carbon atom. The Cu(TMPA) moiety is bent with an angle of 163.8(5) degrees around the cyanide-copper vector. Compound 6 possesses a low-spin iron(III) atom axially coordinated by two cyanide ligands capped on either side by trigonally coordinated [Cu(TMPA)] moieties. The [Cu(1)(TMPA)] unit is twisted somewhat ( angleCu1-N&tbd1;C = 168 degrees ), whereas the [Cu(2)(TMPA)] unit is coordinated in a nearly linear fashion with respect to the cyanide-iron vector ( angleCu2-N&tbd1;C4 = 175 degrees ). (1)H and (2)H NMR spectroscopy on 5 and 6 confirmed the low-spin nature of these iron complexes (pyrrole resonance found at -11.1 and -8 ppm, respectively). The NMR data as well as observed solution magnetic moment (&mgr;(B) = 2.7 for 5; &mgr;(B) = 3.4 for 6) suggest ferromagnetic coupling between the paramagnetic metal ions. This gives rise to an enhancement of the electronic relaxation rate for Cu(II) in both 5 and 6 allowing for the observation of the sharp and downfield shifted TMPA ligand proton signals.
已知一系列小分子,如氰化物,可结合和/或抑制血红素 - 铜氧化酶的活性位点。因此,模型研究旨在阐明配体结合模式及其对衍生配合物光谱性质的后续影响。我们在此描述了两种含Fe - CN - Cu部分的化合物的分离和表征,即(py)(F(8)-TPP)Fe(III)-CN-Cu(II)(TMPA) (5) 和(F(8)-TPP)Fe(III)-(CN)(2)-{Cu(II)(TMPA)}(2) (6) [py = 吡啶,TMPA = 三(2 - 吡啶甲基)胺,(F(8)-TPP) = 四(2,6 - 二氟苯基)卟啉(二价阴离子)]。Cu(II)(TMPA)(CH(3)CN)(2) 和[(py)(F(8)-TPP)Fe(III)(CN)] (3) 反应生成5,而6由[Cu(II)(TMPA)(CN)]PF(6) (2-(PF(6))) 和[(F(8)-TPP)Fe(III)(PF(6))] (4) 反应生成。配合物2-(PF(6)) 结晶于正交晶系空间群Iba2,a = 17.2269(5) Å,b = 17.3143(4) Å,c = 14.4971(4) Å,Z = 8;配合物(5-(Sb/P)F(6))(1.5)(ClO(4))(0.5) 获得于正交晶系空间群P222,a = 17.9541(2) Å,b = 20.5359(1) Å,c = 21.2023(2) Å,Z = 4;6-(PF(6))(3) 结晶于单斜晶系空间群P2(1)/c,a = 15.318(4) Å,b = 33.921(2) Å,c = 19.649(6) Å,β = 109.69(2)°,Z = 4。化合物5具有一个低自旋铁(III) 中心,通过氰化物桥连到铜。铁 - 氰化物向量略微偏离线性(174.6(5)°)。铜(II) 离子由TMPA的N供体原子和氰化物碳原子五配位。Cu(TMPA) 部分围绕氰化物 - 铜向量弯曲,角度为163.8(5)°。化合物6具有一个低自旋铁(III) 原子,由两个氰化物配体轴向配位,两侧由三角配位的[Cu(TMPA)] 部分封端。[Cu(1)(TMPA)] 单元略有扭曲(∠Cu1 - N&C = 168°),而[Cu(2)(TMPA)] 单元相对于氰化物 - 铁向量以近乎线性的方式配位(∠Cu2 - N&C4 = 175°)。对5和6的(1)H和(2)H NMR光谱证实了这些铁配合物的低自旋性质(吡咯共振分别出现在 - 11.1和 - 8 ppm处)。NMR数据以及观察到的溶液磁矩(5的μ(B) = 2.7;6的μ(B) = 3.4) 表明顺磁性金属离子之间存在铁磁耦合。这导致5和6中Cu(II) 的电子弛豫速率增强,从而可以观察到尖锐且向低场移动的TMPA配体质子信号。