Palion-Gazda Joanna, Machura Barbara, Kruszynski Rafal, Grancha Thais, Moliner Nicolás, Lloret Francesc, Julve Miguel
Department of Crystallography, Institute of Chemistry, University of Silesia , Ninth Szkolna Street, 40006 Katowice, Poland.
Department of X-ray Crystallography and Crystal Chemistry, Institute of General and Ecological Chemistry, Lodz University of Technology , 116 Żeromski Street, 90-924 Łódź, Poland.
Inorg Chem. 2017 Jun 5;56(11):6281-6296. doi: 10.1021/acs.inorgchem.7b00360. Epub 2017 May 22.
The preparation and spectroscopic and structural characterization of three cobalt(II) complexes of formulas Co(tppz) (1), [Co(tppz)][Co(NCS)]·MeOH (2), and [Co(tppz)][Co(NCO)]·2HO (3) [tppz = 2,3,5,6-tetrakis(2-pyridyl)pyrazine and dca = dicyanamide] are reported here. Compounds 1-3 have in common the presence of the cationic [Co(tppz)] entity where each mer-tridentate tppz ligand coordinates to the cobalt(II) ion equatorially through two pyridyl donors and axially via the pyrazine, completing the six-coordination. The electroneutrality is achieved by the organic dca group (1) and the anionic tetrakis(thiocyanato-κN)cobaltate(II) (2) and tetrakis(cyanato-κN)cobaltate(II) (3) complexes. Direct current (dc) magnetic susceptibility measurements of 1 in the temperature range 1.9-400 K show the occurrence of a thermally induced spin crossover behavior of the [Co(tppz)] unit from a high spin (S = 3/2) at higher temperatures to a low-spin (S = 1/2) at lower temperatures, with the low spin phase being reached at T ≤ 200 K. X-band electron paramagnetic resonance (EPR) measurements in solution at low temperatures were used to characterize the low spin state. An analytical expression based on the combination of the spin-orbit coupling and both first- and second-order Zeeman effects for a d electronic configuration was used to fit the magnetic data of 1, the values of the best-fit parameters being C = 0.1367(9), λ = -168(2) cm, α = 1.12(1), Δ = 1626(15) cm, and g = 2.12(1). The magnetic behavior of the four-coordinate cobalt(II) ions [Co(NCS)] (2) and [Co(NCO)] (3) with a A ground state overlaps with the spin crossover of the [Co(tppz)] entity, the abrupt decrease of the χT product below 15.0 K being due to zero-field splitting effects between the spin components |±1/2> and |±3/2>. The combined analysis of the dc magnetic data and the Q-band EPR spectra in the solid state of 2 and 3 led to the following sets of best-fit parameters: C = 0.105(5), λ = -170(4) cm, α = 1.10(2), Δ = 1700(25) cm, g = 2.10(1), g = 2.27(1), and |D| = 3.80(2) cm (2) and C = 0.100(1), λ = -169(5) cm, α = 1.10(3), Δ = 1500(30) cm, g = 2.10(1), g = 2.28(1), and |D| = 4.30(2) cm (3). Some evidence of slowing of the relaxation of the magnetization has been found in the out-of-phase ac signal at very low temperatures under applied dc fields of 0.1-0.4 T for 3, suggesting the occurrence of single-ion magnet behavior of its [Co(NCO)] anionic entity.
本文报道了三种化学式为Co(tppz) (1)、[Co(tppz)][Co(NCS)]·MeOH (2)和[Co(tppz)][Co(NCO)]·2H₂O (3)的钴(II)配合物的制备及其光谱和结构表征[tppz = 2,3,5,6 - 四(2 - 吡啶基)吡嗪,dca = 二氰胺]。化合物1 - 3的共同之处在于存在阳离子[Co(tppz)]实体,其中每个面式三齿tppz配体通过两个吡啶供体与钴(II)离子赤道配位,并通过吡嗪轴向配位,形成六配位。通过有机dca基团(1)以及阴离子四(硫氰酸根 - κN)钴酸(II) (2)和四(氰酸根 - κN)钴酸(II) (3)配合物实现电中性。在1.9 - 400 K温度范围内对1进行的直流磁化率测量表明,[Co(tppz)]单元发生了热诱导自旋交叉行为,从较高温度下的高自旋(S = 3/2)转变为较低温度下的低自旋(S = 1/2),在T ≤ 200 K时达到低自旋相。低温下在溶液中进行的X波段电子顺磁共振(EPR)测量用于表征低自旋态。基于自旋轨道耦合以及d电子构型的一阶和二阶塞曼效应的组合的解析表达式用于拟合1的磁性数据,最佳拟合参数值为C = 0.1367(9),λ = -168(2) cm⁻¹,α = 1.12(1),Δ = 1626(15) cm⁻¹,g = 2.12(1)。具有A基态的四配位钴(II)离子[Co(NCS)] (2)和[Co(NCO)] (3)的磁性行为与[Co(tppz)]实体的自旋交叉重叠,χT乘积在15.0 K以下的突然下降是由于自旋分量|±1/2>和|±3/2>之间的零场分裂效应。对2和3的固态直流磁性数据和Q波段EPR光谱的联合分析得出以下最佳拟合参数集:C = 0.105(5),λ = -170(4) cm⁻¹,α = 1.10(2),Δ = 1700(25) cm⁻¹,g₁ = 2.10(1),g₂ = 2.27(1),|D| = 3.80(2) cm⁻¹ (2)以及C = 0.100(1),λ = -169(5) cm⁻¹,α = 1.10(3),Δ = 1500(30) cm⁻¹,g₁ = 2.10(1),g₂ = 2.28(1),|D| = 4.30(2) cm⁻¹ (3)。在0.1 - 0.4 T的外加直流场下,在非常低的温度下对3的异相交流信号中发现了一些磁化弛豫减慢的证据,表明其[Co(NCO)]阴离子实体存在单离子磁体行为。