Busse Susanne, Elias Horst, Fischer Jürgen, Poggemann Markus, Wannowius Klaus J., Boca Roman
Faculty of Chemical Technology, Slovak Technical University, SK-812 37 Bratislava, Slovakia.
Inorg Chem. 1998 Aug 10;37(16):3999-4005. doi: 10.1021/ic9716262.
Visible spectrophotometry was used to study the kinetics of metal substitution in the system Cu(amben)/Ni(DMF)(6)(ClO(4))(2)/R(4)NX in DMF at 298 K and I = 0.2 M (Bu(4)NPF(6)) (H(2)amben = N,N'-ethylenebis(2-aminobenzaldimine); X = Br(-)(), SCN(-), Cl(-); DMF = N,N-dimethylformamide). The rate of nickel for copper substitution is markedly affected by the nature of the anion X, the order of reactivity being ClO(4)- < Br(-) < SCN(-) << Cl(-). For X = Cl(-) and under excess conditions [(Cu(amben)] << [Ni(DMF)(6)(ClO(4))(2)], [BzEt(3)NCl]), the overall process is triphasic and multiwavelength analysis in the range 350-900 nm yields the experimental rate constants k(obsd)(1), k(obsd)(2), and k(obsd)(3). Rate constant k(obsd)(1) is nickel and chloride dependent, whereas k(obsd)(2) and k(obsd)(3) are not. For the rate of disappearance of Cu(amben), v = -d[Cu(amben)]/dt, it is found that v ~ Cl(2) at Ni(DMF)(6)(ClO(4))(2) = constant and v ~ Ni(3) at [nickel]:[chloride] = 1:2 (Cl and Ni refer to the total concentration of chloride and nickel, respectively). These dependencies suggest a second-order rate law, v = k(1)[Cu(amben)]["NiCl(2)"], for the first step, with k(1) = 64 +/- 8 M(-)(1) s(-)(1) at 298 K. In view of the ligand properties of Cu(amben) it is concluded that the species "NiCl(2)" is tetrahedral Ni(DMF)(2)Cl(2) which reacts with Cu(amben) as ligand to form a binuclear adduct in the first step. It is suggested that the observed rate effects of the anions X are linked with their ability to favor the formation of nickel species with reduced coordination number, such as four-coordinate Ni(DMF)(2)X(2). The mechanism of the overall process of nickel for copper substitution in Cu(amben) is discussed. The results of the analysis of the visible spectra of Cu(amben) and Ni(amben) and of MO calculations on the charge distribution in these complexes are reported.
采用可见分光光度法研究了在298K、离子强度I = 0.2M(四丁基六氟磷酸铵)的N,N - 二甲基甲酰胺(DMF)体系中,Cu(amben)/Ni(DMF)₆(ClO₄)₂/R₄NX (H₂amben = N,N'-亚乙基双(2 - 氨基苯甲酰亚胺);X = Br⁻、SCN⁻、Cl⁻;DMF = N,N - 二甲基甲酰胺)中金属取代反应的动力学。镍取代铜的速率受阴离子X性质的显著影响,反应活性顺序为ClO₄⁻ < Br⁻ < SCN⁻ << Cl⁻。对于X = Cl⁻且在过量条件下[(Cu(amben)] << [Ni(DMF)₆(ClO₄)₂],[BzEt₃NCl]时,整个过程为三相,在350 - 900nm范围内的多波长分析得到实验速率常数k(obsd)₁、k(obsd)₂和k(obsd)₃。速率常数k(obsd)₁与镍和氯离子有关,而k(obsd)₂和k(obsd)₃无关。对于Cu(amben)的消失速率v = -d[Cu(amben)]/dt,发现在[Ni(DMF)₆(ClO₄)₂]₀ = 常数时v ~ [Cl]ₜₒₜ²,在[镍]:[氯离子] = 1:2([Cl]ₜₒₜ和[Ni]ₜₒₜ分别指氯离子和镍的总浓度)时v ~ [Ni]ₜₒₜ³。这些相关性表明第一步的速率定律为二级反应,v = k₁[Cu(amben)]["NiCl₂"],在298K时k₁ = 64 ± 8 M⁻¹ s⁻¹。鉴于Cu(amben)的配体性质,得出“NiCl₂”物种为四面体Ni(DMF)₂Cl₂,它在第一步中作为配体与Cu(amben)反应形成双核加合物。有人认为观察到的阴离子X的速率效应与其促进形成低配位数镍物种(如四配位Ni(DMF)₂X₂)的能力有关。讨论了Cu(amben)中镍取代铜的整个过程的机理。报告了Cu(amben)和Ni(amben)可见光谱分析结果以及这些配合物中电荷分布的分子轨道计算结果。