Demsar Alojz, Kosmrlj Janez, Petricek Sasa
Faculty of Chemistry and Chemical Technology, University of Ljubljana, Askerceva 5, SI-1000 Ljubljana, Slovenia.
J Am Chem Soc. 2002 Apr 17;124(15):3951-8. doi: 10.1021/ja016534x.
Tetranuclear complexes [Zn(4)(bdmap)(2)(OOCR)(6)] 1 (R = Me) and 2 (R = Et), where Hbdmap = 1,3-bis(dimethylamino)-2-propanol, were prepared from zinc carboxylates and Hbdmap in tetrahydrofuran (THF). The solid-state structures of isomers 1a and 2a consist of two pairs of zinc atoms, each bridged by two mu-1,2 and one mu-1,1 carboxylate ligands. Two pairs are connected by two tridentate bdmap ligands with oxygen acting as a bridging donating atom. The complexes retain the tetranuclear structure in solution and two dynamic processes are observed from variable-temperature (1)H and (13)C NMR spectra. A low-temperature process (LT dynamics) observed already below 200 K is a coalescence of the mu-1,2 and the mu-1,1 resonances to a single resonance. An additional dynamic process (HT dynamics) is observed above 247 K (1) and 263 K (2), leading to a coalescence of two dimethylamino resonances. Both dynamic processes are rationalized by a mechanism involving changes in the carboxylate coordination mode termed as carboxylate shift. The LT dynamics is ascribed to interconversions of a single mu-1,2 and a single mu-1,1 carboxylate ligation by rotations of 60 degrees. The interconversions involve all carboxylate ligands in 1 and 2. The HT dynamics is ascribed to the exchange of the coordinating geometries of two carboxylate-bridged zinc atoms. We propose a mechanism that starts with a cleavage of the Zn-N coordination bond. The resulting coordinatively unsaturated zinc atom acquires an additional oxygen donor atom by carboxylate shift of mu-1,2 carboxylate to mu-1,1 mode. The activation parameters (DeltaH values in kilocalories per mole, DeltaS values in calories per mole per kelvin) were determined by line-shape analysis of VT NMR spectra: for 1 in THF-d(8), DeltaH(LT) = 8.1(3), DeltaS(LT) = -12(2), DeltaH(HT) = 17.9(2), DeltaS(HT) = 14(1); for 1 in CDCl(3), DeltaH(HT) = 13.6(5), DeltaS(HT) = 3(3); for 1 in CD(2)Cl(2), DeltaH(HT) = 9.9(3), DeltaS(HT) = -8(2); for 2 in THF-d(8), DeltaH(LT) = 11(1), DeltaS(LT) = -5(3), DeltaH(HT) = 19.6(5), DeltaS(HT) = 18(3). Polymeric Zn(4)(bdmap)(2)(OOCMe)(6) 1-catena crystallizes from a dichloromethane solution of 1. In 1-catena, the zinc atoms are linked into a chain through mu-1,2 and mu-1,1 acetate alternated by mu-1,2 acetate and bdmap.
四核配合物[Zn₄(bdmap)₂(OOCR)₆] 1(R = 甲基)和2(R = 乙基),其中Hbdmap = 1,3 - 双(二甲氨基)-2 - 丙醇,由羧酸锌和Hbdmap在四氢呋喃(THF)中制备而成。异构体1a和2a的固态结构由两对锌原子组成,每对锌原子由两个μ - 1,2和一个μ - 1,1羧酸酯配体桥连。两对锌原子通过两个三齿bdmap配体相连,氧作为桥连供体原子。这些配合物在溶液中保持四核结构,并且从变温¹H和¹³C NMR光谱中观察到两个动态过程。在200 K以下观察到的低温过程(LT动力学)是μ - 1,2和μ - 1,1共振合并为一个单一共振。在247 K(1)和263 K(2)以上观察到另一个动态过程(HT动力学),导致两个二甲氨基共振合并。这两个动态过程都通过一种涉及羧酸酯配位模式变化(称为羧酸酯迁移)的机制得到合理解释。LT动力学归因于单个μ - 1,2和单个μ - 1,1羧酸酯配位通过60度旋转的相互转化。这种相互转化涉及1和2中的所有羧酸酯配体。HT动力学归因于两个羧酸酯桥连锌原子配位几何结构的交换。我们提出一种机制,该机制始于Zn - N配位键的断裂。产生的配位不饱和锌原子通过μ - 1,2羧酸酯向μ - 1,1模式的羧酸酯迁移获得一个额外的氧供体原子。通过VT NMR光谱的线形分析确定了活化参数(以千卡每摩尔为单位的ΔH值,以卡每摩尔每开尔文为单位的ΔS值):对于在THF - d₈中的1,ΔH(LT) = 8.1(3),ΔS(LT) = -12(2),ΔH(HT) = 17.9(2),ΔS(HT) = 14(1);对于在CDCl₃中的1,ΔH(HT) = 13.6(5),ΔS(HT) = 3(3);对于在CD₂Cl₂中的1,ΔH(HT) = 9.9(3),ΔS(HT) = -8(2);对于在THF - d₈中的2,ΔH(LT) = 11(1),ΔS(LT) = -5(3),ΔH(HT) = 19.6(5),ΔS(HT) = 18(3)。聚合物[Zn₄(bdmap)₂(OOCMe)₆]ₙ 1 - catena从1的二氯甲烷溶液中结晶。在1 - catena中,锌原子通过μ - 1,2和μ - 1,1乙酸酯以及μ - 1,2乙酸酯和bdmap交替连接成链。