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变温核磁共振光谱法可直接观察羧酸锌配合物中羧酸根的位移。

Variable-temperature nuclear magnetic resonance spectroscopy allows direct observation of carboxylate shift in zinc carboxylate complexes.

作者信息

Demsar Alojz, Kosmrlj Janez, Petricek Sasa

机构信息

Faculty of Chemistry and Chemical Technology, University of Ljubljana, Askerceva 5, SI-1000 Ljubljana, Slovenia.

出版信息

J Am Chem Soc. 2002 Apr 17;124(15):3951-8. doi: 10.1021/ja016534x.

Abstract

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.

摘要

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。

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