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高pH值下生物重要α-氨基酸与钙(II)的配位作用:α-氨基羧酸盐钙晶体结构的见解

Coordination of biologically important alpha-amino acids to calcium(II) at high pH: insights from crystal structures of calcium alpha-aminocarboxylates.

作者信息

Fox Stefan, Büsching Insa, Barklage Walter, Strasdeit Henry

机构信息

Department of Bioinorganic Chemistry, Institute of Chemistry, University of Hohenheim, Garbenstrasse 30, D-70599 Stuttgart, Germany.

出版信息

Inorg Chem. 2007 Feb 5;46(3):818-24. doi: 10.1021/ic061838b.

Abstract

A series of calcium alpha-aminocarboxylates was prepared by refluxing aqueous solutions/suspensions of calcium hydroxide and the respective alpha-amino acid. The colorless, crystalline hydrates Ca(gly)2.H2O (1), Ca(ala)2.3H2O (2), Ca(val)2.H2O (3), Ca(leu)2.3H2O (4), Ca(met)2.nH2O (5, n approximately 2), and Ca(pro)2.H2O (6) have been isolated in yields between 29 and 67% (gly- = glycinate, ala- = rac-alaninate, val- = rac-valinate, leu- = rac-leucinate, met- = rac-methioninate, pro- = rac-prolinate). The compounds 1-6 are readily soluble in water. The 0.10 M solutions have ca. pH 10-11 which is consistent with a noticeable degree of dissociation. The 13C NMR spectra of 1-6 in D2O were measured, and their comparison with those of the corresponding tetramethylammonium alpha-aminocarboxylates point to carboxylate coordination in solution, but no indication of nitrogen coordination was found. Infrared spectra of 1-6 gave similar results for the solid state. Complete single-crystal X-ray structure analyses of 1-4 and preliminary ones of 5 and 6, however, revealed that all aminocarboxylate ligands are N,O-chelating. Crystals of 2 consist of mononuclear complexes, while the other five compounds form three different types of one-dimensional coordination polymers. Structural diversity is also observed with the binding modes of the aminocarboxylate ligands and the calcium environment. Besides terminal aminocarboxylate coordination, there are three different types of aminocarboxylate bridges. The calcium ions are seven- or eight-coordinate in N2O5 and N2O6 coordination environments, respectively; one or three water molecules are part of the first ligand sphere of each metal ion. The crystal structures support conjectures about the existence of the yet undetected solution species [Cax(aa)2x(H2O)n] (aa- = alpha-aminocarboxylate). For example, x = 1 is realized in crystalline [Ca(ala)2(H2O)3] (2), and in 4 [Ca2(leu)4(H2O)4] complexes (x = 2) are linked to infinite chains by bridging aqua ligands.

摘要

通过使氢氧化钙与相应的α-氨基酸的水溶液/悬浮液回流,制备了一系列α-氨基羧酸钙。已分离出无色结晶水合物Ca(gly)₂·H₂O (1)、Ca(ala)₂·3H₂O (2)、Ca(val)₂·H₂O (3)、Ca(leu)₂·3H₂O (4)、Ca(met)₂·nH₂O (5, n约为2) 和Ca(pro)₂·H₂O (6),产率在29%至67%之间(gly⁻ = 甘氨酸根,ala⁻ = 外消旋丙氨酸根,val⁻ = 外消旋缬氨酸根,leu⁻ = 外消旋亮氨酸根,met⁻ = 外消旋蛋氨酸根,pro⁻ = 外消旋脯氨酸根)。化合物1 - 6易溶于水。0.10 M的溶液pH约为10 - 11,这与明显的解离程度一致。测量了1 - 6在D₂O中的¹³C NMR光谱,并将其与相应的四甲基铵α-氨基羧酸盐的光谱进行比较,结果表明溶液中存在羧酸根配位,但未发现氮配位的迹象。1 - 6的红外光谱在固态下给出了类似的结果。然而,对1 - 4进行了完整的单晶X射线结构分析,对5和6进行了初步分析,结果表明所有氨基羧酸配体均为N,O-螯合。2的晶体由单核配合物组成,而其他五种化合物形成三种不同类型的一维配位聚合物。在氨基羧酸配体的结合模式和钙环境中也观察到了结构多样性。除了末端氨基羧酸配位外,还有三种不同类型的氨基羧酸桥。钙离子在N₂O₅和N₂O₆配位环境中分别为七配位或八配位;每个金属离子的第一配体球中含有一个或三个水分子。晶体结构支持了关于尚未检测到的溶液物种[Cax(aa)₂x(H₂O)n](aa⁻ = α-氨基羧酸盐)存在的推测。例如,在晶体[Ca(ala)₂(H₂O)₃] (2) 中实现了x = 1,在4中,[Ca₂(leu)₄(H₂O)₄] 配合物(x = 2)通过桥连水配体连接成无限链。

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