ANALYSIS OF SPECIALTIES OF CRYSTAL STRUCTURE FOR NON-­CHELATE CONFORMATIONS OF ETHYLENE-DIAMINETETRAACETIC ACID AND ITS SALTS WITH ALKALI AND ALKALINE EARTH METALS

Daisuke Noguchi
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Abstract

In the present study, the crystal structures of non-chelating EDTA molecules and their non-chelation salts in a zwitterionic state, along with the EDTA-chelates of alkali and alkaline earth metals, were searched and overviewed. 25 non-chelating molecules of EDTA, and zwitterions of ethylenediammonium-diacetate diacetic acid HOOC-CH2-(-OOC-CH2-)NH+-CH2-CH2-NH+(-CH2-COO-)-CH2-COOH and their salts (ethylenediammonium-tetraace­tic acid (HOOC-CH2-)2NH+-CH2-CH2-NH+(-CH2-COOH)2, ethylenediammonium-acetate triacetic acid (HOOC-CH2-)2NH+-CH2-CH2-NH+(-CH2-COO-)-CH2-COOH, and ethylenediammonium-tetraacetate (-OOC-CH2-)2NH+-CH2-CH2-NH+(-CH2-COO-)2 with counterions), as well as 17 types of EDTA-chelates of alkali metal ions (Li+, Na+, K+, Rb+) and alkaline earth metal ions (Mg2+, Ca2+, Sr2+, Ba2+) were analyzed using data from the Cambridge Crystallographic Data Center (CCDC). Each intramolecular contact distance between nitrogen and oxygen atoms (NH+···O) has been examined and found to be around 2.7 Å. Investigation on the distribution of the intramolecular NH+··· NH+-distances of EDTA and non-chelated salts thereof also revealed that bulky counterion and certain crystal solvent molecules correspond to change in crystal packing, and that they influenced the conformers of EDTA mo­lecules among gauche form to anti form. In the existing crystalline EDTA-chelates of alkali metals as well as alkaline earth metals, various coordination numbers (CN) and the denticity (к) of EDTA anions are displayed; CN 5 to 9, and tri- and hexadentate fashions. Intramolecular contact N···O and N···N distances correspond to the metal ion radii except for the case of Sr-EDTA chelate, probably due to differences of crystal packings in addition to the number of counterions and crystal solvent molecules. The existing data on crystalline EDTA and its salts have been gathered herein, which contributes to a further understanding and exploring applications hereafter.
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乙二胺四乙酸及其盐与碱金属和碱土金属非螯合构象的晶体结构特性分析
本研究对两性离子状态下非螯合EDTA分子及其非螯合盐的晶体结构,以及碱金属和碱土金属的EDTA螯合物进行了研究和综述。25 non-chelating分子的EDTA,既ethylenediammonium-diacetate diacetic酸HOOC-CH2——(-OOC-CH2) NH + -CH2-CH2-NH + (-CH2-COO) -CH2-COOH及其盐(ethylenediammonium-tetraace-tic酸(HOOC-CH2) 2 NH + -CH2-CH2-NH + (-CH2-COOH) 2, ethylenediammonium-acetate triacetic酸(HOOC-CH2) 2 NH + -CH2-CH2-NH + (-CH2-COO) -CH2-COOH,和ethylenediammonium-tetraacetate (-OOC-CH2) 2 NH + -CH2-CH2-NH + (-CH2-COO) 2与抗衡离子),以及17种EDTA-chelates碱金属离子(李+,利用剑桥晶体学数据中心(CCDC)的数据分析了Na+, K+, Rb+)和碱土金属离子(Mg2+, Ca2+, Sr2+, Ba2+)。氮和氧原子之间的每个分子内接触距离(NH+···O)已被检查,发现约为2.7 Å。对EDTA及其非螯合盐的分子内NH+···NH+距离分布的研究也表明,大块的反离子和某些晶体溶剂分子对应于晶体填充的变化,它们影响了EDTA分子在间扭式到反式之间的构象。在现有的碱金属和碱土金属的EDTA螯合物晶体中,EDTA阴离子的配位数(CN)和密度(nm)各不相同;cn5至9,以及三齿和六齿的样式。除Sr-EDTA螯合物外,分子内接触N··O和N··N距离对应于金属离子半径,这可能是由于晶体填料的不同以及反离子和晶体溶剂分子的数量不同所致。本文收集了晶体EDTA及其盐的现有数据,有助于进一步认识和探索其应用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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