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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Synthesis of a large amino-phenolic cage. Synthesis, crystal structures, and acid-base and coordination behavior toward cations and anions
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Synthesis of a large amino-phenolic cage. Synthesis, crystal structures, and acid-base and coordination behavior toward cations and anions

机译:合成了一个大的氨基酚笼。合成,晶体结构,酸碱和对阳离子和阴离子的配位行为

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The synthesis and characterization of the new polyaza-phenolic-macrobicycle 32-hydroxy-1,4,7,10,13,16,19,22-octaazatricyclo-[11.11.7.1(26,30)]-diatriconta-26,28,Delta(30,32)-triene (L) are reported. L incorporates a 2,6-dimethyl-phenolic unit bridging two opposite amine functions of the [24]aneN(8) polyazamacrocyclic base to obtain a large cage. The basicity and binding properties of L toward Cu(II), Zn(II), and Cl- were determined by means of potentiometric measurements in aqueous solution (298.1 +/- 0.1 K, /= 0.15 mol dm(-3)). L can add up to six acidic protons, yielding the H5L5+ species or the H6L6+ species, depending on the ionic medium used. The molecular topology of L permits the formation of a highly positive three-dimensional cavity in the polyprotonated species that is able to host the chloride anion. This was detected both using potentiometric data, log K = 41.33 for the reaction L + 6H(+) + Cl- = H6LCl5+, and in Cl-35 NMR experiments that showed interactions also with the H5L5+ and H4L4+ species. The anion is probably hosted inside the three-dimensional cavity of L, and stabilized by H-bonding interactions with the ammonium groups, as depicted in the crystal structure of the H6L6+ cation reported. L forms mono- and dinuclear complexes with all the metal ions investigated; the dinuclear species are the only existing species with an L:M(II) molar ratio of 1:2 at pH higher than 6. The phenolate oxygen atom coordinates the two metal ions in a bridged disposition, drawing them inside the macrobicyclic cavity. The two metals were found to be quite isolated by the medium, and were coordinated by all the amine groups of L, as shown by the crystal structure of the dinuclear [Zn2H-1L](3+) species. This species can bind guests such as hydroxide and phosphate anions. Studies of anion binding in aqueous solution using pyrochatecol violet as the sensing guest revealed that the [Zn2H-1L](3+) species is able to bind one phosphate at physiological pH.
机译:新型聚氮杂-酚-大环32-羟基-1,4,7,10,13,16,19,22-八氮杂三环-[11.11.7.1(26,30)]-diatriconta-26,28的合成与表征报道了δ(30,32)-三烯(L)。 L结合了一个2,6-二甲基苯酚单元,桥接[24] aneN(8)聚氮杂大环碱的两个相对的胺官能团,以得到一个大的笼子。 L在水溶液(298.1 +/- 0.1 K,/ = 0.15 mol dm(-3))中的电位测定法确定了L对Cu(II),Zn(II)和Cl-的碱性和结合特性。 L最多可以添加六个酸性质子,产生H5L5 +物种或H6L6 +物种,具体取决于所使用的离子介质。 L的分子拓扑结构允许在多质子化的物种中形成一个高度正向的三维空穴,该空穴能够携带氯离子。使用电位计数据检测到这一点,对于反应L + 6H(+)+ Cl- = H6LCl5 +,log K = 41.33,在Cl-35 NMR实验中也显示了与H5L5 +和H4L4 +种类的相互作用。如所报道的H6L6 +阳离子的晶体结构所示,阴离子可能位于L的三维腔内,并通过与铵基团的H键相互作用而稳定。 L与所研究的所有金属离子形成单核和双核配合物;双核物质是仅有的在pH高于6时L:M(II)摩尔比为1:2的物质。酚盐氧原子以桥联方式配位两个金属离子,将它们吸入大双环腔内。发现这两种金属被介质完全隔离,并与L的所有胺基配位,如双核[Zn2H-1L](3+)物种的晶体结构所示。这种物质可以结合客体,例如氢氧根和磷酸根阴离子。使用邻苯二酚紫作为传感客体的水溶液中阴离子结合的研究表明,[Zn2H-1L](3+)物种能够在生理pH下结合一种磷酸盐。

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