Lopera Alberto, Gil-Martínez Ariadna, Pitarch-Jarque Javier, Verdejo Begoña, Blasco Salvador, Clares M Paz, Jiménez Hermas R, García-España Enrique
Instituto de Ciencia Molecular, Universidad de Valencia, c/Catedrático José Beltrán Martínez 2, 46980 Paterna, Valencia, Spain.
Dalton Trans. 2020 Jul 7;49(25):8614-8624. doi: 10.1039/d0dt01056a. Epub 2020 Jun 16.
Three new [1 + 1] macrocycles formed by the reaction of 1H-3,5-bis(chloromethyl)pyrazole with the tosylated amines 1,4,7,10-tetraazadecane (L1), 1,4,8,11-tetraazaundecane (L2) and 1,5,10,14-tetraazatetradecane (L3) are described. Potentiometric studies and HR-ESI-Mass spectrometry show the formation of dimeric binuclear Cu complexes whose organization depends on the type of hydrocarbon chains connecting the amine groups. Furthermore, trinuclear or/and tetranuclear complexes are formed depending also on the length of the polyaminic bridge and on the sequence of the hydrocarbon chains. The crystal structures of the [2 + 2] Cu(H(HL2))·4HO (1) and Cu(HL2) (2) complexes show in both of them two macrocycles self-assembled by the metal ions which interconnect their pyrazolate fragments that behave as bis(monodentate) ligands. While in 1 one central amine of each macrocycle binds to the axial position of a distorted square-pyramid and the other ones remain protonated, in 2 all the amine groups are involved in the coordination giving rise to a strongly distorted octahedral geometry. Paramagnetic H NMR measurements support that these structures also form in solution. Interestingly, tetranuclear complexes Cu(HL4)(OH)BrCl (3) and PdCu(HL4)(OH)ClBr·2.87HO (4) have been isolated for the macrocycle containing the 1,5,9,13-tetraamine chain (L4). 3 has two binucleating units, one of them formed by the pyrazolate moieties and their neighbouring secondary amines and the other by the two central amines of both macrocycles. This latter Cu coordination site is completed by two hydroxide anions as bridging ligands. 4 was obtained from a solution prepared to achieve full formation of the dimeric cage [Cu(H(HL4))] by addition of KPdCl. The Pd ion due to its softer acidic characteristics displaces the Cu ions from the pyrazolate site. UV-vis spectroscopy suggests that the exchange is completed at room temperature after one hour.
描述了由1H-3,5-双(氯甲基)吡唑与对甲苯磺酰化胺1,4,7,10-四氮杂癸烷(L1)、1,4,8,11-四氮杂十一烷(L2)和1,5,10,14-四氮杂十四烷(L3)反应形成的三种新型[1 + 1]大环化合物。电位滴定研究和高分辨电喷雾电离质谱表明形成了二聚双核铜配合物,其结构取决于连接胺基的烃链类型。此外,三核或/和四核配合物的形成还取决于多胺桥的长度和烃链的序列。[2 + 2]Cu(H(HL2))·4H₂O(1)和Cu(HL2)(2)配合物的晶体结构表明,在这两种配合物中,两个大环由金属离子自组装而成,金属离子将吡唑盐片段相互连接,这些吡唑盐片段表现为双(单齿)配体。在1中,每个大环的一个中心胺与一个扭曲的四方锥的轴向位置配位,而其他胺保持质子化;在2中,所有胺基都参与配位,形成严重扭曲的八面体几何结构。顺磁¹H NMR测量结果支持这些结构在溶液中也能形成。有趣的是,对于含有1,5,9,13-四胺链(L4)的大环化合物,分离得到了四核配合物Cu(HL4)(OH)BrCl(3)和PdCu(HL4)(OH)ClBr·2.87H₂O(4)。3有两个双核单元,其中一个由吡唑盐部分及其相邻的仲胺形成,另一个由两个大环的两个中心胺形成。后一个铜配位位点由两个氢氧根阴离子作为桥连配体完成配位。4是通过加入KPdCl₂制备溶液以完全形成二聚笼状化合物[Cu(H(HL4))]而得到的。由于钯离子酸性较弱,它从吡唑盐位点取代了铜离子。紫外可见光谱表明,在室温下一小时后交换完成。