Ahmed Basil M, Mezei Gellert
Department of Chemistry, Western Michigan University , Kalamazoo, Michigan 49008-5413, United States.
Inorg Chem. 2016 Aug 1;55(15):7717-28. doi: 10.1021/acs.inorgchem.6b01172. Epub 2016 Jul 14.
Nanojars are large (2 nm wide) anion-incarcerating coordination complexes of the composition [anion⊂{Cu(μ-OH)(μ-pz)}n] (n = 27-36), formed by the self-assembly of simple Cu(2+), HO(-), and pyrazolate (pz(-) = C3H3N2(-)) ions in the presence of certain anions with large hydration energy (e.g., CO3(2-), SO4(2-), PO4(3-), HPO4(2-)). Nanojars display spectacular chemical properties, such as unparalleled anion binding strength and, as shown herein, extraordinary resistance to extreme alkalinities (10 M NaOH). To shed light on the mechanism of the self-assembly process leading to these distinctive constructs, we employed an array of complementary techniques including mass spectrometry, pH titration, UV-vis and NMR spectroscopies, chemical synthesis, and single-crystal X-ray diffraction. In the reaction of Cu(NO3)2, pyrazole, NaOH, and Na2CO3 in tetrahydrofuran (THF), the first major intermediate is a trinuclear copper pyrazolate complex, [Cu3(μ3-OH)(μ-pz)3(NO3)2(H2O)], which was separately isolated and characterized. As the THF-insoluble NaOH slowly reacts, the nitrate ions are gradually precipitated out as NaNO3 and replaced by hydroxide ions. The resulting species, Cu3(μ3-OH)(μ-pz)3(OH)x(NO3)3-x (x = 1-3), have unstable terminal Cu-OH groups and react with each other to yield OH-bridged units, such as [Cu3(μ3-OH)(μ-pz)3(NO3)2]2(μ-OH) and then [{Cu3(μ3-OH)(μ-pz)3(μ-OH)2}x(NaNO3)y(Na2CO3)z] oligomers. The Cu3(OH)3(pz)3 repeating units of these oligomers have the same composition as the [Cu(OH)(pz)]n (n = 3x) nanojars and rearrange to the final products, Na2[CO3⊂{Cu(μ-OH)(μ-pz)}n] (n = 27, 29, 31), while eliminating the last amounts of NaNO3. pH titration, UV-vis monitoring, and chemical synthesis also confirm the formation of the trinuclear intermediate, followed by its clean transformation to nanojars. While displaying an unusual stability to high pH, nanojars are sensitive to acids stronger than water, a property exploitable for the recovery of the incarcerated anion. On lowering the pH, nanojars first break down to trinuclear complexes and finally to copper ions and pyrazole. This process is fully reversible, and nanojars are reassembled as pH is increased.
纳米罐是一种大型(宽2纳米)的包埋阴离子的配位络合物,其组成为[阴离子⊂{Cu(μ-OH)(μ-pz)}n](n = 27 - 36),由简单的Cu(2+)、HO(-)和吡唑盐(pz(-) = C3H3N2(-))离子在某些具有大水合能的阴离子(如CO3(2-)、SO4(2-)、PO4(3-)、HPO4(2-))存在下自组装形成。纳米罐具有惊人的化学性质,如无与伦比的阴离子结合强度,以及如本文所示的对极端碱度(10 M NaOH)的非凡抗性。为了阐明导致这些独特结构的自组装过程的机制,我们采用了一系列互补技术,包括质谱、pH滴定、紫外可见光谱和核磁共振光谱、化学合成以及单晶X射线衍射。在Cu(NO3)2、吡唑、NaOH和Na2CO3在四氢呋喃(THF)中的反应中,第一个主要中间体是三核铜吡唑盐络合物[Cu3(μ3-OH)(μ-pz)3(NO3)2(H2O)],它被单独分离并表征。随着不溶于THF的NaOH缓慢反应,硝酸根离子逐渐以NaNO3的形式沉淀出来并被氢氧根离子取代。生成的物种Cu3(μ3-OH)(μ-pz)3(OH)x(NO3)3-x(x = 1 - 3)具有不稳定的末端Cu - OH基团,它们相互反应生成OH桥连单元,如[Cu3(μ3-OH)(μ-pz)3(NO3)2]2(μ-OH),然后是[{Cu3(μ3-OH)(μ-pz)3(μ-OH)2}x(NaNO3)y(Na2CO3)z]低聚物。这些低聚物的Cu3(OH)3(pz)3重复单元与[Cu(OH)(pz)]n(n = 3x)纳米罐具有相同的组成,并重新排列成最终产物Na2[CO3⊂{Cu(μ-OH)(μ-pz)}n](n = 27、29、31),同时除去最后残留的NaNO3。pH滴定、紫外可见监测和化学合成也证实了三核中间体的形成,随后它干净地转化为纳米罐。虽然纳米罐在高pH下表现出异常的稳定性,但它们对比水更强的酸敏感,这一性质可用于回收被包埋的阴离子。降低pH时,纳米罐首先分解为三核络合物,最终分解为铜离子和吡唑。这个过程是完全可逆的,随着pH升高,纳米罐会重新组装。