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Substituent effects on the supramolecular aggregation of Ag ~I-pyrazolato trimers

机译:取代基对Ag〜I-吡唑并三聚体超分子聚集的影响

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The interplay of argentophilic and dipolar (π-acid?base) interactions, on one hand, and the presence or absence of interstitial solvent molecules, on the other, determines the supramolecular organization of trinuclear silver-pyrazolato complexes in the solid state. The crystal structures of one gold and six silver metallacyclic complexes of the type [M~I(μ-pz*)]_3, where pz* are the substituted pyrazolato anions 3,5-Ph_2-pz, 3-Me-5-Ph-pz, 4-Br-3,5-Ph _2-pz, 4-Br-3-~tBu-pz and 3-(o-Cl-C_6H _4)-pz and M = Ag and Au, are discussed in the context of their supramolecular organization. Two silver complexes, for which the π-acid character of their Ag_3-faces is maximized by their peripheral electron-withdrawing substituents, show crystal packing dominated by short Ag_3?Br contacts, the first structural manifestation of supramolecular structure via dipolar interactions involving the tunable π-acidity of the Ag_3-face.
机译:一方面,亲银和偶极(π-酸?碱)相互作用的相互作用,另一方面,是否存在间隙溶剂分子,决定了固态的三核银-吡唑并酮络合物的超分子组织。 [M〜I(μ-pz*)] _ 3类型的一金和六银金属环配合物的晶体结构,其中pz *是取代的吡唑基阴离子3,5-Ph_2-pz,3-Me-5-Ph -pz,4-Br-3,5-Ph _2-pz,4-Br-3-〜tBu-pz和3-(o-Cl-C_6H _4)-pz以及M = Ag和Au讨论于他们的超分子组织的背景。两个银配合物,其Ag_3面的π酸特征通过其周围的吸电子取代基而最大化,它们显示出以短Ag_3?Br接触为主的晶体堆积,这是超分子结构的第一个结构表现,是通过涉及可调谐分子的偶极相互作用实现的。 Ag_3面的π酸度。

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