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在稀溶液中组装过程中不同多质子大分子之间的自我识别。

Self-recognition among different polyprotic macroions during assembly processes in dilute solution.

机构信息

Department of Chemistry, Lehigh University, Bethlehem, PA 18015, USA.

出版信息

Science. 2011 Mar 25;331(6024):1590-2. doi: 10.1126/science.1201121.

Abstract

We report a self-recognition phenomenon based on an assembly process in a homogeneous dilute aqueous solution of two nano-scaled, spherical polyprotic metal oxide-based macroions (neutral species in crystals), also called Keplerates of the type [(linker)₃₀(pentagon)₁₂]≡[{M(H₂O)}₃₀{(Mo)Mo₅}₁₂] where M is Fe(III) or Cr(III). Upon deprotonation of the neutral species, the resulting macroions assemble into hollow "blackberry"-type structures through very slow homogeneous dimer-oligomerization processes. Although the geometrical surface structures of the two macroions are practically identical, mixtures of these form homogeneous superstructures, rather than mixed species. The phase separation is based on the difference in macroionic charge densities present during the slow homogeneous dimer or oligomer formation. The surface water ligands' residence times of Cr(III) and Fe(III) differ markedly and lead to very different interfacial water mobilities between the Keplerates.

摘要

我们报告了一种基于自组装过程的自识别现象,该过程发生在两种纳米级、球形多质子金属氧化物基大分子(晶体中的中性物质)在均相稀水溶液中的组装过程中,也称为[(linker)₃₀(pentagon)₁₂]≡[{M(H₂O)}₃₀{(Mo)Mo₅}₁₂]型的 Keplerates,其中 M 为 Fe(III) 或 Cr(III)。在中性物质去质子化后,所得大分子通过非常缓慢的均相二聚体-齐聚体化过程组装成中空“黑莓”型结构。尽管这两种大分子的几何表面结构实际上是相同的,但它们的混合物形成了同相超结构,而不是混合物质。相分离基于在缓慢的均相二聚体或齐聚体形成过程中存在的大分子电荷密度的差异。Cr(III) 和 Fe(III) 的表面水配体的停留时间有显著差异,导致 Keplerates 之间的界面水迁移率非常不同。

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