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首页> 外文期刊>American Chemical Society, Division of Fuel Chemistry, Preprints >TOPOLOGY GUIDED DESIGN AND SYNTHESES OF HIGHLY STABLE MESOPOROUS PORPHYRINIC ZIRCONIUM MOFS WITH ULTRAHIGH SURFACE AREA
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TOPOLOGY GUIDED DESIGN AND SYNTHESES OF HIGHLY STABLE MESOPOROUS PORPHYRINIC ZIRCONIUM MOFS WITH ULTRAHIGH SURFACE AREA

机译:具有超高表面面积的高度稳定的介孔卟啉锆MOFS的拓扑学指导设计和合成

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摘要

Mesoporous metal-organic frameworks (MOFs) have attractedngreat interest in versatile application, such as catalysis, gas storagenand separation and luminescence.1 However, compared with thenwell-explored microporous MOFs, mesoporous MOFs are relativelynunder-developed. This is ascribed to the difficulty in organic linkernextension, challenges in activation of MOFs with ultra-large pores, asnwell as the common appearance of undesired interpenetration.2nMoreover, the stability of the framework becomes difficult tonmaintain after extension of the organic linker, especially fornmesoporous materials whose applications are usually conductednunder aqueous or harsh chemical environments. To improve thenchemical stability of MOFs, hard Lewis acidic species such as Al3+,nFe3+, Cr3+ and Zr4+, which can form much stronger bonds withncarboxylates, are often incorporated.3 Despite this adjustment, asnisoreticular chemistry is applied to augment the internal cavity ofnknown MOF structures, the pore size and stability are usuallyninversely correlated.
机译:介孔金属有机骨架(MOF)引起了人们的广泛兴趣,例如催化,气体储存和分离以及发光等。1然而,与开发良好的微孔MOF相比,介孔MOF相对较不发达。这归因于有机连接子的延伸困难,具有超大孔的MOF活化的挑战以及常见的互穿现​​象。2n此外,有机连接子(尤其是无孔材料)扩展后,骨架的稳定性变得难以维持。其应用通常在水性或苛刻的化学环境下进行。为了提高MOF的化学稳定性,经常掺入可以与羧酸酯形成更强键的硬路易斯酸性物质,例如Al3 +,nFe3 +,Cr3 +和Zr4 +。3尽管进行了这种调整,但仍采用非球面化学来增加MOF结构的内部腔,孔径和稳定性通常不成反比。

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