POMzites: A Family of Zeolitic Polyoxometalate Frameworks from a Minimal Building Block Library
نویسندگان
چکیده
We describe why the cyclic heteropolyanion [P8W48O184]40- (abbreviated as {P8W48}) is an ideal building block for the construction of intrinsically porous framework materials by classifying and analyzing >30 coordination polymers incorporating this polyoxometalate (POM) ligand. This analysis shows that the exocyclic coordination of first-row transition metals (TMs) to {P8W48} typically yields frameworks which extend through {W-O-TM-O-W} bridges in one, two, or three dimensions. However, despite the rich structural diversity of such compounds, the coordination of TMs to the {P8W48} ring is poorly understood, and therefore largely unpredictable, and had not until now been present with any structural classification that could allow rational design. Herein, not only do we present a new approach to understand and classify this new class of materials, we also present three {P8W48}-based frameworks which complement those frameworks which have previously been described. These new compounds help us postulate a new taxonomy of these materials. This is possible because the TM coordination sites of the {P8W48} ring are found, once fully mapped, to lead to well-defined classes of connectivity. Together, analysis provides insight into the nature of the building block connectivity within each framework, to facilitate comparisons between related structures, and to fundamentally unite this family of compounds. Hence we have tentatively named these compounds as "POMzites" to reflect the POM-based composition and zeolitic nature of each family member, although crucially, POMzites differ from zeolites in the modular manner of their preparation. As the synthesis of further POMzites is anticipated, the classification system and terminology introduced here will allow new compounds to be categorized and understood in the context of the established materials. A better understanding of TM coordination to the {P8W48} ring may allow the targeted synthesis of new frameworks rather than the reliance on serendipity apparent in current methods.
منابع مشابه
Structural and catalytic performance of a polyoxometalate-based metal-organic framework having a lanthanide nanocage as a secondary building block.
A polyoxometalate-based lanthanide-organic framework was achieved using the {[Ho(4)(dpdo)(8)(H(2)O)(16)BW(12)O(40)] (H(2)O)(2)}(7+) nanocage as a secondary building block for the heterogeneous catalysis of phosphodiester cleavage in an aqueous solution.
متن کاملOrganic functionalization of polyoxometalate in aqueous solution: self-assembly of a new building block of {VMo6O25} with triethanolamine.
A novel organic-inorganic hybrid of triethanolamine linked covalently with a new building block of {VMo6O25} was synthesized in aqueous solution, and the hybrid was further assembled with copper-triethanolamine complexes to form a ring-like structure. This work represents an advance in the organic functionalization of polyoxometalate performed in aqueous solution instead of an organic solvent.
متن کاملModular inorganic polyoxometalate frameworks showing emergent properties: redox alloys.
The targeted synthesis of new extended modular frameworks exhibiting specific properties is a principal challenge of modern chemistry research. Many inorganic frameworks and metal–organic frameworks (MOFs) have been reported, but the fine manipulation of their electronic properties remains challenging. One such approach could be the development of molecular alloys, analogous to metal alloys, ye...
متن کاملTemplate-directed assembly of polyoxothiometalate scaffolds into nanomolecular architectures.
Polyoxometalate clusters (POMs) represent some of the largest non-biologically derived molecules so far synthesized as they occupy the 1–6 nm size range and exhibit a diverse variety of structures, assembled from a large “virtual combinatorial library” of building blocks. Whilst many tungsten POM clusters can be built in a controlled way, the designed assembly of giant molybdates is more diffic...
متن کاملSelf-assembly and alterable relaxivity of an organic cation-encapsulated gadolinium-containing polyoxometalate.
A new amphiphilic molecule bearing poly(ethylene oxide) (PEO) and quaternary ammonium group, was designed and synthesized to encapsulate paramagnetic Gd(III)-containing polyoxometalate (Gd-POM) through electrostatic interaction for obtaining a water-soluble organic-inorganic hybrid building block based on POM. The yielding organic cation-encapsulated Gd-POM (OCEP-Gd) complex exhibited water-sol...
متن کامل