Assembly, disassembly and reassembly: a "top-down" synthetic strategy towards hybrid, mixed-metal {Mo10Co6} POM clusters

被引:6
|
作者
Healy, Colm [1 ,2 ,3 ]
Steuber, Friedrich W. [1 ,2 ]
Wix, Paul [1 ,2 ]
Macreadie, Lauren K. [1 ,2 ,4 ]
Kathalikkattil, Amal Cherian [1 ,2 ]
Schmitt, Wolfgang [1 ,2 ]
机构
[1] Trinity Coll Dublin, Coll Green, Sch Chem, Dublin 2, Ireland
[2] Trinity Coll Dublin, Coll Green, CRANN, Dublin 2, Ireland
[3] Univ Canterbury, Sch Phys & Chem Sci, MacDiarmid Inst Adv Mat & Nanotechnol, Private Bag 4800, Christchurch 8041, New Zealand
[4] CCSIRO Mfg, Bayview Ave, Clayton, Vic 3168, Australia
基金
欧洲研究理事会; 爱尔兰科学基金会;
关键词
POLYOXOMOLYBDATE CLUSTERS; MASS-SPECTROMETRY; WATER OXIDATION; POLYOXOMETALATE; DRIVEN; FUNCTIONALIZATION; ACCESS; CHARGE;
D O I
10.1039/c9dt00075e
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Polyoxometalates (POMs) are commonly prepared using a bottom-up synthetic procedure. The alternative top-down approach of disassembling a pre-formed POM unit to generate new synthetic intermediates is promising, but relatively comparatively underused. In this paper, a rationale for the top-down method is provided, demonstrating that this approach can generate compounds that are fundamentally inaccessible from simple bottom-up assembly. We demonstrate this principle through the synthesis of a series of 10, new, mixed-metal, hybrid compounds with the general formula [TBA](2)[MoVI10CoII6O(30)(RpPO3)(6)(RcCOO)(2)(L)(x)(H2O)(6)] (TBA = tetrabutylammonium, R-p = phosphonate moiety, R-c = carboxylate moiety, L = pyridyl ligand, and x = 2-4), including a one-dimensional polyoxometalate-based coordination polymer. We propose that these structures are generated from {MoxO3x-1} fragments that cannot be accessed from bottom-up assembly alone. The POM clusters are stabilised by three distinct classes of organic ligand - organophosphonate, carboxylate and pyridyl ligands - which can each be substituted independantly, thus providing a controlled route to ligand functionalisation.
引用
收藏
页码:3018 / 3027
页数:10
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