Supramolecular Aggregation Control in Polyoxometalates Covalently Functionalized with Oligoaromatic Groups

被引:1
|
作者
Knoll, Sebastian [1 ]
Haenle, Matthias [1 ]
Mengele, Alexander K. [1 ]
Sorsche, Dieter [1 ]
Rau, Sven [1 ]
Streb, Carsten [1 ,2 ]
机构
[1] Ulm Univ, Inst Inorgan Chem I, Albert Einstein Allee 11, D-89081 Ulm, Germany
[2] Johannes Gutenberg Univ Mainz, Dept Chem, Duesbergweg 10-14, D-55128 Mainz, Germany
关键词
organic-inorganic hybrid; organofunctionalization; photosensitizer; polyoxometalate; supramolecular; POST-FUNCTIONALIZATION; CATALYST DYADS; VISIBLE-LIGHT; COMPLEXES; CHEMISTRY; PHASE; AZIDE; ACTIVATION; REDUCTION; HYBRIDS;
D O I
10.1002/chem.202203469
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
CLICK-chemistry has become a universal route to covalently link organic molecules functionalized with azides and alkynes, respectively. Here, we report how CLICK-chemistry can be used to attach oligoaromatic organic moieties to Dawson-type polyoxometalates. In step one, the lacunary Dawson anion [alpha(2)-P2W17O61](6-) is functionalized with phosphonate anchors featuring peripheral azide groups. In step two, this organic-inorganic hybrid undergoes microwave-assisted CLICK coupling. We demonstrate the versatility of this route to access a series of Dawson anions covalently functionalized with oligoaromatic groups. The supramolecular chemistry and aggregation of these systems in solution is explored, and we report distinct changes in charge-transfer behavior depending on the size of the oligoaromatic pi-system.
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页数:9
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