| Literature DB >> 29205556 |
Peng Yang1, Hui Li2, Tian Ma1, Fadi Haso2, Tianbo Liu2, Linyuan Fan3, Zhengguo Lin1,3, Changwen Hu3, Ulrich Kortz1.
Abstract
The SrII -centered 12-palladate(II) open-cube {SrPd12 (OAc)3 } has been systematically evolved by substitution of the three acetate ligands by a library of saturated carboxylic acids with increasing chain lengths leading to four novel polyoxopalladates(II) with the formula [SrPd12 O6 (OH)3 (PhAsO3 )6 (L)3 ]4- (SrPd12 L3 , L=Cn H2n+1 COO, n=2 to 5). These first examples of surfactant-type polyoxopalladates with a hydrophilic metal-oxo unit and three hydrophobic alkyl chains were characterized in the solid state (single-crystal XRD, FTIR, TGA), in solution (1 H, 13 C NMR spectroscopy), and in the gas phase (ESI-MS). The two polyanions SrPd12 L3 with chain lengths of 5 and 6 are the first examples of polyoxopalladates that are soluble and stable in organic media. The Na salts of the amphiphilic polyoxopalladates SrPd12 L3 were shown to self-assemble into "blackberry"-type spherical supramolecular structures in dilute solutions, of which an unusual "volcano"-shaped trend of assembly size versus solvent polarity is chiefly influenced by directional hydrogen bonding interactions.Entities:
Keywords: palladium; polyoxometalates; post-functionalization; supramolecular chemistry; vesicles
Year: 2018 PMID: 29205556 DOI: 10.1002/chem.201705303
Source DB: PubMed Journal: Chemistry ISSN: 0947-6539 Impact factor: 5.236