Size and charge effect of guest cations in the formation of polyoxopalladates: a theoretical and experimental study12. Issue 11 (4th October 2017)

• Record Type: Journal Article
• Authors: Lang, Zhongling; Yang, Peng; Lin, Zhengguo; Yan, Likai; Li, Ming-Xing; Carbó, Jorge J.; Kortz, Ulrich; Poblet, Josep M.
• Is Part Of: Chemical science. Volume 8:Issue 11(2017)
• Page Start: 7862
• Page End: 7872
• Publication Date: 2017-10-04
• Subjects: Chemistry -- Periodicals; 540.5
• DOI: 10.1039/c7sc03441e
• Languages: English
• ISSNs: 2041-6520

Abstract

Abstract : The close interplay of theoretical and experimental techniques can facilitate the understanding and rational synthesis of novel inorganic clusters, and here an impressive example is shown for the class of cuboid-shaped polyoxo-12-palladates(ii ) with a central metal ion guest. Abstract : The development of rational synthetic procedures with desired nuclearity and high selectivity is a critical issue in inorganic chemistry. Here we demonstrate a comprehensive understanding of the template effect induced by metal cations in the formation mechanism of the class of polyoxopalladates ({MPd12 L8 } nanocube and {MPd15 L10 } nanostar) by combining computational and experimental techniques. The capture of a M n + guest ion by a peripheral palladium(ii )-oxo shell leads to a competition between the parent Pd 2+ addenda ion and the respective guest metal ion. The present study reveals that (i) the selection of the incorporated guest ion has a thermodynamic control, (ii) the main factors governing the formation of a particular polyanion are the charge and size of the guest cation, (iii) the electrostatic interaction between the cation and the surrounding oxo ligands and (iv) the dehydration ability of the cation. As expected from the number of observed {M n + Pd12 L8 } species, trivalent cations M 3+ were found to be good templates resulting in several examples of {M 3+ Pd12 L8 }, whereas monovalent cations M + are much less prone to form {M + Pd12 L8 }. For tetravalent cations the dehydration energies are very large, however, the formation of {M 4+ Pd12 L8 } nanocubes is found to be still energetic favourable. Fully consistent with computational predictions, four novel polyoxo-12-palladates were synthesized: the La 3+ -centered nanocube [LaPd12 O8 (PhAsO3 )8 ] 5− (LaPd12 -closed ), the La 3+ -centered "open" nanocube [LaPd12 O6 (OH)3 (PhAsO3 )6 (OAc)3 ] 3− (LaPd12 -open ), the Ga 3+ -centered [GaPd12 O8 (PhAsO3 )8 ] 5− (GaPd12 ), and the In 3+ -analogue [InPd12 O8 (PhAsO3 )8 ] 5− (InPd12 ). All four compounds were fully characterized in the solid state and in solution by a multitude of physicochemical techniques, including 71 Ga and 115 In NMR as well as mass spectrometry. The experimentally observed selective incorporation of only In 3+ ions in the presence of Ga 3+ and In 3+ confirmed the thermodynamic control of the formation mechanism, which we had predicted by theory.