TY - JOUR
T1 - Tetravalent metal complexation by Keggin and lacunary phosphomolybdate anions
AU - Copping, Roy
AU - Jonasson, Leif
AU - Gaunt, Andrew J.
AU - Drennan, Dennis
AU - Collison, David
AU - Helliwell, Madeleine
AU - Pirttijarvi, Ross J.
AU - Jones, Chris J.
AU - Huguet, Anne
AU - Apperley, David C.
AU - Kaltsoyannis, Nikolas
AU - May, Iain
PY - 2008/7/7
Y1 - 2008/7/7
N2 - We report the synthesis, spectroscopic and structural characterization, and computational analysis of a series of phosphomolybdate complexes with tetravalent metal cations. The reaction between CeIV and Th IV with phosphomolybdate at the optimum pH for the stabilization of the lacunary heteropolyoxometalate anion, [PMo11O39] 7-, results in the formation of compounds containing the anions [Ce(PMo11O39)2]10- and [Th(PMo 11O39)2]10-, respectively. Single crystal X-ray diffraction analysis was performed on salts of both species, Cs10[Ce(PMo11O39)2]·20H 2O and (NH4)10[Th(PMo11O 39)2]·22H2O. In both anionic complexes the f-block metal cation is coordinated to the four unsaturated terminal lacunary site oxygens of each [PMo11O39]7- anion, yielding 8 coordinate sandwich complexes, analogous to previously prepared related complexes. Spectroscopic characterization points to the stability of these complexes in solution over a reasonably wide pH range. Density functional analysis suggests that the Ce-O bond strength in [Ce(PMo 11O39)2]10- is greater than the Th-O bond strength in [Th(PMo11O39)2] 10-, with the dominant bonding interaction being ionic in both cases. In contrast, under similar reaction conditions, the dominant solid state ZrIV and HfIV complexes formed contain the anions [Zr(PMo12O40)(PMo11O39)] 6- and [Hf(PMo12O40)(PMo11O 39)]6-, respectively. In these complexes the central Group 4 d-block metal cations are coordinated to the four unsaturated terminal lacunary site oxygens of the [PMo11O39]7- ligand and to four bridging oxygens of a plenary Keggin anion, [PMo 12O40]3-. In addition, (NH4) 5{Hf[PMo12O40][(NH4)PMo 11O39]}·23.5H2O can be crystallized as a minor product. The structure of the anion, {Hf[PMo12O 40][(NH4)PMo11O39]}5-, reveals coordination of the central HfIV cation via four bridging oxygens on both the coordinated [PMo11O39]7- and [PMo12O40]3- anions. Unusually, the highly charged lacunary site remains uncoordinated to the Hf metal center but instead interacts with an ammonium cation. 31P NMR indicates that complexation of the Keggin anion, [PMo12O40]3-, to HfIV and ZrIV will stabilize the Keggin anion to a much higher pH than usually observed.
AB - We report the synthesis, spectroscopic and structural characterization, and computational analysis of a series of phosphomolybdate complexes with tetravalent metal cations. The reaction between CeIV and Th IV with phosphomolybdate at the optimum pH for the stabilization of the lacunary heteropolyoxometalate anion, [PMo11O39] 7-, results in the formation of compounds containing the anions [Ce(PMo11O39)2]10- and [Th(PMo 11O39)2]10-, respectively. Single crystal X-ray diffraction analysis was performed on salts of both species, Cs10[Ce(PMo11O39)2]·20H 2O and (NH4)10[Th(PMo11O 39)2]·22H2O. In both anionic complexes the f-block metal cation is coordinated to the four unsaturated terminal lacunary site oxygens of each [PMo11O39]7- anion, yielding 8 coordinate sandwich complexes, analogous to previously prepared related complexes. Spectroscopic characterization points to the stability of these complexes in solution over a reasonably wide pH range. Density functional analysis suggests that the Ce-O bond strength in [Ce(PMo 11O39)2]10- is greater than the Th-O bond strength in [Th(PMo11O39)2] 10-, with the dominant bonding interaction being ionic in both cases. In contrast, under similar reaction conditions, the dominant solid state ZrIV and HfIV complexes formed contain the anions [Zr(PMo12O40)(PMo11O39)] 6- and [Hf(PMo12O40)(PMo11O 39)]6-, respectively. In these complexes the central Group 4 d-block metal cations are coordinated to the four unsaturated terminal lacunary site oxygens of the [PMo11O39]7- ligand and to four bridging oxygens of a plenary Keggin anion, [PMo 12O40]3-. In addition, (NH4) 5{Hf[PMo12O40][(NH4)PMo 11O39]}·23.5H2O can be crystallized as a minor product. The structure of the anion, {Hf[PMo12O 40][(NH4)PMo11O39]}5-, reveals coordination of the central HfIV cation via four bridging oxygens on both the coordinated [PMo11O39]7- and [PMo12O40]3- anions. Unusually, the highly charged lacunary site remains uncoordinated to the Hf metal center but instead interacts with an ammonium cation. 31P NMR indicates that complexation of the Keggin anion, [PMo12O40]3-, to HfIV and ZrIV will stabilize the Keggin anion to a much higher pH than usually observed.
UR - https://www.scopus.com/pages/publications/47949124357
U2 - 10.1021/ic800101t
DO - 10.1021/ic800101t
M3 - Article
AN - SCOPUS:47949124357
SN - 0020-1669
VL - 47
SP - 5787
EP - 5798
JO - Inorganic Chemistry
JF - Inorganic Chemistry
IS - 13
ER -