Article

Rational synthesis and characterization of the mixed-metal organometallic polyoxometalates [Cp*Mo(x)W(6-x)O18]- (x = 0, 1, 5, 6).

CNRS, Laboratoire de Chimie de Coordination, 205 route de Narbonne, BP 44099, F-31077 Toulouse Cedex 4, France.
Inorganic Chemistry (impact factor: 4.6). 04/2012; 51(10):5931-40. DOI:10.1021/ic300578g pp.5931-40
Source: PubMed

ABSTRACT The reaction between the oxometallic complexes Cp*(2)M(2)O(5) and Na(2)M'O(4) (M, M' = Mo, W) in a 1:10 molar ratio in an acidic aqueous medium constitutes a mild and selective entry into the anionic Lindqvist-type hexametallic organometallic mixed oxides [Cp*Mo(x)W(6-x)O(18)](-) [x = 6 (1), 5 (2), 1 (3), 0 (4)]. All of these compounds have been isolated as salts of nBu(4)N(+) (a), nBu(4)P(+) (b), and Ph(4)P(+) (c) cations and two of them (1 and 3) also with the n-butylpyridinium (nBuPyr(+), d) cation. The compounds have been characterized by elemental analyses, thermogravimetric analyses, electrospray mass spectrometry, and IR spectroscopy. The molecular identity and geometry of compounds 1c, 2a, and 2c have been confirmed by single-crystal X-ray diffraction. Density functional theory calculations on models obtained by replacing Cp* with Cp (I-IV) have provided information on the assignment of the terminal M═O and bridging M-O-M vibrations.

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Keywords

acidic aqueous medium
 
anionic Lindqvist-type hexametallic organometallic mixed oxides [Cp*Mo(x)W(6-x)O(18)](-)
 
Cp
 
Density functional theory calculations
 
electrospray mass spectrometry
 
molecular identity
 
n-butylpyridinium
 
single-crystal X-ray diffraction
 
terminal M═O
 
thermogravimetric analyses