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Rational Synthesis and Characterization of the Mixed-Metal Organometallic Polyoxometalates [Cp*MoxW6–xO18] (x = 0, 1, 5, 6)
Author(s) -
G. Taban-Caliskan,
Daniel Mesquita Fernandes,
JeanClaude Daran,
Dominique Agustin,
Funda Demirhan,
Rinaldo Poli
Publication year - 2012
Publication title -
inorganic chemistry
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.348
H-Index - 233
eISSN - 1520-510X
pISSN - 0020-1669
DOI - 10.1021/ic300578g
Subject(s) - chemistry , polyoxometalate , group 2 organometallic chemistry , crystallography , thermogravimetric analysis , x ray crystallography , density functional theory , metal , mass spectrometry , crystal structure , aqueous solution , single crystal , organometallic chemistry , infrared spectroscopy , inorganic chemistry , molecule , diffraction , computational chemistry , catalysis , organic chemistry , physics , chromatography , optics
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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