Research output: Contribution to journal › Article › peer-review
Tetrabutylammonium Salts of [Mo12O28(μ-L)8]4– Polyoxometal Clusters with Pyrazolate and Triazolate Ligands. / Konkova, A. V.; Evtushok, D. V.; Vorotnikov, Y. A. et al.
In: Journal of Structural Chemistry, Vol. 65, No. 3, 03.2024, p. 610-618.Research output: Contribution to journal › Article › peer-review
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TY - JOUR
T1 - Tetrabutylammonium Salts of [Mo12O28(μ-L)8]4– Polyoxometal Clusters with Pyrazolate and Triazolate Ligands
AU - Konkova, A. V.
AU - Evtushok, D. V.
AU - Vorotnikov, Y. A.
AU - Eltsov, I. V.
AU - Yanshole, V. V.
AU - Ivanov, A. A.
AU - Shestopalov, M. A.
N1 - This work was funded by the Russian Science Foundation (project No. 22-23-00660). The authors thank the Ministry of Science and Higher Education of the Russian Federation and A.S. Sukhikh and L.V. Zargarova for providing the data measured at the XRD Facility of the Nikolaev Institute of Inorganic Chemistry, Siberian Branch of the Russian Academy of Sciences.
PY - 2024/3
Y1 - 2024/3
N2 - Abstract: The metathesis of ammonium cations in (NH4)4[Mo12O28(μ-L)8] (L = pz (pyrazolate) and trz (1,2,4-triazolate)) with tetrabutylammonium is performed under boiling in an aqueous solution with Bu4NOH. The substitution of cations and the preservation of the anionic cluster fragment are confirmed by a number of physicochemical methods such as XRD, 1H NMR, and mass spectrometry. The resulting compounds are soluble and stable in organic solvents, so their redox properties are studied. According to the cyclic voltammetry data, the compounds exhibit reversible oxidation with E1/2 = 0.26 V and 0.61 V for L = pz and trz respectively. The electronic structure is studied by quantum chemical calculations. It is shown that the frontier molecular orbitals of these compounds are mainly composed of molybdenum d-orbitals.
AB - Abstract: The metathesis of ammonium cations in (NH4)4[Mo12O28(μ-L)8] (L = pz (pyrazolate) and trz (1,2,4-triazolate)) with tetrabutylammonium is performed under boiling in an aqueous solution with Bu4NOH. The substitution of cations and the preservation of the anionic cluster fragment are confirmed by a number of physicochemical methods such as XRD, 1H NMR, and mass spectrometry. The resulting compounds are soluble and stable in organic solvents, so their redox properties are studied. According to the cyclic voltammetry data, the compounds exhibit reversible oxidation with E1/2 = 0.26 V and 0.61 V for L = pz and trz respectively. The electronic structure is studied by quantum chemical calculations. It is shown that the frontier molecular orbitals of these compounds are mainly composed of molybdenum d-orbitals.
KW - cluster complexes
KW - cyclic voltammetry
KW - molybdenum
KW - polyoxometalates
KW - quantum chemical calculations
UR - https://www.scopus.com/record/display.uri?eid=2-s2.0-85191873876&origin=inward&txGid=4f94e4bcbaa70aad86e20ac969d9b9cf
UR - https://www.mendeley.com/catalogue/7616fc58-b3c7-33d9-b98a-2656c9639e02/
U2 - 10.1134/S0022476624030156
DO - 10.1134/S0022476624030156
M3 - Article
VL - 65
SP - 610
EP - 618
JO - Journal of Structural Chemistry
JF - Journal of Structural Chemistry
SN - 0022-4766
IS - 3
ER -
ID: 61124136