Synthesis of a bowl-type dodecavanadate by the coupling reaction of alkoxohexavanadate and discovery of a chiral octadecavanadate

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Abstract

A new route to an alkoxohexavanadate species leads to the isolation of a bowl-type dodecavanadate without a guest molecule in the cavity. The 1D tetravanadate, [V4O11]2-, is a good precursor for the alkoxohexavanadate, [V6O13(OCH3)6]2-, which is then utilized for the [V6 + V6] coupling reaction to form the dodecavanadate, [V12O42]4-, with a capped dichloromethane molecule at the cavity entrance. We also obtained structural information on a newly discovered octadecavanadate, [V18O46(NO3)]5-, in both the solid and solution states through extended X-ray absorption fine structure (EXAFS) studies. The existence of the chiral inorganic species in acetonitrile with double-stranded V8 chains was confirmed through EXAFS oscillations. © 2009 IUPAC.

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Domae, K., Uchimura, D., Koyama, Y., Inami, S., Hayashi, Y., Isobe, K., … Shimoda, T. (2009). Synthesis of a bowl-type dodecavanadate by the coupling reaction of alkoxohexavanadate and discovery of a chiral octadecavanadate. Pure and Applied Chemistry, 81(7), 1323–1330. https://doi.org/10.1351/PAC-CON-08-08-25

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