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Anodic oxidation of molybdenum and tungsten in alcohols: isolation and X-ray single-crystal study of side products

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TLDR
In this paper, the side products of the anodic dissolution of molybdenum and tungsten metals in alcohols in the presence of LiCl showed them to be [LiMo2O4(OPri)4(OC2H4OMe)] 1 in the case of MeOH and [ LiMo2OC4(OEt)5(EtOH)] 2 in EtOH.
Abstract
The study of the side products of the anodic dissolution of molybdenum and tungsten metals in alcohols in the presence of LiCl showed them to be [LiMo2O2(OMe)7(MeOH)] 1 in the case of MeOH and [LiMo2O4(OEt)5(EtOH)] 2 in EtOH. Treatment of 2 with an excess of PriOH gave [LiMo2O4(OPri)5(PriOH)] 3, the structure of which was confirmed by a study of [{LiMo2O4(OPri)4(OC2H4OMe)}2] 4, the product of partial substitution of OR groups in 3 by 2-methoxyethoxide ligands. Reaction of 2 with an excess of MeOC2H4OH led to an equimolar mixture of [MoO2(OC2H4OMe)2] and [LiMoO2(OC2H4OMe)3] 5. In PriOH a crystalline product identified as [Mo6O10(OPri)12] 6 was isolated. Anodic oxidation of tungsten in MeOH gave a mixture of homometallic W(OMe)6 and [WO(OMe)4]. Electrosynthesis in EtOH gave as major product an amorphous glass-like mass {after separation of crystalline [WO(OEt)4] by filtration and subsequent drying of the filtrate in vacuo}. Treatment of the latter with an excess of HOC2H4OMe led to crystallization of [{LiWO2(OC2H4OMe)3}2· 2Li(HOC2H4OMe)2]2+[W6O19]2– 7. Complexes 1, 4 and 7 were characterized by X-ray single-crystal studies. A GLC-mass spectrometric study of the composition of organic side products indicated that the processes were associated with formation of ethers, alkyl halides, aldehydes or ketones and their derivatives. The nature of the possible side reactions was deduced on the basis of the data obtained.

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Citations
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Journal ArticleDOI

Synthesis of WO3 nanorods by reacting WO(OMe)4 under autogenic pressure at elevated temperature followed by annealing.

TL;DR: The mechanism of the formation of nonstoichiometric W(18)O(49) nanorods is supported by the measured analytical data and several control experiments.
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The use of sacrificial anodes for the electrochemical synthesis of metallic complexes

TL;DR: In this paper, a compilation of electrochemically prepared metallic complexes is presented, all of them were synthesized by using a single step electrolytic process, which is useful in the syntheses of homoleptic and heteroleptic complexes.
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Electrochemical synthesis, X-ray single crystal, IR spectroscopic, and quantum chemical investigation of molybdenum and tungsten hexamethoxides.

TL;DR: The anodic oxidation of molybdenum metal in MeOH at both low anodic and cathodic current density and electrolyte temperatures kept below 20 degrees C provides an efficient approach to Mo(OMe)6 (I), which can be obtained from the electrolytes via anodic dissolution of tungsten, by fractional crystallization.
Journal ArticleDOI

Construct Polyoxometalate Frameworks through Covalent Bonds.

TL;DR: This work forges a link among polymer science, POM chemistry, and open-framework materials by demonstrating that it is possible to use covalent bonds according to polymer chemistry principles to construct crystalline 3D open- framework POM materials.
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Isolation, X-ray single crystal and theoretical study of quinquevalent metal oxoisopropoxides, Nb6O8(iPrO)14(iPrOH)2 and Re4O6(OiPr)10

TL;DR: In this paper, the stability of oxoalkoxide derivatives of rhenium(V,VI) and niobium (V,V) and poor stability for those of tantalum(V) are discussed based on the results of quantum-chemical calculations.
References
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Revised effective ionic radii and systematic studies of interatomic distances in halides and chalcogenides

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Journal ArticleDOI

Reactions of Metal-Metal Multiple Bonds. 10. Reactions of Mo2(OR)6 (M Triple Bond M) and (M(OR)4)x Compounds with Molecular Oxygen. Preparation and Characterization of Oxo-Alkoxides of Formula MoO2(OR)2, MoO2(OR)2(bpy), MoO(OR)4, Mo3O(OR)10, Mo4O8(OR)4(py)4 and Mo6O10(OR)12.

TL;DR: In this paper, it has been shown that the Mo=Mo bond in M02(OR)6 compounds is labile toward a number of oxidative-addition reactions, including those involving molecular oxygen.
Journal ArticleDOI

Crystal and Molecular Structure of Titanium (IV) Ethoxide

TL;DR: In this article, it was shown that the trimeric titanium (IV) ethoxide is a tetramer in the solid, and hence that this long-awaited X-ray analysis of a titanium(IV) alkoxide not only fails to confirm one of the proposed structures, but also makes unreasonable the assumption, implicit in much of the recent discussions, that the species in solution are identical with those precipitated from solution.
Journal ArticleDOI

Low-nuclearity titanium oxoalkoxides: the trititanates [Ti3O](OPri)10 and [Ti3O](OPri)9(OMe)

TL;DR: The tritinate [Ti3O](OPri)9(OMe) was isolated from the reaction of Ti(OPri),4 with water and methanol in isopropanol solution and characterized by elemental analysis, multinuclear NMR spectroscopy, and single-crystal X-ray diffraction (a = 23.295(5), b = 19.560(4), c = 18.661(4) A, β = 108.39(3)°; Z = 8 ; space group P21/c-C2h
Journal ArticleDOI

Crystal structure of lithium niobium ethoxide (LiNb(OCH2CH3)6: a precursor for lithium niobate ceramics

TL;DR: In this paper, a complete crystallographic study of these crystals was carried out, and the results were presented in the form of a 2-5 mm in length and a transparent crystal.
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