The ring opening polymerization reaction of tetrahydrofuran (thf) by WCl6 was investigated under different conditions, and the polymeric material was characterized by NMR and SEC (Size Exclusion Chromatography) analyses. The mixed valence complex [(thf)(2)(mu-H)][{WOCl3(thf)}(2)(mu-O)], 3, was isolated from the reactions of WCl6 with 4-8 equivalents of thf in dichloromethane at room temperature, and crystallographically characterized. The formation of 3 was preceded by that of WOCI4(thf), 2, while Cl (CH2)(4)Cl and Cl(CH2)(4)O(CH2)(4)Cl were identified as the prevalent organic side products. The 1:1 M reaction of WCl6 with meO(CH2)(2)OH, in CH2Cl2 at room temperature, afforded the complexes (WOCl4)(2)(mu-kappa(2)-1,4-dioxane), 4, and WCl5(OCH2CH2OMe), 5, in admixture with Cl(CH2)(2)Cl, MeO(CH2)(2)OMe and MeCl. Also complex 4, resulting from a C-O bond forming process, was characterized by X-ray crystallography. (C) 2016 Elsevier Ltd. All rights reserved.

The reactivity of tungsten hexachloride with tetrahydrofuran and 2-methoxyethanol

BORTOLUZZI, Marco;
2016-01-01

Abstract

The ring opening polymerization reaction of tetrahydrofuran (thf) by WCl6 was investigated under different conditions, and the polymeric material was characterized by NMR and SEC (Size Exclusion Chromatography) analyses. The mixed valence complex [(thf)(2)(mu-H)][{WOCl3(thf)}(2)(mu-O)], 3, was isolated from the reactions of WCl6 with 4-8 equivalents of thf in dichloromethane at room temperature, and crystallographically characterized. The formation of 3 was preceded by that of WOCI4(thf), 2, while Cl (CH2)(4)Cl and Cl(CH2)(4)O(CH2)(4)Cl were identified as the prevalent organic side products. The 1:1 M reaction of WCl6 with meO(CH2)(2)OH, in CH2Cl2 at room temperature, afforded the complexes (WOCl4)(2)(mu-kappa(2)-1,4-dioxane), 4, and WCl5(OCH2CH2OMe), 5, in admixture with Cl(CH2)(2)Cl, MeO(CH2)(2)OMe and MeCl. Also complex 4, resulting from a C-O bond forming process, was characterized by X-ray crystallography. (C) 2016 Elsevier Ltd. All rights reserved.
2016
117
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/10278/3680712
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