A new ring-like arrangement of vanadyl(IV) groups bridged by monodentate alkoxides: cyclo-decakis(μ-cyclohexylmethanolato)pentakis[oxidovanadium(IV)]

The pentanuclear title compound, [V5(C7H13O)10O5], has a metal–oxygen core that consists of five vanadyl(IV) centres bridged by the O atoms of cyclohexylmethanolate ligands. This particular ring topology is new to oxovanadium(IV) chemistry and resembles the structure proposed for [V5O15]5− on the ba...

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Published inActa crystallographica. Section C, Crystal structure communications Vol. 68; no. 12; pp. m353 - m355
Main Authors Stinghen, Danilo, Ferreira, Janaina G., Nunes, Giovana G., Soares, Jaísa F.
Format Journal Article
LanguageEnglish
Published 5 Abbey Square, Chester, Cheshire CH1 2HU, England International Union of Crystallography 01.12.2012
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Abstract The pentanuclear title compound, [V5(C7H13O)10O5], has a metal–oxygen core that consists of five vanadyl(IV) centres bridged by the O atoms of cyclohexylmethanolate ligands. This particular ring topology is new to oxovanadium(IV) chemistry and resembles the structure proposed for [V5O15]5− on the basis of 51V NMR studies in aqueous solution. The bulky cyclohexylmethanolate ligands adopt chair‐like conformations and project outwards from the central cyclic core. The title compound crystallizes in a centrosymmetric triclinic unit cell, which contains four independent but chemically identical molecules in the asymmetric unit. The crystal structure is devoid of any significant intermolecular interactions.
AbstractList The pentanuclear title compound, [V5(C7H13O)10O5], has a metal-oxygen core that consists of five vanadyl(IV) centres bridged by the O atoms of cyclohexylmethanolate ligands. This particular ring topology is new to oxovanadium(IV) chemistry and resembles the structure proposed for [V5O15]5- on the basis of 51V NMR studies in aqueous solution. The bulky cyclohexylmethanolate ligands adopt chair-like conformations and project outwards from the central cyclic core. The title compound crystallizes in a centrosymmetric triclinic unit cell, which contains four independent but chemically identical molecules in the asymmetric unit. The crystal structure is devoid of any significant intermolecular interactions.
The pentanuclear title compound, [V5(C7H13O)10O5], has a metal–oxygen core that consists of five vanadyl(IV) centres bridged by the O atoms of cyclohexylmethanolate ligands. This particular ring topology is new to oxovanadium(IV) chemistry and resembles the structure proposed for [V5O15]5− on the basis of 51V NMR studies in aqueous solution. The bulky cyclohexylmethanolate ligands adopt chair‐like conformations and project outwards from the central cyclic core. The title compound crystallizes in a centrosymmetric triclinic unit cell, which contains four independent but chemically identical molecules in the asymmetric unit. The crystal structure is devoid of any significant intermolecular interactions.
The pentanuclear title compound, [V(5)(C(7)H(13)O)(10)O(5)], has a metal-oxygen core that consists of five vanadyl(IV) centres bridged by the O atoms of cyclohexylmethanolate ligands. This particular ring topology is new to oxovanadium(IV) chemistry and resembles the structure proposed for [V(5)O(15)](5-) on the basis of (51)V NMR studies in aqueous solution. The bulky cyclohexylmethanolate ligands adopt chair-like conformations and project outwards from the central cyclic core. The title compound crystallizes in a centrosymmetric triclinic unit cell, which contains four independent but chemically identical molecules in the asymmetric unit. The crystal structure is devoid of any significant intermolecular interactions.
The pentanuclear title compound, [V5(C7H13O)10O5], has a metal-oxygen core that consists of five vanadyl(IV) centres bridged by the O atoms of cyclohexylmethanolate ligands. This particular ring topology is new to oxovanadium(IV) chemistry and resembles the structure proposed for [V5O15]5- on the basis of 51V NMR studies in aqueous solution. The bulky cyclohexylmethanolate ligands adopt chair-like conformations and project outwards from the central cyclic core. The title compound crystallizes in a centrosymmetric triclinic unit cell, which contains four independent but chemically identical molecules in the asymmetric unit. The crystal structure is devoid of any significant intermolecular interactions. [PUBLICATION ABSTRACT]
The pentanuclear title compound, [V 5 (C 7 H 13 O) 10 O 5 ], has a metal–oxygen core that consists of five vanadyl(IV) centres bridged by the O atoms of cyclohexylmethanolate ligands. This particular ring topology is new to oxovanadium(IV) chemistry and resembles the structure proposed for [V 5 O 15 ] 5− on the basis of 51 V NMR studies in aqueous solution. The bulky cyclohexylmethanolate ligands adopt chair-like conformations and project outwards from the central cyclic core. The title compound crystallizes in a centrosymmetric triclinic unit cell, which contains four independent but chemically identical molecules in the asymmetric unit. The crystal structure is devoid of any significant intermolecular interactions.
Author Stinghen, Danilo
Soares, Jaísa F.
Nunes, Giovana G.
Ferreira, Janaina G.
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Snippet The pentanuclear title compound, [V5(C7H13O)10O5], has a metal–oxygen core that consists of five vanadyl(IV) centres bridged by the O atoms of...
The pentanuclear title compound, [V(5)(C(7)H(13)O)(10)O(5)], has a metal-oxygen core that consists of five vanadyl(IV) centres bridged by the O atoms of...
The pentanuclear title compound, [V 5 (C 7 H 13 O) 10 O 5 ], has a metal–oxygen core that consists of five vanadyl(IV) centres bridged by the O atoms of...
The pentanuclear title compound, [V5(C7H13O)10O5], has a metal-oxygen core that consists of five vanadyl(IV) centres bridged by the O atoms of...
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StartPage m353
SubjectTerms Alkoxides
Aqueous solutions
Asymmetry
Crystal structure
Crystallization
Ligands
Positioning
Unit cell
Title A new ring-like arrangement of vanadyl(IV) groups bridged by monodentate alkoxides: cyclo-decakis(μ-cyclohexylmethanolato)pentakis[oxidovanadium(IV)]
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