. "synthesis; redox-active ferrocenyl groups; ferrocene"@en . . . . "Synthesis, structural characterisation and bonding in an anionic hexavanadate bearing redox-active ferrocenyl groups at the periphery"@en . . "GB - Spojen\u00E9 kr\u00E1lovstv\u00ED Velk\u00E9 Brit\u00E1nie a Severn\u00EDho Irska" . "Gyepes, Robert" . "4"^^ . "[6F4F5041772E]" . . "1144-0546" . . "1"^^ . "C\u00EDsa\u0159ov\u00E1, I." . . "RIV/61388955:_____/10:00437165!RIV15-AV0-61388955" . "Synthesis, structural characterisation and bonding in an anionic hexavanadate bearing redox-active ferrocenyl groups at the periphery" . . . . "Amide FcCONHC(CH2OH)(3) (1; Fc = ferrocenyl), prepared from fluorocarbonylferrocene and tris(hydroxymethyl)methylamine, reacts with (Bu4N)(3)[H3V10O28] in N, N-dimethylacetamide to afford a salt containing a bis(triolato) capped hexavanadate anion bearing two ferrocenyl groups at its periphery, (Bu4N)(2)[{FcC(O)NHC(CH2O)(3)}(2)V6O13] (2). Compounds 1 and 2 were characterised by elemental analysis, spectroscopic methods (IR, NMR, and MS) and by cyclic voltammetry; the crystal structures of 1.1/2CH(3)CO(2)Et and (Bu4N)(2)[{FcC(O)NHC(CH2O)(3)}(2)V6O13]center dot 2Me(2)NCHO were determined by X-ray diffraction analysis. Single-point DFT calculations performed for the isolated hexavanadate anion revealed the presence of 3-centre 4-electron (3c4e) O-V-O bonds on the hexavanadate cage, which are responsible for the high energy of the occupied frontier orbitals. The upper eleven occupied molecular orbitals including the HOMO are all delocalized over the hexavanadate cage and, therefore, any electrochemical oxidation can be expected to occur preferentially at the hexavanadate anion without affecting the pendant ferrocene moieties." . "\u0160t\u011Bpni\u010Dka, P." . "New Journal of Chemistry" . "10.1039/c0nj00421a" . . "P(LC06070), Z(AV0Z40400503)" . "Synthesis, structural characterisation and bonding in an anionic hexavanadate bearing redox-active ferrocenyl groups at the periphery"@en . "12" . "8"^^ . "RIV/61388955:_____/10:00437165" . . . . "34" . "Schulz, J." . . "291564" . "Synthesis, structural characterisation and bonding in an anionic hexavanadate bearing redox-active ferrocenyl groups at the periphery" . . "Amide FcCONHC(CH2OH)(3) (1; Fc = ferrocenyl), prepared from fluorocarbonylferrocene and tris(hydroxymethyl)methylamine, reacts with (Bu4N)(3)[H3V10O28] in N, N-dimethylacetamide to afford a salt containing a bis(triolato) capped hexavanadate anion bearing two ferrocenyl groups at its periphery, (Bu4N)(2)[{FcC(O)NHC(CH2O)(3)}(2)V6O13] (2). Compounds 1 and 2 were characterised by elemental analysis, spectroscopic methods (IR, NMR, and MS) and by cyclic voltammetry; the crystal structures of 1.1/2CH(3)CO(2)Et and (Bu4N)(2)[{FcC(O)NHC(CH2O)(3)}(2)V6O13]center dot 2Me(2)NCHO were determined by X-ray diffraction analysis. Single-point DFT calculations performed for the isolated hexavanadate anion revealed the presence of 3-centre 4-electron (3c4e) O-V-O bonds on the hexavanadate cage, which are responsible for the high energy of the occupied frontier orbitals. The upper eleven occupied molecular orbitals including the HOMO are all delocalized over the hexavanadate cage and, therefore, any electrochemical oxidation can be expected to occur preferentially at the hexavanadate anion without affecting the pendant ferrocene moieties."@en . "000284544800008" .