Syntéza, roztok a krystal. struktura 2jaderného oxo-peroxovanadičnatého komplexu s kyselinou mandelátovou: (NR4)2[V2O2(O2)2(mand)2] . xH2O [R=H, Me, Et; MAND=mandelato(2-)=C8H6O3 2-].

Kód výsledku v IS VaVaI

<a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00216224%3A14310%2F04%3A00009932" target="_blank" >RIV/00216224:14310/04:00009932 - isvavai.cz</a>

Výsledek na webu

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DOI - Digital Object Identifier

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Jazyk výsledku

angličtina

Název v původním jazyce

Synthesis, solution and crystal structures of dinuclear vanadium(V) oxo monoperoxo complexes with mandelic acid: (NR4)2[V2O2(O2)2(mand)2] . xH2O [R=H, Me, Et; MAND=mandelato(2-)=C8H6O3 2-]

Popis výsledku v původním jazyce

Vanadium(V) oxo peroxo mandelato complexes were prepared from aqueous solution and characterized by elemental analysis, IR, UV-Vis and 51V NMR spectroscopies. The single crystal X-ray studies of (NMe4)2[V2O2 (O2)2(R,S-mand)2].6.5H2O (3), (NMe4)(NH4)[V2O2(O2)2(R,S-mand)2].2H2O (4) and (NEt4)2[V2O2(O2)2(R-mand)2] (8) revealed that the mandelato ligand behaves as a bidentate chelator adopting the (O-, COO-) donor set. The complex anions in structures of 3 and 8 contain a dinuclear V2O2 core with cyclic arrangement of two vanadium atoms and two hydroxyl oxygen atoms from the bridging mand ligands. Each vanadium atom is coordinated by six oxygen atoms arising from two hydroxyl and one carboxyl groups, 2-peroxo ligand and one end-bonded oxo ligand. The coordination polyhedron can be described as distorted pentagonal pyramid. The structure of 4 is unique as it contains in the unit cell differently coordinated water molecules in two types of dinuclear anions: [V2O2(O2)2(R-mand)2(H2O)]2-, with

Název v anglickém jazyce

Synthesis, solution and crystal structures of dinuclear vanadium(V) oxo monoperoxo complexes with mandelic acid: (NR4)2[V2O2(O2)2(mand)2] . xH2O [R=H, Me, Et; MAND=mandelato(2-)=C8H6O3 2-]

Popis výsledku anglicky

Vanadium(V) oxo peroxo mandelato complexes were prepared from aqueous solution and characterized by elemental analysis, IR, UV-Vis and 51V NMR spectroscopies. The single crystal X-ray studies of (NMe4)2[V2O2 (O2)2(R,S-mand)2].6.5H2O (3), (NMe4)(NH4)[V2O2(O2)2(R,S-mand)2].2H2O (4) and (NEt4)2[V2O2(O2)2(R-mand)2] (8) revealed that the mandelato ligand behaves as a bidentate chelator adopting the (O-, COO-) donor set. The complex anions in structures of 3 and 8 contain a dinuclear V2O2 core with cyclic arrangement of two vanadium atoms and two hydroxyl oxygen atoms from the bridging mand ligands. Each vanadium atom is coordinated by six oxygen atoms arising from two hydroxyl and one carboxyl groups, 2-peroxo ligand and one end-bonded oxo ligand. The coordination polyhedron can be described as distorted pentagonal pyramid. The structure of 4 is unique as it contains in the unit cell differently coordinated water molecules in two types of dinuclear anions: [V2O2(O2)2(R-mand)2(H2O)]2-, with

Druh

J_x - Nezařazeno - Článek v odborném periodiku (Jimp, Jsc a Jost)

CEP obor

CA - Anorganická chemie

OECD FORD obor

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Projekt

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Návaznosti

Z - Vyzkumny zamer (s odkazem do CEZ)

Rok uplatnění

2004

Kód důvěrnosti údajů

S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Název periodika

Polyhedron

ISSN

0277-5387

e-ISSN

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Svazek periodika

23

Číslo periodika v rámci svazku

4

Stát vydavatele periodika

GB - Spojené království Velké Británie a Severního Irska

Počet stran výsledku

9

Strana od-do

655-663

Kód UT WoS článku

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EID výsledku v databázi Scopus

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