http://www.cnr.it/ontology/cnr/individuo/prodotto/ID192072
New structures based on the mixed valence polyoxometalate cluster [V12B18O60H6]n2 (Articolo in rivista)
- Type
- Label
- New structures based on the mixed valence polyoxometalate cluster [V12B18O60H6]n2 (Articolo in rivista) (literal)
- Anno
- 2012-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1039/c2ce25436k (literal)
- Alternative label
Patricio Hermosilla-Ibanez, Pierre Emmanuel Car, Andres Vega, Juan Costamagna, Francesco Caruso,
Jean-Yves Pivan, Eric Le Fur, Evgenia Spodine Diego Venegas-Yazigi (2012)
New structures based on the mixed valence polyoxometalate cluster [V12B18O60H6]n2
in CrystEngComm (Camb., Online)
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Patricio Hermosilla-Ibanez, Pierre Emmanuel Car, Andres Vega, Juan Costamagna, Francesco Caruso,
Jean-Yves Pivan, Eric Le Fur, Evgenia Spodine Diego Venegas-Yazigi (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://pubs.rsc.org/en/Content/ArticleLanding/2012/DT/c1dt11519g (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Facultad de Qu?mica y Biolog?a, Universidad de Santiago de Chile,
USACH, Chile.; CEDENNA, Chile; ENSCR, CNRS, UMR 6226, Rennes, France; Universite´ Europeenne de Bretagne, France; Universidad Andres Bello, Departamento de Ciencias Qu?´micas, Facultad
de Ciencias Exactas, Chile; Instituto di Chimica Biomolecolare, CNR, c/o Universita` di Roma ''La
Sapienza'', Rome, Italy; Facultad de Ciencias Qu?´micas y Farmace´uticas, Universidad de Chile,
Chile (literal)
- Titolo
- New structures based on the mixed valence polyoxometalate cluster [V12B18O60H6]n2 (literal)
- Abstract
- Hydrothermal synthesis was used to obtain four new crystalline lattices derived from the
functionalization of the [V12B18O60H6]n2 cluster: Na8(H3O){[Ni(H2O)5][V12B18O60H6]}?12.5H2O (1),
Na5 (H3O)4{[Ni (H2O)3(en)][V12B18O60H6]}?9H2O (2), and Na9(H3O){Zn0.5[V12B18O60H6]}?11H2O
(3), [Hen][H2en]{[Zn(en)2]3 [V12B18O60H6]}?3H2O (4). All four compounds crystallize in the space
group C2/c. Compounds (1) (2) and (4) are 0D species, while for (3) there is some degree of covalent
connectivity between the anionic units, due to the presence of ZnII cations with partial occupation
between them. On the basis of structural data and BVS calculations, these functionalized cluster
species present mixed-valence ratios of 11VIV/1VV for (1), (2) and (3) and 9VIV/3VV for compound (4).
Compounds (1), (2) and (3) present sodium and hydronium ions in the crystalline lattice, while
protonated ethylenediamine is observed in compound (4). These cations balance the negative charge
of the corresponding clusters and stabilize the crystalline lattice by electrostatic interactions. In the
studied compounds, NiII ions coordinate to the vanadyl oxygen atoms, whereas the ZnII cations
coordinate both to the vanadyl oxygen atoms and to the oxygen atoms bonded to boron centres. The
electronic spectra in the low energy range are dominated by the IVCT phenomenon, since the
functionalization of the cluster [V12B18O60H6]n2 by different transition metal ions does not affect the
observed absorption bands. (literal)
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