http://www.cnr.it/ontology/cnr/individuo/prodotto/ID18299
Chelated hydrazido(3-)rhenium(V) complexes: On the way to the nitridoM(V) Core (M = Tc, Re) (Articolo in rivista)
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- Label
- Chelated hydrazido(3-)rhenium(V) complexes: On the way to the nitridoM(V) Core (M = Tc, Re) (Articolo in rivista) (literal)
- Anno
- 2002-01-01T00:00:00+01:00 (literal)
- Alternative label
Mevellec F.1, Lepareur N. 2, Roucoux A. 3, Noiret N. 4, Patin H. 5, Bandoli G. 6, Porchia M. 7, Tisato F.8 (2002)
Chelated hydrazido(3-)rhenium(V) complexes: On the way to the nitridoM(V) Core (M = Tc, Re)
in Inorganic chemistry
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Mevellec F.1, Lepareur N. 2, Roucoux A. 3, Noiret N. 4, Patin H. 5, Bandoli G. 6, Porchia M. 7, Tisato F.8 (literal)
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- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#descrizioneSinteticaDelProdotto
- Studio di base sulla riduzione dello ione perrenato e introduzione del gruppo nitruro. Questa reattività è importante per capire come gli ioni perrenato e pertecnetato si riducono nei generatori 99-Mo/99m-Tc e 188W/188Re che si utilizzano negli ospedali (literal)
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- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- 7,8 ICIS-CNR; 6,Università di Padova; 1,2,3,4,5 ENSCR - Università di Rennes, Rennes - Francia (literal)
- Titolo
- Chelated hydrazido(3-)rhenium(V) complexes: On the way to the nitridoM(V) Core (M = Tc, Re) (literal)
- Abstract
- Neutral and asymmetrical hydrazido(3-)rhenium(V) heterocomplexes of the
type [Re(Ø2-L4)(Ln)(PPh3)] (Ø2-L4 = NNC(SCH3)S; H2L1 = S-methyl-Ò-N-(2-
hydroxyphenylethylidene)dithiocarbazate, 1, H2L2 = S-methyl-Ò-N-(2-
hydroxyphenylmethylidene) dithiocarbazate, 2) are prepared via ligand-
exchange reactions in ethanolic solutions starting from [ReV(O)Cl4]- in
the presence of PPh3, or from [ReV(O)Cl3(PPh3)2]. The distorted
octahedral coordination sphere of these compounds is saturated by a
chelated hydrazido group, a facially ligated ONS-Schiff base and PPh3.
Reduction-substitution reactions starting from [NH4][ReVIIO4] in acidic
ethanolic mixtures containing PPh3 and H2Ln (or its dithiocarbazic acid
precursor H3L4) produce another example of chelated hydrazido(3-) rhenium
(V) derivative, namely [RenvØ2-L4)Cl2(PPh3)2] 3. On the contrary, the N-
methyl substituted dithiocarbazic acid H2L3 reacts with perrhenate to
give the known nitrido complex [Re(N)Cl2(PPh3)2]. Rhenium(V) complexes
incorporating the robust Ø2-hydrazido moiety represent key intermediates
helpful for the comprehension of the reaction pathway which generates
nitrido-rhenium(V) species starting from oxo precursors. An essential
requirement for the stabilization of such chelated hydrazido-Re(V) units
is the triple deprotonation at the hydrazine nitrogens, thereby providing
efficient à-electron circulation in the resulting five-membered ring. The
thermal stability of these units is affected by the nature of the
anchoring donor, thione sulfur ensuring stronger chelation than nitrogen
and oxygen. The Ø2-hydrazido complexes are characterized by conventional
physicochemical techniques, including the X-ray crystal structure
determination of 1 and 3.
(literal)
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