http://www.cnr.it/ontology/cnr/individuo/prodotto/ID48284
Low-Temperature Nucleophilic Attack of Me3SiO- and MeO- on Rhenium(I) and Rhenium(0) Carbonyl Complexes (Articolo in rivista)
- Type
- Label
- Low-Temperature Nucleophilic Attack of Me3SiO- and MeO- on Rhenium(I) and Rhenium(0) Carbonyl Complexes (Articolo in rivista) (literal)
- Anno
- 2009-01-01T00:00:00+01:00 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#doi
- 10.1021/om8007162 (literal)
- Alternative label
Lucenti, E.; D'Alfonso, G.; Dragonetti, C.; Roberto, D.; Sironi, A.; Ugo, R. (2009)
Low-Temperature Nucleophilic Attack of Me3SiO- and MeO- on Rhenium(I) and Rhenium(0) Carbonyl Complexes
in Organometallics
(literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#autori
- Lucenti, E.; D'Alfonso, G.; Dragonetti, C.; Roberto, D.; Sironi, A.; Ugo, R. (literal)
- Pagina inizio
- Pagina fine
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#url
- http://pubs.acs.org/doi/abs/10.1021/om8007162 (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#numeroVolume
- Rivista
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#pagineTotali
- Note
- Scopu (literal)
- ISI Web of Science (WOS) (literal)
- Http://www.cnr.it/ontology/cnr/pubblicazioni.owl#affiliazioni
- Institute of Molecular Science and Technology of CNR, Via Golgi 19, 20133 Milan, Italy, Department of
Inorganic, Metallorganic, and Analytical Chemistry \"Lamberto Malatesta\" and Department of Structural
Chemistry and Inorganic Stereochemistry, UniVersity of Milan, Via Venezian 21, 20133 Milan, Italy, and
Italian InteruniVersity Consortium on Materials Science and Technology (INSTM) - Research Unit of
Milan, Via Giusti 9, 50121 Firenze, Italy (literal)
- Titolo
- Low-Temperature Nucleophilic Attack of Me3SiO- and MeO- on Rhenium(I) and Rhenium(0) Carbonyl Complexes (literal)
- Abstract
- The reactivity of [Re(CO)5Cl] and [Re2(CO)10] with nucleophiles such as Me3SiO- and MeO- has been investigated by low-temperature NMR and by infrared spectroscopy particularly aimed at detecting the [Re(CO)5OR] species, which so far have eluded isolation, proposed as intermediates in the synthesis of the dimeric species [Re2(CO)6(mu-OR)3]- (R = SiMe3, Me). For both nucleophiles the first step involves an interaction with one specific carbonyl ligand and formation of new anionic complexes carrying a metal carboxy silyl or methyl ester, such as cis-[Re(CO)4(COOSiMe3)Cl]-, cis-[Re(CO)4(COOMe)Cl]-, [Re2(CO)9(COOSiMe3)]-, and [Re2(CO)9(COOMe)]-. The Re(I) complexes, stable only at low temperature, by further nucleophilic attack generate the well-known dimeric [Re2(CO)6(mu-OR)3]- complexes. The Re(0) metal carboxy-methyl esters derived from [Re2(CO)10] are thermally more stable and can be isolated in the solid state. In particular, the new complex [Re2(CO)9(COOMe)][NBu4] has been fully characterized by X-ray diffraction. In contrast, when the nucleophilic attack involves a weaker OR- nucleophile such as [(c-C6H11)7Si8O12O]- or a Re(I) pentacarbonyl substrate which bears a better leaving group such as the triflate, the low-temperature nucleophilic attack on a specific carbonyl ligand does not occur. (literal)
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