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Synthesis of Oligosilanyl Compounds of Group 4 Metallocenes with the Oxidation State +3

[Image: see text] Recently, we showed that titanocene silyls are much more stable with Ti in the oxidation state +3. The current study demonstrates that analogous Zr and Hf compounds can also be obtained by reaction of a suitable metalate precursor with an oligosilanyl dianion. As the obtained compl...

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Detalles Bibliográficos
Autores principales: Arp, Henning, Zirngast, Michaela, Marschner, Christoph, Baumgartner, Judith, Rasmussen, Kenneth, Zark, Patrick, Müller, Thomas
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Chemical Society 2012
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3377365/
https://www.ncbi.nlm.nih.gov/pubmed/22723723
http://dx.doi.org/10.1021/om3001873
Descripción
Sumario:[Image: see text] Recently, we showed that titanocene silyls are much more stable with Ti in the oxidation state +3. The current study demonstrates that analogous Zr and Hf compounds can also be obtained by reaction of a suitable metalate precursor with an oligosilanyl dianion. As the obtained complexes formally possess a d(1) electron configuration, they were investigated using EPR spectroscopy. The corresponding spectra indicate that the compounds can be considered to also exhibit some cyclosilanyl radical anion character. In order to understand the strong preference of disilylated titan(IV)ocenes for reductive elimination, a theoretical study of the thermodynamics of these reactions was conducted, revealing that this behavior is essentially caused by the weak Si–Ti(IV) bond.