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Título : Rhodium and iridium olefin complexes with bulky cyclopentadienyl and hydrotris(pyrazolyl)borate ligands
Autor : Conejero Iglesias, Salvador, Esqueda Oliva, Ana Cristina, Villar Valpuesta, José E., Álvarez, Eleuterio, Carmona Guzmán, Ernesto
Palabras clave : Rhodium
C-H activation
Fecha de publicación : 10-May-2009
Editor: Elsevier
Resumen: The synthesis of a series of rhodium and iridium complexes bearing bulky cyclopentadienyl or hydro(trispyrazolyl)borate ligands is described. The rhodium cyclopentadienyl and hydrotris(pyrazolyl)borate diene compounds, [(η5-C5Me4But)Rh(η4-2,3-MeRC4H4] (R = H, 1; Me, 2) and TpMsRh(η4-2,3-MeRC4H4) (R = H, 3; Me, 4; TpMs is hydrotris(3-mesitylpyrazol-1-yl)borate), respectively, have been prepared from the corresponding Rh(I) diene precursors and Zn(C5Me4But)2 (for 1 and 2), or TlTpMs (for 3 and 4), as effective C5Me4But or TpMs transfer reagents. In contrast with these results, attempts to obtain a bis(ethylene) derivative of the TptolIr(I) unit (Tptol stands for hydrotris(3-p-tolylpyrazol-1-yl)borate) have provided instead the Ir(III) complex [(κ4-N,N′,N″,C-Tptol)-Ir(C2H5)(C2H4)] (5), whose formation requires C–H bond activation of a molecule of ethylene and of one of the Tptol p-tolyl substituents. In refluxing toluene 5 experiences metalation of a second p-tolyl substituent to give [(κ5-N,N′,N″,C,C′-Tptol)-Ir(C2H4)] (6), which features unusual κ5-Tptol coordination. The latter compound reacts with carbon monoxide to yield the corresponding carbonyl, 7.
Descripción : 7 páginas, 3 figuras, 6 esquemas.
Versión del editor:
ISSN: 0020-1693
DOI: 10.1016/j.ica.2009.05.002
Citación : Inorganica Chimica Acta 362(12): 4539-4545 (2009)
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