Issue 6, 2008

Isoelectronic caesium compounds: the triphosphenide Cs[tBu3SiPPPSitBu3] and the enolate Cs[OCH[double bond, length as m-dash]CH2]

Abstract

The caesium triphosphenide Cs[tBu3SiPPPSitBu3] was accessible from the reaction of CsF with the sodium triphosphenide Na[tBu3SiPPPSitBu3] in tetrahydrofuran at room temperature. In contrast to the preparation of tetrahydrofuran-solvated silanides M[SitBu3] (M = Li, Na, K), our efforts to synthesize the caesium silanide Cs[SitBu3] as a tetrahydrofuran complex failed. When tBu3SiBr was treated with an excess of caesium metal in tetrahydrofuran at room temperature, the caesium enolate Cs[OCH[double bond, length as m-dash]CH2] and the supersilane tBu3SiH formed rather than the silanide Cs[SitBu3]. X-Ray quality crystals of the enolate Cs[OCH[double bond, length as m-dash]CH2] (orthorhombic, Pnma) were obtained from tetrahydrofuran at ambient temperature. In contrast to the structures of its homologues M[tBu3SiPPPSitBu3] (M = Na, K), the caesium triphosphenide Cs[tBu3SiPPPSitBu3] features a polymer in the solid state (orthorhombic, Cmcm).

Graphical abstract: Isoelectronic caesium compounds: the triphosphenide Cs[tBu3SiPPPSitBu3] and the enolate Cs[OCH [[double bond, length as m-dash]] CH2]

Supplementary files

Article information

Article type
Paper
Submitted
17 Sep 2007
Accepted
09 Nov 2007
First published
29 Nov 2007

Dalton Trans., 2008, 787-792

Isoelectronic caesium compounds: the triphosphenide Cs[tBu3SiPPPSitBu3] and the enolate Cs[OCH[double bond, length as m-dash]CH2]

H. Lerner, I. Sänger, F. Schödel, A. Lorbach, M. Bolte and M. Wagner, Dalton Trans., 2008, 787 DOI: 10.1039/B714339G

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