Oxorhenium(V) Complexes with Ketiminato Ligands: Coordination Chemistry and Epoxidation of Cyclooctene
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- 作者：Albert Schrckeneder ; Pedro Traar ; Georg Raber ; Judith Baumgartner ; Ferdinand Belaj ; Nadia C. Msch-Zanetti
- 刊名：Inorganic Chemistry
- 出版年：2009
- 出版时间：December 21, 2009
- 年：2009
- 卷：48
- 期：24
- 页码：11608-11614
- 全文大小：822K
- 年卷期：v.48,no.24(December 21, 2009)
- ISSN：1520-510X
文摘
Rhenium(V) oxo complexes of the type [ReOX(L)2] (1−7; X = Cl, Br) containing β-ketiminate ligands (L = CH3C(O)CH2C(NAr)CH3: Ar = Ph (APOH), 2-MePh (MPOH), 2,6-Me2Ph (DPOH), 2,6-iPr2Ph (DiPOH)) have been prepared by reaction of [ReOX3(OPPh3)(SMe2)] (X = Cl, Br) with the lithium salts of the corresponding ligands. All compounds have been spectroscopically characterized, showing [ReOX(DiPO)2] (X = Cl (1), Br (5)), [ReOX(DPO)2] (X = Cl (2), Br (6)), and [ReOX(APO)2] (X = Cl (4), Br (7)) to be isomerically pure, in contrast to complex [ReOCl(MPO)2] (3), which exhibits a mixture of isomers. Compounds 2, 3, 5, and 7 were crystallographically characterized, showing similar octahedral coordination spheres with trans O═Re−O and cis O═Re−Cl bonds. However, the coordination of the nitrogen atoms vs each other is found to be cis or trans. Compounds 2 and 5 showed a trans-N,N configuration, for compound 3 both isomers (trans-N,N 3 and cis-N,N 3) were structurally characterized, and 7 gave a cis-N,N configuration. Compounds 1−6 are catalyst precursors for the epoxidation of cis-cyclooctene with 3 equiv of tert-butyl hydroperoxide (TBHP). Yields of the formed epoxide were up to 55% with all precursors, except with 2 and 6, where only up to 13% of epoxide was obtained under analogous conditions.