Phosphine promoted substituent redistribution reactions of B-chlorocatechol borane:: Molecular structures of ClBcat, BrBcat and L•ClBcat (cat=1,2-O2C6H4; L = PMe3, PEt3, PBut3, PCy3, NEt3)

被引:49
作者
Coapes, RB
Souza, FES
Fox, MA
Batsanov, AS
Goeta, AE
Yufit, DS
Leech, MA
Howard, JAK
Scott, AJ
Clegg, W
Marder, TB
机构
[1] Univ Durham, Dept Chem, Durham DH1 3LE, England
[2] Univ Waterloo, Dept Chem, Waterloo, ON N2L 3G1, Canada
[3] Newcastle Univ, Dept Chem, Newcastle Upon Tyne NE1 7RU, Tyne & Wear, England
来源
JOURNAL OF THE CHEMICAL SOCIETY-DALTON TRANSACTIONS | 2001年 / 08期
关键词
D O I
10.1039/b010025k
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
In order to evaluate the potential for side reactions when using B-chlorocatechol borane (ClBcat) in stoichiometric or catalytic transformations involving metal phosphine complexes, we examined the interaction between ClBcat and a series of PR3 compounds. Reactions of ClBcat with the basic phosphines PMe3, PEt3, PMe2Ph and PBu3t, in exactly 1 & ratio;1 stoichiometry, all afforded crystalline adducts of the form R3P . ClBcat, which have been characterised spectroscopically. All display broad singlets at room temperature in both B-11{H-1} and P-31{H-1} NMR spectra with no B-P coupling observed. The low temperature B-11{H-1} and P-31{H-1} NMR spectra, however, do show B-P coupling, suggesting rapid dissociation at room temperature. The compounds ClBcat, BrBcat, and the adducts between ClBcat and PMe3, PEt3 and PBu3t have been characterised by single crystal X-ray diffraction. In ClBcat and BrBcat, the halogen contributes little pi -bonding to boron as the B-O bond lengths are identical in both compounds. The reaction of ClBcat with a small excess of PCy3 yielded Cy3P . ClBcat, which has also been characterised by single crystal X-ray diffraction and shows considerable distortion. The reaction between ClBcat and the less basic phosphines PPh3 and PPh2Me yielded only the redistribution products R3P . BCl3 and B(2)cat(3). In fact, reaction of all of the phosphines with an excess of ClBcat gave only redistribution products, although there was evidence for an intermediate in the B-11{H-1} NMR spectra, with PMe3 and PEt3. The isolated R3P . ClBcat adducts proved unstable, even at low temperature in the solid state, eventually leading to R3P . BCl3 and B(2)cat(3). Reaction of ClBcat with NEt3 afforded Et3N . ClBcat, which was characterised spectroscopically and by single crystal X-ray diffraction. This adduct is stable both in solution and in the solid state.
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页码:1201 / 1209
页数:9
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