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Lookup NU author(s): Dr Keith Izod, Dr Stephen Liddle, Emeritus Professor William McFarlane, Professor William Clegg
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Metathesis between LaI3 and two equivalents of {R(C6H4-2-CH2NMe2)P}K gives the heteroleptic complex {R(C6H4-2-CH2NMe2)P}2LaI (1), which reacts in situ with one equivalent of KOR′ to give the corresponding mixed phosphide/alkoxide complexes {R(C6H4-2-CH2NMe2)P}2La(OR′) [R = (Me3Si)2CH, R′ = t-Bu (2), i-Pr (3)]. A similar in situ reaction between 1 and one equivalent of any of the alkali metal organometallics R′K [R′ = PhCH2, Me3SiCH2, (Me3Si)2CH] yields the cyclometalated product {([Me3Si]2CH)(C6H4-2-CH2NMe2)P}La(THF)[P(C6H4-2-CH2NMe2)[CH{SiMe3}{SiMe2CH2}] (4) and R′H. Reaction between the homoleptic tris(alkyl) {(Me3Si)2CH}3La and two equivalents of the secondary phosphine R(C6H4-2-CH2NMe2)PH yields 4 as the exclusive product, suggesting that the cyclometalation reaction is intramolecular in nature. Compounds 2 – 4 have been characterized by multi-element NMR spectroscopy and X-ray crystallography. Variable-temperature 31P and 1H NMR spectra and 2-D NMR experiments reveal that 4 is subject to dynamic processes in toluene solution which may be attributed to rapid, reversible inversion at phosphorus, which results in rapid equilibria between stereoisomers; La C cleavage is slow on the NMR timescale.
Author(s): Izod K, Liddle ST, McFarlane W, Clegg W
Publication type: Article
Publication status: Published
Journal: Organometallics
Year: 2004
Volume: 23
Issue: 11
Pages: 2734-2743
ISSN (print): 0276-7333
ISSN (electronic): 1520-6041
Publisher: American Chemical Society
URL: http://dx.doi.org/10.1021/om0498798
DOI: 10.1021/om0498798
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