OXIDATIVE COUPLING OF PHOSPHINOMETHANIDE LIGANDS ON TITANOCENE AND BISMUTH CENTERS - SELECTIVE C-C, P-C AND P-P BOND FORMATION

Citation
Hh. Karsch et al., OXIDATIVE COUPLING OF PHOSPHINOMETHANIDE LIGANDS ON TITANOCENE AND BISMUTH CENTERS - SELECTIVE C-C, P-C AND P-P BOND FORMATION, Journal of organometallic chemistry, 459(1-2), 1993, pp. 95-105
Citations number
42
Categorie Soggetti
Chemistry Inorganic & Nuclear","Chemistry Inorganic & Nuclear
ISSN journal
0022328X
Volume
459
Issue
1-2
Year of publication
1993
Pages
95 - 105
Database
ISI
SICI code
0022-328X(1993)459:1-2<95:OCOPLO>2.0.ZU;2-A
Abstract
The reaction of Cp2TiCl2 with two equivalents of Lithium-phosphinometh anides is described. The reaction with LiCH2PMe2 leads to a C-C coupli ng product Cp2Ti[Me2PCH2CH2PMe2], whereas with {(TMEDA)Li[CH(PMe2)(SiM e3)]}2, the P-C coupling product Me3SiCH2PMe2=C(PMe2)(SiMe3), a P-ylid e, is formed. An anlogous P-C coupling is observed with Li[CH(PMe2)2], whereby a novel titanocene heterocycle (Cp2Ti(H)[(Me2P)2C-PMe2-CH2-PM e2)]}, with an agostic Ti ... H ... C interaction, may be characterize d as an intermediate. In contrast, with Li[CH(PMe2)(SiMe3)] (without T MEDA) P-P coupling, yielding [(Me3Si)-(H)C=PMe2]2, is observed exclusi vely. An analogous result is obtained with Li[C(PMe2)(SiMe3)2], leadin g to [(Me3Si)2C=PMe2]2, and, likewise, in the similar reaction of Cp2T iCl2 with Li[C(PMe2)2(SiMe3)], P-P Coupling is observed leading to [(M e2P)(Me3Si)C=PMe2]2 and (CP2Ti(III)[(Me2P)2C(SiMe3)]}. With (TMEDA)Li[ HC(PPh2)2], both P-P (34%) and P-C (66%) coupling are observed, yieldi ng the P-ylides [(Ph2P)HC=PPh2]2 and Ph2PCH2PPh2=C(PPh2)2, respectivel y. The results are compared with the respective coupling reactions at bismuth centers: BiCl3 reacts with LiCH2PMe2 to give Bi(CH2PMe2)3; wit h {(TMEDA)Li[CH(PMe2)(SiMe3)]}2 only 5% of the P-C coupling product Me 3SiCH2PMe2=C(PMe2)(SiMe3) are found, whereas 95% of the P-P coupling p roduct [(Me3Si)(H)C-PMe2]2 are obtained. Exclusive P-P coupling is als o observed from BiCl3 and (TMEDA)Li[C(PMe2)(SiMe3)2] and Li[C(PMe2)2(S iMe3)], respectively. The results clearly indicate that a metal-center ed process, sensitive to steric and coordination effects, is active. S elective C-C, P-C and P-P coupling reactions are possible by selecting the appropriate combinations of reagents. The novel P-ylides are char acterized by use of NMR spectroscopy; (Cp2Ti(III)[(Me2P)2C(Si-Me3)]} a nd [(Me3Si)2C=PMe2]2 are further characterized by X-ray structure dete rminations.