TY - JOUR
T1 - η5-cyclopentadienyl and η5-methylcyclopentadienyl 1,2-bis(dimethylphosphino)ethane complexes of titanium(II). The crystal structure of Ti(C5H4Me)2(dmpe)
AU - Girolami, Gregory S.
AU - Wilkinson, Geoffrey
AU - Thornton-Pett, Mark
AU - Hursthouse, Michael B.
PY - 1984
Y1 - 1984
N2 - The interaction of the titanium(II) complex trans-TiCl2(dmpe)2 with 2 equivalents of Na(C5H5) or Na(C5H4Me) in diethyl ether gives the dark orange cyclopentadienyl compounds Ti(C5H4R)2(dmpe) (R = H or Me, dmpe = Me2PCH2CH2PMe2). These diamagnetic 18-electron species give n.m.r. spectra consistent with a bent metallocene structure, confirmed by the X-ray structure analysis of Ti(C5H4Me)2(dmpe) for which Ti-P 2.533(6) Å (mean), Ti-C 2.310(5)-2.441 (6) Å, P-Ti-P 76.9(2)°, and centroid-Ti-centroid = 135.3(2)°. The cyclopentadienyl rings are very slightly tilted towards the dmpe ligand due to non-bonding contacts between the ring-bound methyl groups.
AB - The interaction of the titanium(II) complex trans-TiCl2(dmpe)2 with 2 equivalents of Na(C5H5) or Na(C5H4Me) in diethyl ether gives the dark orange cyclopentadienyl compounds Ti(C5H4R)2(dmpe) (R = H or Me, dmpe = Me2PCH2CH2PMe2). These diamagnetic 18-electron species give n.m.r. spectra consistent with a bent metallocene structure, confirmed by the X-ray structure analysis of Ti(C5H4Me)2(dmpe) for which Ti-P 2.533(6) Å (mean), Ti-C 2.310(5)-2.441 (6) Å, P-Ti-P 76.9(2)°, and centroid-Ti-centroid = 135.3(2)°. The cyclopentadienyl rings are very slightly tilted towards the dmpe ligand due to non-bonding contacts between the ring-bound methyl groups.
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U2 - 10.1039/DT9840002347
DO - 10.1039/DT9840002347
M3 - Article
AN - SCOPUS:37049111122
SN - 1472-7773
SP - 2347
EP - 2350
JO - Journal of the Chemical Society, Dalton Transactions
JF - Journal of the Chemical Society, Dalton Transactions
IS - 10
ER -