TY - JOUR
T1 - Syntheses and Chemistry of the diynyl Complexes M(C CC CH)(CO)(3)(eta-C5H5) (M = MO, W)
T2 - Crystal Structures of W(C CC CSiMe3)(CO)(3) (eta-C5H5), W{C CC[CH=C(CN)(2)]=C(CN)(2)}(CO)(3)(eta-C5H5), and cis-W(C CPh)(CO)(2)(PPh3)(eta-C5H5)
AU - Bruce, MI
AU - Ke, MZ
AU - Low, PJ
AU - Skelton, BW
AU - White, AH
PY - 1998/8/3
Y1 - 1998/8/3
N2 - Reactions of buta-1,3-diyne with appropriate metal halides, carried out in the presence of CuI in NHEt2, have given high yields of M(C=CC=CH)(CO)(n)Cp [M = W (1-W), Mo (1-Mo), n = 3; M = Fe, n = 2 (2)]. Complex 1-W was metalated with LiNPr2i; subsequent reactions with SiClMe3 or PClPh2 gave W(C=CC=CR)(CO)(3)Cp [R = SiMe3 (3) or P(O)Ph-2 (4)] in modest to high yield. Coupling of 1 with iodoarenes, catalyzed by a mixed Cu-I-Pd-0 catalyst, gave M(C=CC=CAr) (CO)(3)Cp [M = W, Ar = Ph (5-W), tol (6), C6H4OMe-4 (7), C6H4CO2Me-4 (8); M = Mo, Ar = Ph (5-Mo)]. Oxidative coupling of 1 (CuCl-tmed-O-2) gave {M(CO)(3)Cp}(2) (mu-C-8) [M = W(9-W), Mo (9-Mo)]. Addition of tetracyanoethene to 1-W occurred at the C=C triple bond further from the metal atom, to give W{C=CC[=C(CN)(2)]CH=C(CN)(2)}(CO)(3)Cp (10). Substitution of CO by PPh3 was difficult, but the Me3NO-induced reaction with 5-W afforded cis-W(C=CC=CPh)(CO)(2)(PPh3)Cp (11) in low yield. The X-ray crystal structures of 3 and 10, together with that of cis-W(C=CPh)(CO)(2)(PPh3)Cp (12), are reported.
AB - Reactions of buta-1,3-diyne with appropriate metal halides, carried out in the presence of CuI in NHEt2, have given high yields of M(C=CC=CH)(CO)(n)Cp [M = W (1-W), Mo (1-Mo), n = 3; M = Fe, n = 2 (2)]. Complex 1-W was metalated with LiNPr2i; subsequent reactions with SiClMe3 or PClPh2 gave W(C=CC=CR)(CO)(3)Cp [R = SiMe3 (3) or P(O)Ph-2 (4)] in modest to high yield. Coupling of 1 with iodoarenes, catalyzed by a mixed Cu-I-Pd-0 catalyst, gave M(C=CC=CAr) (CO)(3)Cp [M = W, Ar = Ph (5-W), tol (6), C6H4OMe-4 (7), C6H4CO2Me-4 (8); M = Mo, Ar = Ph (5-Mo)]. Oxidative coupling of 1 (CuCl-tmed-O-2) gave {M(CO)(3)Cp}(2) (mu-C-8) [M = W(9-W), Mo (9-Mo)]. Addition of tetracyanoethene to 1-W occurred at the C=C triple bond further from the metal atom, to give W{C=CC[=C(CN)(2)]CH=C(CN)(2)}(CO)(3)Cp (10). Substitution of CO by PPh3 was difficult, but the Me3NO-induced reaction with 5-W afforded cis-W(C=CC=CPh)(CO)(2)(PPh3)Cp (11) in low yield. The X-ray crystal structures of 3 and 10, together with that of cis-W(C=CPh)(CO)(2)(PPh3)Cp (12), are reported.
KW - X-RAY STRUCTURES
KW - TRANSITION-METAL COMPLEXES
KW - SIGMA-ACETYLIDE COMPLEXES
KW - CYCLO-ADDITION REACTIONS
KW - RUTHENIUM COMPLEXES
KW - ALLENYLIDENE-RUTHENIUM
KW - MOLECULAR-STRUCTURE
KW - CARBONYL-COMPLEXES
KW - LIGAND
KW - CENTERS
U2 - 10.1021/om980031r
DO - 10.1021/om980031r
M3 - Article
SN - 0276-7333
VL - 17
SP - 3539
EP - 3549
JO - Organometallics
JF - Organometallics
IS - 16
ER -