TRANSITION-METAL-SUBSTITUTED ACYLPHOSPHANES AND PHOSPHAALKENES .18. P-METALATED IMINOPHOSPHIRANES BY ISOCYANIDE ADDITION TO A METALLOPHOSPHAALKENE - X-RAY STRUCTURE DETERMINATION OF (ETA-5-C5ME5)(CO)2FEPC(SIME3)2C=NPH
L. Weber et al., TRANSITION-METAL-SUBSTITUTED ACYLPHOSPHANES AND PHOSPHAALKENES .18. P-METALATED IMINOPHOSPHIRANES BY ISOCYANIDE ADDITION TO A METALLOPHOSPHAALKENE - X-RAY STRUCTURE DETERMINATION OF (ETA-5-C5ME5)(CO)2FEPC(SIME3)2C=NPH, Organometallics, 12(11), 1993, pp. 4653-4656
The reaction of (eta5-C5Me5)(CO)2FeP=C(SiMe3)2 (1) with the isocyanide
s arylNC (2: aryl = Ph (a), 2-MeC6H4 (b), 2,6-Me2C6H3 (c)) in benzene
at 20-degrees-C afforded the transition-metal-functionalized iminophos
phiranes 3a-c as red crystalline solids. The novel compounds were char
acterized by elemental analyses and spectroscopic methods (IR, H-1, C-
13, and P-31 NMR, and mass spectroscopy). The molecular structure of t
he iminophosphirane (eta5-C5Me5)(CO)2FePC-(SiMe3)2C=NPh (3a) was estab
lished by a complete single-crystal diffraction study (space group, C2
/c; Z = 8, a = 27.214(4) angstrom, b = 15.146(2) angstrom, c = 15.854(
2) angstrom, beta = 114.350(10)-degrees).