@article {2772,
	title = {CRYSTAL AND MOLECULAR-STRUCTURES OF OS3(CO)9[MU(3)-(C5H4PR)FE(C5H4)] (R = FC OR PH), 2 MOLECULES WITH FE -] OS BONDS},
	journal = {Journal of Organometallic Chemistry},
	volume = {452},
	number = {1-2},
	year = {1993},
	note = {ISI Document Delivery No.: LM427Times Cited: 12Cited Reference Count: 16},
	month = {Jun},
	pages = {97-103},
	type = {Article},
	abstract = {{The thermal reaction between Os3(CO)12 and Fe(C5H4)2PPh affords Os3(CO)9[mu3-(C5H4PPh)Fe(C5H4)](5b) (70\%) as the only major product. Heating a solution of Os3(CO)11(PFc2Ph) (FcH = (eta-C5H5)2Fe) in octane for 3 h gives the related molecule Os3(CO)9[mu3-(C5H4PFc)Fe(C5H4)] (5a) in low yield (5\%). The structures of 5a and 5b have been established by X-ray crystallography, revealing in each case that a closed Os3-triangle is capped on one face by the ferrocenyl phosphido moiety acting as an overall six-electron donor. It is bonded to the cluster via one phosphorus atom, one carbon atom from the C5H4 ring, and the iron atom. Two semibridging carbonyls are also present in each structure. Crystals of {mu3-[eta5-C5H4)2Fe]P[(eta3-C5H4)Fe(eta5-C5H5)]-Fe,P,P,C}Os3(CO)9 (5a) are triclinic, a 12.304(1), b 12.336(2), c 10.886(2) angstrom, alpha 115.38(2), beta 92.34(1), gamma 91.76(1)-degrees},
	keywords = {CLEAVAGE, CLUSTERS, CONVERSION},
	isbn = {0022-328X},
	url = {<Go to ISI>://A1993LM42700016},
	author = {Cullen, W. R. and Rettig, S. J. and Zheng, T. C.}
}
