COMPLEXATION OF 1,4,5,8,9,10-HEXAHYDROANTHRACENE (HHA) TO IRON OR RUTHENIUM - A BIS(DIENE)DIIRON HHA GEOMETRY, HYDROAROMATIC RUTHENIUM COMPOUNDS RELATED TO RU(ETA-6-THA)CL2(DMSO) (THA = 1,4,9,10-TETRAHYDROANTHRACENE - DMSO = DIMETHYL-SULFOXIDE), AND RU3(CO)12-CATALYZED HHA REARRANGEMENTS
Tj. Beasley et al., COMPLEXATION OF 1,4,5,8,9,10-HEXAHYDROANTHRACENE (HHA) TO IRON OR RUTHENIUM - A BIS(DIENE)DIIRON HHA GEOMETRY, HYDROAROMATIC RUTHENIUM COMPOUNDS RELATED TO RU(ETA-6-THA)CL2(DMSO) (THA = 1,4,9,10-TETRAHYDROANTHRACENE - DMSO = DIMETHYL-SULFOXIDE), AND RU3(CO)12-CATALYZED HHA REARRANGEMENTS, Organometallics, 12(11), 1993, pp. 4599-4606
The nonconjugated tetraene 1,4,5,8,9,10-hexahydroanthracene (HHA; I) r
eacts with Fe(CO)5 to afford mono- and bis(tricarbonyliron) derivative
s 1 and 2, in which the hydrocarbon fragment is bound to iron as a eta
4-diene (respectively lo[4.4.0.0(3,8)]tetradeca1(10),3(8),5,11-tetraen
e) iron (1) and eta4:1,10,11,12-eta4)-tricyclo[8.4.0.0.3,8]tetrade ca-
1(10),3(8),4,11-tetraene) diiron (2)). Complex 2, which crystallizes i
n the space group P2(1)/c (a = 11.0617(7) angstrom, b = 12.239(2) angs
trom, c = 6.9928(5) angstrom, beta = 105.82(6)-degrees, V = 910.9(9) a
ngstrom3, Z = 2), has been characterized by using X-ray diffraction, e
stablishing the anti disposition of the two Fe(CO)3 groups. Compounds
1 and 2 have been further characterized by using C-13 NMR spectroscopy
. In the presence of Ru3(CO)12, HHA is converted catalytically to othe
r anthracenes, mainly by isomerization. With hydrated ruthenium(III) c
hloride, HHA binds to Ru as a eta6-arene (i.e. 1,4,9,10-tetrahydroanth
racene (THA; II), via aromatization in one terminal ring), as is illus
trated in the crystal structure of the product Ru(eta6-THA)Cl2(L) (4,
L = DMSO; space group P2(1)/n, a = 10.821(3) angstrom, b = 12.472(4) a
ngstrom, c = 12.738(4) angstrom, beta = 107.63(7)-degrees, V = 1638(2)
angstrom3, Z = 4), from which facile displacement of DMSO may be acco
mplished to give 6 (L = Me2pzH, pzH = pyrazole), 7 (L = PPh3), 8 (L =
P(OEt)3), 9 (L = PMePh2), and 10(L = PCy3, Cy = cyclohexyl). The H-1 a
nd C-13 NMR spectra of compounds 7-10 show different and shielding of
H6,7 of the THA ligand attributable to ring current effects due to the
proximity of the PPh3 ligand and identify selective coupling of C8a,1
0a to the P-31 nucleus in 7, i.e. consistent with the existence of an
energy minimum during eta6-THA rotation.