Xj. Lei et al., CLUSTERS AS LIGANDS .5. TRICOBALT CLUSTER ALKOXYCARBOXYLATES OF TITANIUM AND ZIRCONIUM EXHIBITING NOVEL STRUCTURES AND PROPERTIES, Organometallics, 16(24), 1997, pp. 5289-5301
The protonolysis of group 4 M(IV)(OR)(4), M = Ti, Zr, organic alkyl- o
r aryloxides with the cluster acid (CO)(9)Co-3(mu(3)-CCO2H) leads to a
series of novel tricobalt cluster M(IV) alkoxy- or aryloxycarboxylate
s, most of which contain bridging oxo ligands. The compounds, which ar
e isolated in good yield as crystalline substances and characterized s
pectroscopically as well as crystallographically, are Co-3(mu(3)-CCO2)
}(2){(CO)(9)-Co-3(mu(3)-CCO2)}(2), 1; mu(3)-O)(4)(OR)(4){mu-(CO)(9)Co-
3(mu(3)-CCO2)}(4), 2 (R = CH(CH3)(2), 2a; (CH2)(3)CH3, 2b; C6H5, 2c; 2
,6-(CH3)(2)-C6H3, 2d); H3)(4)(OCH2CH3)(8){mu-(CO)(9)Co-3(mu(3)-CCO2)}(
4), 3; and 2)(1,2-O2C6H4)(4){mu-(CO)(9)Co-3(mu(3)-CCO2)}(4)], 4. Furth
er, the mixed-metal derivatives )(OCH(CH3)(2))(2){mu-(CO)(9)Co-3(mu(3)
-CCO2)}(4)], 5, and THF){mu(CO)(9)Co-3(mu(3)-CCO2)}(3)}(2)(O-2-CCO2)].
2HOCH(3) . 2THF, 6, in which the Co(II) ions are derived from in situ
tricobalt cluster degradation, are characterized in similar fashion.
Some of the distinguishing features of an inorganic cluster as a ligan
d substituent are revealed by a comparison of the observed chemistry w
ith that known for reactions of organic acids with M(IV)(OR)(4).