Abstract
A novel scandium(III) complex with disulfonates as counter anions, [Sc(μ-OH)(H 2O) 5] 2[O 3S(CF 2) 3SO 3] 2 ( 5), was prepared from scandium oxides (Sc 2O 3) and perfluoropropane-1,3-disulfonic acid ( 1, HO 3SCF 2CF 2CF 2SO 3H). By X-ray analysis, 5 was found to be a μ-OH-bridged dimeric structure bearing two perfluoropropane-1,3-disulfonates without bonding to scandium(III) centers. A series of lanthanide(III) complexes were also prepared from 1 and lanthanide oxides (Ln 2O 3; Ln = La, Nd, Sm, and Gd). In sharp contrast to the dimeric scandium(III) complex, the corresponding lanthanide(III) complexes had monomeric structures. Interestingly, the dimeric scandium(III) complex, but not the monomeric lanthanide complexes, with perfluoropropane-1,3-disulfonates served as an efficient Lewis acid catalyst for the hydrolysis of esters.
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