Spectoscopic and structural studies on charge-transfer complexes of lanthanum(III)acetylacetonate with σ-acceptor iodine and π-acceptor DDQ

Abstract

The interaction of the donor La(III)acetylacetonate, [La(acac)3], with iodine as a r-acceptor and with 2,3- dichloro-5,6 dicyano-1,4-benzoquinone, (DDQ) as a p-acceptor have been studied in the solvents CH2Cl2, CHCl3 and CCl4 at room temperature. The obtained results indicate the formation of 1:1 charge-transfer complexes. The electronic and infrared absorptions and elemental analysis of the formed complexes indicate that the complexes are formulated as the triiodide [(La(acac)3)2I]+ I

3 and [La(acac)3(DDQ)]. Far-infrared spectrum shows that the triiodide ion is nonlinear with C2v symmetry. The values of the equilibrium constants (K) and obsorptivities (e) for both the formed CT-complexes are calculated and discussed in term of reaction stoichiometry values and molecular steric hindrance. Mid infrared spectra suggest that the electron donation from [La(acac)3] to the donors I2 or DDQ could mainly take place through the oxygen atoms in addition to the acac ring p-molecular orbitals.