화학공학소재연구정보센터
Journal of Physical Chemistry A, Vol.101, No.28, 5046-5053, 1997
Europium(III) Luminescence and Intramolecular Energy-Transfer Studies of Polyoxometalloeuropates
The photoexcitation in the oxygen-to-metal (M = Nb or W) charge transfer (O-->M lmct) bands of two X-ray crystallographically characterized polyoxometalloeuropates, Na7H19{[Eu3O(OH)(3)(H2O)(3)](2)Al-2(Nb6O19)(5)}.47H(2)O and [Eu(H2O)(8)](3)K2H3[(GeTi3W9O37)(2)O-3].13H(2)O, induced Eu3+ emission due to the D-5(0)-->F-7(J) (J = 0-4) transition with a single-exponential decay. In the latter compound an additional D-5(1)-->F-7(J) transition with a weak intensity (with the relative intensity of about 9% of the D-5(0)-->F-7(J) emission at 4.2 K) was observed. No observation of the D-5(1)-->F-7(J) emission in the former compound was ascribed to the D-5(1)-D-5(0) cross-relaxation : Eu3+(D-5(1)) + Eu3+(F-7(0)) --> Eu3+(D-5(0)) + Eu3+(F-7(3)). Both nonradiative deactivation of the D-5(0) state and intramolecular energy transfer from the O-->M lmct states to Eu3+ are discussed together with the luminescence properties of four other structurally characterized polyoxotungsto(or molybdo)europates, Na-9[Eu(W5O18)(2)].32H(2)O, K15H3[Eu-3(H2O)(3)(SbW9O33)(W5O18)(3)].25.5H(2)O, [NH4](12)H2H[Eu-4(H2O)(16)(MoO4)(Mo7O24)(4)].13H(2)O, and [Eu-2(H2O)(12)][Mo8O27].6H(2)O, on the basis of differences in the number of aqua and hydroxo ligands at the first coordination sphere of the Eu3+ site, the Eu ... Eu distance in the molecule, and the structure of the polyoxometalate ligands among six compounds. A plot of the deviation of the reciprocal D-5(0) lifetime from that of Na-9[Eu(W5O18)(2)].32H(2)O containing an anhydrous Eu3+ Site versus total number of aqua and hydroxo ligands coordinating Eu3+ indicates a good linearity irrespective of the coordination geometry, if the mean distance between Eu and aqua or hydroxo oxygen atoms is less than 2.5 Angstrom. The kinetic analysis of the luminescence reveals that the highly symmetrical polyoxometalate ligand favors the effective nonradiative deactivation of the O-->M lmct excitation energy due to a small disparity between the O-->M lmct excited and ground states and that the energy transfer into the D-5(0) and D-5(1) states in the polyoxometaloeuropates occurs via the O-->M lmct triplet states.