Abstract

The selective synthesis of heteroleptic (heteronuclear) sandwich-type lanthanide phthalocyanines has been accomplished. Double-decker complexes BuPcLnPc, and BuPcLnPc Cl (Ln = Lu, Eu; BuPc = 2,3,9,10,16,17,23,24-octabutylphthalocyaninate; Pc = phthalocyaninate, ClPc = 2,3,9,10,16,17,23,24-octachlorophthalocyaninate) were obtained in good yields by a direct interaction of metal-free ligand BuPcH 2 with the monophthalocyanines PcLnOAc or ClPcLnOAc. Heteronuclear triple-decker phthalocyanines PcEu RPcLu RPc, ClPcEu RPcLu RPc and BuPcEu RPcLu RPc ( RPc = BuPc, tBu Pc; tBu Pc = 2(3),9(10),16(17),23(24)-tetra- tert-butylphthalocyaninate) were obtained from the corresponding mono-(PcEuOAc, ClPcEuOAc, BuPcEuOAc) and bisphthalocyanines ( RPc 2Lu) under similar conditions.

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