Sensitised near-infrared luminescence from lanthanide(<scp>iii</scp>) centres using Re(<scp>i</scp>) and Pt(<scp>ii</scp>) diimine complexes as energy donors in d–f dinuclear complexes based on 2,3-bis(2-pyridyl)pyrazine

Abstract

The luminescent transition metal complexes [Re(CO)(3)Cl(bppz)] and [Pt(CC-C(6)H(4)CF(3))(2)(bppz)] [bppz = 2,3-bis(2-pyridyl)pyrazine], in which one of the diimine binding sites of the potentially bridging ligand bppz is vacant, have been used as 'complex ligands' to make heterodinuclear d-f complexes by attachment of a {Ln(dik)(3)} fragment (dik = a 1,3-diketonate) at the vacant site. When Ln = Pr, Nd, Er or Yb the lanthanide centre has low-energy f-f excited states capable of accepting energy from the (3)MLCT excited state of the Pt(II) or Re(I) centre, quenching the (3)MLCT luminescence and affording sensitised lanthanide(III)-based luminescence in the near-IR region. UV/Vis and luminescence spectroscopic titrations allowed measurement of (i) the association constants for binding of the {Ln(dik)(3)} fragment at the vacant diimine site of [Re(CO)(3)Cl(bppz)] or [Pt(CC-C(6)H(4)CF(3))(2)(bppz)], and (ii) the degree of quenching of the (3)MLCT luminescence according to the nature of the Ln(III) centre. In all cases Nd(III) was found to be the most effective of the series at quenching the (3)MLCT luminescence of the d-block component because the high density of f-f excited states of the appropriate energy make it a particularly effective energy-acceptor.