Electronic energy transfer in conjugated polymers is of both theoretical and practical importance. At the theoretical level, the study of on-chain and interchain energy transfer is helping reveal the mechanism of exciton migration in conjugated polymers, [1] which is of fundamental importance for their application in many optoelectronic devices. Interest at the practical level extends from color tuning in light-emitting devices [2] to applications in chemical and biological sensors. [3,4] Fluorene-based copolymers are particularly attractive as energy donors in Förster Resonance Energy Transfer (FRET), because their high fluorescence quantum yields and blue emission allow efficient transfer to acceptors, emitting over the whole visible and near-infrared spectrum.[5] In addition, using complexes containing heavy metals, such as Ir, Pt, or Ru, it is possible to capture both singletand triplet-state energy, and produce high efficiency electrophosphorescent devices.[6] Whilst triplet-energy transfer to metal complexes normally involves the short-range Dexter (exchange) mechanism, [7] it is anticipated that the efficiency of this process can be optimized if both this and the long-range Förster(dipoledipole) [8] mechanisms are involved. Conjugated polyelectrolytes (CPE), conjugated polymers containing charged groups, are of particular interest, and are finding applications which include chemical and biological sensors, [3,4] light-emitting devices, [9] charge injection, and transport layers.[10] In addition, they self-assemble with oppositely charged species, such as surfactants, to build up complex multilayered structures, which have interesting materials properties with potential for molecular-electronics applications.[11] These tend to cluster in aqueous solutions, [12c] but we have shown that with the fluorene-based anionic poly{1,4-phenylene-[9,9-bis(4-phenoxy-butylsulfonate)]fluorene-2,7-diyl} (PBS-PFP), the clusters can be broken up by addition of nonionic surfactants, such as pentaethylene glycol monododecyl ether (C 12 E 5 ), to form cylindrical micelles, in which the CPE is present as isolated chains. [12a,b,d] Polypyridylruthenium(II) complexes are amongst the most widely studied systems in inorganic photochemistry, [13] and are used in areas such as photovoltaic devices [14] and optical sensors, [15] in addition to showing potential as light-emitting electrochemical cells and other devices.[16] The emission spectrum of PBS-PFP has a near-perfect overlap with the lowest singlet-singlet transition in the absorption spectrum of tris(2,2-bipyridyl)ruthenium(II) (Ru(bpy) 3 2þ ). In addition, intersystem crossing in this metal complex to the emitting 3 MLCT (metal-toligand charge transfer) state occurs on a sub-picosecond time scale, [17] such that all electronic energy from excited singlet or triplet states of donor or acceptor will be funneled to the triplet state of the metal complex. Phase segregation is a problem in many systems involving conjugated polymers and metal complexes. However, it is ant...