Materials　with　aggregation-induced　emission　(AIE)　properties　have　received　increased　attention　recently　due　to　their　potential　applications　in　light-emitting　devices,　chemo/biosensors　and　biomedical　diagnostics.　In　general,　AIE　requires　the　forced　aggregation　of　the　AIEgens　induced　by　the　poor　solvent　or　close　arrangement　of　AIEgens　covalently　attached　to　polymer　chains.　Here,　we　report　two　coordination-enhanced　fluorescent　supramolecular　complexes　featuring　hierarchically　restricted　intramolecular　motions　via　the　self-assembly　of　tetraphenylethylene　(TPE)-based　tetra-dentate　(L-a)　and　bidentate　(L-b)　ligands　and　the　cis-Pd(en)(NO3)(2)　(en　=　ethylenediamine)　unit.　While　the　free　ligands　are　non-emissive　in　dilute　solution　and　show　typical　AIE　properties　in　both　mixed　solvent　system　and　the　solid　state,　the　self-assembled　complexes　maintain　their　fluorescent　nature　in　the　solution　state.　In　particular,　the　Pd-4(L-a)(2)　complex　shows　remarkable　6-fold　fluorescent　enhancement　over　L-a　in　dilute　solution.　We　anticipate　that　these　kinds　of　coordination-enhanced　emissive　supramolecules　will　find　applications　in　biomedical　sensing　or　labeling.