Rotation Restricted Emission and Antenna Effect in Single Metal–Organic Frameworks

Abstract

Aggregation induced-emission (AIE) and antenna effects are important luminescence behaviors. Thus, investigating their emission mechanisms and revealing their behaviors have become critical but challenging. Here we design and prepare metal-organic frameworks (MOFs) with an AIE ligand (i.e., tetrakis(4-carboxyphenyl)pyrazine (<b>L1</b>)) and Ln³⁺ ions (including Eu³⁺, Tb³⁺, and Gd³⁺). The emission from <b>L1</b> is gradually enhanced during the formation of the MOFs because coordination restricts the intramolecular rotation. Thus, the emission is called as coordination-induced emission (CIE) with the same restriction of intramolecular rotation mechanism as AIE. Meanwhile, benzene rings twist to adapt to the MOFs' rigid structure, so the emission blueshifts gradually, as an additional evidence of CIE. Both AIE and CIE are "rotation-restricted emission (RRE)". Eu³⁺ ions exhibit the strongest emission with gradually enhanced intensity during the formation of <b>L1</b>-Eu MOF. Combined with emission properties from Tb³⁺ and Gd³⁺ ions, the antenna effect is verified. We also validate the conditions for the efficient sensitization of Ln³⁺ ions experimentally and refresh the threshold value of the energy gap between triplet state of a ligand and excited state of Ln³⁺ ions to 3000 cm^-1. Thus, RRE and antenna effects are revealed and validated simultaneously. Because CIE of <b>L1</b> and antenna effect emission from Eu³⁺ ions are enhanced simultaneously as strong dual emissions, ratiometric fluorescence detection is realized with the detection of arginine as a model. Our results incorporate AIE and CIE into RRE, which provides explicit information for the construction and application of emission systems with AIE ligands as building blocks. MOFs are also extended to explore the emission mechanism and the energy transfer between ligands and metal ions.