Rare Earth pcu Metal-Organic Framework Platform Based on RE4(μ3-OH)4(COO)62+ Clusters: Rational Design, Directed Synthesis, and Deliberate Tuning of Excitation Wavelengths

被引:107
作者
Luo, Tian-Yi [1 ]
Liu, Chong [1 ]
Eliseeva, Svetlana V. [2 ]
Muldoon, Patrick F. [1 ]
Petoud, Stephane [1 ,2 ]
Rosi, Nathaniel L. [1 ]
机构
[1] Univ Pittsburgh, Dept Chem, Pittsburgh, PA 15260 USA
[2] CNRS, UPR 4301, Ctr Biophys Mol, F-45071 Orleans, France
关键词
STRUCTURAL-CHARACTERIZATION; HYDROLYTIC SYNTHESIS; ENERGY-TRANSFER; COMPLEXES; COORDINATION; PH; FLUOROPHORES; FLUORESCENCE; CHEMISTRY; MOFS;
D O I
10.1021/jacs.7b04532
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
The T-d point group symmetry of rare earth (RE3+) metal clusters RE4(mu(3)-OH)(4)(COO)(6)(2+) makes them attractive building blocks for creating metal-organic frameworks (MOFs) with controllable topologies. Herein, we describe the design and synthesis of a series of isoreticular MOFs featuring pcu topology [MOF-1114(RE) and MOF-1115(RE)] with variable rare earth metal ions (RE3+ = Y3+, Sm3+, Eu3+, Gd3+, Tb3+,Dy3+, Ho3+, Er3+, Tm3+, Yb3+) and linear amino-functionalized dicarboxylate linkers of different lengths. In total, we report 22 MOFs that vary in both composition and structure yet share the same RE4(mu(3)-OH)(4) cluster motif. We demonstrate that these pcu MOFs are cationic and that anion exchange can be used to affect the MOF properties. We also investigate the luminescence properties of a representative member of this MOF series [MOF-1114(Yb)] that exhibits near-infrared emission. We show that the excitation energy for Yb3+ sensitization can be carefully adjusted to lower energy via covalent postsynthetic modification at the amino group sites within the MOF.
引用
收藏
页码:9333 / 9340
页数:8
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