Series d–f Heteronuclear Metal–Organic Frameworks: Color Tunability and Luminescent Probe with Switchable Properties

• Published in: Inorganic chemistry 2017-02, Vol.56 (3), p.1713-1721
• Main Authors: Feng, Xun, Feng, Yuquan, Guo, Nan, Sun, Yiling, Zhang, Tian, Ma, Lufang, Wang, Liya
• Format: Article
• Language: English
• ISSN: 0020-1669; 1520-510X
• DOI: 10.1021/acs.inorgchem.6b02851

A series of five unique d–f heteronuclear luminescent metal–organic frameworks (MOFs) in an entangled polyrotaxane array and the light-harvesting block homonuclear zinc compound have been isolated successfully and characterized. The series of isostructural polymers feature 3,4-connected (4.82)­(4.83.92)­(6.8.9)2(6.92)­(83) topology and high stability, exhibiting diverse void spaces. By taking advantage of the isostructural MOFs 2 and 3, the intensities of red and green emissions can be modulated by adjusting the ratios of EuIII and TbIII ions correspondingly, and white-light emission can be generated by a combination of different doped TbIII and EuIII concentrations. The Tb–Zn-based framework {[Tb3Zn6(bipy2)2(Hmimda)7 (H2O)3]·5H2O} n (3; H3mimda = 2-methyl-1-H-imidazole-4,5-dicarboxylic acid and bipy = 4,4′-bipyridine) can detect trace MgII ion with relatively high sensitivity and selectivity. Dehydrated MOF 3a shows a remarkable emission quenching effect through the introduction of I2 solids. Further investigation indicates that it exhibits turn on/off switchable properties for small solvent molecules or heavy-metal ions. Steady/transient-state near-IR luminescence properties for MOFs 1, 4, and 5 were investigated under visible-light excitation.