Citation: Chen Guanghui, He Yanping, Zhang Lei, Zhang Jian. Syntheses and Structural Studies of a Series of Ti4(embonate)6-based Complexes[J]. Acta Chimica Sinica, ;2020, 78(12): 1411-1417. doi: 10.6023/A20070337 shu

Syntheses and Structural Studies of a Series of Ti4(embonate)6-based Complexes

  • Corresponding author: He Yanping, hyp041@163.com Zhang Jian, zhj@fjirsm.ac.cn
  • Received Date: 31 July 2020
    Available Online: 6 August 2020

    Fund Project: Project supported by the National Natural Science Foundation of China (No.21935010)the National Natural Science Foundation of China 21935010

Figures(6)

  • Metal-organic cages (MOCs) as a new type of molecular containers have attracted great interest because of their special cavities and wide applications in molecule recognition and separation, drug delivery and catalysis, etc. However, in the past decades, most researchers just devote to constructing discrete MOCs with special functions. Since many cage compounds are not soluble and stable in the solvent, the further assembly of cages into advanced materials is relatively less developed. In our previous study, we reported a water-soluble and ultrastable Ti4L6 (L=embonate) tetrahedron with coordination assembly function, which has been applied as the starting material to realize coordination assembly with different metal ions through two-step reaction. In this work, by employing the Ti4L6 cages to assemble with Mn2+, Nd3+, Ba2+ and Ca2+ ions, respectively, a series of Ti4L6-based complexes have been synthesized under different solvothermal reaction conditions, namely, (Me2NH2)9(Me4N)[Mn3(Ti4L6)2(H2O)9(DMF)6]·Guests (PTC-241, DMF=N, N-dimethylformamide); (Me2NH2)5- [Nd(Ti4L6)(H2O)2(DMF)5]·Guests (PTC-242); (Me2NH2)2[Ba4(Ti4L6)(OH)2(H2O)8(TEA)5]·Guests (PTC-243, TEA=Triethanolamine); (Me2NH2)2[Ca3(Ti4L6)(H2O)8(DEA)2]·Guests (PTC-242, DEA=Diethanolamine); (Me2NH2)2[Ca3(Ti4L6)-(H2O)15]·Guests (PTC-245). Their structures were characterized by X-ray single crystal diffraction, thermo gravimetric analyzer (TGA), infrared spectroscopy (IR) and powder X-ray diffraction (PXRD). Single-crystal analysis reveals that PTC-241 is a supramolecular homochiral architecture formed by the staggered accumulation of ΔΔΔΔ-[Ti4L6] and ΔΔΔΔ-[Ti4L6]-Mn3 cages by weak interactions (such as hydrogen bonding and π-π stacking). PTC-242 is also a supramolecular structure, in which the Ti4L6-Nd cages are linked by (Me2NH2)+ cations and ethanediamine (en) molecules via the weak N-H…O hydrogen bonding force, giving rise to a 3D H-bonding framework with a honeycomb lattice of hexagonal channels along the b axis. PTC-243 is a linear Ti4L6-Ba4 chain structure. Both PTC-242 and PTC-245 are two-dimensional (2D) Ti4L6-Ca3 layers with honeycomb-like structures. In addition, we also investigated the fluorescent properties of PTC-242 and PTC-245 in the solid state, and the results show that both of them display strong emitting bands in the visible region.
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