Anisotropic lanthanide-based nano-clusters for imaging applications† †Electronic supplementary information (ESI) available: Characterization details for clusters 1–3. CCDC 1450317–1450319. For ESI and crystallographic data in CIF or other electronic format see DOI: 10.1039/c6fd00018e Click here for additional data file. Click here for additional data file.

نویسندگان

  • Xiaoping Yang
  • Shiqing Wang
  • Tyler L. King
  • Christopher J. Kerr
  • Clement Blanchet
  • Dmitri Svergun
  • Robert Pal
  • Andrew Beeby
  • Jamuna Vadivelu
  • Katherine A. Brown
  • Richard A. Jones
  • Lijie Zhang
  • Shaoming Huang
چکیده

We have developed a new class of lanthanide nano-clusters that self-assemble using flexible Schiff base ligands. Cd-Ln and Ni-Ln clusters, [Ln8Cd24(L1)12(OAc)39Cl7(OH)2] (Ln = Nd, Eu), [Eu8Cd24(L1)12(OAc)44], [Ln8Cd24(L2)12(OAc)44] (Ln = Nd, Yb, Sm) and [Nd2Ni4(L3)2(acac)6(NO3)2(OH)2], were constructed using different types of flexible Schiff base ligands. These molecular nano-clusters exhibit anisotropic architectures that differ considerably depending upon the presence of Cd (nano-drum) or Ni (square-like nano-cluster). Structural characterization of the self-assembled particles has been undertaken using crystallography, transmission electron microscopy and small-angle X-ray scattering. Comparison of the metric dimensions of the nano-drums shows a consistency of size using these techniques, suggesting that these molecules may share similar structural features in both solid and solution states. Photophysical properties were studied by excitation of the ligand-centered absorption bands in the solid state and in solution, and using confocal microscopy of microspheres loaded with the compounds. The emissive properties of these compounds vary depending upon the combination of lanthanide and Cd or Ni present in these clusters. The results provide new insights into the construction of novel high-nuclearity nano-clusters and offer a promising foundation for the development of new functional nanomaterials.

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عنوان ژورنال:

دوره 191  شماره 

صفحات  -

تاریخ انتشار 2016