期刊
MOLECULES
卷 23, 期 5, 页码 -出版社
MDPI
DOI: 10.3390/molecules23051006
关键词
symmetric bis(salamo)-type tetraoxime; heterobimetalic complex; synthesis; crystal structure; spectroscopic study
资金
- Program for Excellent Team of Scientific Research in Lanzhou Jiaotong University [201706]
- National Natural Science Foundation of China [21761018]
A novel heterotrinuclear complex [Cu-2(L)Na(mu-NO3)].CH3OH.CHCl3 derived from a symmetric bis(salamo)-type tetraoxime H4L having a naphthalenediol unit, was prepared and structurally characterized via means of elemental analyses, UV-Vis, FT-IR, fluorescent spectra and single-crystal X-ray diffraction. The heterobimetallic Cu(II)-Na(I) complex was acquired via the reaction of H4L with 2 equivalents of Cu(NO3)(2)2H(2)O and 1 equivalent of NaOAc. Clearly, the heterotrinuclear Cu(II)-Na(I) complex has a 1:2:1 ligand-to-metal (Cu(II) and Na(I)) ratio. X-ray diffraction results exhibited the different geometric behaviors of the Na(I) and Cu(II) atoms in the heterotrinuclear complex; the both Cu(II) atoms are sited in the N2O2 coordination environments of fully deprotonated (L)(4-) unit. One Cu(II) atom (Cu1) is five-coordinated and possesses a geometry of slightly distorted square pyramid, while another Cu(II) atom (Cu2) is four-coordination possessing a square planar coordination geometry. Moreover, the Na(I) atom is in the O-6 cavity and adopts seven-coordination with a geometry of slightly distorted single triangular prism. In addition, there are abundant supramolecular interactions in the Cu(II)-Na(I) complex. The fluorescence spectra showed the Cu(II)-Na(I) complex possesses a significant fluorescent quenching and exhibited a hypsochromic-shift compared with the ligand H4L.
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