期刊
INORGANIC CHEMISTRY
卷 54, 期 10, 页码 4724-4736出版社
AMER CHEMICAL SOC
DOI: 10.1021/acs.inorgchem.5b00040
关键词
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资金
- Core Research for Evolutional Science and Technology (CREST) program of the Japan Science and Technology Agency (JST)
- Advanced Photon Science Alliance (APSA) from the Ministry of Education, Culture, Sports, Science and Technology of Japan (MEXT)
- Global Science course from MEXT
- Cryogenic Research Center, The University of Tokyo
- Center for Nano Lithography and Analysis, The University of Tokyo - MEXT
- JSPS (JSPS Kakenhi) [15H05697]
- Polish National Science Centre [DEC-2011/01/B/ST5/00716]
- Foundation for Polish Science within the START
- Grants-in-Aid for Scientific Research [15K13666] Funding Source: KAKEN
Complexes of lanthanides(III) (Ce-Yb) with 2,2'-bis(2-oxazoline) (Box) combined with octacyanidomolybdate(V) gave a series of magneto-luminescent coordination polymers, {[Ln(III)(Box)(n)(DMF)(m)][Mo-V(CN)(8)]}.x(solvent) (1-12). They are built of cyanido-bridged layers of a mixed 4- and 8-metal rings topology and show unique sliding of layers dependent on a 4f metal ion. For light lanthanides, dominant phase A, {[Ln(III)(Box)(2)(DMF)(2)]-[Mo-V(CN)(8)]}.1.5MeCN (Ln = Ce, 1; Pr, 2; Nd, 3), consists of ideally aligned, not shifted layers, giving large channels (13.7 x 14.0 angstrom). Intermediate lanthanides reveal phase B, {[Ln(III)(Box)(2)(DMF)(2)] [Mo-V(CN)(8)]}.H2O (Ln = Sm, 4; Eu, 5; Gd, 6; Tb, 7; Dy, 8), of smaller pores (8.4 x 10.6 angstrom) due to layer-H2O hydrogen bonding, which induces sliding of CN-bridged layers. Heavy lanthanides show phase C, {[Ln(III)(Box)(DMF)(3)][Mo-V(CN)(8)]}.MeCN (Ln = Ho, 9; Er, 10; Tm, 11; Yb, 12), with large channels (13.7 x 13.7 angstrom) of a similar size to light lanthanides. This effect comes from the changes in Ln(III) coordination sphere affecting solvent-layer interactions. Compounds 1-12 reveal diverse emission depending on the interaction between Ln(III) and Box luminophors. For 2-5, 9, and 12, the ligand-to-metal energy-transfer-induced visible f-centered emission ranging from green for HoIII-based 9, orange from SmIII-based 4, to red for PrIII- and EuIII-containing 2 and 5, respectively. Near-infrared emission was found for 2-4, 9, and 12. Red phosphorescence of Box was detected for GdIII-based 6, whereas the selective excitation of ligand or Ln(III) excited states resulting in the switchable red to green emission was found for TbIII-based 7. The materials revealed Ln(III)-MoV magnetic coupling leading to ferromagnetism below 2.0 and 2.2 K for 4 and 7, respectively. The onset of magnetic ordering at low temperatures was found for 6 and 8. Compounds 1-12 form a unique family of cyanido-bridged materials of a bifunctional magneto-luminescence character combined with dynamic structural features.
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