Multifunctional chiral metal hydrogen-bonded organic frameworks constructed from lanthanide ions with a trigonal prismatic coordination environment

被引:0
|
作者
Peng, Guo [1 ]
Zhou, Guo-Xing [1 ]
Dong, Xiang-Tao [1 ]
Peng, Yong-Bo [1 ]
Zhang, Rong-Yan [1 ]
Ma, Ying-Zhao [2 ]
Ren, Xiao-Ming [1 ,3 ]
机构
[1] Nanjing Tech Univ, Sch Chem & Mol Engn, State Key Lab Mat Oriented Chem Engn, Nanjing 211816, Peoples R China
[2] Chongqing Normal Univ, Coll Chem, Chongqing Key Lab Green Synth & Applicat, Chongqing 401331, Peoples R China
[3] Nanjing Univ, State Key Lab Coordinat Chem, Nanjing 210093, Peoples R China
基金
中国国家自然科学基金;
关键词
SLOW MAGNETIC-RELAXATION; BEHAVIOR; DY; LUMINESCENCE; PHOSPHONATES; BLOCKING; CHAINS;
D O I
10.1039/d4dt02131b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two pairs of chiral enantiomers D/L-Dy(PMP)(3)center dot 2H(2)O (D-1/L-1) and D/L-Yb(PMP)(3)center dot 2H(2)O (D-2/L-2) were synthesized by the introduction of enantiomerically pure D/L-PMP (PMP = (phosphonomethyl)proline) ligands into lanthanide coordination chemistry. The chiral characteristics of these products were confirmed by single crystal X-ray diffraction, second harmonic generation (SHG) measurements and circular dichroism (CD) spectroscopy. These complexes are composed of 1D chains constructed from lanthanide ions with a trigonal prismatic coordination geometry and PMP ligands. The assembly of the 1D chains led to the formation of a lanthanide hydrogen-bonded organic framework with 1D water chains filled in the channels. Zero-field slow relaxation of magnetization was detected in L-1, whereas L-2 showed field-induced single-molecule magnet (SMM) behavior. Complexes D-1, L-1 and L-2 show proton conductive ability and their conductivity values reach the order of 10(-5) S cm(-1) at 90 degrees C and 98% relative humidity.
引用
收藏
页码:152 / 158
页数:7
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