Lanthanide(iii) (Er/Ho) coordination polymers for a photocatalytic CO2 cycloaddition reaction

被引:5
作者
Alzard, Reem H. H. [1 ]
Siddig, Lamia A. A.
Abdelhamid, Abdalla S. S.
Paz, Alejandro Perez [1 ]
Nguyen, Ha L. L. [2 ,3 ]
Sethupathi, K. [4 ]
Sreejith, P. K. [4 ]
Alzamly, Ahmed [1 ]
机构
[1] UAE Univ, Dept Chem, POB 15551, Al Ain, U Arab Emirates
[2] Univ Calif Berkeley, Kavli Energy Nanosci Inst, Berkeley, CA 94720 USA
[3] Berkeley Global Sci Inst, Berkeley, CA 94720 USA
[4] Indian Inst Technol Madras, Dept Phys, Low Temp Phys Lab, Chennai 600036, India
关键词
METAL-ORGANIC FRAMEWORKS; SLOW MAGNETIC-RELAXATION; CYCLIC CARBONATES; COMPLEXES; EPOXIDES; CRYSTAL; CONVERSION; PYROLYSIS; CHEMISTRY; DESIGN;
D O I
10.1039/d3dt01269g
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two new isostructural carboxylate-bridged lanthanide ribbons having the chemical formula [Ln(2)(4-ABA)(6)](n) [4-ABA = 4-aminobenzoate, Ln: holmium (Ho) and erbium (Er)] were synthesized by a solvothermal method and fully characterized using multiple analytical, spectroscopic, and computational techniques. Single-crystal X-ray diffraction analysis reveals that both lanthanide coordination polymers (Ln-CPs) exhibit linear ribbon-like structures built up by dinuclear Ln(2)(4-ABA)(6) units and bridged by carboxylate groups. Ln-CPs showed remarkably high thermal and chemical stabilities. Ho-CP and Er-CP exhibited similar band gaps of 3.21 eV and 3.22 eV, respectively, showing their photocatalytic ability under UV light. The photocatalytic activities of Ln-CPs were examined in the CO2 cycloaddition of epoxides to cyclic carbonates under solvent-free conditions, and full conversion (yields up to 99.9%) to the product was achieved. Ln-CP photocatalysts retained the same product yields over five consecutive cycles. Additionally, the experimental magnetic studies indicated that both Ln-CP crystals are antiferromagnetic at low T, which is confirmed by density functional theory calculations.
引用
收藏
页码:8473 / 8487
页数:15
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