Structures and multiple properties of two polar metal-organic frameworks based on achiral N,O-coordinated ligands: toward multifunctional materials

被引:27
|
作者
Liu, Guang-Ning [1 ]
Zhang, Ming-Jian [2 ]
Liu, Wan-Qing [1 ]
Sun, Hui [1 ]
Li, Xin-Yu [1 ]
Li, Ke [1 ]
Ren, Cai-Ze [1 ]
Zhang, Zhen-Wei [1 ]
Li, Cuncheng [1 ]
机构
[1] Univ Jinan, Sch Chem & Chem Engn, Key Lab Chem Sensing & Anal Univ Shandong, Jinan 250022, Shandong, Peoples R China
[2] Peking Univ, Shenzhen Grad Sch, Sch Adv Mat, Shenzhen 518055, Peoples R China
关键词
COORDINATION POLYMERS; MAGNETIC-PROPERTIES; PHOTOCATALYTIC DEGRADATION; PROTON CONDUCTIVITY; CRYSTAL-STRUCTURES; CADMIUM COMPLEXES; HYDROGEN STORAGE; LIGHT EMISSION; MOF; 2,2'-BIPYRIDINE;
D O I
10.1039/c5dt02374b
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Two novel metal-organic frameworks (MOFs) [Cd-3(padc)(Hpadc)(H(2)padc)(H2O)](n)center dot nH(2)O (1, H(3)padc = pyrazole-3,5-dicarboxylic acid) and [Co-4(pidc)(2)(Hpidc)(4)(H2O)(3)](n)center dot 12nH(2)O (2, H(2)pidc = pyridine-2,5-dicarboxylic acid), that both crystallize in polar space groups, were solvothermally synthesized by using achiral N, O-coordinated ligands. Compound 1 consists of trinuclear Cd(II)-based units that are further bridged by the backbone of H(3)padc ligands to form a three-dimensional (3-D) (4,6)-connected fsc topology network, while compound 2 features two types of double-helical tubes with different chiralities connecting with each other alternatively to construct a typical 2-D (3,6)-connected kgd topology network. Importantly, 1 exhibits combined properties of photoluminescence (PL) and second harmonic generation (SHG), and represents the first noncentrosymmetric H(3)padc-based MOF that was obtained without any ancillary ligands. While 2 shows strong antiferromagnetic interactions between paramagnetic Co(II) centers, and the aqueous solution of 2 exhibits effective homogeneous photocatalysis properties under visible irradiation. Further, the mechanisms of the physical properties of 1 and 2 are discussed in detail.
引用
收藏
页码:18882 / 18892
页数:11
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