Syntheses, Structural Evolutions, and Properties of Cd(II) Coordination Polymers Induced by Bis(pyridyl) Ligand with Chelated or Protonated Spacer and Diverse Counteranions

被引:14
|
作者
Ge, Fa-Yuan [1 ]
Ma, Xin [1 ]
Guo, Dan-Dan [1 ]
Zhu, Li-Na [1 ]
Deng, Zhao-Peng [1 ]
Huo, Li-Hua [1 ]
Gao, Shan [1 ]
机构
[1] Heilongjiang Univ, Sch Chem & Mat Sci, Key Lab Funct Inorgan Mat Chem, Minist Educ, Harbin 150080, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
METAL-ORGANIC FRAMEWORKS; CRYSTAL-STRUCTURES; GAS-ADSORPTION; SILVER(I); NETWORKS; DESIGN; CO2;
D O I
10.1021/acs.cgd.7b00174
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Hydrothermal reaction of Cd(II) metal salts, diverse organic acids, as well as flexible bis(pyridyl) ligand leads to the formation of 10 complexes, namely, [Cd2LCl4] (1), [Cd(H2L)(SO4)(2)(H2O)(2)](n)center dot 6nH(2)O (2), [CdL(malonate)](n)center dot 5nH(2)O (3), [Cd2L(malonate)Cl-2(H2O)](n)center dot nH(2)O (4), [Cd-2(H2L)(succinate)(3)](n)center dot 4nH(2)O (5), [Cd2L(fumarate)(2)(H2O)(2)](n)center dot 2nH(2)O (6), [Cd2L(m-BDC2-)(2)](n)center dot 2nH(2)O (7), [Cd-2(L)(p-BDC2-)(2)(H2O)(3)](n)center dot 3nH(2)O (8), [Cd-3(L)(2)(p-BDC2-)(3)(H2O)(n)center dot nH(2)O (9), and [Cd-3(H2L)(p-BDC2-)(2) (SO4)(2)(H2O)(3)](n)center dot 2nH(2)O (10) (L = N,M-bis(pyridin-3-ylmethyl)ethane-1,2diamine, m-BDC2- = m -benzene dicarboxylate dianion, P-BDC2- = p -benzene dicarboxylate dianion), which have been characterized by elemental analysis, infrared, thermogravimetric analysis, PL, powder and single-crystal X-ray diffraction: Structural analyses indicate that the diverse coordination modes of the bis(pyridyl) ligand with a chelated or protonated spacer, the feature of different inorganic and organic anions, can effectiyely influence the topological Structures of these complexes. Complex 1 presents a three-dimensional (3D) hybrid network which is accomplished by the interconnection of adjacent Cd(II) cations through L molecules and mu(2)-Cl- anions. Complex 2 exhibits an interesting pseudo 2-fold interpenetrated network formed by the interconnection of.a [Cd-H2L2+] pcu net and [SO42+ -H2O](n) pcu net. In complexes 3 and 4, adjacent Cd(II) cations are all bridged by dicarboxylate and L to generate a sill layer. In contrast, complex 5 presents 3-fold parallel interpenetrated sql layer owing to the protonated spacer of H2L2+ cation which extends, the size of the quadrate window. The organic dicarboxylates in complexes 6 and 7 present more -abundant coordination modes which join adjacent Cd(II) cations;together with, L molecules, thus giving rise to a different 3D framework with sra and-snk topology. The p-BDC2- dianions in complexes 8, 9, and 10 present different coordination modes and join adjacent Cd(II) cations together with t molecules and H2L2+ cations to frirm a diverse ladder chain, tfc and new (4(4).6(11))(6(6)) topology. Luminescent investigation reveals that the emiSsion maximum of these 10 complexes varies from 376 to 450 nm.
引用
收藏
页码:2667 / 2681
页数:15
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