Concomitant Metal Organic Frameworks of Cobalt(II) and 3-(4-Pyridyl)benzoate: Optimized Synthetic Conditions of Solvatochromic and Thermochromic Systems

被引:44
作者
Mehlana, Gift [1 ]
Bourne, Susan A. [1 ]
Ramon, Gaelle [1 ]
Ohrstrom, Lars [2 ]
机构
[1] Univ Cape Town, Dept Chem, Ctr Supramol Chem Res, ZA-7701 Rondebosch, South Africa
[2] Chalmers, Dept Chem & Biol Engn, S-41296 Gothenburg, Sweden
基金
新加坡国家研究基金会;
关键词
SUPRAMOLECULAR ISOMERISM; THERMOGRAVIMETRIC DATA; COORDINATION POLYMERS; STRUCTURAL DIVERSITY; POLYMORPHISM; INCLUSION; TEMPERATURE; STABILITY; CHEMISTRY; KINETICS;
D O I
10.1021/cg301312v
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Two coordination networks, {[Co-(34pba)(2)]center dot DMF}(n) (1 and 2), where 34pba is 3-(4-pyridy1)benzoate, were prepared by solvothermal methods. 1 is a three-dimensional metal organic framework formed by linking [Co-2(34pba)(8)] clusters in a bcu net. 2 consists of single [Co(34pba)(4)] units in a tetragonal plane net of sql topology. The thermal conditions leading to their selective synthesis were established: 120 degrees C for 1 and 75 degrees C for 2. Their structures were solved and their thermal behavior was investigated. Further experiments established the activation energy for the desorption of the DMF molecules entrapped in their framework: 76(6)-106(16) kJ mol(-1) for 1 and 49(3)-58(3) kJ mol(-1) for 2. For 1, sorption experiments were carried out to demonstrate the ability of the coordination network to absorb different solvents, and the framework solvatochromic response was also ascertained.
引用
收藏
页码:633 / 644
页数:12
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