高等学校化学学报 ›› 2011, Vol. 32 ›› Issue (3): 527.

• 研究论文 • 上一篇    下一篇

钴(Ⅲ)-胺配合物模板导向合成新型草酸盐化合物[Co(dien)2][NaCo2(C2O4)4]·H2O

潘勤鹤1,陈强2,韩义德3,胡同亮2,卜显和2   

  1. 1. 海南大学材料与化工学院, 海南优势资源化工材料应用技术教育部重点实验室, 海口 570228;
    2. 南开大学化学系, 金属与分子基材料化学天津市重点实验室, 天津 300071;
    3. 吉林大学无机合成与制备化学国家重点实验室, 长春 130021
  • 收稿日期:2010-10-18 修回日期:2010-12-27 出版日期:2011-03-10 发布日期:2011-02-23
  • 通讯作者: 潘勤鹤;胡同亮 E-mail:panqinhe@163.com; tlhu@nankai.edu.cn
  • 基金资助:

    国家自然科学基金(批准号: 20801029, 51073079)、 天津市自然科学基金(批准号: 10JCZD JC22100)和海南大学科研启动基金(批准号: kyqd1051)资助.

Template-directed Synthesis of a Novel Oxalate Compound [Co(dien)2][NaCo2(C2O4)4] Using Co(Ⅲ) Complex as Template

PAN Qin-He1*, CHEN Qiang2, HAN Yi-De3, HU Tong-Liang2*, BU Xian-He2   

  1. 1. Department of Materials and Chemical Engineering, Ministry of Education Key Laboratory of Application Technology of Hainan Superior Resources Chemical Materials, Hainan University,  Haikou 570228, China;
    2. Department of Chemistry,  Tianjin Key Laboratory of Metal & Molecule\|based Material Chemistry, Nankai University, Tianjin 300071, China;
    3. State Key Laboratory of Inorganic Synthesis and Preparative Chemistry, Jilin University, Changchun 130012, China
  • Received:2010-10-18 Revised:2010-12-27 Online:2011-03-10 Published:2011-02-23
  • Contact: PAN Qin-He;HU Tong-Liang E-mail:panqinhe@163.com; tlhu@nankai.edu.cn
  • Supported by:

    国家自然科学基金(批准号: 20801029, 51073079)、 天津市自然科学基金(批准号: 10JCZD JC22100)和海南大学科研启动基金(批准号: kyqd1051)资助.

摘要: 以Co(dien)2?Cl3为模板剂,在水热条件下导向合成出一例新型草酸盐化合物[Co(dien)2][NaCo2(C2O4)4]?H2O. 并通过X-射线单晶结构分析、元素分析、ICP以及X-射线粉末衍射分析对该化合物的结构进行了标征. 结果表明,属于单斜晶系,C2/c空间群,晶胞参数a = 1.3805(3) nm,b = 1.3017(3) nm,c = 1.5913(3) nm,β = 104.41(3)°, V = 2.7695(10) nm3,Z = 4. 在这个结构中,二价Co2+离子先与草酸基团相互交替连接形成一个常见链状结构基元[Co(C2O4)2]n2n-,这些链状结构基元进一步被散布于链间的Na+离子连接成三维草酸盐开放骨架结构[NaCo2(C2O4)4]n3n-. 金属配合物离子Co(dien)23+存在于孔道中扮演模板剂的作用.  

关键词: 草酸盐, 金属配合物, 水热合成, 主客体体系

Abstract: By using Co(dien)2?Cl3 as the template, a novel oxalate compound [Co(dien)2][NaCo2(C2O4)4]?H2O has been synthesized under hydrothermal conditional. Its structure is determined by single-crystal X-ray diffraction analysis, elemental analyses, ICP, and X-ray powder diffraction. It crystallizes in monoclinic, space group C2/c with a = 1.3805(3) nm, b = 1.3017(3) nm, c = 1.5913(3) nm, β = 104.41(3)°, V = 2.7695(10) nm3, Z = 8. In this structure, the Co2+ cations are first linked to oxalate ligands to form a familiar chain-like building unit [Co(C2O4)2]n2n-, and then those chain-like building units are further connected by Na+ cations, which are dispersed between the chains, to construct a three dimensional oxalate open-framework of [NaCo2(C2O4)4]n3n-. The complex cations Co(dien)23+ are encapsulated inside the channels as template.

Key words: Oxalate, Metal complex, Hydrothermal synthesis, Host-guest system

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