Bauer Sebastian, Bein Thomas, Stock Norbert
Institute of Inorganic Chemistry, Christian-Albrechts-University, Germany.
Inorg Chem. 2005 Aug 8;44(16):5882-9. doi: 10.1021/ic0505089.
High-throughput methods have been employed to study the system Co(2+)/(H(2)O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH/NaOH in detail. The use of the phosphonocarboxylic acid (H(2)O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH has led to several new cobalt carboxyaryl phosphonates under hydrothermal conditions. In addition to the effect of the pH of the starting mixture, the influence of the counterions of the cobalt salts on the product formation was investigated. Thus, reaction trends as well as fields of formation could be identified. Four new compounds Co(2)[(O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH].H(2)O (1), Co[(O(3)PCH(2))(OCH)NCH(2)C(6)H(4)COOH].H(2)O (2), Co[H(2)(O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH] (3), and [Co(2)(O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH].3.5H(2)O (4) were obtained, and compounds 1 and 2 could be isolated as single crystals suitable for single-crystal X-ray diffraction. The counterions of the cobalt salts have an influence on the structure of the resulting compounds. This is due to the effect on the initial pH as well as the possibility of the counterions to take part in redox reactions. Compounds 1 and 4 are formed under more basic conditions, and the phosphonic acid group is fully deprotonated. The structure of 1 is a rare example of the family of inorganic-organic hybrid materials with iminobis(methylphosphonic acid) units wherein the nitrogen coordinates to the metal center. Compound 2 is the result of an in situ oxidation of one of the P-C bonds; the organic building unit is stabilized by complexation of the cobalt ion. On the basis of spectroscopic, thermogravimetric, elemental chemical analysis, and EDX-analysis data, compound 3 has been characterized as Co[H(2)(O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH] and compound 4 as [Co(2)(O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH].3.5H(2)O. X-ray powder diffraction and IR-spectroscopic studies show that thermal treatment of 4 leads to the title compound 1. This transformation is accompanied by a change of color from pink to deep blue.
已采用高通量方法详细研究了Co(2+)/(H(2)O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH/NaOH体系。在水热条件下,使用膦酰基羧酸(H(2)O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH生成了几种新型钴羧芳基膦酸盐。除了起始混合物pH值的影响外,还研究了钴盐抗衡离子对产物形成的影响。由此可以确定反应趋势以及生成范围。得到了四种新化合物Co(2)[(O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH].H(2)O (1)、Co[(O(3)PCH(2))(OCH)NCH(2)C(6)H(4)COOH].H(2)O (2)、Co[H(2)(O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH] (3)和[Co(2)(O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH].3.5H(2)O (4),化合物1和2可以分离得到适合单晶X射线衍射分析的单晶。钴盐的抗衡离子对所得化合物的结构有影响。这是由于其对初始pH值的影响以及抗衡离子参与氧化还原反应的可能性。化合物1和4在碱性更强的条件下形成,膦酸基团完全去质子化。化合物1的结构是具有亚氨基双(甲基膦酸)单元的无机-有机杂化材料家族中的一个罕见例子,其中氮与金属中心配位。化合物2是P-C键之一原位氧化的结果;有机结构单元通过钴离子的络合作用得以稳定。基于光谱、热重、元素化学分析和能谱分析数据,化合物3被表征为Co[H(2)(O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH],化合物4被表征为[Co(2)(O(3)PCH(2))(2)NCH(2)C(6)H(4)COOH].3.5H(2)O。X射线粉末衍射和红外光谱研究表明,对化合物4进行热处理可得到标题化合物1。这种转变伴随着颜色从粉红色变为深蓝色。