期刊文献+

硝酸钍氧化膦取代杯芳烃配合物的合成与结构 被引量:10

Synthesis and Crystal Structure of a Thorium(Ⅳ) Nitrate Complex with Phosphinoxide[-CH_2P(O)Ph_2]-substituted Calix[4]arene
在线阅读 下载PDF
导出
摘要 合成了一种硝酸钍与氧化膦取代杯芳烃衍生物的配合物 ,[L·Th(OH2 ) (NO3 ) 2 ] [Th(NO3 ) 6]·CH3 CN {L =四 (亚甲基二苯基氧化膦 )杯 [4 ]芳烃 }.通过元素分析和红外光谱对配合物进行了表征 .用X射线单晶衍射法测定了其晶体结构 .晶体属三斜晶系 ,P 1空间群 ,晶胞参数a =1 990 ( 7)nm ,b =2 2 17( 8)nm ,c =2 890 ( 10 )nm ;α =10 4 92 ( 12 )° ,β =10 0 76( 14 )° ,γ =93 13 ( 10 )° ,Z =4;V =12 0 3 3 ( 7)nm3 ,R1=0 0 90 1,wR2 =0 190 7.此配合物由配阳离子和配阴离子构成 .配阳离子中 ,1个Th4+ 与杯芳烃中的 4个磷氧键上的氧原子 ,2个双齿配位的硝酸根中的 4个氧原子 ,以及 1个水分子的氧原子配位 ,构成 1个九配位的单帽四方反棱柱体 ;配阴离子中 ,1个Th4+ 与 A thorium(Ⅳ) nitrate complex with phosphinoxide[-CH 2P(O)Ph 2]-substituted calixarene [L·Th^(OH 2)(NO 3) 2][Th(NO 3) 6]·CH 3CN has been prepared and characterized by elemental analysis and IR spectroscopy. Its crystal structure was determined by X-ray diffraction method. It belongs to triclinic crystal system, space group P 1, with a=1.990(7) nm, b=2.217(8) nm, c=2.890(10) nm; α=104.92(12)°, β=100.76(14)°, γ=93.13(10)°, Z=4, V=12.033(7) nm 3, R 1=0.0901, wR 2=0.1907. The complex consists of a coordination cation and a coordination anion. In the cation the thorium(Ⅳ) is coordinated to the four phosphinoxide oxygen atoms of the calixarene, four oxygen atoms from two bidentate nitrate anions and one oxygen from a water molecule forming a nine-coordinate monocapped square antiprism. In the coordination anion, the thorium(Ⅳ) is coordinated to six bidentate nitrate. In addition, an acetonitrile molecule was encapsulated in the cavity of calixarene.
出处 《化学学报》 SCIE CAS CSCD 北大核心 2004年第13期1260-1264,J004,共6页 Acta Chimica Sinica
关键词 硝酸钍 氧化膦取代杯芳烃 配合物 合成 晶体结构 thorium(Ⅳ) nitrate complex, phosphinoxide[-CH 2P(O)Ph 2]-substituted calix[4]arene, crystal structure
  • 相关文献

参考文献13

  • 1[1]Gutsche, C. D. Calixarenes, The Royal Society of Chemistry, Cambridge, England, 1989.
  • 2[2]Vicens, J.; Bhmer, V. E. Calixarenes-A Versatile Class of Macrocyclic Compounds, Kluwer, Academic Press, Dordrecht, 1991.
  • 3[3]Dieleman, C. B.; Matt, D.; Jones, P. G. J. Org. Chem. 1997, 461, 545.
  • 4[4]Dieleman, C. B.; Lober, C.; Matt, D.; Cian, A. D.;Fischer, J. J. Chem. Soc., Dalton Trans. 1995, 3097.
  • 5[5]Yaftian, M. R.; Burgard, M.; Matt, D.; Wieser, C.; Dieleman, C. B. J. Phenom. Mol. Recognit. Chem. 1997, 27, 127.
  • 6[6]Yaftian, M. R.; Burgard, M.; Matt, D.; Wieser, C.; Dieleman, C. B. J. Phenom. Mol. Recognit. Chem. 1997, 29, 137.
  • 7[7]Yaftian, M. R.; Burgard, M.; Matt, D. J. Membr. Sci. 1998, 144, 57.
  • 8[8]Arnaud-Neu, F.; Browne, J. K.; Byrne, D.; Mckervey, M. A.; O'Hagan, P.; Schwing-Weill, M. J.; Walker, A. Chem. Eur. J. 1999, 5(1), 175.
  • 9[9]Leatitia, L.; Saulnier, S. V. J. Chem. Soc., Dalton Trans. 1999, 3919.
  • 10[10]Gutshe, C. D.; Iqbal, M.; Stewart, D. J. Org. Chem. 1986, 51, 742~745.

同被引文献205

引证文献10

二级引证文献29

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部