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从配位聚合物到单分子化合物的转化:Demko-Sharpless四唑合成法制备两个新颖的Co(Ⅱ)配合物(英文) 被引量:1

From Coordination Polymer to Monomeric Complex:Two Cobalt Complexes from a Single Demko-Sharpless's Tetrazole Synthesis Reaction
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摘要 The reaction of CoCl2·6H2O with 4-cyanopyridine N-oxide in the present of NaN3 affords two novel complexes, {[(POTZ)(H2O)2N3]Co(H2O)} (1) and Co(POTZ)2(H2O)4 (2) (POTZ=4-tetrazolyl pyridine N-oxide), which are two different phases yielded at different stages of a single Demko-Sharpless' tetrazole synthesis reaction. Surprisingly the 1D chain coordination polymer 1 is almost completely converted into monomeric complex 2 in this reaction, and, in a separate test, 2 also can be converted into 1. CCDC: 641222, 1; 641223, 2. The reaction of CoCl2·6H2O with 4-cyanopyridine N-oxide in the present of NaN3 affords two novel complexes, {[(POTZ)(H2O)2N3]Co(H2O)} (1) and Co(POTZ)2(H2O)4 (2) (POTZ=4-tetrazolyl pyridine N-oxide), which are two different phases yielded at different stages of a single Demko-Sharpless' tetrazole synthesis reaction. Surprisingly the 1D chain coordination polymer 1 is almost completely converted into monomeric complex 2 in this reaction, and, in a separate test, 2 also can be converted into 1. CCDC: 641222, 1; 641223, 2.
作者 瞿志荣
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2007年第6期1117-1120,共4页 Chinese Journal of Inorganic Chemistry
基金 东南大学启动基金资助项目。
关键词 配位聚合物 四唑 晶体结构 coordination polymer tetrazole crystal structure
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参考文献16

  • 1Xiong R G,Zhang J,Chen Z F,et al.J.Chem.Soc.,Dalton Trans.,2001:780~782
  • 2Singh H,Chawla A S,Kapoor V K,et al.Prog.Med.Chem.,1980,17:151~183
  • 3Demko Z P,Sharpless K B.J.Org.Chem.,2001,66:7945~7950
  • 4Xiong R G,Xue X,Zhao H.et al.Angew.Chem.,Int.Ed.,2002,41:3800~3803
  • 5Xue X,Wang X S,Wang L Z,et al.Inorg.Chem.,2002,41:6544~6546
  • 6Xue X,Abrahams B F,Xiong R G,et al.Aust.J.Chem.,2002,55:495~497
  • 7Qu Z R,Zhao H,Wang X S,et al.Inorg.Chem.,2003,42:7710~7712
  • 8Wang L Z,Qu Z R,Zhao H.et al.Inorg.Chem.,2003,42:3969~3971
  • 9王立中,王锡森,李咏华,白志平,熊仁根,熊明,李国武.Sharpless四唑合成中捕获双四唑锌配合物(英文)[J].无机化学学报,2002,18(12):1191-1199. 被引量:6
  • 10王锡森,唐云志,熊仁根.原位水热合成一个新颖的银四唑配位聚合物(英文)[J].无机化学学报,2005,21(7):1025-1029. 被引量:3

二级参考文献135

  • 1王锡森,黄雪峰,熊仁根.5-取代-1-氢四唑合成中捕获的一个新奇的三维镉配聚物(英文)[J].无机化学学报,2005,21(7):1020-1024. 被引量:6
  • 2王锡森,唐云志,熊仁根.原位水热合成一个新颖的银四唑配位聚合物(英文)[J].无机化学学报,2005,21(7):1025-1029. 被引量:3
  • 3王锡森,宋玉梅,熊仁根.在Demko-Sharpless四唑合成反应中的一个意外的不同配位模式的铀配合物(英文)[J].无机化学学报,2005,21(7):1030-1034. 被引量:4
  • 4[4](a)Xiong R.-G., Xue X., Zhao H., You X. -Z., Abrahams B. F., Xue Z. Angew. Chem. Int. Ed., 2001,41, 3800;(b)Xue X., Abrahams B. F., Xiong R.-G., You X.-Z. Aust. J. Chem., 2002, 55,495;(c)Xue X., Wang X. -S., Wang L. -Z., Xiong R. -G., You X. -Z., Che C. -M., Xue Z. Inorg. Chem., 2002, in press.
  • 5[5]Crystal Data for 1: C13H18N10O4Zn, Mr =443.74, monoclinic, P21/c, a= 12.5705(18), b = 16.078(2),c=9.1921(13)A, β=95.010(3)°, V=1850.7(5)A3,Z=4, Dc=1.593Mg @ m-3, R1 =0.0501, wR2=0. 1442,T=293K, μ=1.372mm-1, S=1.025.
  • 6[6](a)Xiong R. -G., Zuo J. -L., You X. -Z., Abrahams B. F., Bai Z.-P., Che C.-M., Fun H.-K. Chem. Commun.,2000, 2061;(b)Xiong R. -G., Zuo J. -L., You X. -Z., Fun H. -K., Raj S. S. S. Organometallics, 2000, 19, 4183;(c)Fun H. -K., Raj S. S. S., Xiong R. -G., Zuo J. -L., Yu Z., You X.-Z. J. Chem. Soc., Dalton Trans., 1999, 1915;(d)Zhang J., Lin W. B., Chen Z. -F., Xiong R. -G., Abrahams B. F., Fun H. -K. J. Chem. Soc., Dalton Trans.,2001, 1804.
  • 7[1](a)Carlucci L., Ciani G., Proserpio D.M. Angew. Chem. Int. Ed., 1999, 38, 3488;(b)Singh H., Chawla A. S., Kapoor V. K., Paul D., Malhotra R.K. Prog. Med. Chem., 1980, 17, 151;(c)Ostrovskii V. A.,Pevzner M.S., Kofmna T. P., Shcherbinin M. B., Tselinskii I.V. Targets Heterocycl. Syst., 1999, 3,467;(d)Janiak C., Scharmann T. G., Gunter W., Girgsdies F., Hemling H., Hinrichs W., Lentz D. Chem. Eur. J.,1995, 1,637;(e)Bhandari S., Mahon M. F., Molloy K. C., Palmer J. S., Sayers S. F. J. Chem. Soc. Dalton Trans., 2000, 1053.
  • 8[2](a)Demko Z. P., Sharpless K.B. J. Org. Chem., 2001,66, 7945;(b)Demko Z. P., Sharpless K.B. Org. Lett., 2001, 3,4091.
  • 9[3](a)Xiong R. -G., You X. -Z., Abrahams B. F., Xue Z., Che C.-M. Angew. Chem. Int. Ed., 2001,40,4422;(b)Xiong R.-G., Zhang J., Chen Z. -F., You X,-Z., Che C.-M., Fun H.-K. J. Chem. Soc. Dalton. Trans., 2001, 780;(c)Xue X., Wang X.-S., Xiong R.-G., You X.-Z., Abra- hams B. F., Che C. -M., Ju H. -X. Angew. Chem. Int. Ed., 2002, 41, 2944;(d)Zeng X. -R., Xiong R. -G., You X. -Z., Raj S. S. S., Fun H.-K. Chin. J. Inorg. Chem., 2000, 16,641.
  • 10Demko Z P, Sharpless K B. Org. Lett., 2001,3:4091~4094.

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