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Sharpless四唑合成中捕获双四唑锌配合物(英文) 被引量:6

Trapping of Zn-Complex with Bis(tetrazole) Ligand during the Demko-Sharpless' Tetrazole Synthesis
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摘要 The reaction of malononitrile with Z nCl 2 and NaN 3 in the presence of 2,2’-bipyridine a nd water affords the first bis(tetrazole)Zn-complex intermediate,mono(2,2’-bipyridine)bis(tetrazolyl)methane aqua zinc*",[Zn(2,2’ -bpy)(BTZ)(H 2 O)]·(H 2 O) 2 (1)which gives a clue for Demko-Sharple ss’ tetrazole synthesis.Crystal data for1:C 13 H 18 N 10 O 4 Zn,M r =443.74,monoclinic,space group P2 1 /c,a=12.5705(18),b=16.078(2),c=9.1921(13)*!,β=95.010(3)°,V=1850.7(5)*! 3 ,Z =4.CCDC:197788. The reaction of malononitrile with Z nCl 2 and NaN 3 in the presence of 2,2'-bipyridine a nd water affords the first bis(tetrazole)Zn-complex intermediate,mono(2,2'-bipyridine)bis(tetrazolyl)methane aqua zinc*',[Zn(2,2' -bpy)(BTZ)(H 2 O)]·(H 2 O) 2 (1)which gives a clue for Demko-Sharple ss' tetrazole synthesis.Crystal data for1:C 13 H 18 N 10 O 4 Zn,M r =443.74,monoclinic,space group P2 1 /c,a=12.5705(18),b=16.078(2),c=9.1921(13)*!,β=95.010(3)°,V=1850.7(5)*! 3 ,Z =4.CCDC:197788.
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2002年第12期1191-1199,共9页 Chinese Journal of Inorganic Chemistry
基金 国家重点基础研究发展规划资助项目(G2000077500) 国家自然科学基金资助项目 教育部优秀青年教师资助计划项目。
关键词 Sharpless四唑 双四唑 水热合成 锌配位聚合物 bis-tetrazole hydrother mal synthesis zinc coordination polymer
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  • 1[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.
  • 2[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.
  • 3[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.
  • 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.

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