期刊文献+

氢键和π-π诱导的三重穿插的二维Zn(Ⅱ)配位聚合物的晶体结构和荧光性能(英文) 被引量:1

Structure and Photoluminescent Property of Three-Fold Interpenetrated 2D Zn(Ⅱ) Coordination Polymer Induced by H-Bonding and π-π Interaction
下载PDF
导出
摘要 本文以(4-羧基苄基)-4,4′-二羧基二苯胺(H3L)和1,10-菲罗啉(Phen)为配体,溶剂热合成了一个二维锌配位聚合物[Zn(HL)(Phen)]n(1),对其进行了红外、热重、粉末单晶衍射等表征,配合物属于三斜晶系,空间群P21/c。相邻的Zn(Ⅱ)离子通过连接HL2-和Phen形成一维之字形的链,该一维链通过氢键和π-π作用进一步形成三重穿插的二维超分子结构。此外,还研究了配合物的荧光性能。 Solvothermal reaction of 4,4'-[(4-carboxybenzyl)nitrilo]dibenzoate (H3L) with 1,10-phenanthroline (Phen) produced a two dimensional (2D) zinc(II) coordination polymer [Zn(HL)(Phen)]n (1). The complex was characterized by elemental analysis, IR spectroscopy, and X-ray single-crystal diffraction. It crystallizes in the monoclinie system, space group P21/c. The neighboring Zn(II) ions are linked by HL2- anions and Phen to form infinitely 1D zigzag chain, the 1D chains further linked each other to form interaction. In addition, the fluorescence property 3-fold interpenetrated 2D wavelike sheet by H-bonding and or-or of 1 was also studied. CCDC: 901345.
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2013年第1期123-126,共4页 Chinese Journal of Inorganic Chemistry
基金 国家自然基金(No.21071004) 安徽理工大学博士启动和青年基金(No.11227,2012QNZ08) 江苏省新型环保重点实验室开放课题基金(No.AE201107)资助项目
关键词 配位聚合物 氢键 Π-Π作用 荧光性质 coordination polymer H-bonding 7r-lr interaction fluorescence
  • 相关文献

参考文献11

  • 1Ma Y, Cheng A L, Gao E Q. Cryst. Growth Des., 2010,10(7): 2832-2834.
  • 2Fu J H, Li H J, Mu Y J, et al. Chem. Commun., 2011,47 (18):5271-5273.
  • 3Feng R, Jiang F L, Chen L, et al. Chem. Commun., 2009,45: 5296-5298.
  • 4Bi Y F, Wang X T, Wang B W, et al. Dalton Trans., 2009, 12:2250-2254.
  • 5Sarma R, Deka H, Boudalis A K, et al. Cryst. Growth Des., 2011,11:547-554.
  • 6Corma A, Garca H, Llabr6s i Xamena F X. Chem. Rev., 2010,110(8):4606-4655.
  • 7Huang Y B, Liu T F, Lin J X, et al. lnorg. Chem., 2008,50 (15):2191-2198.
  • 8Lin J B, Zhang J P, Chen X M. J. Am. Chem. Soc., 2010, 132(19):6654-6656.
  • 9Chen S S, Chen M, Takamizawa S, et al. Chem. Commun., 2011,47(17) :4902-4904.
  • 10Lan Y Q, Li S L, Shao K Z, et al. Cryst. Growth Des., 2010, 10(8):3490-3492.

同被引文献27

  • 1Guo S, Sivaram H, Yuan D, et al. Organomet allics, 2013,32 (l 3):3685-3696.
  • 2Blase V, Flores-Figueroa A, Hahn F E, et al. Organomet allics, 2014,33(17):4471-4478.
  • 3Aher S B, Muskawar P N, Bhagat P R. Eur. J. Med. Chem., 2014,81:408-419.
  • 4Huang H J, Lee W C, Ong T G, et al. J. Orgartomet. Chem., 2014,761:64-73.
  • 5Chang W C, Chen H S, Li W R, et al. A ngew. Chem. Int. Ed., 2010,49(44):8161-8164.
  • 6Ma X, Wang H, Chen W.J. Org. Chem., 2014,79(18):8652.
  • 7Zhao N, Hou G H, Deng X B, et al. Dalton Trans., 2014,43 (22):8261-8272.
  • 8Catalano V J, Moore A L, Shearer J, et al. Inorg. Chem., 2009,48(23): 11362-11375.
  • 9Liu B, Pan S, Liu B, et al. Inorg. Chem., 2014,53(19):10485 - 10497.
  • 10Schick S, Pape T, Hahn F E. Organomet allics, 2014,33(15): 4035-4041.

引证文献1

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