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4, 4′-二羧基二苯基砜的镧系配合物的合成和结构 被引量:3

Synthesis and Structure of Lanthanide Complexes with 4,4'-dicarboxybiphenyl Sulfone
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摘要 合成了V型半刚性配体4,4′-二羧基二苯基砜的3个新的镧系配合物[Nd2(dbsf)3(DMF)2.25(H2O)1.75]·1.25DMF·0.5MeOH(1),[Yb2(dbsf)3(H2O)2]·1.5H2O(2)和[Er2(dbsf)3(H2O)2]·0.75H2O(3)(H2dbsf=4,4′-二羧基二苯基砜,DMF=N,N-二甲基甲酰胺,MeOH=甲醇),并测定了它们的晶体结构。结构表明配合物1具有一维孔道的三维镧系金属-有机骨架结构(LnOF),未配位的DMF和MeOH填充在孔道中;配合物2和3也具有三维的LnOF结构,但晶格水存在于洞穴里。它们的形成与结构特征可能与半刚性V型配体H2dbsf和镧系收缩效应有关。 Three new lanthanide complexes with semi-rigid V-shape 4,4'-dicarboxybiphenyl sulfone, [Ndffdbsf)3 (DMF)225 (H20)1.75] · 1.25DMF ·0.5MeOH (1), [Yb2 (dbsf)3 (H2O)2] ·1.5H20 (2) and [Er2 (dbsf)3 (H20)2]·0.75H20 (3) (H2dbsf=4,4'-dicarboxybiphenyl sulfone, DMF=N,N-dimethyl formamide, MeOH=methanol) were synthesized and characterized by X-ray diffraction single-crystal structural analysis. The crystal structures show that complex 1 is composed of 3D lanthanide-organic framework (LnOF) with 1D channels, in which uncoordinated DMF and MeOH molecules are filled; while the complexes 2 and 3 have 3D LnOFs with cavities, in which lattice water molecules are located. Their formation and structural characteristics are possibly due to the semi-rigid V-shape ligand H2dbsf and lanthanide contraction effect. CCDC: 683617, 1; 683618, 2; 683619, 3.
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2008年第8期1305-1310,共6页 Chinese Journal of Inorganic Chemistry
基金 国家自然科学基金资助项目(No.0331010 20501003)
关键词 镧系配合物:V型配体:晶体结构 lanthanide complex V-shape ligand crystal structure
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  • 1Batten S R, Robson R. A ngew. Chem. Int. Ed., 1998,37: 1460- 1494.
  • 2Kitaura R, Kitagawa S, Kubota Y, et al. Science, 2002,298: 2358-2361.
  • 3Halder G J, Kepert C J, Moubaraki M, et al. Science, 2002, 298:1762-1765.
  • 4Yaghi O M, Okeeffe M, Ockwig N W, et al. Nature, 2003, 423:705-714.
  • 5Chae H K, Siberio-Perez D Y, Kim J, et al. Nature, 2004, 427:523-527.
  • 6Rosi N L, Eckert J, Eddaoudi M, et al. Science, 2003,300: 1127-1129.
  • 7Ferey G, Mellot-Draznieks C, Serre C, et al. Science, 2005, 309:2040-2042.
  • 8Zaworotko M J. Angew. Chem. Int. Ed., 2000,39:3052-3054.
  • 9Kitagawa S, Kitaura R, Noro S I. Angew. Chem. Int. Ed., 21104,43:2334-2375.
  • 10Zou R Q, Sakurai H, Xu Q. A ngew. Chem. Int. Ed., 2006, 45:2542-2546.

同被引文献53

  • 1Hu J S, Zhu C L, Song X M, et al. Mendeleev Commun.,2012,22:310-311.
  • 2Pramanik S, Zheng C, Zhang X, et al. J. Am. Chem. Soc.,2011,133:4153-4155.
  • 3Rajput L, Kim D, Lah M S. CrystEngComm, 2013,15:259-264.
  • 4Ma L F, Han M L, Qin J H, et al. Inorg. Chem., 2012,51:9431-9442.
  • 5Agarwal R A, Aijaz A, Saudo C, et al. Cryst. Growth Des.,2013,13:1238-1245.
  • 6Li J R, Zhou H C. Nat. Chem., 2010,2:893-898.
  • 7Zhang H X, Wang F, Yang H, et al. J. Am. Chem. Soc.,2011,133:11884-11887.
  • 8Chu Q, Su Z, Fan J, et al. Cryst. Growth Des., 2011,50:3885-3894.
  • 9Xiao D R, Yuan R, Sun D Z, et al. J. Mol. Struct., 2009,936:264-269.
  • 10Bruker 2000, SMART (Version 5.0), SAINT-plus (Version6), SHELXTL (Version 6.1), and SADABS (Version 2.03);Bruker AXS Inc.: Madison, WI.

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