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以5-甲基-3-吡唑甲酸为配体的钴(Ⅱ)、镍(Ⅱ)配合物的合成、晶体结构和性质(英文) 被引量:3

Syntheses,Crystal Structures and Properties of Cobalt(Ⅱ) and Nickel(Ⅱ) Complexes Based on 5-Methyl-1H-pyrazole-3-carboxylic Acid Ligand
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摘要 以5-甲基-3-吡唑甲酸(H2MPCA)为主配体,桥联配体4,4′-联吡啶(4,4′-bpy)和吡嗪(pyz)为辅助配体,合成了2个新的配合物{[Co(HMPCA)2(4,4′-bpy)]2·5H_2O}n(1)和{[Ni(HMPCA)2(pyz)]·5H_2O}n(2),并用元素分析、红外光谱、X射线单晶衍射结构分析、热重分析等对其进行了表征。配合物1属于正交晶系,空间群为Pccn,配合物2属于单斜晶系,空间群为P2/c。在1和2中,金属离子都位于一个扭曲的八面体配位环境中,分别由4,4′-联吡啶(1)和吡嗪(2)两端的氮原子桥联2个相邻的金属离子,形成一维链状聚合物。考察了配合物1和2的热稳定性、荧光性能和磁性。 Two new 1D chain-typed coordination polymers, {[Co(HMPCA)2(4,4'-bpy)]25H2O}n (1) and {[Ni(HMPCA)2(pyz)]5H2O}n(2) (H2MPCA=5-methyl-1H-pyrazole-3-carboxylic acid, 4,4'-bpy=4,4'-bipyridine, pyz=pyrazine), have been synthesized and characterized by elemental analysis, IR spectra, single crystal X-ray diffraction and thermogravimetric analysis. Complex 1 crystallizes in the orthorhombic system, space group Pccn, and 2 crystallizes in the monoclinic system, space group P2/c. In 1 and 2, metal ions are both located in an octahedral geometry, coordinated by two nitrogen atoms and two oxygen atoms from two HMPCA-anions, and linked by two nitrogen atoms from 4,4'-bpy ligands (1) and pyz ligands (2), respectively, forming a 1D chain-typed coordination polymer. The thermal stability, luminescent properties and magnetic properties of them have also been investigated.
出处 《无机化学学报》 SCIE CAS CSCD 北大核心 2016年第8期1457-1466,共10页 Chinese Journal of Inorganic Chemistry
基金 国家自然科学基金(No.21101018,20971060) 江苏省高校自然科学研究面上项目(No.13KJB150001) 南京大学配位化学国家重点实验室开放课题 江苏省先进催化与绿色制造协同创新中心创新型人才支持项目资助
关键词 5-甲基-3-吡唑甲酸 晶体结构 荧光 磁性 cobalt(Ⅱ) nickel(Ⅱ) 5-methyl-1H-pyrazole-3-carboxylic acid crystal structure photoluminescence magnetic properties
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参考文献40

  • 1Cook T R, Zheng Y R, Stang P J. Chem. Rev., 2013,113(1): 734-777.
  • 2Hu X Y, Xiao T X, Lin C, et al. Acc. Chem. Res., 2014,47 (7):2041-2051.
  • 3Liu Q, Liu X X, Shi C D, et al. Dalton Trans., 2015,44: 19175-19184.
  • 4Liu X X, Shi C D, Zhai C W, et al. A CS Appl. Mater.Interfaces, 20111,8(7):4585-4591.
  • 5Santra A, Senkovska I, Kaskel S, et al. Inorg. Chem., 2013, 52(13):7358-7366.
  • 6Gipson T J, Beobide G, Castillo O, et al. Cryst. Growth Des., 2014,14(8):4019-4029.
  • 7Hu S, He K H, Zeng M H, et al. Inorg. Chem., 2008,47(12): 5218-5224.
  • 8Chatterjee B, Noveron C J, Resendiz E J M, et al. J. Am. Chem. Soc., 2004,126(34):10645-10656.
  • 9Brown J C, Miller M G, Johnson W M, et al. J. Am. Chem. Soc., 2011,133(31): 11964-11966.
  • 10Hagen M C, Ludovic V P, Gabor L, et al. Organometallics, 2005,24(8): 1819-1831.

二级参考文献125

  • 1Chui S S Y, Lo S M F, Charmant J P H, et al. Science, 1999,283:1148-1150.
  • 2Yazaydin A, Snurr R Q, Park T H, et al. J. Am. Chem. Soc., 2009,131(5): 18198-18199.
  • 3Gu Z Y, Yan X P. Angew. Chem. Int. Ed., 2010,49:1477- 1480.
  • 4He Q W, Miller E W, Wong A P, et al. J. Am. Chem. Soc., 2006,128:9316-9317.
  • 5Glover T G, Peterson G W, Schindler B J, et al. Chem. Eng. Sci., 2010,66:163-170.
  • 6Sanna D, Micera G, Buglyo P, et al. Inorg. Chim. Acta, 1998,268:297-305.
  • 7Sava D F, Kravtsov V C, Nouar F, et al. J. Am. Chem. Soc., 2008,130:3768-3770.
  • 8Beobide G, Wang W G, Castillo O, et al. Inorg. Chem., 2008,47(12):5267 -5277.
  • 9Chen C, Sun J K, Li W, et al. Chem. Commun., 2011,47: 6683-6685.
  • 10Hua Y, Xiong L S.J. Inorg. Chem., 2009,25(5):893-899.

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