Metal-Dependent Phase Selection in Coordination Polymers Derived from a C2v-Symmetric Tricarboxylate

被引:55
作者
Lim, Choong-Sun
Schnobrich, Jennifer K.
Wong-Foy, Antek G.
Matzger, Adam J. [1 ]
机构
[1] Univ Michigan, Dept Chem, Ann Arbor, MI 48109 USA
基金
美国国家科学基金会;
关键词
FRAMEWORK; SUBSTITUTION; BEHAVIOR; LN;
D O I
10.1021/ic100378p
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Reacting biphenyl-3,4',5-tricarboxylic acid (H3BHTC) with the appropriate metal salt yields the microporous coordination polymers (MCPs) Mn-3(BHTC)(2) (1), Mg-3(BHTC)(2) (2), and Co-3(BHTC)(2) (3) containing hourglass metal clusters. The addition of Cu to reactions with Co-II, Fe-III, or Mn-II leads to the formation of heterobimetallic UMCM-150 isostructural analogues Co1Cu2(BHTC)(2) (4), Fe1Cu2(BHTC)(2) (5), and Mn1Cu2(BHTC)(2) (6) containing both paddlewheel and trinuclear metal clusters. X-ray diffraction analysis of the crystals of the heterobimetallic MCPs suggests that Cu on the trinuclear site of UMCM-150 was replaced by the other metal, whereas Cu in paddlewheel sites remains unchanged. N-2 sorption isotherms were measured for the mixed-metal UMCM-150 analogues, and it was confirmed that there is no structural collapse after the metal replacement.
引用
收藏
页码:5271 / 5275
页数:5
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