作者:P.A. Prasad、S. Neeraj、R. Vaidhyanathan、Srinivasan Natarajan
DOI:10.1006/jssc.2002.9568
日期:2002.6
β=93.796(1)°, Z=4; [Cd(C2O4)2(C3N2H4)3(H2O)]∞ (II): monoclinic, space group P21/c (no. 14), a=7.8614(2) Å, b=14.9332(3) Å, c=15.9153(4) Å β=94.587(1)°, Z=4; [Cd(C2O4)2(C3N2H4)3(H2O)]∞ (III): monoclinic, space group P21/c (no. 14), a=11.844(2) Å, b=9.066(1) Å, c=18.583(2) Å, β=103.84(2)°, Z=4. While the structure of I is made from CdO5N distorted octahedra linked with oxalate, II and III are built-up
在咪唑存在下,已经合成了三种新的草酸镉配位聚合物I–III,具有扩展的层状结构。I是草酸咪唑鎓与Cd反应制得的,而II和III是用水热法从它们的成分合成的。[Cd(C 2 O 4)(C 3 N 2 H 4)] ∞(I):单斜晶系,空间群P 2 1 / c(编号14),a = 8.7093(1)Å,b = 9.9477(3) )Å,c = 8.4352Å,β = 93.796(1)°,Z = 4; [镉(C 2 O 4)2(C 3 N 2 H 4)3(H 2 O)] ∞(II):单斜,空间群P 2 1 / c(no。14 ),a = 7.8614(2)Å,b = 14.9332(3)埃,ç = 15.9153(4)β = 94.587(1)°,ž = 4; [Cd(C 2 O 4)2(C 3 N 2 H 4)3(H 2 O)] ∞(III):单斜,空间群P 2 1/ c(第14号),a = 11