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Novel dioxotetrazamacrocyclic 'sandwich' complexes - synthesis and structural characterization

机译:新型二氧四氮杂大环“三明治”配合物-合成与结构表征

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摘要

Reaction of 1,4,7,10-tetraazacyclododecane-2,9-dione with copper and cobalt perchlorate in water at 1:1 molar ratio afforded two new crystal-engineered 1:2 'Sandwich' type complexes. Both of them are isostructural analogues. Copper complex crystallized in monoclinic space group P2_1/c with a = 9.6888(12), b = 12.2956(16), c = 10.5661(13), #beta# = 104.965(2) deg, V = 1216.0(3) A~3, and Z = 2. The Cu(II) ions are six-coordinated by four nitrogen atoms and two amide oxygen atoms. Their coordination geometry can be described as Jahn-Teller distorted octahedral, with elongated Cu-O distances. (2.310(2) A) Cobalt complex crystallized in monoclinic space group P2_1/c with a = 9.7560(12), b = 12.237(16), c = 10.7130(13), #beta# = 105.194(3) deg, V = 1234.2(4) A~3, and Z = 2. The Co(II) ions are also six-coordinated by similar atoms as found in copper complex. But the bond lengths of Co-O 2.0881(13) A are slightly shorter than respective Co-N.
机译:1,4,7,10-四氮杂十二环十二烷-2,9-二酮与铜和高氯酸钴在水中的摩尔比为1:1的反应生成了两种新的晶体工程的1:2的“三明治”型配合物。它们都是同构类似物。在单斜空间群P2_1 / c中结晶的铜络合物,a = 9.6888(12),b = 12.2956(16),c = 10.5661(13),#beta#= 104.965(2)度,V = 1216.0(3)A〜 3,Z =2。Cu(II)离子由四个氮原子和两个酰胺氧原子六配位。它们的配位几何形状可以描述为Jahn-Teller扭曲的八面体,具有较长的Cu-O距离。 (2.310(2)A)在单斜空间群P2_1 / c中结晶的钴配合物,a = 9.7560(12),b = 12.237(16),c = 10.7130(13),#beta#= 105.194(3)度,V = 1234.2(4)A〜3,Z =2。Co(II)离子也与铜络合物中的相似原子六配位。但是Co-O 2.0881(13)A的键长略短于相应的Co-N。

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