吉林师范大学学报(自然科学版)
吉林師範大學學報(自然科學版)
길림사범대학학보(자연과학판)
JILIN NORMAL UNIVERSITY JOURNAL(NATURAL SCIENCE EDITION)
2014年
3期
128-131
,共4页
张文通%杨旭%阮晓文%张兴晶%李秀颖%车广波
張文通%楊旭%阮曉文%張興晶%李秀穎%車廣波
장문통%양욱%원효문%장흥정%리수영%차엄파
锌(Ⅱ)配合物%镉(Ⅱ)配合物%二吡啶3,2-a:2',3'-c并吩嗪%2,3-f吡嗪并1,10菲罗啉%晶体结构
鋅(Ⅱ)配閤物%鎘(Ⅱ)配閤物%二吡啶3,2-a:2',3'-c併吩嗪%2,3-f吡嗪併1,10菲囉啉%晶體結構
자(Ⅱ)배합물%력(Ⅱ)배합물%이필정3,2-a:2',3'-c병분진%2,3-f필진병1,10비라람%정체결구
zinc(Ⅱ)complex%cadmium(Ⅱ)complex%dipyrido[3,2-a:2’,3’-c]phenazine%pyrazino[2,3-f ] [1,10]phenanthroline%crystal structure
以多氮杂环配体二吡啶[3,2-a:2',3'-c]并吩嗪(DPPZ)和[2,3-f]吡嗪并[1,10]菲罗啉(Pyphen)为配体,采用水热法合成了两个配合物[Zn(DPPZ)2 SO4]·2H2 O(1)和[Cd(Pyphen)2 Cl2](2),利用元素分析和单晶 X-射线衍射对其结构进行了表征.分析结果表明,配合物(1)和(2)都属于单斜晶系,空间群都为 C2/ c.配合物1的晶胞参数为:a =17.5007(9)?,b =7.2344(5)?,c =23.1822(14)?,β=94.942(5)°,V =2924.1(3)?3,Z =4;配合物(2)的晶胞参数为:a =8.5098(17)?,b =12.524(3)?,c =22.683(5)?,β=95.31(3)°,V =2407.0(8)?3,Z =4.配合物(1)和(2)均为零维结构单元,配合物(1)的单元之间通过π-π堆积作用形成二维层状结构,层与层之间通过氢键作用形成三维超分子结构.配合物(2)的配位单元之间通过 Pyphen 配体的π-π堆积作用构筑成一个二维超分子结构.
以多氮雜環配體二吡啶[3,2-a:2',3'-c]併吩嗪(DPPZ)和[2,3-f]吡嗪併[1,10]菲囉啉(Pyphen)為配體,採用水熱法閤成瞭兩箇配閤物[Zn(DPPZ)2 SO4]·2H2 O(1)和[Cd(Pyphen)2 Cl2](2),利用元素分析和單晶 X-射線衍射對其結構進行瞭錶徵.分析結果錶明,配閤物(1)和(2)都屬于單斜晶繫,空間群都為 C2/ c.配閤物1的晶胞參數為:a =17.5007(9)?,b =7.2344(5)?,c =23.1822(14)?,β=94.942(5)°,V =2924.1(3)?3,Z =4;配閤物(2)的晶胞參數為:a =8.5098(17)?,b =12.524(3)?,c =22.683(5)?,β=95.31(3)°,V =2407.0(8)?3,Z =4.配閤物(1)和(2)均為零維結構單元,配閤物(1)的單元之間通過π-π堆積作用形成二維層狀結構,層與層之間通過氫鍵作用形成三維超分子結構.配閤物(2)的配位單元之間通過 Pyphen 配體的π-π堆積作用構築成一箇二維超分子結構.
이다담잡배배체이필정[3,2-a:2',3'-c]병분진(DPPZ)화[2,3-f]필진병[1,10]비라람(Pyphen)위배체,채용수열법합성료량개배합물[Zn(DPPZ)2 SO4]·2H2 O(1)화[Cd(Pyphen)2 Cl2](2),이용원소분석화단정 X-사선연사대기결구진행료표정.분석결과표명,배합물(1)화(2)도속우단사정계,공간군도위 C2/ c.배합물1적정포삼수위:a =17.5007(9)?,b =7.2344(5)?,c =23.1822(14)?,β=94.942(5)°,V =2924.1(3)?3,Z =4;배합물(2)적정포삼수위:a =8.5098(17)?,b =12.524(3)?,c =22.683(5)?,β=95.31(3)°,V =2407.0(8)?3,Z =4.배합물(1)화(2)균위령유결구단원,배합물(1)적단원지간통과π-π퇴적작용형성이유층상결구,층여층지간통과경건작용형성삼유초분자결구.배합물(2)적배위단원지간통과 Pyphen 배체적π-π퇴적작용구축성일개이유초분자결구.
Two different complexes[Zn(DPPZ)2 SO4 ]·2(H2 O)(1)and[Cd(Pyphen)2 Cl2 ](2)based on the multi-nitrogen heterocyclic ligands dipyrido[3,2-a:2',3'-c]phenazine(DPPZ)or pyrazino[2,3-f][1,10] phenanthroline have been synthesized under hydrothermal conditions and characterized by elemental analysis and single-crystal X-ray diffraction. Two complexes crystallizes in monoclinic crystal space group C 2 / c,with complex (1)a = 17. 500 7(9)?,b = 7. 234 4(5)?,c = 23. 182 2(14)?,β = 94. 942(5)°,V = 2 924. 1(3)?3 ,Z = 4 and complex(2)a = 8. 509 8(17)?,b = 12. 524(3)?,c = 22. 683(5)?,β = 95. 31(3)°,V = 2 407. 0(8) ?3 ,Z = 4. The structure of the title compounds(1)and(2)is mononuclear 0D unit. In complex(1),a 2D layer structure is formed through the π-π interactions between the adjacent independent units,and the layers are linked through hydrogen bonds to form a 3D supramolecular structure. Complex(2)is stacked through π-π interactions between the Pyphen ligands to form a 2D supramolecular structure.