物理化学学报
物理化學學報
물이화학학보
ACTA PHYSICO-CHIMICA SINICA
2014年
7期
1354-1362
,共9页
李婕%熊萍萍%步怀宇%陈三平
李婕%熊萍萍%步懷宇%陳三平
리첩%웅평평%보부우%진삼평
过渡金属配合物%晶体结构%抑菌活性%DNA裂解活性%DNA插入
過渡金屬配閤物%晶體結構%抑菌活性%DNA裂解活性%DNA插入
과도금속배합물%정체결구%억균활성%DNA렬해활성%DNA삽입
Transition metal compound%Crystal structure%Antifungal activity%DNA cleavage activity%DNA intercalation
以4-(1H-1,2,4-三唑-1-亚甲基)苯甲酸(HL)为配体,水热合成了三个过渡金属配合物[Cu0.5L]n (1),{[Ni(L)2?(H2O)2]?(H2O)2}n (2),{[Co(L)2?(H2O)2]?(H2O)2}n (3);运用红外光谱、元素分析、单晶X射线衍射、热分析、紫外光谱和荧光光谱等手段对化合物进行了表征.结构分析表明,配合物1呈现一维(1D)的链状结构,而同构的配合物2和3则通过链间的氢键连接为三维(3D)网状结构.抑菌活性研究表明,配合物对镰刀菌、苹果腐烂病菌、苹果轮纹病菌、梨炭疽病菌和烟草赤星病菌均有良好的抑菌效果,特别是配合物1的抑菌效果最为显著.质粒DNA(pUC 18)裂解活性实验结果表明,相比较于化合物2和3,化合物1能更有效地促进质粒DNA裂解.进一步采用光谱法检测三种配合物对DNA的结合作用.结果显示三种配合物均可插入DNA分子中,其中配合物1的插入作用最为强烈.
以4-(1H-1,2,4-三唑-1-亞甲基)苯甲痠(HL)為配體,水熱閤成瞭三箇過渡金屬配閤物[Cu0.5L]n (1),{[Ni(L)2?(H2O)2]?(H2O)2}n (2),{[Co(L)2?(H2O)2]?(H2O)2}n (3);運用紅外光譜、元素分析、單晶X射線衍射、熱分析、紫外光譜和熒光光譜等手段對化閤物進行瞭錶徵.結構分析錶明,配閤物1呈現一維(1D)的鏈狀結構,而同構的配閤物2和3則通過鏈間的氫鍵連接為三維(3D)網狀結構.抑菌活性研究錶明,配閤物對鐮刀菌、蘋果腐爛病菌、蘋果輪紋病菌、梨炭疽病菌和煙草赤星病菌均有良好的抑菌效果,特彆是配閤物1的抑菌效果最為顯著.質粒DNA(pUC 18)裂解活性實驗結果錶明,相比較于化閤物2和3,化閤物1能更有效地促進質粒DNA裂解.進一步採用光譜法檢測三種配閤物對DNA的結閤作用.結果顯示三種配閤物均可插入DNA分子中,其中配閤物1的插入作用最為彊烈.
이4-(1H-1,2,4-삼서-1-아갑기)분갑산(HL)위배체,수열합성료삼개과도금속배합물[Cu0.5L]n (1),{[Ni(L)2?(H2O)2]?(H2O)2}n (2),{[Co(L)2?(H2O)2]?(H2O)2}n (3);운용홍외광보、원소분석、단정X사선연사、열분석、자외광보화형광광보등수단대화합물진행료표정.결구분석표명,배합물1정현일유(1D)적련상결구,이동구적배합물2화3칙통과련간적경건련접위삼유(3D)망상결구.억균활성연구표명,배합물대렴도균、평과부란병균、평과륜문병균、리탄저병균화연초적성병균균유량호적억균효과,특별시배합물1적억균효과최위현저.질립DNA(pUC 18)렬해활성실험결과표명,상비교우화합물2화3,화합물1능경유효지촉진질립DNA렬해.진일보채용광보법검측삼충배합물대DNA적결합작용.결과현시삼충배합물균가삽입DNA분자중,기중배합물1적삽입작용최위강렬.
Three novel transition metal compounds [Cu0.5L]n (1),{[Ni(L)2?(H2O)2]?(H2O)2}n (2), and{[Co(L)2?(H2O)2]?(H2O)2}n (3), were hydrothermal y synthesized with 4-(1H-1,2,4-triazol-1-ylmethyl) benzoic acid (HL) and characterized by infrared spectroscopy, elemental analyses, single-crystal X-ray diffraction, thermal analyses, UV-Vis spectroscopy, and fluorescence spectroscopy. Structural analyses reveal that compound 1 features a one-dimensional (1D) chain, while isomorphic 2 and 3 exhibit a three-dimensional (3D) network structure with interchain hydrogen-bonding. Antifungal activities tests reveal that 1 has the highest antifungal effect on the five fungi (Fusarium graminearum, Vasa mali, Macrophoma kawatsukai, Col etotrichum gloeosporioides, and Alternaria alternate) among the three compounds. Furthermore, DNA cleavage experiments indicate that compound 1 has more efficient DNA (pUC 18) cleavage activity than compounds 2 and 3. The binding properties of the three compounds with DNA were also investigated by absorption. The results show that the three compounds can intercalate into DNA, and the interaction of compound 1 is the strongest.