摘要
水热条件下采用Sm(NO3)3.6H2O,1-萘乙酸和5,5'-二甲基-2,2'-联吡啶作为反应物合成出一个双核钐金属配合物Sm2(1-npac)6(dmpy)2.(H2O)3(1)(1-npac=1-萘乙酸,dmpy=5,5′-二甲基-2,2′-联吡啶),并分别用元素分析、红外光谱、差热分析、X-射线粉末衍射,紫外-可见光谱和X-射线单晶衍射等表征了该结构。晶体结构分析结果表明:化合物1为双核钐髥配合物,通过分子间的氢键作用以及C-H…π和π…π的堆积作用,双核分子进一步被连接成三维超分子结构。荧光分析表明常温固态下配合物1发射橙色荧光,荧光寿命为0.87μs(598 nm)。
A complex Smffl-npac)6 (dmpy)2(H20)3 (1), (1-npac=l-naphthaleneacetate, dmpy=5,5'-dimethyl-2,2'- bipyridine) has been hydrothermally synthesized and characterized by elemental analysis, IR, TGA, powder X-ray diffraction, UV-Vis and single-crystal X-ray diffraction. Structural determination reveals that the samarium ions are bridged by two bidentate and two terdentate carboxylato groups to give centrosymmetric dimers with Sm..-Sm separation of 0.3925 (2) nm, which is further extended to a 3D supramolecular structure by hydrogen bonds, C-π and π ... πr stacking interactions. Solid-state 1 emits the intensive orange luminescence of Sm3+ ion with fluorescence lifetime of 0.87 us (598 nm) at room temperature. CCDC: 898378.
出处
《无机化学学报》
SCIE
CAS
CSCD
北大核心
2013年第5期1065-1071,共7页
Chinese Journal of Inorganic Chemistry
基金
安徽高校省级自然科学研究项目(No.KJ2012Z310,KJ2011A210,KJ2012Z306)
阜阳师范学院博士启动基金(No.29709004)
阜阳师范学院分析化学重点学科基金(No.2010xk7-02)资助项目