کد مقاله | کد نشریه | سال انتشار | مقاله انگلیسی | نسخه تمام متن |
---|---|---|---|---|
1304768 | 974849 | 2008 | 6 صفحه PDF | دانلود رایگان |

The reaction of 1,4-dihydro-2,3-quinoxalinedione (H2L′) with CuCl2 in the presence of LiOH in DMF has led to the 3D coordination polymer [Cu3L2Cl2(DMF)4]n (1) with an (82 · 10)-a, lig (LiGe), topology, where L2− is 2,3-dioxyquinoxalinate(−2). This compound is the first coordination polymer of any transition metal featuring L2− and contains the ligand in a novel 3.1111 (Harris notation) coordination mode. IR data are discussed in terms of the chemical composition of the polymer and the coordination mode of L2−. Variable-temperature (2–300 K) magnetic susceptibility and variable-field (0–5 T) magnetization studies reveal that L2− propagates weak antiferromagnetic exchange interactions through its “quinoxaline” moiety.
The 3:2 CuCl2/1,4-dihydro-2,3-quinoxalinedione reaction system in DMF in the presence of OH−s gives a structurally and magnetically interesting 3D coordination polymer possessing the 2,3-dioxyquinoxalinate(-2) ligand (L2−) and exhibiting the extremely rare (82 · 10)-a [lig (LiGe)] topology. Complex [Cu3L2Cl2(DMF)4]n is the first coordination polymer of any metal with L2− and contains the dianionic ligand in the novel 3.1111 mode.Figure optionsDownload as PowerPoint slide
Journal: Inorganic Chemistry Communications - Volume 11, Issue 2, February 2008, Pages 186–191