Versatile coordination mode of dicyanamide in nickel(II) complexes containing polyamines as blocking ligands

被引:36
作者
Boca, R [1 ]
Boca, M
Gembicky, M
Jäger, L
Wagner, C
Fuess, H
机构
[1] Slovak Univ Technol Bratislava, Dept Inorgan Chem, SK-81237 Bratislava, Slovakia
[2] Slovak Acad Sci, Inst Inorgan Chem, SK-81237 Bratislava, Slovakia
[3] Tech Univ Darmstadt, D-64287 Darmstadt, Germany
[4] Univ Halle Wittenberg, Dept Chem, D-06099 Halle An Der Saale, Germany
关键词
crystal structure; nickel(II) complexes; magnetism; pseudohalides;
D O I
10.1016/j.poly.2004.06.022
中图分类号
O61 [无机化学];
学科分类号
070301 ; 081704 ;
摘要
Triethylenetetramine (L-4) and dipropylenetriamine (L-3) were used as blocking ligands (tetradentate and tridentate, respectively) that, after complexation with Ni(II), leave two or three sites ready for ligation with N(CN)(2)(-) (dicyanamide, abbr. dca). The formed complexes are mononuclear, binuclear or polymeric. This was proven by the X-ray structure analysis for [NiL4(dca)(2)] (mononuclear, 1), [(dca)(LNi)-Ni-3(dca)(2)NiL3(dca)] (binuclear, 2) and [NiL4(dca)](ClO4) (polymeric, 3). The magnetic susceptibility measurements for 1 confirm that the Curie law is obeyed at higher temperatures whereas the zero-field splitting is effective below 10 K (D/hc = -4 cm(-1)); 2 shows a weak anti ferromagnetic coupling (J/hc = -0.6 cm(-1)); 3 exhibits a negligible exchange coupling (J/hc approximate to 0). (C) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:2337 / 2348
页数:12
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