Department of Chemistry and MacDiarmid Institute for Advanced Materials and Nanotechnology, University of Otago, P.O. Box 56, Dunedin 9054, New Zealand.
Inorg Chem. 2012 May 7;51(9):5058-69. doi: 10.1021/ic202537c. Epub 2012 Apr 6.
Four bis-tetradentate N(4)-substituted-3,5-{bis[bis-N-(2-pyridinemethyl)]aminomethyl}-4H-1,2,4-triazole ligands, L(Tz1)-L(Tz4), differing only in the triazole N(4) substituent R (where R is amino, pyrrolyl, phenyl, or 4-tertbutylphenyl, respectively) have been synthesized, characterized, and reacted with M(II)(BF(4))(2)·6H(2)O (M(II) = Cu, Ni or Co) and Co(SCN)(2). Experiments using all 16 possible combinations of metal salt and L(TzR) were carried out: 14 pure complexes were obtained, 11 of which are dinuclear, while the other three are tetranuclear. The dinuclear complexes include two copper(II) complexes, Cu(II)(2)(L(Tz2))(H(2)O)(4)(4) (2), Cu(II)(2)(L(Tz4))(BF(4))(2)(2) (4); two nickel(II) complexes, Ni(II)(2)(L(Tz1))(H(2)O)(3)(CH(3)CN)(4)·0.5(CH(3)CN) (5) and Ni(II)(2)(L(Tz4))(H(2)O)(4)(4)·H(2)O (8); and seven cobalt(II) complexes, Co(II)(2)(L(Tz1))(μ-BF(4))(3)·H(2)O (9), Co(II)(2)(L(Tz2))(μ-BF(4))(3)·2H(2)O (10), Co(II)(2)(L(Tz3))(H(2)O)(2)(4) (11), Co(II)(2)(L(Tz4))(μ-BF(4))(3)·3H(2)O (12), [Co(II)(2)(L(Tz1))(SCN)(4)]·3H(2)O (13), [Co(II)(2)(L(Tz2))(SCN)(4)]·2H(2)O (14), and [Co(II)(2)(L(Tz3))(SCN)(4)]·H(2)O (15). The tetranuclear complexes are Cu(II)(4)(L(Tz1))(2)(H(2)O)(2)(BF(4))(2)(6) (1), Cu(II)(4)(L(Tz3))(2)(H(2)O)(2)(μ-F)(2)(6)·0.5H(2)O (3), and Ni(II)(4)(L(Tz3))(2)(H(2)O)(4)(μ-F(2))(6)·6.5H(2)O (7). Single crystal X-ray structure determinations revealed different solvent content from that found by microanalysis of the bulk sample after drying under a vacuum and confirmed that 5', 8', 9', 11', 12', and 15' are dinuclear while 1' and 7' are tetranuclear. As expected, magnetic measurements showed that weak antiferromagnetic intracomplex interactions are present in 1, 2, 4, 7, and 8, stabilizing a singlet spin ground state. All seven of the dinuclear cobalt(II) complexes, 9-15, have similar magnetic behavior and remain in the [HS-HS] state between 300 and 1.8 K.
四种双齿四氮唑配体 L(Tz1)-L(Tz4),分别用氨基、吡咯基、苯基和 4-叔丁基苯基取代三唑氮原子 N(4),与 M(II)(BF(4))(2)·6H(2)O(M(II) = Cu、Ni 或 Co)和 Co(SCN)(2)反应,合成、表征。实验采用了 16 种可能的金属盐和 L(TzR)组合:得到了 14 种纯配合物,其中 11 种为双核,另外 3 种为四核。双核配合物包括两个铜(II)配合物Cu(II)(2)(L(Tz2))(H(2)O)(4)(4)(2)和Cu(II)(2)(L(Tz4))(BF(4))(2)(2)(4);两个镍(II)配合物Ni(II)(2)(L(Tz1))(H(2)O)(3)(CH(3)CN)(4)·0.5(CH(3)CN)(5)和Ni(II)(2)(L(Tz4))(H(2)O)(4)(4)·H(2)O(8);以及七个钴(II)配合物Co(II)(2)(L(Tz1))(μ-BF(4))(3)·H(2)O(9)、Co(II)(2)(L(Tz2))(μ-BF(4))(3)·2H(2)O(10)、Co(II)(2)(L(Tz3))(H(2)O)(2)(4)(11)、Co(II)(2)(L(Tz4))(μ-BF(4))(3)·3H(2)O(12)、[Co(II)(2)(L(Tz1))(SCN)(4)]·3H(2)O(13)、[Co(II)(2)(L(Tz2))(SCN)(4)]·2H(2)O(14)和[Co(II)(2)(L(Tz3))(SCN)(4)]·H(2)O(15)。四核配合物为Cu(II)(4)(L(Tz1))(2)(H(2)O)(2)(BF(4))(2)(6)(1)、Cu(II)(4)(L(Tz3))(2)(H(2)O)(2)(μ-F)(2)(6)·0.5H(2)O(3)和Ni(II)(4)(L(Tz3))(2)(H(2)O)(4)(μ-F(2))(6)·6.5H(2)O(7)。单晶 X 射线结构测定显示,与真空干燥后通过微分析发现的溶剂含量不同,证实了 5'、8'、9'、11'、12'和 15'是双核的,而 1'和 7'是四核的。正如预期的那样,磁测量表明,1、2、4、7 和 8 中存在弱的反铁磁内络合相互作用,稳定了单重态自旋基态。七个双核钴(II)配合物 9-15 的磁行为相似,在 300 和 1.8 K 之间保持[HS-HS]状态。