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首页> 外文期刊>Russian Journal of Coordination Chemistry >Complexes Fe(HTrz)3B_(10)H_(10) · H2O and Fe(NH2Trz)3B_(10)H_(10) · H2O (HTrz = 1,2,4-Triazole and NH2Trz = 4-Amino-1,2,4-Triazole). The Spin Transition ~1A_1 ←→ ~5T_2 in Fe(HTrz)3B_(10)H_(10) · H2O
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Complexes Fe(HTrz)3B_(10)H_(10) · H2O and Fe(NH2Trz)3B_(10)H_(10) · H2O (HTrz = 1,2,4-Triazole and NH2Trz = 4-Amino-1,2,4-Triazole). The Spin Transition ~1A_1 ←→ ~5T_2 in Fe(HTrz)3B_(10)H_(10) · H2O

机译:Fe(HTrz)3B_(10)H_(10)·H2O和Fe(NH2Trz)3B_(10)H_(10)·H2O(HTrz = 1,2,4-三唑和NH2Trz = 4-氨基-1,2 ,4-三唑)。 Fe(HTrz)3B_(10)H_(10)·H2O中的自旋跃迁〜1A_1←→〜5T_2

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摘要

Methods for the synthesis of iron(II) complexes with 1,2,4-triazole (HTrz) and 4-amino-1,2,4-tria-zole (NH2Trz) containing the decahydro-closo-decaborate ion [B_(10)H_(10)]~2- were developed. The empirical formulas of the complexes were Fe(HTrz)3B_(10)H_(10) · H2O (I) and Fe(NH2Trz)3B_(10)H_(10) · H2O (II). The complexes were examined by static magnetic susceptibility measurements (2-300 K) and Moessbauer, IR, and electronic spectroscopy. Complex I exhibits the reversible spin transition ~1A_1 ←→ ~5T_2 and pink ←→ white thermo-chromism. The temperatures of the forward and reverse transitions in complex I were 246 and 233 K, respectively. Complex II remained in the high-spin state over the whole temperature range. The sharp decrease in its effective magnetic moment at T < 78 K was attributed to antiferromagnetic exchange interactions between Fe~(2+) ions.
机译:含有十氢-氯杂-十恶酸盐离子的1,2,4-三唑(HTrz)和4-氨基-1,2,4-三唑(NH2Trz)的铁(II)配合物的合成方法)H_(10)]〜2-被开发出来。配合物的经验公式为Fe(HTrz)3B_(10)H_(10)·H2O(I)和Fe(NH2Trz)3B_(10)H_(10)·H2O(II)。通过静态磁化率测量(2-300 K)以及Moessbauer,IR和电子光谱对复合物进行了检查。复合体I表现出可逆的自旋跃迁〜1A_1←→〜5T_2和粉红色←→白色热致变色。配合物I中正向和反向跃迁的温度分别为246和233K。复合物II在整个温度范围内均保持高旋转状态。其有效磁矩在T <78 K时急剧下降归因于Fe〜(2+)离子之间的反铁磁交换相互作用。

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