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Anion coordination directed synthesis patterns for [Ni4] aggregates: structural changes for thiocyanate coordination and ligand arm hydrolysis

机译:[Ni4]聚集体的阴离子协调定向合成模式:硫氰酸酯配位和配体臂水解的结构变化

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摘要

The coordination reactivity of ligand H _(5) L1 (2,6-bis-{(1,3-dihydroxy-2-methylpropan-2-ylimino)methyl}-4-methylphenol) toward nickel( II ) ions in the presence of two different anions resulted in cubane and fused dicubane types of tetranuclear coordination aggregates. In the first case, utilization of two carboxylate (R = Me and Et in RCO _(2) ~(?) ) anions led to cubane type Ni _(4) O _(4) aggregates [Ni _(4) (H _(4) L1) _(2) (μ _(3) -OH) _(2) (μ _(1,3) -O _(2) CCH _(3) ) _(2) ](NO _(3) )(CH _(3) COO)·3H _(2) O ( 1 ) and [Ni _(4) (H _(4) L1) _(2) (μ _(3) -OH) _(2) (μ _(1,3) -O _(2) CC _(2) H _(5) ) _(2) ](NO _(3) )(C _(2) H _(5) COO)·CH _(3) CN·1.5H _(2) O ( 2 ). Whereas the use of thiocyanate anions triggered single imine arm hydrolysis of H _(5) L1 and gave partial dicubane type Ni _(4) N _(2) O _(4) aggregates [Ni _(4) (H _(2) L2) _(2) (HAMP) _(2) (μ _(1,1) -NCS) _(2) ](NO _(3) ) _(2) ( 3a ) and [Ni _(4) (H _(2) L2) _(2) (HAMP) _(2) (μ _(1,1) -NCS) _(2) ]Cl _(2) ·CH _(3) OH·H _(2) O ( 3b ) (H _(2) L2 = 3-{(1,3-dihydroxy-2-methylpropan-2-ylimino)methyl}-2-hydroxy-5-methylbenzaldehyde). Liberated 2-amino-2-methyl-1,3-propanediol from imine arm hydrolysis was successfully trapped in 3a and 3b for the growth and stabilization of different molecular architectures. Mass spectral evidence established that two types of dinuclear fragments Ni _(2) (H _(4) L1) and Ni _(2) (H _(2) L2), from the originally used and partially hydrolyzed ligand anions have been self-assembled for two types of Ni ~(II) based coordination aggregates. Two sets of complexes were characterized by elemental analysis, FT-IR and optical spectroscopy, variable temperature magnetic measurements, and single crystal X-ray analysis. The magnetic behavior examined through the temperature interval of 1.9–300 K with experimental and theoretical corroboration support the exchange pathways within the two types of [Ni _(4) ] coordination aggregates.
机译:配体H的协调反应_(5)L1(2,6-双 - {(1,3-二羟基-2-甲基丙-2-基亚氨基)甲基} -4-甲基苯酚)朝向镍(II)离子在存在两种不同的阴离子导致立方烷和融合dicubane类型四核配骨料。在第一种情况下,利用两个羧酸酯的(R =我和Et在RCO _(2)〜(?))导致立方烷型Ni阴离子_(4)O _(4)聚集体的Ni _(4)(H _(4)L1)_(2)(μ_(3)-OH)_(2)(μ_(1,3)-O _(2)CCH _(3))_(2)](NO _(3))(CH _(3)COO)·3H _(2)O(1)和[镍_(4)(H _(4)L1)_(2)(μ_(3)-OH )_(2)(μ_(1,3)-O _(2)CC _(2)H _(5))_(2)](NO _(3))(C _(2)H _ (5)COO)·CH _(3)CN·1.5H _(2)O(2)。而使用硫氰酸根阴离子的触发为h _(5)L1单亚胺臂水解,并给部分dicubane型Ni _(4)N _(2)O _(4)聚集体的Ni _(4)(H _(2 )L2)_(2)(HAMP)_(2)(μ_(1,1)-NCS)_(2)](NO _(3))_(2)(3a)和[镍_(4- )(H _(2)L2)_(2)(HAMP)_(2)(μ_(1,1)-NCS)_(2)]氯_(2)·CH _(3)OH·H _(2)O(图3b)(H _(2)L2 = 3 - {(1,3-二羟基-2-甲基丙-2-基亚氨基)甲基} -2-羟基-5-甲基苯甲醛)。释放的2-氨基-2-甲基-1,3-丙二醇,从亚胺臂水解成功被困在图3a和3b为不同的分子结构的生长和稳定化。质谱证据证实,两种类型的双核片段的镍_(2)(H _(4)L1)和Ni _(2)(H _(2)L2),从最初使用的和部分水解的配体阴离子已经自-assembled两种类型的Ni〜(II)的基于协调聚集体。通过元素分析两组配合物进行了表征,FT-IR和光学光谱法,变温磁性测量,和单晶X射线分析。磁性行为通过1.9-300的K用实验和理论佐证支持两种类型的[镍_(4)]协调聚集体的内部的交换途径中的温度间隔检查。

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  • 来源
    《New Journal of Chemistry》 |2018年第20期|共12页
  • 作者单位

    Department of Chemistry Indian Institute of Technology;

    Division of Biologically Active Complexes and Molecular Magnets Regional Centre of Advanced Technologies and Materials Faculty of Science Palacky University in Olomouc;

    Division of Biologically Active Complexes and Molecular Magnets Regional Centre of Advanced Technologies and Materials Faculty of Science Palacky University in Olomouc;

    Dipartimento di Scienze Chimiche e Farmaceutiche Centro di Strutturistica Diffrattometrica University of Ferrara;

    Department of Chemistry Indian Institute of Technology;

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