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Embracing ligands. Synthesis, characterisation and the correlation between 59Co NMR and ligand field parameters of Co(III) complexes with a new class of nitrogen-thioether multidentate ligand

机译:拥抱配体。新型一类氮-硫醚多齿配体的Co(III)配合物的59Co NMR的合成,表征及相关性

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摘要

The syntheses of the hexadentate ligands 2,2,10,10-tetra(methyleneamine)-4,8-dithiaundecane (PrN(4)S(2)amp), 2,2,11,11-tetra(methyleneamine)-4,9-dithiadodecane (BuN(4)S(2)amp), and 1,2-bis(4,4-methyleneamine)-2-thiapentyl)benzene (XyN(4)S(2)amp) are reported and the complexes [Co(RN(4)S(2)amp)](3+) (R = Pr, Bu, Xy) characterised by single crystal X-ray study. The low-temperature (11 K) absorption spectra have been measured in Nafion films. From the observed positions of both spin-allowed (1)A(1g) --> T-1(1g) and (1)A(1g) --> T-1(2g) and spin forbidden (1)A(1g) --> T-3(1g) and (1)A(1g) --> T-3(2g) bands, octahedral ligand-field parameters (10D(q), B and C) have been determined. DFT calculations suggest that significant interaction between the d-d and CT excitations occurs for the complexes. The calculations offer an explanation for the observed deviations from linearity of the relationship between Co-59 magnetogyric ratio and beta(DeltaE)(-1) (beta = the nephelauxetic ratio; DeltaE the energy of the (1)A(1g) --> T-1(1g) transition) for a series of amine and mixed amine/thioether donor complexes.
机译:六齿配体2,2,10,10-四(亚甲基胺)-4,8-​​二硫十一碳烷(PrN(4)S(2)amp),2,2,11,11-四(亚甲基胺)-4的合成报道了1,9-二硫十二烷(BuN(4)S(2)amp)和1,2-双(4,4-亚甲基胺)-2-噻吩基)苯(XyN(4)S(2)amp)配合物[Co(RN(4)S(2)amp)](3+)(R = Pr,Bu,Xy)的特征在于单晶X射线研究。在Nafion膜中已测量了低温(11 K)吸收光谱。从观察到的位置都允许自旋(1)A(1g)-> T-1(1g)和(1)A(1g)-> T-1(2g)和自旋禁止(1)A( 1g)-> T-3(1g)和(1)A(1g)-> T-3(2g)带,已确定八面体配体场参数(10D(q),B和C)。 DFT计算表明,配合物在d-d和CT激发之间发生了显着的相互作用。这些计算为观察到的Co-59磁氧比率与beta(DeltaE)(-1)之间的关系的线性偏离提供了解释(beta =肾上腺皮质激素比率; DeltaE(1)A(1g)的能量- > T-1(1g)过渡),用于一系列胺和混合的胺/硫醚供体配合物。

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