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首页> 外文期刊>Inorganic Chemistry: A Research Journal that Includes Bioinorganic, Catalytic, Organometallic, Solid-State, and Synthetic Chemistry and Reaction Dynamics >Solvent-Induced Change of Electronic Spectra and Magnetic Susceptibility of Co-II Coordination Polymer with 2,4,6-Tris(4-pyridyl)-1,3,5-triazine
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Solvent-Induced Change of Electronic Spectra and Magnetic Susceptibility of Co-II Coordination Polymer with 2,4,6-Tris(4-pyridyl)-1,3,5-triazine

机译:溶剂引起的Co-II配位聚合物与2,4,6-Tris(4-吡啶基)-1,3,5-三嗪的电子光谱变化和磁化率

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摘要

One-dimensional coordination polymer [Co(Piv)(2)(4-ptz)(C2H5OH)(2)]n (compound 1, Piv(-) = pivalate, 4-ptz = 2,4,6-tris(4-pyridyl)-1,3,5-triazine) was synthesized by interaction of Co(II) pivalate with 4-ptz. Desolvation of 1 led to formation of [Co(Piv)(2)(4-ptz)]n (compound 2), which adsorbed N-2 and H-2 at 78 K as a typical microporous sorbent. In contrast, absorption of methanol and ethanol by 2 at 295 K led to structural transformation probably connected with coordination of these alcohols to Co(II). Formation of 2 from 1 was accompanied by change of color of sample from orange to brown and more than 2-fold decrease of molar magnetic susceptibility (chi(M)) in the temperature range from 2 to 300 K. Resolvation of 2 by ethanol or water resulted in restoration of spectral characteristics and chi(M) values almost to the level of that of 1. chi T-M versus T curves for 1 and samples, obtained by resolvation of 2 by H2O or C2H5OH, were fitted using a model for Co(II) complex with zero-field splitting of this ion.
机译:一维配位聚合物[Co(Piv)(2)(4-ptz)(C2H5OH)(2)] n(化合物1,Piv(-)=新戊酸酯,4-ptz = 2,4,6-tris(4 -吡啶基)-1,3,5-三嗪)是通过新戊酸钴(II)与4-ptz的相互作用合成的。 1的去溶剂化导致形成[Co(Piv)(2)(4-ptz)] n(化合物2),该化合物以典型的微孔吸附剂在78 K下吸附N-2和H-2。相反,在295 K下2吸收甲醇和乙醇会导致结构转变,可能与这些醇与Co(II)的配位有关。从1形成2伴随着样品颜色从橙色变为棕色,并且在2至300 K的温度范围内摩尔磁化率(chi(M))降低了2倍以上。用乙醇或水溶解2水导致光谱特征恢复,并且chi(M)值几乎恢复到1的水平。1的chi TM与T曲线通过使用H2O或C2H5OH溶解2的样品拟合,使用Co( II)与该离子的零场分裂复合。

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