Electronic Structure, Reactivity, And Some Magnetic Properties of Paramagnetic Tetrahedral Di Nuclear Cobaltous Complexes. (Theoretical Study)

None Ali K. Almansori, None Falah S. Abd-Suhail
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Abstract

The tetrahedral paramagnetic di-cobaltous complex is an important class of coordination compounds that have many applications in various fields such as catalysis, single molecular magnet SMM, and spintronics[1], using BP86 functional[24] with def2-TZVP[25], basis set, while the broken symmetry theoretical method was conducted by B3LYP functional, the reactivity of the synthesized paramagnetic di cobaltous [Co2LI2OH] + complex[2] can be enhanced by the lowering HOMO-LUMO gap effect of oxo bridging ligand instead hydroxo ligand, also from the different theoretical approaches for calculating the exchange coupling constant to tetrahedral paramagnetic di-cobaltous complex, we found that the best approach was achieved by Noodlman treatment[3], also for such chemical environments the best calculated spin population was generated by Mulliken spin analysis.
顺磁性四面体二钴核配合物的电子结构、反应性和一些磁性能。(理论研究)
四面体顺磁性二钴配合物是一类重要的配位化合物,在催化、单分子磁体SMM、自旋电子学等各个领域都有广泛的应用[1],采用BP86泛函[24],def2-TZVP[25],基集,而破缺对称性理论方法采用B3LYP泛函,合成的顺磁性二钴[Co2LI2OH] +配合物[2]的反应性可以通过降低氧桥接配体的HOMO-LUMO间隙效应而不是羟基配体来增强,并且从计算与四面体顺磁性二钴配合物交换偶联常数的不同理论方法中,我们发现采用noolman处理获得的方法最好[3]。对于这样的化学环境,用Mulliken自旋分析得到了最佳的自旋居数。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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