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结合开壳卟啉嗪环境和 Co(II) 自旋交叉:钴氧代verdazyl 化合物中的自旋聚交错。

Combining Open-Shell Verdazyl Environment and Co(II) Spin-Crossover: Spinmerism in Cobalt Oxoverdazyl Compound.

机构信息

Laboratoire de Chimie Quantique, UMR 7177 Université de Strasbourg CNRS, 4 rue Blaise Pascal, 67000, Strasbourg, FR.

Laboratoire de Physique et Chimie Quantiques, UMR 5626 Université Paul Sabatier, 118 route de Narbonne, 31062, Toulouse, FR.

出版信息

Chemphyschem. 2022 May 4;23(9):e202100801. doi: 10.1002/cphc.202100801. Epub 2022 Mar 16.

Abstract

The spin states of a Co(II) oxoverdazyl compound are investigated by means of wavefunction-based calculations. Within a ca. 233 K energy window, the ground state and excited states display a structure-sensitive admixture of low-spin S =1/2 in a dominant high-spin S =3/2 Co(II) ion as indicated by the localized molecular orbitals. The puzzling spin zoology that results from the coupling between open-shell radical ligands and a spin-crossover metal ion gives rise to this unusual scenario, which extends the views in molecular magnetism. In agreement with experimental observation, the low-energy spectroscopy is very sensitive to deformations of the coordination sphere, and a growing admixture of Co(II) low-spin is evidenced from the calculations. In analogy with mesomerism that accounts for charge delocalization, entanglement combines different local spin states to generate a given total spin multiplicity, a spinmerism phenomenon.

摘要

通过基于波函数的计算研究了 Co(II)氧代verdazyl 化合物的自旋态。在大约 233 K 的能量窗口内,基态和激发态显示出低自旋 S =1/2 和主导的高自旋 S =3/2 Co(II)离子的结构敏感混合,这是由局域分子轨道表明的。来自开壳自由基配体和自旋交叉金属离子之间耦合的令人费解的自旋动物学导致了这种不寻常的情况,这扩展了分子磁学的观点。与实验观察一致,低能光谱对配位球的变形非常敏感,并且从计算中可以证明 Co(II)低自旋的混合增加。类似于解释电荷离域的mesomerism,entanglement 将不同的局部自旋态组合在一起以产生给定的总自旋多重性,这是一种spinmerism 现象。

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