Issue 29, 2020

Spin-symmetrised structures and vibrational frequencies of iron–sulfur clusters

Abstract

Calculations of relaxed geometries of multi-centre transition metal compounds are routinely carried out using Broken Symmetry Density Functional Theory. The resulting low-spin open shell electronic state is described by one single Slater determinant and is affected by spin contamination. To alleviate this symmetry breaking, the Extended Broken Symmetry (EBS) approach can be applied to complexes with an arbitrary number of local high-spin metal ions. The actual symmetry is therefore reconstructed through minimization of an effective Hamiltonian leading to a relaxed geometry consistent with the magnetic couplings. In the present work we extend the approach already introduced by [Chu et al., J. Chem. Theory Comput., 2017, 13, 4675] to the calculation of vibrational frequencies. As prototypes we have considered the iron–sulfur clusters Fe2S2Cl42− and Fe4S4Cl4. We have compared the results obtained for different spin states (high spin, broken symmetry and extended broken symmetry) and by using different DFT functionals (B3LYP, OPBE, BP, M06 and B2PLYP) and a post-HF method (SCS-MP2). The data have shown that for specific vibrational modes the EBS technique produces shifts up to 40 cm−1 with respect to the routinely used Broken Symmetry approach, indicating that the use of a consistent spin-symmetrised state is a crucial ingredient for an accurate description of vibrational properties, as certified by the comparison with the experimental data for the Fe2S2Cl42− cluster.

Graphical abstract: Spin-symmetrised structures and vibrational frequencies of iron–sulfur clusters

Supplementary files

Article information

Article type
Paper
Submitted
29 رجب 1441
Accepted
11 ذو القعدة 1441
First published
11 ذو القعدة 1441

Phys. Chem. Chem. Phys., 2020,22, 16655-16664

Spin-symmetrised structures and vibrational frequencies of iron–sulfur clusters

F. Cappelluti, L. Bencivenni and L. Guidoni, Phys. Chem. Chem. Phys., 2020, 22, 16655 DOI: 10.1039/D0CP01591A

To request permission to reproduce material from this article, please go to the Copyright Clearance Center request page.

If you are an author contributing to an RSC publication, you do not need to request permission provided correct acknowledgement is given.

If you are the author of this article, you do not need to request permission to reproduce figures and diagrams provided correct acknowledgement is given. If you want to reproduce the whole article in a third-party publication (excluding your thesis/dissertation for which permission is not required) please go to the Copyright Clearance Center request page.

Read more about how to correctly acknowledge RSC content.

Social activity

Spotlight

Advertisements