Correction: ⁵⁷Fe Mössbauer spectroscopy and high-pressure structural analysis for the mechanism of pressure-induced unique magnetic behaviour in (cation)[Fe^IIFe^III(dto)₃] (cation = Ph₄P and ⁿPrPh₃P; dto = 1,2-dithiooxalato)

Abstract

Correction for ‘⁵⁷Fe Mössbauer spectroscopy and high-pressure structural analysis for the mechanism of pressure-induced unique magnetic behaviour in (cation)[Fe^IIFe^III(dto)₃] (cation = Ph₄P and ⁿPrPh₃P; dto = 1,2-dithiooxalato)’ by Ryosuke Taniai et al., Dalton Trans., 2023, 52, 8368–8375.

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The authors regret that several errors were published in the original article. The correct details are given below.

In the first paragraph of “Synthetic procedures” on page 8369, “C₃₀H₂₀Fe₂O₆PS₆” should read “C₂₇H₂₂Fe₂O₆PS₆”.

In the third paragraph of the section “Crystal structures” on page 8370, the sentence “the nearest C6⋯S2^b and C7⋯O2^c distances were 3.62(3) and 3.28(3) Å, respectively”, should read “the nearest C6⋯S2^b and C4⋯O1^a distances were 3.62(3) and 3.26(3) Å, respectively”.

In addition, the authors regret that an incorrect version of Fig. 2 was included in the original article. The correct version of Fig. 2 is presented here.

Fig. 2 (a) Coordination environment of O₆ and S₆ atoms for the two Fe ions in 3. Colour codes: gray, red, yellow, purple and navy represent C, O, S, P, and Fe atoms, respectively. A 2-D honeycomb layer in the ab plane is shown. (b) Layered structure along the c axis. One side of two disordered configurations is shown in the ⁿPrPh₃P position. Symmetry codes: (a) 1 + x, 1 + y, +z; (b) 1 + y, 1−x + y, 1/2 + z.

The Royal Society of Chemistry apologises for these errors and any consequent inconvenience to authors and readers.

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