4.6 Article

Exploring the influence of counterions on a hysteretic spin-transition in isomorphous iron(ii) complex salts

期刊

JOURNAL OF MATERIALS CHEMISTRY C
卷 10, 期 43, 页码 16353-16362

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ROYAL SOC CHEMISTRY
DOI: 10.1039/d2tc03654a

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资金

  1. University of Leeds (Brotherton Scholarship)
  2. EPSRC
  3. Research Council of Norway [301619]

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This study found that [FeL2]X-2 center dot 2H(2)O (L = 2,6-bis{5-methyl-1H-pyrazol-3-yl}pyridine; X- = BF4- or ClO4-) can be dehydrated by mild heating. The anhydrous [FeL2][BF4](2) exhibits a spin transition with thermal hysteresis, while the isomorphous [FeL2][ClO4](2) remains high spin on cooling, likely due to kinetic inhibition of its spin transition.
[FeL2]X-2 center dot 2H(2)O (L = 2,6-bis{5-methyl-1H-pyrazol-3-yl}pyridine; X- = BF4- or ClO4-) are readily dehydrated upon mild heating. Anhydrous [FeL2][BF4](2) exhibits an abrupt spin-transition at T-1/2 = 205 K, with a 65 K thermal hysteresis loop which narrows upon repeated scanning. The isomorphous ClO4- salt remains high-spin on cooling, however, which is investigated further in this study. Unlike the iron complex, [ZnL2][ClO4](2)center dot 2H(2)O undergoes single-crystal-to-single-crystal dehydration; the tetragonal anhydrous crystals transform to a new triclinic phase upon cooling. The phase change is apparently sluggish and transition temperatures between 268 K and <200 K were measured by different techniques, implying it depends on the measurement conditions or sample history. Powder diffraction shows the zinc complex is a good model for the structural chemistry of [FeL2][ClO4](2). The spin states of mixed-anion salts of the iron complex [FeL2][BF4](z)[ClO4](2-z) (z = 1.5 and 1.0) are also investigated. Their spin-transitions evolve more slowly on repeated scanning, as z decreases, and efficient thermally induced kinetic trapping is observed below 120 K when z = 1.0. Taken together, these data imply structural rearrangements in the anhydrous materials during thermal cycling occur more slowly in the presence of the larger ClO4- ion. Hence, rather than reflecting any structural differences with the SCO-active BF4- salt, the high-spin nature of [FeL2][ClO4](2) is probably caused by kinetic inhibition of its putative spin-transition.

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