Boldog, Ishtvan

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orcid::0000-0001-6077-4524
  • Boldog, Ishtvan (2)

Author's Bibliography

Solvent-triggered relaxative spin state switching of [Fe(HB(pz)(3))(2)] in a closed nano-confinement of NH2-MIL-101(Al)

Zhao, Tian; Boldog, Ishtvan; Spasojević, Vojislav; Rotaru, Aurelian; Garcia, Yann; Janiak, Christoph

(2016)

TY  - JOUR
AU  - Zhao, Tian
AU  - Boldog, Ishtvan
AU  - Spasojević, Vojislav
AU  - Rotaru, Aurelian
AU  - Garcia, Yann
AU  - Janiak, Christoph
PY  - 2016
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/1168
AB  - The synthesis of the NH2-MIL-101(Al) Metal-Organic Framework (MOF) with bis(hydrotris(pyrazolyl)borato)iron(II), [Fe(HB(pz)(3))(2)], added to the reaction medium yielded [Fe(HB(pz)(3))(2)]"NH2-MIL101(Al) encapsulation products, denoted as S"Ms, in the course of a bottle-around-the-ship assembly. [Fe(HB(pz)(3))(2)] is a spin-crossover (SCO) compound with a gradual spin transition at 290-440 K for the bulk material (repeated cycles), associated with a pronounced colour change from the red low spin (LS) state to the white high-spin (HS) state. The identity of S"Ms, with a maximum loading of the iron complex at similar to 11 wt% (0.16 molecules per Al3OL3 moiety), was confirmed by PXRD and spectroscopic measurements. The entrapped complex, which is stable in air and cannot be removed by vacuum drying, is confined in the cages of the framework. N-2 and CO2 gas adsorption measurements on the dry S"M composite with different iron complex loadings confirm the absence of most of the initial NH2-MIL-101(Al) porosity. The S"M composite material demonstrates a gradual thermally induced transition from the red low-spin (LS) state to the light yellow HS state, associated with the colour of the matrix, chiefly over the range 300-450 K, which is close to the 290-440 K temperature range for [Fe(HB(pz)(3))(2)]. The thermally induced HS form of S"M does not return to the LS upon cooling to room temperature, and the metastable HS form relaxes only very slowly, which becomes noticeable only after weeks of storage. Rapid and almost complete relaxation and decrease of magnetic moment for up to similar to 97% of the whole sweep could be triggered by the addition of n-hexane, as evidenced by the change of colour and magnetic measurements. Via mechanical stress akin to the action of capillary forces, the adsorbed liquid effectively amplifies the otherwise very weak matrix effect by increasing the effective local pressure imposed on the transiting molecules, thus favouring even further the LS state. The immersion of the dried composites into practically any typical solvents, including MeOH, DMSO, DMF, (PrOH)-Pr-i, BuOH, t-BuOH, THF, ethylacetate, CH2Cl2, CHCl3 CCl4, toluene, mesitylene, and cyclohexane, also induces a spin state change, which is evidenced by the change of colour. The effect is fully reversible: the metastable HS state could be reinstated upon drying the sample at elevated temperature and subsequent cooling. The materials were thoroughly characterized by AAS, PXRD, gas sorption analysis, IR spectroscopy, magnetic measurements, and optical reflectivity measurements. Therefore, a novel MOF-based material with isolated SCO units is proposed, which demonstrates a salient relaxative solvent assisted matrix-effect on metastable entrapped sites, potentially suitable for light-driven single-unit addressability.
T2  - Journal of Materials Chemistry. C
T1  - Solvent-triggered relaxative spin state switching of [Fe(HB(pz)(3))(2)] in a closed nano-confinement of NH2-MIL-101(Al)
VL  - 4
IS  - 27
DO  - 10.1039/c6tc01297c
ER  - 
@article{
author = "Zhao, Tian and Boldog, Ishtvan and Spasojević, Vojislav and Rotaru, Aurelian and Garcia, Yann and Janiak, Christoph",
year = "2016",
abstract = "The synthesis of the NH2-MIL-101(Al) Metal-Organic Framework (MOF) with bis(hydrotris(pyrazolyl)borato)iron(II), [Fe(HB(pz)(3))(2)], added to the reaction medium yielded [Fe(HB(pz)(3))(2)]"NH2-MIL101(Al) encapsulation products, denoted as S"Ms, in the course of a bottle-around-the-ship assembly. [Fe(HB(pz)(3))(2)] is a spin-crossover (SCO) compound with a gradual spin transition at 290-440 K for the bulk material (repeated cycles), associated with a pronounced colour change from the red low spin (LS) state to the white high-spin (HS) state. The identity of S"Ms, with a maximum loading of the iron complex at similar to 11 wt% (0.16 molecules per Al3OL3 moiety), was confirmed by PXRD and spectroscopic measurements. The entrapped complex, which is stable in air and cannot be removed by vacuum drying, is confined in the cages of the framework. N-2 and CO2 gas adsorption measurements on the dry S"M composite with different iron complex loadings confirm the absence of most of the initial NH2-MIL-101(Al) porosity. The S"M composite material demonstrates a gradual thermally induced transition from the red low-spin (LS) state to the light yellow HS state, associated with the colour of the matrix, chiefly over the range 300-450 K, which is close to the 290-440 K temperature range for [Fe(HB(pz)(3))(2)]. The thermally induced HS form of S"M does not return to the LS upon cooling to room temperature, and the metastable HS form relaxes only very slowly, which becomes noticeable only after weeks of storage. Rapid and almost complete relaxation and decrease of magnetic moment for up to similar to 97% of the whole sweep could be triggered by the addition of n-hexane, as evidenced by the change of colour and magnetic measurements. Via mechanical stress akin to the action of capillary forces, the adsorbed liquid effectively amplifies the otherwise very weak matrix effect by increasing the effective local pressure imposed on the transiting molecules, thus favouring even further the LS state. The immersion of the dried composites into practically any typical solvents, including MeOH, DMSO, DMF, (PrOH)-Pr-i, BuOH, t-BuOH, THF, ethylacetate, CH2Cl2, CHCl3 CCl4, toluene, mesitylene, and cyclohexane, also induces a spin state change, which is evidenced by the change of colour. The effect is fully reversible: the metastable HS state could be reinstated upon drying the sample at elevated temperature and subsequent cooling. The materials were thoroughly characterized by AAS, PXRD, gas sorption analysis, IR spectroscopy, magnetic measurements, and optical reflectivity measurements. Therefore, a novel MOF-based material with isolated SCO units is proposed, which demonstrates a salient relaxative solvent assisted matrix-effect on metastable entrapped sites, potentially suitable for light-driven single-unit addressability.",
journal = "Journal of Materials Chemistry. C",
title = "Solvent-triggered relaxative spin state switching of [Fe(HB(pz)(3))(2)] in a closed nano-confinement of NH2-MIL-101(Al)",
volume = "4",
number = "27",
doi = "10.1039/c6tc01297c"
}
Zhao, T., Boldog, I., Spasojević, V., Rotaru, A., Garcia, Y.,& Janiak, C.. (2016). Solvent-triggered relaxative spin state switching of [Fe(HB(pz)(3))(2)] in a closed nano-confinement of NH2-MIL-101(Al). in Journal of Materials Chemistry. C, 4(27).
https://doi.org/10.1039/c6tc01297c
Zhao T, Boldog I, Spasojević V, Rotaru A, Garcia Y, Janiak C. Solvent-triggered relaxative spin state switching of [Fe(HB(pz)(3))(2)] in a closed nano-confinement of NH2-MIL-101(Al). in Journal of Materials Chemistry. C. 2016;4(27).
doi:10.1039/c6tc01297c .
Zhao, Tian, Boldog, Ishtvan, Spasojević, Vojislav, Rotaru, Aurelian, Garcia, Yann, Janiak, Christoph, "Solvent-triggered relaxative spin state switching of [Fe(HB(pz)(3))(2)] in a closed nano-confinement of NH2-MIL-101(Al)" in Journal of Materials Chemistry. C, 4, no. 27 (2016),
https://doi.org/10.1039/c6tc01297c . .
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Water effect on the spin-transition behavior of Fe(II) 1,2,4-triazole 1D chains embedded in pores of MCM-41

Zhao, Tian; Cuignet, Laure; Dirtu, Marinela Maria; Wolff, Mariusz; Spasojević, Vojislav; Boldog, Ishtvan; Rotaru, Aurelian; Garcia, Yann; Janiak, Christoph

(2015)

TY  - JOUR
AU  - Zhao, Tian
AU  - Cuignet, Laure
AU  - Dirtu, Marinela Maria
AU  - Wolff, Mariusz
AU  - Spasojević, Vojislav
AU  - Boldog, Ishtvan
AU  - Rotaru, Aurelian
AU  - Garcia, Yann
AU  - Janiak, Christoph
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/672
AB  - The spin-crossover (SCO) compounds [Fe(Htrz)(3)](BF4)(2)center dot H2O (SCO-1) and [Fe(Htrz)(2)trz]BF4 (SCO-2) (Htrz = 1,2,4-triazole) were embedded in the pores of mesostructured silica MCM-41 to yield SCO"MCM composites as evidenced by electron microscopy, gas sorption studies, powder X-ray diffractometry, atomic absorption and infrared spectrometry. Studies of the temperature-induced spin crossover behavior of the composites by temperature-variable Fe-57 Mossbauer spectroscopy, magnetic and differential scanning calorimetry measurements and optical reflectivity indicate that the spin transition of the composites was significantly shifted for SCO-1"MCM to higher temperature in comparison to bulk SCO-1 compounds while the shift for SCO-2 was negligible. These shifts in the transition temperature for SCO-1"MCM [versus bulk SCO-1] amounted to T-c(up arrow) = 371/376 K [282/291 K] and T-c(down arrow) = 340/345 K [276/286 K] (magnetic/optical reflectivity data) with a broadening of the hysteresis by 25-26 K relative to bulk SCO-1 (varying slightly with the used method). The significant difference in the SCO behavior of the similar materials SCO-1 and SCO-2 when embedded in the MCM-41 matrix is assigned to the hydration of the SCO-1"MCM material. Water is apparently crucial in transmitting the confinement pressure or matrix effect on the spin transition when the SCO compound is embedded between the pore walls.
T2  - Journal of Materials Chemistry. C
T1  - Water effect on the spin-transition behavior of Fe(II) 1,2,4-triazole 1D chains embedded in pores of MCM-41
VL  - 3
IS  - 30
SP  - 7802
EP  - 7812
DO  - 10.1039/c5tc00311c
ER  - 
@article{
author = "Zhao, Tian and Cuignet, Laure and Dirtu, Marinela Maria and Wolff, Mariusz and Spasojević, Vojislav and Boldog, Ishtvan and Rotaru, Aurelian and Garcia, Yann and Janiak, Christoph",
year = "2015",
abstract = "The spin-crossover (SCO) compounds [Fe(Htrz)(3)](BF4)(2)center dot H2O (SCO-1) and [Fe(Htrz)(2)trz]BF4 (SCO-2) (Htrz = 1,2,4-triazole) were embedded in the pores of mesostructured silica MCM-41 to yield SCO"MCM composites as evidenced by electron microscopy, gas sorption studies, powder X-ray diffractometry, atomic absorption and infrared spectrometry. Studies of the temperature-induced spin crossover behavior of the composites by temperature-variable Fe-57 Mossbauer spectroscopy, magnetic and differential scanning calorimetry measurements and optical reflectivity indicate that the spin transition of the composites was significantly shifted for SCO-1"MCM to higher temperature in comparison to bulk SCO-1 compounds while the shift for SCO-2 was negligible. These shifts in the transition temperature for SCO-1"MCM [versus bulk SCO-1] amounted to T-c(up arrow) = 371/376 K [282/291 K] and T-c(down arrow) = 340/345 K [276/286 K] (magnetic/optical reflectivity data) with a broadening of the hysteresis by 25-26 K relative to bulk SCO-1 (varying slightly with the used method). The significant difference in the SCO behavior of the similar materials SCO-1 and SCO-2 when embedded in the MCM-41 matrix is assigned to the hydration of the SCO-1"MCM material. Water is apparently crucial in transmitting the confinement pressure or matrix effect on the spin transition when the SCO compound is embedded between the pore walls.",
journal = "Journal of Materials Chemistry. C",
title = "Water effect on the spin-transition behavior of Fe(II) 1,2,4-triazole 1D chains embedded in pores of MCM-41",
volume = "3",
number = "30",
pages = "7802-7812",
doi = "10.1039/c5tc00311c"
}
Zhao, T., Cuignet, L., Dirtu, M. M., Wolff, M., Spasojević, V., Boldog, I., Rotaru, A., Garcia, Y.,& Janiak, C.. (2015). Water effect on the spin-transition behavior of Fe(II) 1,2,4-triazole 1D chains embedded in pores of MCM-41. in Journal of Materials Chemistry. C, 3(30), 7802-7812.
https://doi.org/10.1039/c5tc00311c
Zhao T, Cuignet L, Dirtu MM, Wolff M, Spasojević V, Boldog I, Rotaru A, Garcia Y, Janiak C. Water effect on the spin-transition behavior of Fe(II) 1,2,4-triazole 1D chains embedded in pores of MCM-41. in Journal of Materials Chemistry. C. 2015;3(30):7802-7812.
doi:10.1039/c5tc00311c .
Zhao, Tian, Cuignet, Laure, Dirtu, Marinela Maria, Wolff, Mariusz, Spasojević, Vojislav, Boldog, Ishtvan, Rotaru, Aurelian, Garcia, Yann, Janiak, Christoph, "Water effect on the spin-transition behavior of Fe(II) 1,2,4-triazole 1D chains embedded in pores of MCM-41" in Journal of Materials Chemistry. C, 3, no. 30 (2015):7802-7812,
https://doi.org/10.1039/c5tc00311c . .
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