Janiak, Christoph

Link to this page

Authority KeyName Variants
orcid::0000-0002-6288-9605
  • Janiak, Christoph (5)
Projects

Author's Bibliography

Synthesis and structural characterization of Cd(II) complexes with 2-acetylpyridine-aminoguanidine - a novel coordination mode

Radanović, Mirjana M.; Novaković, Slađana B.; Rodić, Marko V.; Vojinović-Ješić, Ljiljana S.; Janiak, Christoph; Leovac, Vukadin M.

(2022)

TY  - JOUR
AU  - Radanović, Mirjana M.
AU  - Novaković, Slađana B.
AU  - Rodić, Marko V.
AU  - Vojinović-Ješić, Ljiljana S.
AU  - Janiak, Christoph
AU  - Leovac, Vukadin M.
PY  - 2022
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/11173
AB  - The structures of the first two complexes with bidentate coordination of aminoguanidine Schiff base, i.e., 2-acetylpyridine-aminoguanidine (L), are reported. The complex of the formula [Cd2Cl6(HL)2] (1) was obtained in the reaction of warm aqueous solutions of chloride salts of Cd(II), Zn(II) and the ligand, while the reaction of cadmium bromide and the ligand in the presence of deprotonating agent as well as ammonium thiocyanate resulted in the formation of the complex in which Schiff base has both the role of the ligand and the counterion, viz., [HL][Cd(HL)(NCS)2XY]·H2O (2), where X is Cl- or Br-, and Y Br- or SCN-. The complexes were characterized by IR spectroscopy, elemental analysis, conductometric measurements and single crystal X-ray diffraction. The unusual bidentate coordination of the Schiff base lead to significant changes in the geometry of this molecule (from almost planar in free form and as a tridentate ligand to twisted as a bidentate ligand). Besides, in complex 1 relatively rare bridging coordination of Cl- in octahedral Cd(II) is found, while the crystal structure of complex 2 exhibits substitutional disorder, and contains four different anions: [Cd(HL)(NCS)2Br(SCN)]- (ca. 61 %), [Cd(HL)(NCS)2Cl(SCN)]- (ca. 35 %), [Cd(HL)(NCS)2Br2]- (ca. 3 %) and [Cd(HL)(NCS)2ClBr]- (ca. 1 %).
T2  - Journal of the Serbian Chemical Society
T1  - Synthesis and structural characterization of Cd(II) complexes with 2-acetylpyridine-aminoguanidine - a novel coordination mode
VL  - 87
IS  - 11
SP  - 1259
EP  - 1272
DO  - 10.2298/JSC220613072R
ER  - 
@article{
author = "Radanović, Mirjana M. and Novaković, Slađana B. and Rodić, Marko V. and Vojinović-Ješić, Ljiljana S. and Janiak, Christoph and Leovac, Vukadin M.",
year = "2022",
abstract = "The structures of the first two complexes with bidentate coordination of aminoguanidine Schiff base, i.e., 2-acetylpyridine-aminoguanidine (L), are reported. The complex of the formula [Cd2Cl6(HL)2] (1) was obtained in the reaction of warm aqueous solutions of chloride salts of Cd(II), Zn(II) and the ligand, while the reaction of cadmium bromide and the ligand in the presence of deprotonating agent as well as ammonium thiocyanate resulted in the formation of the complex in which Schiff base has both the role of the ligand and the counterion, viz., [HL][Cd(HL)(NCS)2XY]·H2O (2), where X is Cl- or Br-, and Y Br- or SCN-. The complexes were characterized by IR spectroscopy, elemental analysis, conductometric measurements and single crystal X-ray diffraction. The unusual bidentate coordination of the Schiff base lead to significant changes in the geometry of this molecule (from almost planar in free form and as a tridentate ligand to twisted as a bidentate ligand). Besides, in complex 1 relatively rare bridging coordination of Cl- in octahedral Cd(II) is found, while the crystal structure of complex 2 exhibits substitutional disorder, and contains four different anions: [Cd(HL)(NCS)2Br(SCN)]- (ca. 61 %), [Cd(HL)(NCS)2Cl(SCN)]- (ca. 35 %), [Cd(HL)(NCS)2Br2]- (ca. 3 %) and [Cd(HL)(NCS)2ClBr]- (ca. 1 %).",
journal = "Journal of the Serbian Chemical Society",
title = "Synthesis and structural characterization of Cd(II) complexes with 2-acetylpyridine-aminoguanidine - a novel coordination mode",
volume = "87",
number = "11",
pages = "1259-1272",
doi = "10.2298/JSC220613072R"
}
Radanović, M. M., Novaković, S. B., Rodić, M. V., Vojinović-Ješić, L. S., Janiak, C.,& Leovac, V. M.. (2022). Synthesis and structural characterization of Cd(II) complexes with 2-acetylpyridine-aminoguanidine - a novel coordination mode. in Journal of the Serbian Chemical Society, 87(11), 1259-1272.
https://doi.org/10.2298/JSC220613072R
Radanović MM, Novaković SB, Rodić MV, Vojinović-Ješić LS, Janiak C, Leovac VM. Synthesis and structural characterization of Cd(II) complexes with 2-acetylpyridine-aminoguanidine - a novel coordination mode. in Journal of the Serbian Chemical Society. 2022;87(11):1259-1272.
doi:10.2298/JSC220613072R .
Radanović, Mirjana M., Novaković, Slađana B., Rodić, Marko V., Vojinović-Ješić, Ljiljana S., Janiak, Christoph, Leovac, Vukadin M., "Synthesis and structural characterization of Cd(II) complexes with 2-acetylpyridine-aminoguanidine - a novel coordination mode" in Journal of the Serbian Chemical Society, 87, no. 11 (2022):1259-1272,
https://doi.org/10.2298/JSC220613072R . .
1

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 . .
1
36
24
32

Charge-Density Distribution and Electrostatic Flexibility of ZIF-8 Based on High-Resolution X-ray Diffraction Data and Periodic Calculations

Novaković, Slađana B.; Bogdanović, Goran A.; Heering, Christian; Makhloufi, Gamall; Francuski, Đorđe D.; Janiak, Christoph

(2015)

TY  - JOUR
AU  - Novaković, Slađana B.
AU  - Bogdanović, Goran A.
AU  - Heering, Christian
AU  - Makhloufi, Gamall
AU  - Francuski, Đorđe D.
AU  - Janiak, Christoph
PY  - 2015
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/452
AB  - The electron-density distribution in a prototypical porous coordination polymer ZIF-8 has been obtained in an approach combining high-resolution X-ray diffraction data and Invariom refinement. In addition, the periodic quantum-chemical calculation has been used to describe the theoretical density features of ZIF-8 in the same geometry (m1) and also in a high-pressure form of ZIF-8 (m2) characterized by conformational change with respect to the methylimidazolate linker. A thorough comparison of the electronic and electrostatic properties in two limiting structural forms of ZIF-8 proposes additional aspects on diffusion and adsorption processes occurring within the framework. The dimensions of the four-membered (FM) and six-membered (SM) apertures of the beta cage are reliably determined from the total electron-density distribution. The analysis shows that FM in m2 becomes competitive in size to the SM aperture and should be considered for the diffusion of small molecules and cations. Baders topological analysis (quantum theory of atoms in molecules) shows similar properties of both ZIF-8 forms. On the other hand, analysis of their electrostatic properties reveals tremendous differences. The study suggests exceptional electrostatic flexibility of the ZIF-8 framework, where small conformational changes lead to a significantly different electrostatic potential (EP) distribution, a feature that could be important for the function and dynamics of the ZIF-8 framework. The cavity surface in m1 contains 38 distinct regions with moderately positive, negative, or neutral EP and weakly positive EP in the cavity volume. In contrast to m1, the m2 form displays only two regions of different EP, with the positive one taking the whole cavity surface and the strong negative one localized entirely in the FM apertures. The EP in the cavity volume is also more positive than that in m1. A pronounced influence of the linker reorientation on the EP of the ZIF-8 forms is related to the high symmetry of the system and to an amplification of the electrostatic properties by cooperative effects of the proximally arranged structural fragments.
T2  - Inorganic Chemistry
T1  - Charge-Density Distribution and Electrostatic Flexibility of ZIF-8 Based on High-Resolution X-ray Diffraction Data and Periodic Calculations
VL  - 54
IS  - 6
SP  - 2660
EP  - 2670
DO  - 10.1021/ic5028256
ER  - 
@article{
author = "Novaković, Slađana B. and Bogdanović, Goran A. and Heering, Christian and Makhloufi, Gamall and Francuski, Đorđe D. and Janiak, Christoph",
year = "2015",
abstract = "The electron-density distribution in a prototypical porous coordination polymer ZIF-8 has been obtained in an approach combining high-resolution X-ray diffraction data and Invariom refinement. In addition, the periodic quantum-chemical calculation has been used to describe the theoretical density features of ZIF-8 in the same geometry (m1) and also in a high-pressure form of ZIF-8 (m2) characterized by conformational change with respect to the methylimidazolate linker. A thorough comparison of the electronic and electrostatic properties in two limiting structural forms of ZIF-8 proposes additional aspects on diffusion and adsorption processes occurring within the framework. The dimensions of the four-membered (FM) and six-membered (SM) apertures of the beta cage are reliably determined from the total electron-density distribution. The analysis shows that FM in m2 becomes competitive in size to the SM aperture and should be considered for the diffusion of small molecules and cations. Baders topological analysis (quantum theory of atoms in molecules) shows similar properties of both ZIF-8 forms. On the other hand, analysis of their electrostatic properties reveals tremendous differences. The study suggests exceptional electrostatic flexibility of the ZIF-8 framework, where small conformational changes lead to a significantly different electrostatic potential (EP) distribution, a feature that could be important for the function and dynamics of the ZIF-8 framework. The cavity surface in m1 contains 38 distinct regions with moderately positive, negative, or neutral EP and weakly positive EP in the cavity volume. In contrast to m1, the m2 form displays only two regions of different EP, with the positive one taking the whole cavity surface and the strong negative one localized entirely in the FM apertures. The EP in the cavity volume is also more positive than that in m1. A pronounced influence of the linker reorientation on the EP of the ZIF-8 forms is related to the high symmetry of the system and to an amplification of the electrostatic properties by cooperative effects of the proximally arranged structural fragments.",
journal = "Inorganic Chemistry",
title = "Charge-Density Distribution and Electrostatic Flexibility of ZIF-8 Based on High-Resolution X-ray Diffraction Data and Periodic Calculations",
volume = "54",
number = "6",
pages = "2660-2670",
doi = "10.1021/ic5028256"
}
Novaković, S. B., Bogdanović, G. A., Heering, C., Makhloufi, G., Francuski, Đ. D.,& Janiak, C.. (2015). Charge-Density Distribution and Electrostatic Flexibility of ZIF-8 Based on High-Resolution X-ray Diffraction Data and Periodic Calculations. in Inorganic Chemistry, 54(6), 2660-2670.
https://doi.org/10.1021/ic5028256
Novaković SB, Bogdanović GA, Heering C, Makhloufi G, Francuski ĐD, Janiak C. Charge-Density Distribution and Electrostatic Flexibility of ZIF-8 Based on High-Resolution X-ray Diffraction Data and Periodic Calculations. in Inorganic Chemistry. 2015;54(6):2660-2670.
doi:10.1021/ic5028256 .
Novaković, Slađana B., Bogdanović, Goran A., Heering, Christian, Makhloufi, Gamall, Francuski, Đorđe D., Janiak, Christoph, "Charge-Density Distribution and Electrostatic Flexibility of ZIF-8 Based on High-Resolution X-ray Diffraction Data and Periodic Calculations" in Inorganic Chemistry, 54, no. 6 (2015):2660-2670,
https://doi.org/10.1021/ic5028256 . .
2
34
30
34

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 . .
47
36
44

N-o-Vanillylidene-L-histidine: Experimental Charge Density Analysis of a Double Zwitterionic Amino Acid Schiff-Base Compound

Drašković, Bojana M.; Bogdanović, Goran A.; Neelakantan, M. A.; Chamayou, Anne-Christine; Thalamuthu, S.; Avadhut, Yamini S.; Guenne, Joern Schmedt Auf Der; Banerjee, Sharmila; Janiak, Christoph

(2010)

TY  - JOUR
AU  - Drašković, Bojana M.
AU  - Bogdanović, Goran A.
AU  - Neelakantan, M. A.
AU  - Chamayou, Anne-Christine
AU  - Thalamuthu, S.
AU  - Avadhut, Yamini S.
AU  - Guenne, Joern Schmedt Auf Der
AU  - Banerjee, Sharmila
AU  - Janiak, Christoph
PY  - 2010
UR  - https://vinar.vin.bg.ac.rs/handle/123456789/3938
AB  - A double zwitterionic Schiff base was synthesized using the amino acid L-histidine and o-vanillin (2-hydroxy-3-methoxy benzaldehyde). Both the phenol and carboxyl groups are deprotonated, and the imine nitrogen atom and histidine-imidazole ring are protonated to give the double zwitterion with an intramolecular (imine)N-H(+)center dot center dot center dot(-)O(phenol) hydrogen bond (ketoamine form). Such a ketoamine form in a double zwitterion is assumed in the catalytic cycle of enzymatic transformations of amino acids with the cofactor (vitamin B6) pyridoxal-5-phosphate (PLP). A high-resolution, low-temperature, single-crystal X-ray diffraction data set on N-o-vanillylidene-l-histidine (also named 3-methoxysalicylidene-l-histidine or N-(2-oxy-3-methoxy-benzylidene)-L-histidine, OVHIS) is used in the analysis of molecular electrostatic properties and intermolecular interactions. All oxygen atoms in the molecule (four in total) are mutually almost coplanar and located (externally) on the same side of molecule. These four O atoms carry significant negative charge and form a large area of strong negative electrostatic potential (appropriate for bonding to a metal atom). The protonated and, thus, positively charged imidazole ring is situated on the opposite side of the molecule from the area of the O atoms. Consequently, the OVHIS molecule is highly polarized and has a very high molecular dipole moment of 42.4 D in the solid state (calculated from experimental X-ray data). Two strong intermolecular charge-assisted N-H(+)center dot center dot center dot(-)O hydrogen bonds (with H center dot center dot center dot O distances of 1.61 angstrom) together with other D-H center dot center dot center dot O interactions (D = N, C) contribute to a large molecular dipole enhancement which occurs upon crystallization. The topologies of the bonding within the molecule as well as its hydrogen bonds have been investigated according to Baders quantum theory of atoms in molecules (QTAIM). (1)H solid-state magic angle spinning nuclear magnetic resonance (MAS NMR) was used to confirm the zwitterionic structure in the solid state.
T2  - Crystal Growth and Design
T1  - N-o-Vanillylidene-L-histidine: Experimental Charge Density Analysis of a Double Zwitterionic Amino Acid Schiff-Base Compound
VL  - 10
IS  - 4
SP  - 1665
EP  - 1676
DO  - 10.1021/cg901239v
ER  - 
@article{
author = "Drašković, Bojana M. and Bogdanović, Goran A. and Neelakantan, M. A. and Chamayou, Anne-Christine and Thalamuthu, S. and Avadhut, Yamini S. and Guenne, Joern Schmedt Auf Der and Banerjee, Sharmila and Janiak, Christoph",
year = "2010",
abstract = "A double zwitterionic Schiff base was synthesized using the amino acid L-histidine and o-vanillin (2-hydroxy-3-methoxy benzaldehyde). Both the phenol and carboxyl groups are deprotonated, and the imine nitrogen atom and histidine-imidazole ring are protonated to give the double zwitterion with an intramolecular (imine)N-H(+)center dot center dot center dot(-)O(phenol) hydrogen bond (ketoamine form). Such a ketoamine form in a double zwitterion is assumed in the catalytic cycle of enzymatic transformations of amino acids with the cofactor (vitamin B6) pyridoxal-5-phosphate (PLP). A high-resolution, low-temperature, single-crystal X-ray diffraction data set on N-o-vanillylidene-l-histidine (also named 3-methoxysalicylidene-l-histidine or N-(2-oxy-3-methoxy-benzylidene)-L-histidine, OVHIS) is used in the analysis of molecular electrostatic properties and intermolecular interactions. All oxygen atoms in the molecule (four in total) are mutually almost coplanar and located (externally) on the same side of molecule. These four O atoms carry significant negative charge and form a large area of strong negative electrostatic potential (appropriate for bonding to a metal atom). The protonated and, thus, positively charged imidazole ring is situated on the opposite side of the molecule from the area of the O atoms. Consequently, the OVHIS molecule is highly polarized and has a very high molecular dipole moment of 42.4 D in the solid state (calculated from experimental X-ray data). Two strong intermolecular charge-assisted N-H(+)center dot center dot center dot(-)O hydrogen bonds (with H center dot center dot center dot O distances of 1.61 angstrom) together with other D-H center dot center dot center dot O interactions (D = N, C) contribute to a large molecular dipole enhancement which occurs upon crystallization. The topologies of the bonding within the molecule as well as its hydrogen bonds have been investigated according to Baders quantum theory of atoms in molecules (QTAIM). (1)H solid-state magic angle spinning nuclear magnetic resonance (MAS NMR) was used to confirm the zwitterionic structure in the solid state.",
journal = "Crystal Growth and Design",
title = "N-o-Vanillylidene-L-histidine: Experimental Charge Density Analysis of a Double Zwitterionic Amino Acid Schiff-Base Compound",
volume = "10",
number = "4",
pages = "1665-1676",
doi = "10.1021/cg901239v"
}
Drašković, B. M., Bogdanović, G. A., Neelakantan, M. A., Chamayou, A., Thalamuthu, S., Avadhut, Y. S., Guenne, J. S. A. D., Banerjee, S.,& Janiak, C.. (2010). N-o-Vanillylidene-L-histidine: Experimental Charge Density Analysis of a Double Zwitterionic Amino Acid Schiff-Base Compound. in Crystal Growth and Design, 10(4), 1665-1676.
https://doi.org/10.1021/cg901239v
Drašković BM, Bogdanović GA, Neelakantan MA, Chamayou A, Thalamuthu S, Avadhut YS, Guenne JSAD, Banerjee S, Janiak C. N-o-Vanillylidene-L-histidine: Experimental Charge Density Analysis of a Double Zwitterionic Amino Acid Schiff-Base Compound. in Crystal Growth and Design. 2010;10(4):1665-1676.
doi:10.1021/cg901239v .
Drašković, Bojana M., Bogdanović, Goran A., Neelakantan, M. A., Chamayou, Anne-Christine, Thalamuthu, S., Avadhut, Yamini S., Guenne, Joern Schmedt Auf Der, Banerjee, Sharmila, Janiak, Christoph, "N-o-Vanillylidene-L-histidine: Experimental Charge Density Analysis of a Double Zwitterionic Amino Acid Schiff-Base Compound" in Crystal Growth and Design, 10, no. 4 (2010):1665-1676,
https://doi.org/10.1021/cg901239v . .
80
74
79