Other — Magnetic and electrical behaviors of the homo-and heterometallic 1d and 3d coordination polymers based on the partial decomposition of the [cr(C2o4)3]3− building block

Measurement evidence

Other

Magnetic and electrical behaviors of the homo-and heterometallic 1d and 3d coordination polymers based on the partial decomposition of the [cr(C2o4)3]3− building block · Kanizaj L., Senjug P., Pajic D. et al. · Materials · 2020 · 1-20

6 measurement groups · 14 results

Reported values remain attached to the sample, method, conditions, extraction quality and source location that produced them.

SQUID magnetometry using MPMS 5

Compound 1 yellow crystals / polycrystalline pressed pellet · Pellet

compound 1 polycrystalline powder; 2-300 K; fields up to 5 T; M(T), ZFC/FC and M(H) measurements

Temperature
2-300
Geometry
polycrystalline powder in sample holder/ampoule
Context
pristine coordination polymer
Measurement source
5 · 2.4. Magnetic Study
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Compound 1 intra-chain super-exchange interactionJ = (-3.26 ± 0.01) K±0.01 KText
Exact Reported
11 and 16 · 3.4. Magnetization Study; Conclusions · Figure 8
Compound 1 inter-chain interactionj' = (-0.02 ± 0.01) K±0.01 KText
Exact Reported
12 · 3.4. Magnetization Study

SQUID magnetometry using MPMS 5

Compound 2 green prismatic crystals / polycrystalline pressed pellet · Pellet

compound 2 polycrystalline powder; 2-300 K; fields up to 5 T; M(T), ZFC/FC and M(H) measurements

Temperature
2-300
Geometry
polycrystalline powder in sample holder/ampoule
Context
pristine coordination polymer
Measurement source
5 · 2.4. Magnetic Study
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Compound 2 saturation magnetisationμs = 8.2 μB/f.u.Text
Rounded Reported
13 · 3.4. Magnetization Study · Figure 10

SQUID magnetometry using MPMS 5

Compound 3 dark green prismatic crystals / polycrystalline pressed pellet · Pellet

compound 3 polycrystalline powder; 2-300 K; fields up to 5 T; M(T), ZFC/FC and M(H) measurements

Temperature
2-300
Geometry
polycrystalline powder in sample holder/ampoule
Context
pristine coordination polymer
Measurement source
5 · 2.4. Magnetic Study
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Compound 3 Cu-Cr dimer exchange constantJ = (7.1 ± 0.1) K±0.1 KText
Exact Reported
14 · 3.4. Magnetization Study · Figure 11
Compound 3 inter-dimer interactionzj = (0.078 ± 0.001) K±0.001 KText
Exact Reported
15 · 3.4. Magnetization Study · Figure 11

simultaneous thermogravimetric analysis (TG) and differential thermal analysis (DTA)

Compound 1 yellow crystals / polycrystalline pressed pellet · Pellet

compound 1 crystalline sample in nitrogen atmosphere up to 1100 C; heating rate 10 C min-1

Atmosphere
nitrogen
Context
pristine coordination polymer
Measurement source
3 and 10 · 2.1. Materials and Methods; 3.3. Molecular and Crystal Structures · Figure S5; Table S6
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Compound 1 final decomposition/degradation endpointaround 700 °C973.15 KText
Approximate
10 · 3.3. Molecular and Crystal Structures of Compounds 1-3 · Figure S5; Table S6
Compound 1 framework mass-loss step70.4% over 270-400 °C; loss bpy, CO + CO2; DTAmax 356 exoSI Table
Exact Reported
6 · Table S6 · Table S6
Compound 1 solvent mass-loss step8.49% over 30-270 °C; loss 1.5H2O; DTAmax 33 exoSI Table
Exact Reported
6 · Table S6 · Table S6

simultaneous thermogravimetric analysis (TG) and differential thermal analysis (DTA)

Compound 2 green prismatic crystals / polycrystalline pressed pellet · Pellet

compound 2 crystalline sample in nitrogen atmosphere up to 1100 C; heating rate 10 C min-1

Atmosphere
nitrogen
Context
pristine coordination polymer
Measurement source
3 and 10 · 2.1. Materials and Methods; 3.3. Molecular and Crystal Structures · Figure S5; Table S6
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Compound 2 final decomposition/degradation endpointaround 960 °C1233.15 KText
Approximate
10 · 3.3. Molecular and Crystal Structures of Compounds 1-3 · Figure S5; Table S6
Compound 2 framework mass-loss step63.57% over 220-570 °C; loss 4bpy, 7(CO + CO2); DTAmax 236, 282, 307 exoSI Table
Exact Reported
6 · Table S6 · Table S6
Compound 2 solvent mass-loss step9.99% over 35-220 °C; loss 2H2O, 2CH3OH, CH2Cl2; DTAmax 52 exoSI Table
Exact Reported
6 · Table S6 · Table S6

simultaneous thermogravimetric analysis (TG) and differential thermal analysis (DTA)

Compound 3 dark green prismatic crystals / polycrystalline pressed pellet · Pellet

compound 3 crystalline sample in nitrogen atmosphere up to 1100 C; heating rate 10 C min-1

Atmosphere
nitrogen
Context
pristine coordination polymer
Measurement source
3 and 10 · 2.1. Materials and Methods; 3.3. Molecular and Crystal Structures · Figure S5; Table S6
PropertyReported valueNormalised valueUncertaintyOrigin and qualitySource
Compound 3 final decomposition/degradation endpointaround 900 °C1173.15 KText
Approximate
10 · 3.3. Molecular and Crystal Structures of Compounds 1-3 · Figure S5; Table S6
Compound 3 framework mass-loss step71.12% over 235-945 °C; loss 4phen, 6(CO + CO2); DTAmax 243, 305, 386 exoSI Table
Exact Reported
6 · Table S6 · Table S6
Compound 3 solvent mass-loss step11.25% over 30-235 °C; loss 2H2O, 4CH3CN; DTAmax 48, 234 exoSI Table
Exact Reported
6 · Table S6 · Table S6