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65249129293
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The differences in color between phases II (IP) and III (LS) are too small to follow the low-temperature transition by optical microscopy
-
The differences in color between phases II (IP) and III (LS) are too small to follow the low-temperature transition by optical microscopy.
-
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12
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65249127049
-
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The front direction probably corresponds to the c direction (i.e., the direction of the 1-D supramolecular chains). The faces found at the edges of the longest dimension of the crystal were difficult to index since their indices seemed to vary. Near room temperature, these faces were approximately (104) and (104) but should have been (102) and (102) since the normal to these planes is found nearly along the c direction.
-
The front direction probably corresponds to the c direction (i.e., the direction of the 1-D supramolecular chains). The faces found at the edges of the longest dimension of the crystal were difficult to index since their indices seemed to vary. Near room temperature, these faces were approximately (104) and (104) but should have been (102) and (102) since the normal to these planes is found nearly along the c direction.
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13
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65249114324
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Given per metal ion involved in the transition
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Given per metal ion involved in the transition.
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Both recrystallized samples (b) and (c) show comparable high values at room temperature
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Both recrystallized samples (b) and (c) show comparable high values at room temperature.
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Note that the singularity in the relaxation curve around 40 K might indicate a two-step relaxation process, but its magnitude is comparable with the experimental incertitude.
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Note that the singularity in the relaxation curve around 40 K might indicate a two-step relaxation process, but its magnitude is comparable with the experimental incertitude.
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The synthesis is done in presence of traces of ascorbic acid to avoid aerial oxidation of Fe(II) into FeIII, although it can also be performed under an inert atmosphere, for which ascorbic acid is not required
-
The synthesis is done in presence of traces of ascorbic acid to avoid aerial oxidation of Fe(II) into Fe(III), although it can also be performed under an inert atmosphere, for which ascorbic acid is not required.
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48
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65249124198
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The infrared spectrum of various samples of type (a) are always identical to that of crushed single crystals of 1 [i.e., sample (b) after grinding], and their powder X-ray diffraction spectrum at room temperature (Figure 6) fits well with the spectrum calculated for phase I.
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The small variations of T the HS phase after each cycle (as shown in Figure 5) can be interpreted as a small displacement of the loosely packed crystals in the sampler holder until the most stable arrangement is attained.
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The small variations of T the HS phase after each cycle (as shown in Figure 5) can be interpreted as a small displacement of the loosely packed crystals in the sampler holder until the most stable arrangement is attained.
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