Abstract
In this chapter an outline is presented of the principal features of electronic spin crossover. The development of the subject is traced and the various modes of manifestation of spin transitions are presented. The role of cooperativity in influencing solid state behaviour is considered and the various strategies to strengthen it are addressed along with the chemical and physical perturbations which affect crossover behaviour. The role of intermediate spin states is discussed together with spin crossover in five-coordinate systems. The various techniques applied to monitoring a transition are presented briefly. An introduction to theoretical treatments is given and likely areas for future developments are suggested. Relevant review articles in the field are listed and reference to later chapters in the series is given where appropriate.
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Abbreviations
- abpt:
-
4-Amino-3,5-bis(pyridin-2-yl)-1,2,4-triazole
- bpy:
-
2,2′-Bipyridine
- btr:
-
4,4′-Bis(1,2,4-triazole)
- Cp :
-
Heat capacity
- DSC:
-
Differential scanning calorimetry
- EPR:
-
Electron paramagnetic resonance
- HS:
-
High spin
- LS:
-
Low spin
- LIESST:
-
Light induced excited spin state trapping
- mephen:
-
2-Methyl-1,10-phenanthroline
- NIESST:
-
Nuclear decay induced excited spin state trapping
- NMR:
-
Nuclear magnetic resonance
- ox:
-
The oxalate ion
- paptH:
-
2-(Pyridin-2-yl-amino)-4-(pyridin-2-yl)thiazole
- phen:
-
1,10-Phenanthroline
- phy:
-
1,10-Phenanthroline-2-carbaldehyde phenylhydrazone
- pic:
-
2-Picolylamine
- PM-BiA:
-
N-(2-Pyridylmethylene)aminobiphenyl
- ptz:
-
1-n-Propyl-tetrazole
- py:
-
Pyridine
- SCO:
-
Spin crossover
- ST:
-
Spin transition
- T1/2 :
-
Spin transition temperature (temperature of 505% conversion of all “SCO-active” complex molecules)
- TCNQ:
-
Tetracyanodiquinomethane
- trpy:
-
2,2′:6′,2″-Terpyridine
- trzH:
-
1,2,4-Triazole
- ZFS:
-
Zero field splitting
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Gütlich, P., Goodwin, H.A. Spin Crossover—An Overall Perspective. In: Gütlich, P., Goodwin, H. (eds) Spin Crossover in Transition Metal Compounds I. Topics in Current Chemistry, vol 233. Springer, Berlin, Heidelberg. https://doi.org/10.1007/b13527
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