Search results for "cooperative effects"

showing 3 items of 3 documents

Cooperative phenomena and light-induced bistability in iron(II) spin-crossover compounds

1999

In iron(II) spin-crossover compounds, the transition from the 1A1 low-spin state at low temperatures to the 5T2 high-spin state at elevated temperatures is accompanied by a large increase in metal-ligand bond lengths. The resulting elastic interactions may be pictured as an internal pressure which is proportional to the concentration of the low-spin species. Because pressure stabilises the low-spin state relative to the high-spin state this results in a positive feedback. Thermal transition curves in neat iron(II) spin-crossover compounds are thus invariable much steeper than in diluted mixed crystals, and the high-spin→low-spin relaxation following the light-induced population of the high-…

Phase transitioneducation.field_of_studyCooperative effectsCondensed matter physicsBistabilityChemistryRelaxation (NMR)PopulationInternal pressureIron(II) coordination compoundsLIESSTInorganic ChemistryChemical physicsSpin crossoverddc:540Materials ChemistryHigh-spinlow-spin relaxationCondensed Matter::Strongly Correlated ElectronsBistabilityPhysical and Theoretical ChemistrySpin-crossoverGround stateeducationCoordination Chemistry Reviews
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Cooperative High-Temperature Spin Crossover Accompanied by a Highly Anisotropic Structural Distortion

2016

Spin transitions are a spectacular example of molecular switching that can provoke extreme electronic and structural reorganizations in coordination compounds. A new 3D cyanoheterometallic framework, [Fe(pz)(Au(CN)2)2], has been synthesized in which a highly cooperative spin crossover has been observed at 367 and 349 K in heating and cooling modes, respectively. Mössbauer spectroscopy revealed a complete transition between the diamagnetic and paramagnetic states of the iron centres. The low-spin-to-high-spin transition induced a drastic structural distortion involving a large one-directional expansion (ca. 10.6%) and contraction (ca. 9.6%) of the lattice. Negative thermal expansion along th…

chemistry.chemical_classificationCondensed matter physicsCooperative effects010405 organic chemistryChemistryTransition temperatureIronMetal-organic frameworks010402 general chemistrySpin crossover01 natural sciences0104 chemical sciencesCoordination complexInorganic ChemistryParamagnetismNuclear magnetic resonanceNegative thermal expansionSpin crossoverQD156Mössbauer spectroscopyMagnetic propertiesQD473DiamagnetismAnisotropy
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Progression of Diiminopyridines: From Single Application to Catalytic Versatility

2015

Diiminopyridyl metal complexes, first characterized several decades ago, found practical application in 1998 when they were used as precatalysts in coordinative ethylene polymerization. This discovery contributed to the so-called postmetallocene revolution and triggered the large-scale experimental and theoretical research aimed at understanding diversified diiminopyridine chemistry. The results of this quest, some of which were intriguing and difficult to anticipate, are discussed and summarized in the current Review.

redox reactiontransition metal complexChemistrySingle applicationTheoretical researchNanotechnologyGeneral ChemistryCatalysisdiiminopyridinechemistry.chemical_compoundaluminum alkylEthylene polymerizationcooperative effectsOrganic chemistryOlefin polymerizationAluminum alkylolefin polymerizationDiiminopyridineACS Catalysis
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