Decoupling of the molecular spin-state and the crystallographic phase in the spin-crossover complex [Fe(ptz)6](BF4)2 studied by Raman spectroscopy

2005 ◽  
Vol 402 (4-6) ◽  
pp. 503-509 ◽  
Author(s):  
Nawel Ould Moussa ◽  
Gábor Molnár ◽  
Xavier Ducros ◽  
Antoine Zwick ◽  
Takeshi Tayagaki ◽  
...  
2021 ◽  
Author(s):  
Yongfeng Tong ◽  
Massine Kelaï ◽  
Kaushik Bairagi ◽  
Vincent Repain ◽  
Jérôme Lagoute ◽  
...  

Abstract Bistable spin-crossover molecules are particularly interesting to the development of innovative electronic and spintronic devices as they present two spin states that can be controlled by external stimuli. In this purpose, being able to switch at will the spin state of a single molecule in a dense molecular array is a key milestone. However, the elastic interactions between the molecules favour more cooperative behaviour where patches of neighbouring molecules switches simultaneously. We demonstrate here that the interaction of iron II spin-crossover molecules with a metallic substrate can strongly reduce their cooperative behaviour until addressing independently single molecular spin state. Mechanoelastic model is able to reproduce well such findings.


2012 ◽  
Vol 2013 (5-6) ◽  
pp. 1001-1008 ◽  
Author(s):  
Antoine Tissot ◽  
Helena J. Shepherd ◽  
Loic Toupet ◽  
Eric Collet ◽  
Joelle Sainton ◽  
...  

2018 ◽  
Vol 10 (37) ◽  
pp. 31580-31585 ◽  
Author(s):  
Filip Schleicher ◽  
Michał Studniarek ◽  
Kuppusamy Senthil Kumar ◽  
Etienne Urbain ◽  
Kostantine Katcko ◽  
...  

2014 ◽  
Vol 50 (86) ◽  
pp. 13015-13018 ◽  
Author(s):  
Iurii Suleimanov ◽  
José Sánchez Costa ◽  
Gábor Molnár ◽  
Lionel Salmon ◽  
Azzedine Bousseksou

Nanocomposite spin crossover materials with gold nanoparticles were synthesized and plasmon-enhanced photothermal spin state switching was evidenced using Raman spectroscopy.


2016 ◽  
Vol 55 (11) ◽  
pp. 5254-5265 ◽  
Author(s):  
Philipp Stock ◽  
Eva Deck ◽  
Silvia Hohnstein ◽  
Jana Korzekwa ◽  
Karsten Meyer ◽  
...  

2021 ◽  
Vol 7 (3) ◽  
pp. 37
Author(s):  
Thilini K. Ekanayaka ◽  
Guanhua Hao ◽  
Aaron Mosey ◽  
Ashley S. Dale ◽  
Xuanyuan Jiang ◽  
...  

Nonvolatile, molecular multiferroic devices have now been demonstrated, but it is worth giving some consideration to the issue of whether such devices could be a competitive alternative for solid-state nonvolatile memory. For the Fe (II) spin crossover complex [Fe{H2B(pz)2}2(bipy)], where pz = tris(pyrazol-1-yl)-borohydride and bipy = 2,2′-bipyridine, voltage-controlled isothermal changes in the electronic structure and spin state have been demonstrated and are accompanied by changes in conductance. Higher conductance is seen with [Fe{H2B(pz)2}2(bipy)] in the high spin state, while lower conductance occurs for the low spin state. Plausibly, there is the potential here for low-cost molecular solid-state memory because the essential molecular thin films are easily fabricated. However, successful device fabrication does not mean a device that has a practical value. Here, we discuss the progress and challenges yet facing the fabrication of molecular multiferroic devices, which could be considered competitive to silicon.


2021 ◽  
Vol 50 (10) ◽  
pp. 3464-3467
Author(s):  
Rafal Kulmaczewski ◽  
Mark J. Howard ◽  
Malcolm A. Halcrow

The temperature of the solution-phase spin-crossover equilibrium in iron(ii) complexes of 4-alkylsulfanyl-2,6-di{pyrazol-1-yl}pyridine (bppSR) complexes depends strongly on the alkylsulfanyl substituent.


2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Julia Villalva ◽  
Aysegul Develioglu ◽  
Nicolas Montenegro-Pohlhammer ◽  
Rocío Sánchez-de-Armas ◽  
Arturo Gamonal ◽  
...  

AbstractSpin crossover (SCO) molecules are promising nanoscale magnetic switches due to their ability to modify their spin state under several stimuli. However, SCO systems face several bottlenecks when downscaling into nanoscale spintronic devices: their instability at the nanoscale, their insulating character and the lack of control when positioning nanocrystals in nanodevices. Here we show the encapsulation of robust Fe-based SCO molecules within the 1D cavities of single-walled carbon nanotubes (SWCNT). We find that the SCO mechanism endures encapsulation and positioning of individual heterostructures in nanoscale transistors. The SCO switch in the guest molecules triggers a large conductance bistability through the host SWCNT. Moreover, the SCO transition shifts to higher temperatures and displays hysteresis cycles, and thus memory effect, not present in crystalline samples. Our results demonstrate how encapsulation in SWCNTs provides the backbone for the readout and positioning of SCO molecules into nanodevices, and can also help to tune their magnetic properties at the nanoscale.


2014 ◽  
Vol 26 (18) ◽  
pp. 2889-2893 ◽  
Author(s):  
Edna M. Hernández ◽  
Carlos M. Quintero ◽  
Olena Kraieva ◽  
Christophe Thibault ◽  
Christian Bergaud ◽  
...  

Molecules ◽  
2021 ◽  
Vol 26 (14) ◽  
pp. 4155
Author(s):  
Alexander V. Shokurov ◽  
Daria S. Kutsybala ◽  
Andrey P. Kroitor ◽  
Alexander A. Dmitrienko ◽  
Alexander G. Martynov ◽  
...  

Coordination-induced spin crossover (CISCO) in nickel(II) porphyrinates is an intriguing phenomenon that is interesting from both fundamental and practical standpoints. However, in most cases, realization of this effect requires extensive synthetic protocols or extreme concentrations of extra-ligands. Herein we show that CISCO effect can be prompted for the commonly available nickel(II) tetraphenylporphyrinate, NiTPP, upon deposition of this complex at the air/water interface together with a ruthenium(II) phthalocyaninate, CRPcRu(pyz)2, bearing two axial pyrazine ligands. The latter was used as a molecular guiderail to align Ni···Ru···Ni metal centers for pyrazine coordination upon lateral compression of the system, which helps bring the two macrocycles closer together and forces the formation of Ni–pyz bonds. The fact of Ni(II) porphyrinate switching from low- to high-spin state upon acquiring additional ligands can be conveniently observed in situ via reflection-absorption UV-vis spectroscopy. The reversible nature of this interaction allows for dissociation of Ni–pyz bonds, and thus, change of nickel cation spin state, upon expansion of the monolayer.


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