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Drastic effect of lattice propionitrile molecules on the spin-transition temperature of a 2,2'-dipyridylamino/s-triazine-based iron(II) complex

Authors :
Institución Catalana de Investigación y Estudios Avanzados
Ministerio de Economía y Competitividad (España)
Khon Kaen University
Thailand Research Fund
Center of Excellence for Innovation in Chemistry (Thailand)
Office of the Higher Education Commission (Thailand)
Ministry of Education (Thailand)
Department of Energy (US)
Wannarit, Nanthawat
Masciocchi, Norberto
Youngme, Sujittra
Roubeau, Olivier
Teat, Simon J.
Gamez, Patrick
Institución Catalana de Investigación y Estudios Avanzados
Ministerio de Economía y Competitividad (España)
Khon Kaen University
Thailand Research Fund
Center of Excellence for Innovation in Chemistry (Thailand)
Office of the Higher Education Commission (Thailand)
Ministry of Education (Thailand)
Department of Energy (US)
Wannarit, Nanthawat
Masciocchi, Norberto
Youngme, Sujittra
Roubeau, Olivier
Teat, Simon J.
Gamez, Patrick
Publication Year :
2014

Abstract

Reaction of iron(II) selenocyanate (obtained from Fe(ClO4)2 and KNCSe) with 2-(N,N-bis(2-pyridyl)amino)-4,6-bis(pentafluorophenoxy)-(1,3,5)triazine (L1F) in propionitrile produces the compound [Fe(L1F)2(NCSe)2].2CH3CH2CN (1NCSe.2PrCN), which shows spin-crossover (SCO) properties characterized by a T1/2 of 283 K and a ?T80 (i.e., temperature range within which 80% of the transition considered occurs) of about 65 K. Upon air exposure, 1NCSe.2PrCN gradually converts to a new SCO species that exhibits different properties, as reflected by T1/2 = 220 K and ?T80 = 70 K. Various characterization techniques, namely, IR spectroscopy, thermogravimetric analysis, and thermodiffractometric studies, reveal that the new phase is obtained through the loss of the lattice propionitrile molecules within several days upon air exposure or several hours upon heating above 390 K.

Details

Database :
OAIster
Notes :
English
Publication Type :
Electronic Resource
Accession number :
edsoai.on1104773509
Document Type :
Electronic Resource