Bałanda, Maria ; Tomkowicz, Zbigniew ; Haase, Wolfgang ; Rams, Michał (2024)
Single-chain magnet features in 1D [MnR₄TPP][TCNE] compounds.
In: Journal of Physics: Conference Series, 2011, 303 (1)
doi: 10.26083/tuprints-00020753
Artikel, Zweitveröffentlichung, Verlagsversion
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Kurzbeschreibung (Abstract)
Molecular chains of antiferrimagnetically coupled MnIII-ion (S = 2) and TCNE (tetracyanoethylene) radical moments (s = ½) show different behaviour depending on group R substituted to TPP (tetraphenylporphyrin) and on the substitution site. The compound with R = F in Ortho position is a Single-Chain Magnet (SCM) with blocking temperature Tb = 6.6K, while that with R = F in Meta position shows both blocking (Tb = 5.4 K) and magnetic ordering transition (Tc = 10 K). For bulky groups R = OCnH2n+1, the magnetically ordered phase is observed (Tc ≈ 22 K), which does not however prevent slow relaxation at T <8 K. Magnetic hysteresis with coercive field Hc of 2 T at 2.3 K is like that of SCM. The frequency dependent AC susceptibility in the superimposed DC field reveals common features of all systems. The energy of intrachain ferromagnetic coupling between effective spin units 3/2, relevant at low temperatures, is determined for all compounds and the interchain dipolar coupling is estimated. It is concluded that slow relaxation is inherent for all quasi one-dimensional compounds and for the magnetically ordered ones shows up in the high enough magnetic field.
Typ des Eintrags: | Artikel |
---|---|
Erschienen: | 2024 |
Autor(en): | Bałanda, Maria ; Tomkowicz, Zbigniew ; Haase, Wolfgang ; Rams, Michał |
Art des Eintrags: | Zweitveröffentlichung |
Titel: | Single-chain magnet features in 1D [MnR₄TPP][TCNE] compounds |
Sprache: | Englisch |
Publikationsjahr: | 23 Januar 2024 |
Ort: | Darmstadt |
Publikationsdatum der Erstveröffentlichung: | 2011 |
Ort der Erstveröffentlichung: | Bristol |
Verlag: | IOP Publishing |
Titel der Zeitschrift, Zeitung oder Schriftenreihe: | Journal of Physics: Conference Series |
Jahrgang/Volume einer Zeitschrift: | 303 |
(Heft-)Nummer: | 1 |
Kollation: | 14 Seiten |
DOI: | 10.26083/tuprints-00020753 |
URL / URN: | https://tuprints.ulb.tu-darmstadt.de/20753 |
Zugehörige Links: | |
Herkunft: | Zweitveröffentlichung DeepGreen |
Kurzbeschreibung (Abstract): | Molecular chains of antiferrimagnetically coupled MnIII-ion (S = 2) and TCNE (tetracyanoethylene) radical moments (s = ½) show different behaviour depending on group R substituted to TPP (tetraphenylporphyrin) and on the substitution site. The compound with R = F in Ortho position is a Single-Chain Magnet (SCM) with blocking temperature Tb = 6.6K, while that with R = F in Meta position shows both blocking (Tb = 5.4 K) and magnetic ordering transition (Tc = 10 K). For bulky groups R = OCnH2n+1, the magnetically ordered phase is observed (Tc ≈ 22 K), which does not however prevent slow relaxation at T <8 K. Magnetic hysteresis with coercive field Hc of 2 T at 2.3 K is like that of SCM. The frequency dependent AC susceptibility in the superimposed DC field reveals common features of all systems. The energy of intrachain ferromagnetic coupling between effective spin units 3/2, relevant at low temperatures, is determined for all compounds and the interchain dipolar coupling is estimated. It is concluded that slow relaxation is inherent for all quasi one-dimensional compounds and for the magnetically ordered ones shows up in the high enough magnetic field. |
Status: | Verlagsversion |
URN: | urn:nbn:de:tuda-tuprints-207530 |
Zusätzliche Informationen: | Joint European Magnetic Symposia – JEMS 2010 23–28 August 2010, Krakow, Poland |
Sachgruppe der Dewey Dezimalklassifikatin (DDC): | 500 Naturwissenschaften und Mathematik > 530 Physik 500 Naturwissenschaften und Mathematik > 540 Chemie |
Fachbereich(e)/-gebiet(e): | 07 Fachbereich Chemie 07 Fachbereich Chemie > Eduard Zintl-Institut > Fachgebiet Physikalische Chemie |
Hinterlegungsdatum: | 23 Jan 2024 10:07 |
Letzte Änderung: | 24 Jan 2024 07:32 |
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