Fluoride bridges as structure-directing motifs in 3d-4f cluster chemistry

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Fluoride bridges as structure-directing motifs in 3d-4f cluster chemistry. / Birk, Torben; Pedersen, Kasper Steen; Thuesen, Christian Aagaard; Weyhermüller, Thomas; Schau-Magnussen, Magnus; Piligkos, Stergios; Weihe, Høgni; Mossin, Susanne L.; Evangelisti, Marco; Bendix, Jesper.

I: Inorganic Chemistry, Bind 51, Nr. 9, 2012, s. 5435-5443.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Harvard

Birk, T, Pedersen, KS, Thuesen, CA, Weyhermüller, T, Schau-Magnussen, M, Piligkos, S, Weihe, H, Mossin, SL, Evangelisti, M & Bendix, J 2012, 'Fluoride bridges as structure-directing motifs in 3d-4f cluster chemistry', Inorganic Chemistry, bind 51, nr. 9, s. 5435-5443. https://doi.org/10.1021/ic300421x

APA

Birk, T., Pedersen, K. S., Thuesen, C. A., Weyhermüller, T., Schau-Magnussen, M., Piligkos, S., Weihe, H., Mossin, S. L., Evangelisti, M., & Bendix, J. (2012). Fluoride bridges as structure-directing motifs in 3d-4f cluster chemistry. Inorganic Chemistry, 51(9), 5435-5443. https://doi.org/10.1021/ic300421x

Vancouver

Birk T, Pedersen KS, Thuesen CA, Weyhermüller T, Schau-Magnussen M, Piligkos S o.a. Fluoride bridges as structure-directing motifs in 3d-4f cluster chemistry. Inorganic Chemistry. 2012;51(9):5435-5443. https://doi.org/10.1021/ic300421x

Author

Birk, Torben ; Pedersen, Kasper Steen ; Thuesen, Christian Aagaard ; Weyhermüller, Thomas ; Schau-Magnussen, Magnus ; Piligkos, Stergios ; Weihe, Høgni ; Mossin, Susanne L. ; Evangelisti, Marco ; Bendix, Jesper. / Fluoride bridges as structure-directing motifs in 3d-4f cluster chemistry. I: Inorganic Chemistry. 2012 ; Bind 51, Nr. 9. s. 5435-5443.

Bibtex

@article{68be513c83bb448181f703523fff8fd2,
title = "Fluoride bridges as structure-directing motifs in 3d-4f cluster chemistry",
abstract = "The use of kinetically robust chromium(III) fluorido complexes as synthons for mixed 3d-4f clusters is reported. The tendency toward linear {Cr(III)-F-Ln(III)} units dictates the cluster topology. Specifically, we show that reaction of cis-[Cr(III)F(2)(NN)(2)]NO(3) (NN = 1,10-phenanthroline ({"}phen{"}) or 2,2'-bipyridine ({"}bpy{"})) with Ln(NO(3))(3)·xH(2)O produces isostructural series of molecular {Ln(2)Cr(2)} squares (1-9) with linear fluoride bridges. In a parallel fashion, fac-[Cr(III)F(3)L], where L = N,N',N¿-trimethyl-1,4,7-triazacyclononane ({"}Me(3)tacn{"}), reacts with Nd(NO(3))(3)·6H(2)O to form a fluoride-centered penta-nuclear complex and fac-[Cr(III)F(3)L'], with L' = 1,1,1-tris-((methylamino)methylethane) ({"}Me(3)tame{"}), reacts with [Ln(hfac)(3)(H(2)O)(2)] (hfacH = 1,1,1,5,5,5-hexafluoroacetylacetone) to yield an isostructural series of {Ln(3)Cr(2)} (10-14) trigonal bipyramids with no central ligand. The formation of the latter is accompanied by a partial solvolysis of the Cr(III) precursor but without formation of insoluble LnF(3). The magnetic properties of the gadolinium containing clusters allow quantification of fluoride-mediated, antiferromagnetic Gd-Cr exchange interactions of magnitude between 0.14 cm(-1) and 0.71 cm(-1) (H = J(12)S(1)·S(2) formalism) and vanishingly small J(Gd-Gd) of 0.06(0) cm(-1). The large spin and small anisotropy together with weak exchange interactions in the {Gd(3)Cr(2)} (11) cluster give rise to a very large magneto-caloric effect of -¿S(m) = 28.7 J kg(-1) K(-1) (µ(0)H = 90 to 0 kOe).",
keywords = "Chromium, Fluorides, Kinetics, Lanthanoid Series Elements, Magnetic Phenomena, Models, Molecular, Molecular Conformation, Organometallic Compounds, Temperature",
author = "Torben Birk and Pedersen, {Kasper Steen} and Thuesen, {Christian Aagaard} and Thomas Weyherm{\"u}ller and Magnus Schau-Magnussen and Stergios Piligkos and H{\o}gni Weihe and Mossin, {Susanne L.} and Marco Evangelisti and Jesper Bendix",
year = "2012",
doi = "10.1021/ic300421x",
language = "English",
volume = "51",
pages = "5435--5443",
journal = "Inorganic Chemistry",
issn = "0020-1669",
publisher = "American Chemical Society",
number = "9",

}

RIS

TY - JOUR

T1 - Fluoride bridges as structure-directing motifs in 3d-4f cluster chemistry

AU - Birk, Torben

AU - Pedersen, Kasper Steen

AU - Thuesen, Christian Aagaard

AU - Weyhermüller, Thomas

AU - Schau-Magnussen, Magnus

AU - Piligkos, Stergios

AU - Weihe, Høgni

AU - Mossin, Susanne L.

AU - Evangelisti, Marco

AU - Bendix, Jesper

PY - 2012

Y1 - 2012

N2 - The use of kinetically robust chromium(III) fluorido complexes as synthons for mixed 3d-4f clusters is reported. The tendency toward linear {Cr(III)-F-Ln(III)} units dictates the cluster topology. Specifically, we show that reaction of cis-[Cr(III)F(2)(NN)(2)]NO(3) (NN = 1,10-phenanthroline ("phen") or 2,2'-bipyridine ("bpy")) with Ln(NO(3))(3)·xH(2)O produces isostructural series of molecular {Ln(2)Cr(2)} squares (1-9) with linear fluoride bridges. In a parallel fashion, fac-[Cr(III)F(3)L], where L = N,N',N¿-trimethyl-1,4,7-triazacyclononane ("Me(3)tacn"), reacts with Nd(NO(3))(3)·6H(2)O to form a fluoride-centered penta-nuclear complex and fac-[Cr(III)F(3)L'], with L' = 1,1,1-tris-((methylamino)methylethane) ("Me(3)tame"), reacts with [Ln(hfac)(3)(H(2)O)(2)] (hfacH = 1,1,1,5,5,5-hexafluoroacetylacetone) to yield an isostructural series of {Ln(3)Cr(2)} (10-14) trigonal bipyramids with no central ligand. The formation of the latter is accompanied by a partial solvolysis of the Cr(III) precursor but without formation of insoluble LnF(3). The magnetic properties of the gadolinium containing clusters allow quantification of fluoride-mediated, antiferromagnetic Gd-Cr exchange interactions of magnitude between 0.14 cm(-1) and 0.71 cm(-1) (H = J(12)S(1)·S(2) formalism) and vanishingly small J(Gd-Gd) of 0.06(0) cm(-1). The large spin and small anisotropy together with weak exchange interactions in the {Gd(3)Cr(2)} (11) cluster give rise to a very large magneto-caloric effect of -¿S(m) = 28.7 J kg(-1) K(-1) (µ(0)H = 90 to 0 kOe).

AB - The use of kinetically robust chromium(III) fluorido complexes as synthons for mixed 3d-4f clusters is reported. The tendency toward linear {Cr(III)-F-Ln(III)} units dictates the cluster topology. Specifically, we show that reaction of cis-[Cr(III)F(2)(NN)(2)]NO(3) (NN = 1,10-phenanthroline ("phen") or 2,2'-bipyridine ("bpy")) with Ln(NO(3))(3)·xH(2)O produces isostructural series of molecular {Ln(2)Cr(2)} squares (1-9) with linear fluoride bridges. In a parallel fashion, fac-[Cr(III)F(3)L], where L = N,N',N¿-trimethyl-1,4,7-triazacyclononane ("Me(3)tacn"), reacts with Nd(NO(3))(3)·6H(2)O to form a fluoride-centered penta-nuclear complex and fac-[Cr(III)F(3)L'], with L' = 1,1,1-tris-((methylamino)methylethane) ("Me(3)tame"), reacts with [Ln(hfac)(3)(H(2)O)(2)] (hfacH = 1,1,1,5,5,5-hexafluoroacetylacetone) to yield an isostructural series of {Ln(3)Cr(2)} (10-14) trigonal bipyramids with no central ligand. The formation of the latter is accompanied by a partial solvolysis of the Cr(III) precursor but without formation of insoluble LnF(3). The magnetic properties of the gadolinium containing clusters allow quantification of fluoride-mediated, antiferromagnetic Gd-Cr exchange interactions of magnitude between 0.14 cm(-1) and 0.71 cm(-1) (H = J(12)S(1)·S(2) formalism) and vanishingly small J(Gd-Gd) of 0.06(0) cm(-1). The large spin and small anisotropy together with weak exchange interactions in the {Gd(3)Cr(2)} (11) cluster give rise to a very large magneto-caloric effect of -¿S(m) = 28.7 J kg(-1) K(-1) (µ(0)H = 90 to 0 kOe).

KW - Chromium

KW - Fluorides

KW - Kinetics

KW - Lanthanoid Series Elements

KW - Magnetic Phenomena

KW - Models, Molecular

KW - Molecular Conformation

KW - Organometallic Compounds

KW - Temperature

U2 - 10.1021/ic300421x

DO - 10.1021/ic300421x

M3 - Journal article

C2 - 22497590

VL - 51

SP - 5435

EP - 5443

JO - Inorganic Chemistry

JF - Inorganic Chemistry

SN - 0020-1669

IS - 9

ER -

ID: 41963441