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@ARTICLE{Dulcevscaia:22291,
author = {Dulcevscaia, G.M. and Filippova, I.G. and Speldrich, M. and
Leusen, J. van and Kravtsov, V.C. and Baca, S.G. and
Kögerler, P. and Liu, S.-X. and Decurtins, S.},
title = {{C}luster-based {N}etworks: 1{D} and 2{D} {C}oordination
{P}olymers {B}ased on {{M}n{F}e2(µ3-{O})}-type {C}lusters},
journal = {European journal of inorganic chemistry},
volume = {51},
issn = {1434-1948},
address = {Weinheim},
publisher = {Wiley-VCH},
reportid = {PreJuSER-22291},
pages = {5110 -5117},
year = {2012},
note = {Financial support from the Swiss National Science
Foundation (SCOPES $IZ73Z0_127925),$ the German Federal
Ministry of Education and Research (project MDA 08/022), the
Academy of Sciences of Moldova (project No. 09.820.05.10GF),
the Supreme Council for Science and Technological
Development of the Republic of Moldova (projects
09.836.05.02A and 11.817.05.03A), and the EU (POLYMAG, IIF
contract no. 252984) are acknowledged. We thank Prof. H.
Stoeckli-Evans for the collection of crystallographic data
sets for compound 1.},
abstract = {A straightforward approach to heterometallic Mn-Fe
cluster-based coordination polymers is presented. By
employing a mixed-valent μ(3)-oxo trinuclear
manganese(II/III) pivalate cluster, isolated as
[Mn(II)Mn(III)(2)O(O(2)CCMe(3))(6)(hmta)(3)]·(solvent)
(hmta = hexamethylenetetramine; solvent = n-propanol (1),
toluene (2)) in the reaction with a μ(3)-oxo trinuclear
iron(III) pivalate cluster compound,
[Fe(3)O(O(2)CCMe(3))(6)(H(2)O)(3)]O(2)CCMe(3)·2Me(3)CCO(2)H,
three new heterometallic {Mn(II)Fe(III)(2)} cluster-based
coordination polymers were obtained: the one-dimensional
polymer chain compounds
{[MnFe(2)O(O(2)CCMe(3))(6)(hmta)(2)]·0.5MeCN}(n) (3) and
{[MnFe(2)O(O(2)CCMe(3))(6)(hmta)(2)]·Me(3)CCO(2)H·(n-hexane)}(n)
(4) and the two-dimensional layer compound
{[MnFe(2)O(O(2)CCMe(3))(6)(hmta)(1.5)]·(toluene)}(n) (5).
Single-crystal X-ray diffraction analysis reveals a
μ(3)-oxo trinuclear pivalate cluster building block as the
main constituent in all polymer compounds. Different M:hmta
ratios in 1-5 are related to the different structural
functions of the N-containing ligand. In clusters 1 and 2,
three hmta ligands are monodentate, whereas in chains 3 and
4 two hmta ligands act as bridging ligands and one is a
monodentate ligand; in 5, all hmta molecules act as
bidentate bridges. Magnetic studies indicate dominant
antiferromagnetic interactions between the metal centers in
both homometallic {Mn(3)}-type clusters 1 and 2 and
heterometallic {MnFe(2)}-type coordination polymers 3-5.
Modeling of the magnetic susceptibility data to a isotropic
model Hamiltonian yields least-squares fits for the
following parameters: J(1)(Mn(II)-Mn(III)) = -6.6 cm(-1) and
J(2)(Mn(III)-Mn(III)) = -5.4 cm(-1) for 1; J(1) = -5.5
cm(-1) and J(2)(Mn(III)-Mn(III)) = -3.9 cm(-1) for 2;
J(1)(Mn(II)-Fe(III)) = -17.1 cm(-1) and
J(2)(Fe(III)-Fe(III)) = -43.7 cm(-1) for 3; J(1) = -23.8
cm(-1) and J(2) = -53.4 cm(-1) for 4; J(1) = -13.3 cm(-1)
and J(2) = -35.4 cm(-1) for 5. Intercluster coupling plays a
significant role in all compounds 1-5.},
keywords = {J (WoSType)},
cin = {PGI-6},
ddc = {540},
cid = {I:(DE-Juel1)PGI-6-20110106},
pnm = {Grundlagen für zukünftige Informationstechnologien /
POLYMAG - Magnetic Coordination Cluster Polymers (252984)},
pid = {G:(DE-Juel1)FUEK412 / G:(EU-Grant)252984},
shelfmark = {Chemistry, Inorganic $\&$ Nuclear},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:22524248},
UT = {WOS:000303952900032},
doi = {10.1021/ic202644t},
url = {https://juser.fz-juelich.de/record/22291},
}