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            <subfield code="a">10.1039/c8dt05044a</subfield>
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            <subfield code="2">sideral</subfield>
            <subfield code="a">111507</subfield>
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            <subfield code="a">Bartolomé, E.</subfield>
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        <datafield tag="245" ind1=" " ind2=" ">
            <subfield code="a">Slow relaxation in a {Tb 2 Ba(a-fur) 8 } :N polymer with Ln = Tb(iii) non-Kramers ions</subfield>
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            <subfield code="c">2019</subfield>
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            <subfield code="a">We report the synthesis, crystal structure and magnetic properties of a new heteronuclear polymeric complex based on non-Kramers Tb ions and carboxylic a-fur = C 4 H 3 OCOO ligands: {[Tb 2 Ba(a-fur) 8 (H 2 O) 4 ]·2H 2 O} n . The a-furoate ligands consolidate 1D zig-zag chains running along the c-axis, formed by Tb 2 dimers separated by Ba ions. Ab initio calculations, in combination with the fit of experimental data, predict that the single-ion magnetic ground state is highly anisotropic and consists of a quasi-doublet with a ¿ Tb /k B = 3.22 K gap, well separated from the next excited state, while the gap for the Tb 2 dimer is ¿ 2Tb /k B = 2.58 K. Static magnetization and heat capacity measurements show that, magnetically, the system can be modeled as dimers of non-Kramers Tb ions, coupled by an antiferromagnetic intradimer interaction J'*/k B = -1.6 K. Dipolar interactions couple the Tb ions in the dimer with their first neighbour ions along the chain, with J''*/k B = -0.15 K, and with the surrounding ions out of the chain, with maximum J'''*/k B = -0.03 K. Ac susceptibility measurements in H = 0 performed down to 50 mK temperatures have enabled us to observe slow relaxation of magnetization, with an Orbach-like activation energy of U/k B = 1.1 K. It is assigned to the sluggish response of the 3D spin system due to a short-range ordering, possibly enhanced by the presence of disorder caused by defects in the polymeric chains. Under the application of a magnetic field, the system slowly relaxes by two distinct direct processes, strongly affected by a phonon bottleneck effect. We discuss the different relaxational phenomenology of the new complex in comparison with that of the isostructural {[Dy 2 Ba(a-fur) 8 (H 2 O) 4 ]·2H 2 O} n , differing only in the Kramers nature of the ions, and the mononuclear {Ln(a-fur) 3 (H 2 O) 3 } n (Ln = Tb, Dy) complexes, previously reported.</subfield>
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            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/MAT2014-53921-R</subfield>
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            <subfield code="9">info:eu-repo/grantAgreement/ES/MINECO/MAT2017-83468-R</subfield>
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            <subfield code="a">All rights reserved</subfield>
            <subfield code="u">http://www.europeana.eu/rights/rr-f/</subfield>
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            <subfield code="a">4.174</subfield>
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            <subfield code="a">Inorganic Chemistry</subfield>
            <subfield code="c">2019</subfield>
            <subfield code="d">Q1</subfield>
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            <subfield code="0">(orcid)0000-0002-5999-341X</subfield>
            <subfield code="a">Arauzo, A.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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        <datafield tag="700" ind1=" " ind2=" ">
            <subfield code="0">(orcid)0000-0002-9208-0807</subfield>
            <subfield code="a">Luzón, J.</subfield>
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            <subfield code="a">Melnic, S.</subfield>
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            <subfield code="a">Shova, S.</subfield>
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            <subfield code="a">Prodius, D.</subfield>
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            <subfield code="0">(orcid)0000-0002-0047-1772</subfield>
            <subfield code="a">Bartolomé, J.</subfield>
            <subfield code="u">Universidad de Zaragoza</subfield>
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            <subfield code="a">Amann, A.</subfield>
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            <subfield code="a">Nallaiyan, M.</subfield>
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            <subfield code="a">Spagna, S.</subfield>
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            <subfield code="1">2003</subfield>
            <subfield code="2">395</subfield>
            <subfield code="a">Universidad de Zaragoza</subfield>
            <subfield code="b">Dpto. Física Materia Condensa.</subfield>
            <subfield code="c">Área Física Materia Condensada</subfield>
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            <subfield code="g">48, 15 (2019), 5022-5034</subfield>
            <subfield code="p">Dalton Trans.</subfield>
            <subfield code="t">Dalton Transactions</subfield>
            <subfield code="x">1477-9226</subfield>
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