“…However, the deviation between the two magnetic entropy changes could be attributed to the presence of antiferromagnetic interaction between Gd III ions and Al III ions, as well. Accordingly, the Gd 6 Al cluster demonstrates its potential for practical applications as a magnetic cooling system. − …”
The self-assembly of the lanthanide metal−organic frameworks presents a formidable challenge but profound significance. Compared with the metal−organic frameworks based on 4f−3d ions, the chemistry of 4f−3p metal−organic frameworks has not been fully explored so far. In this study, two lanthanide− aluminum-based clusters [Ln 6 Al(IN) Ln = Gd, abbreviated as Gd 6 Al; x = 2.5, Ln = Eu, abbreviated as Eu 6 Al; HIN = isonicotinic acid) have been meticulously designed and obtained by hydrothermal reaction at low pH. The crystallographic study revealed that both Gd 6 Al and Eu 6 Al clusters exhibit an unprecedented sandwiched metal−organic framework holding a highly ordered honeycomb network. To our knowledge, it is the first case of Ln−Al-based cluster-organic frameworks. Furthermore, magnetic investigation of Gd 6 Al manifests a decent magnetic entropy change of −ΔS m max = 28.8 J kg −1 K −1 at 2 K for ΔH = 7.0 T. Significantly, the introduction of Al III ions into the lanthanide metal−organic frameworks displays excellent solid-state luminescent capability with a lifetime of 371.6 μs and quantum yield of 6.64%. The construction and investigation of these two Ln−Al clusters represent great progress in the 4f−3p metal−organic framework.
“…However, the deviation between the two magnetic entropy changes could be attributed to the presence of antiferromagnetic interaction between Gd III ions and Al III ions, as well. Accordingly, the Gd 6 Al cluster demonstrates its potential for practical applications as a magnetic cooling system. − …”
The self-assembly of the lanthanide metal−organic frameworks presents a formidable challenge but profound significance. Compared with the metal−organic frameworks based on 4f−3d ions, the chemistry of 4f−3p metal−organic frameworks has not been fully explored so far. In this study, two lanthanide− aluminum-based clusters [Ln 6 Al(IN) Ln = Gd, abbreviated as Gd 6 Al; x = 2.5, Ln = Eu, abbreviated as Eu 6 Al; HIN = isonicotinic acid) have been meticulously designed and obtained by hydrothermal reaction at low pH. The crystallographic study revealed that both Gd 6 Al and Eu 6 Al clusters exhibit an unprecedented sandwiched metal−organic framework holding a highly ordered honeycomb network. To our knowledge, it is the first case of Ln−Al-based cluster-organic frameworks. Furthermore, magnetic investigation of Gd 6 Al manifests a decent magnetic entropy change of −ΔS m max = 28.8 J kg −1 K −1 at 2 K for ΔH = 7.0 T. Significantly, the introduction of Al III ions into the lanthanide metal−organic frameworks displays excellent solid-state luminescent capability with a lifetime of 371.6 μs and quantum yield of 6.64%. The construction and investigation of these two Ln−Al clusters represent great progress in the 4f−3p metal−organic framework.
“…Oxydiacetato (O–(CH 2 –COO − ) 2 , oda 2− ) is a versatile tridentate ligand that bears five donor oxygen atoms and forms a wide variety of mononuclear and polynuclear complexes with both d and f transition metal ions. 1–3 The flexible tridentate O-donor motif, formed by the simultaneous coordination of one ether and two carboxylate groups, makes this ligand especially suited for Ln, i.e. , lanthanide and yttrium ions, affording the stable nine-coordinated anionic unit [Ln(oda) 3 ] 3− .…”
Section: Introductionmentioning
confidence: 99%
“…, lanthanide and yttrium ions, affording the stable nine-coordinated anionic unit [Ln(oda) 3 ] 3− . 2,4–17 This building block has also been extensively used as a synthon to prepare heteronuclear complexes. 2,18–48 In the formed [Ln 2 M 3 (oda) 6 (H 2 O) 6 ]· n H 2 O, the [Ln(oda) 3 ] 3− units remain undisturbed but are additionally connected through free carboxylate oxygen atoms to M( ii ) cations.…”
Section: Introductionmentioning
confidence: 99%
“…2,4–17 This building block has also been extensively used as a synthon to prepare heteronuclear complexes. 2,18–48 In the formed [Ln 2 M 3 (oda) 6 (H 2 O) 6 ]· n H 2 O, the [Ln(oda) 3 ] 3− units remain undisturbed but are additionally connected through free carboxylate oxygen atoms to M( ii ) cations. The synthesis and structural characterization of these heteronuclear compounds has been expanded to all lanthanide ions and Y and to various +2 metal ions.…”
Section: Introductionmentioning
confidence: 99%
“…The synthesis and structural characterization of these heteronuclear compounds has been expanded to all lanthanide ions and Y and to various +2 metal ions. 2,18–48 Interestingly, this large family of heteronuclear compounds comprises two structural motifs with slight differences, which are attributed to the geometry of the carboxylate bridge that connects [Ln(oda) 3 ] 3− to M( ii ) cations. If a μ- syn – anti carboxylate bridge is formed, a porous hexagonal structure belonging to the P 6/ mcc space group is obtained.…”
Here, we present the synthesis and crystal structure of a series of heteronuclear metal-organic frameworks, which consists of cobalt(II) and lanthanide(III) ions or yttrium(III), connected by oxydiacetato (oda2-) as ligand....
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