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Studies of two lanthanide coordination polymers built up from dinuclear units 被引量:2
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作者 B.Benmerad K.Aliouane +3 位作者 n.rahahlia A.Guehria-Ladoudi S.Dahaoui C.Lecomte 《Journal of Rare Earths》 SCIE EI CAS CSCD 2013年第1期85-93,共9页
The two three-dimensional oxo-bfidged lanthanides {[Ln2(C4H2O4)3(H20)4]· 3H2O}3, with Ln=Ho3+ (1); Gd3+ (2), are isomorphous. They have layer-type structures built up from non-centrosymrnetric dinuclear... The two three-dimensional oxo-bfidged lanthanides {[Ln2(C4H2O4)3(H20)4]· 3H2O}3, with Ln=Ho3+ (1); Gd3+ (2), are isomorphous. They have layer-type structures built up from non-centrosymrnetric dinuclear unit Ln2O12(H2O)4, beside three lattice H20 molecules stabilizing the 3D open-frmnework. The building entities are linked through one classical syn-anti g2-carboxylato-K1O:K^1O' bridge. Within the bi-polyhedra, two double μ2-O'; K2O,O' bridges and a syn-syn classical one, support the magnetic measurements carried out on holmium compound indicating relatively weak anti-ferromagnetic interactions. The compari- son with magnetic studies on the almost similar reported Gd(III) compound, suggested that concomitant antiferromagnetic and ferro- magnetic properties could not be excluded. The two distinct thermal behaviors evidenced the higher metal-water bond strength with the smaller cation, and revealed the great supramolecular effects generated by hydrogen-bonding patterns. 展开更多
关键词 lanthanide organic frameworks crystal structure thermal behavior magnetic interactions rare earths
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