Palacios María A, Titos-Padilla Silvia, Ruiz José, Herrera Juan Manuel, Pope Simon J A, Brechin Euan K, Colacio Enrique
Departamento de Química Inorgánica, Facultad de Ciencias, Universidad de Granada , Avda. Fuentenueva s/n, 18071 Granada, Spain.
Inorg Chem. 2014 Feb 3;53(3):1465-74. doi: 10.1021/ic402597s. Epub 2013 Dec 17.
There were new dinuclear Zn(II)-Ln(III) complexes of general formulas [Zn(μ-L)(μ-OAc)Ln(NO3)2] (Ln(III) = Tb (1), Dy (2), Er (3), and Yb (4)), [Zn(μ-L)(μ-NO3)Er(NO3)2] (5), [Zn(H2O)(μ-L)Nd(NO3)3]·2CH3OH (6), [Zn(μ-L)(μ-9-An)Ln(NO3)2]·2CH3CN (Ln(III) = Tb (7), Dy (8), Er (9), Yb(10)), [Zn(μ-L)(μ-9-An)Yb(9-An)(NO3)3]·3CH3CN (11), [Zn(μ-L)(μ-9-An)Nd(9-An)(NO3)3]·2CH3CN·3H2O (12), and [Zn(μ-L)(μ-9-An)Nd(CH3OH)2(NO3)]ClO4·2CH3OH (13) prepared from the reaction of the compartmental ligand N,N',N″-trimethyl-N,N″-bis(2-hydroxy-3-methoxy-5-methylbenzyl)diethylenetriamine (H2L), with ZnX2·nH2O (X = NO3(-) or OAc(-)) salts, Ln(NO3)3·nH2O, and, in some instances, 9-anthracenecarboxylate anion (9-An). In all these complexes, the Zn(II) ions invariably occupy the internal N3O2 site whereas the Ln(III) ions show preference for the O4 external site, giving rise to a Zn(μ-diphenoxo)Ln bridging fragment. Depending on the Zn(II) salt and solvent used in the reaction, a third bridge can connect the Zn(II) and Ln(III) metal ions, giving rise to triple-bridged diphenoxoacetate in complexes 1-4, diphenoxonitrate in complex 5, and diphenoxo(9-anthracenecarboxylate) in complexes 8-13. Dy(III) and Er(III) complexes 2, 8 and 3, 5, respectively, exhibit field induced single molecule magnet (SMM) behavior, with Ueff values ranging from 11.7 (3) to 41(2) K. Additionally, the solid-state photophysical properties of these complexes are presented showing that ligand L(2-) is able to sensitize Tb(III)- and Dy(III)-based luminescence in the visible region through an energy transfer process (antenna effect). The efficiency of this process is much lower when NIR emitters such as Er(III), Nd(III), and Yb(III) are considered. When the luminophore 9-anthracene carboxylate is incorporated into these complexes, the NIR luminescence is enhanced which proves the efficiency of this bridging ligand to act as antenna group. Complexes 2, 3, 5, and 8 can be considered as dual materials as they combine SMM behavior and luminescent properties.
通过使用隔室配体N,N',N″-三甲基-N,N″-双(2-羟基-3-甲氧基-5-甲基苄基)二亚乙基三胺(H₂L)与ZnX₂·nH₂O(X = NO₃⁻或OAc⁻)盐、Ln(NO₃)₃·nH₂O以及在某些情况下的9-蒽甲酸根阴离子(9-An)反应,制备了通式为Zn(μ-L)(μ-OAc)Ln(NO₃)₂、Zn(μ-L)(μ-NO₃)Er(NO₃)₂、[Zn(H₂O)(μ-L)Nd(NO₃)₃]·2CH₃OH(6)、[Zn(μ-L)(μ-9-An)Ln(NO₃)₂]·2CH₃CN(Ln(III)=Tb(7)、Dy(8)、Er(9)、Yb(10))、[Zn(μ-L)(μ-9-An)Yb(9-An)(NO₃)₃]·3CH₃CN(11)、[Zn(μ-L)(μ-9-An)Nd(9-An)(NO₃)₃]·2CH₃CN·3H₂O(12)和[Zn(μ-L)(μ-9-An)Nd(CH₃OH)₂(NO₃)]ClO₄·2CH₃OH(13)的新型双核Zn(II)-Ln(III)配合物。在所有这些配合物中,Zn(II)离子始终占据内部N₃O₂位点,而Ln(III)离子则优先占据外部O₄位点,从而产生一个Zn(μ-二苯氧基)Ln桥连片段。根据反应中使用的Zn(II)盐和溶剂的不同,第三条桥可以连接Zn(II)和Ln(III)金属离子,在配合物1-4中产生三桥连的二苯氧基乙酸根、在配合物5中产生二苯氧基硝酸根以及在配合物8-13中产生二苯氧基(9-蒽甲酸根)。Dy(III)和Er(III)配合物2、8和3、5分别表现出场诱导单分子磁体(SMM)行为,Ueff值范围为11.7(3)至41(2)K。此外,还展示了这些配合物的固态光物理性质,表明配体L²⁻能够通过能量转移过程(天线效应)在可见光区域敏化基于Tb(III)和Dy(III)的发光。当考虑诸如Er(III)、Nd(III)和Yb(III)等近红外发射体时,该过程的效率要低得多。当将发光体9-蒽甲酸掺入这些配合物中时,近红外发光增强,这证明了这种桥连配体作为天线基团的效率。配合物2、3、5和8可被视为双功能材料,因为它们兼具SMM行为和发光性质。