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Ln(III)(双恶唑啉)-[Mo(V)(CN)₈](Ln = Ce - Yb)磁性配位聚合物的可见到近红外发射:氰基桥连层呈现出依赖镧系元素的异常滑动

Visible to Near-Infrared Emission from Ln(III)(Bis-oxazoline)-[Mo(V)(CN)8] (Ln = Ce-Yb) Magnetic Coordination Polymers Showing Unusual Lanthanide-Dependent Sliding of Cyanido-Bridged Layers.

作者信息

Chorazy Szymon, Arczynski Mirosław, Nakabayashi Koji, Sieklucka Barbara, Ohkoshi Shin-Ichi

机构信息

‡Department of Chemistry, School of Science, The University of Tokyo, 7-3-1 Hongo, Bunkyo-ku, Tokyo 113-0033, Japan.

†Faculty of Chemistry, Jagiellonian University, Ingardena 3, 30-060 Krakow, Poland.

出版信息

Inorg Chem. 2015 May 18;54(10):4724-36. doi: 10.1021/acs.inorgchem.5b00040. Epub 2015 May 6.

Abstract

Complexes of lanthanides(III) (Ce-Yb) with 2,2'-bis(2-oxazoline) (Box) combined with octacyanidomolybdate(V) gave a series of magneto-luminescent coordination polymers, {[Ln(III)(Box)n(DMF)m][Mo(V)(CN)8]}·x(solvent) (1-12). They are built of cyanido-bridged layers of a mixed 4- and 8-metal rings topology and show unique sliding of layers dependent on a 4f metal ion. For light lanthanides, dominant phase A, {[Ln(III)(Box)2(DMF)2][Mo(V)(CN)8]}·1.5MeCN (Ln = Ce, 1; Pr, 2; Nd, 3), consists of ideally aligned, not shifted layers, giving large channels (13.7 × 14.0 Å). Intermediate lanthanides reveal phase B, {[Ln(III)(Box)2(DMF)2] [Mo(V)(CN)8]}·H2O (Ln = Sm, 4; Eu, 5; Gd, 6; Tb, 7; Dy, 8), of smaller pores (8.4 × 10.6 Å) due to layer-H2O hydrogen bonding, which induces sliding of CN(-)-bridged layers. Heavy lanthanides show phase C, {[Ln(III)(Box)(DMF)3][Mo(V)(CN)8]}·MeCN (Ln = Ho, 9; Er, 10; Tm, 11; Yb, 12), with large channels (13.7 × 13.7 Å) of a similar size to light lanthanides. This effect comes from the changes in Ln(III) coordination sphere affecting solvent-layer interactions. Compounds 1-12 reveal diverse emission depending on the interaction between Ln(III) and Box luminophors. For 2-5, 9, and 12, the ligand-to-metal energy-transfer-induced visible f-centered emission ranging from green for Ho(III)-based 9, orange from Sm(III)-based 4, to red for Pr(III)- and Eu(III)-containing 2 and 5, respectively. Near-infrared emission was found for 2-4, 9, and 12. Red phosphorescence of Box was detected for Gd(III)-based 6, whereas the selective excitation of ligand or Ln(III) excited states resulting in the switchable red to green emission was found for Tb(III)-based 7. The materials revealed Ln(III)-Mo(V) magnetic coupling leading to ferromagnetism below 2.0 and 2.2 K for 4 and 7, respectively. The onset of magnetic ordering at low temperatures was found for 6 and 8. Compounds 1-12 form a unique family of cyanido-bridged materials of a bifunctional magneto-luminescence character combined with dynamic structural features.

摘要

镧系元素(III)(铈 - 镱)与2,2'-双(2 - 恶唑啉)(Box)和八氰基钼酸盐(V)形成的配合物产生了一系列磁光配位聚合物{[Ln(III)(Box)n(DMF)m][Mo(V)(CN)8]}·x(溶剂)(1 - 12)。它们由混合的4 - 和8 - 金属环拓扑结构的氰基桥连层构成,并表现出取决于4f金属离子的独特层间滑动。对于轻镧系元素,主要相A,{[Ln(III)(Box)2(DMF)2][Mo(V)(CN)8]}·1.5MeCN(Ln = Ce,1;Pr,2;Nd,3),由理想排列且未移位的层组成,形成大通道(13.7×14.0 Å)。中间镧系元素呈现相B,{[Ln(III)(Box)2(DMF)2][Mo(V)(CN)8]}·H2O(Ln = Sm,4;Eu,5;Gd,6;Tb,7;Dy,8),由于层与水的氢键作用,其孔较小(8.4×10.6 Å),这导致了氰基桥连层的滑动。重镧系元素显示相C,{[Ln(III)(Box)(DMF)3][Mo(V)(CN)8]}·MeCN(Ln = Ho,9;Er,10;Tm,11;Yb,12),具有与轻镧系元素类似大小的大通道(13.7×13.7 Å)。这种效应源于镧系元素(III)配位球的变化影响了溶剂 - 层相互作用。化合物1 - 12根据镧系元素(III)与Box发光体之间的相互作用呈现出多样的发射。对于2 - 5、9和12,配体到金属的能量转移诱导的可见f中心发射,从基于钬(III)的9的绿色,基于钐(III)的4的橙色,到分别基于镨(III)和铕(III)的2和5的红色。在2 - 4、9和12中发现了近红外发射。基于钆(III)的6检测到Box的红色磷光,而基于铽(III)的7发现了配体或镧系元素(III)激发态的选择性激发导致的可切换红色到绿色发射。这些材料显示出镧系元素(III) - 钼(V)磁耦合,分别导致4和7在2.0和2.2 K以下呈现铁磁性。在6和8中发现了低温下的磁有序开始。化合物1 - 12形成了一类独特的氰基桥连材料家族,具有双功能磁光特性并结合了动态结构特征。

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