Morimoto Masakazu, Miyasaka Hitoshi, Yamashita Masahiro, Irie Masahiro
Department of Chemistry, Graduate School of Science, Tohoku University, 6-3 Aramaki-Aza-Aoba, Aoba-ku, Sendai 980-8578, Japan.
J Am Chem Soc. 2009 Jul 22;131(28):9823-35. doi: 10.1021/ja903366d.
To achieve reversible photoswitching of the magnetic properties of single-molecule magnets (SMMs), coordination assemblies of a mixed valence tetranuclear [Mn(II)(2)Mn(III)(2)] complex linked by open- and closed-ring isomers of a photochromic diarylethene ligand were synthesized: [Mn(4)(hmp)(6)(dae-o)(2)(ClO(4))(2)] x 6 H(2)O (open-ring form; 1o) and Mn(4)(hmp)(6)(dae-c)(2)(H(2)O)(2)(2) x CH(3)CN x 4 H(2)O (closed-ring form; 1c), where Hhmp is 2-hydroxymethylpyridine, and H(2)dae-o and H(2)dae-c are open- and closed-ring isomers of 1,2-bis(5-carboxyl-2-methyl-3-thienyl)perfluorocyclopentene (H(2)dae), respectively. From X-ray crystallographic analyses, 1o and 1c have one-dimensional (1-D) chain structures with a repeating unit of [-{Mn(4)}-(dae)-], in which the [Mn(4)] units are bridged by the diarylethene ligands coordinated to the Mn(II) sites via carboxylate groups. Magnetic measurements involving direct-current (dc) and alternating-current (ac) techniques showed that each [Mn(4)] cluster in the 1-D chains had an S(T) = 9 ground state due to two kinds of intracluster ferromagnetic exchange interactions and behaved as SMMs. Both 1o and 1c underwent photochromic reactions in the crystalline phase, and their colors reversibly changed between reddish-brown and blue upon irradiation with ultraviolet (UV) and visible light. For 1o, no significant change in the magnetic properties was observed after the photocyclization of the dae-o moiety by UV irradiation. In contrast, the photocycloreversion of the dae-c moiety by visible irradiation enhanced inter-[Mn(4)] unit interactions in 1c, which was triggered by the geometrical change in the diarylethene moiety during the photoreaction and the subsequent change in the inter-[Mn(4)] arrangement between the neighboring 1-D chains. This work illustrates the usefulness of photochromic molecules for photoswitching the magnetic behavior of complexes, even superparamagnetic systems, with SMM units.
为实现单分子磁体(SMMs)磁性的可逆光开关,合成了由光致变色二芳基乙烯配体的开环和闭环异构体连接的混合价四核[Mn(II)₂Mn(III)₂]配合物的配位组装体:[Mn₄(hmp)₆(dae-o)₂(ClO₄)₂]·6H₂O(开环形式;1o)和Mn₄(hmp)₆(dae-c)₂(H₂O)₂₂·CH₃CN·4H₂O(闭环形式;1c),其中Hhmp为2-羟甲基吡啶,H₂dae-o和H₂dae-c分别为1,2-双(5-羧基-2-甲基-3-噻吩基)全氟环戊烯(H₂dae)的开环和闭环异构体。通过X射线晶体学分析,1o和1c具有一维(1-D)链状结构,其重复单元为[-{Mn₄}-(dae)-],其中[Mn₄]单元由通过羧酸根基团与Mn(II)位点配位的二芳基乙烯配体桥连。涉及直流(dc)和交流(ac)技术的磁性测量表明,由于两种簇内铁磁交换相互作用,1-D链中的每个[Mn₄]簇具有S(T)=9的基态,并表现为SMMs。1o和1c在结晶相中均发生光致变色反应,在用紫外光(UV)和可见光照射时,它们的颜色在红棕色和蓝色之间可逆变化。对于1o,在用UV照射使dae-o部分发生光环化后,未观察到磁性有明显变化。相反,通过可见光照射使dae-c部分发生光环化反转增强了1c中[Mn₄]单元间的相互作用,这是由光反应过程中二芳基乙烯部分的几何变化以及相邻1-D链之间[Mn₄]排列的随后变化引发的。这项工作说明了光致变色分子对于光开关具有SMM单元的配合物甚至超顺磁体系的磁行为的有用性。