Institute for Materials Research, Tohoku University, 2-1-1 Katahira, Aoba-ku, Sendai 980-8577, Japan.
Dalton Trans. 2018 Aug 29;47(34):11760-11768. doi: 10.1039/c8dt01566j.
A donor (D)/acceptor (A) assembly reaction using the paddlewheel-type diruthenium(ii,ii) complex [Ru2(3,5-F2PhCO2)4(THF)2] (3,5-F2PhCO2- = 3,5-difluorobenzoate; abbreviated hereafter as [Ru2]) as D and 7,7,8,8-tetracyano-p-quinodimethane derivatives (TCNQRx; 2,5-R-substituted TCNQ) as A in a DCM/TCE or DCE solvent system (DCM = dichloromethane, TCE = 1,1,2,2-tetrachloroethane, DCE = 1,2-dichloroethane) led to the formation of D2A-type two-dimensional layered compounds [{Ru2(3,5-F2PhCO2)4}2{TCNQRx}]·nsolv (Rx = H2 (1), Rx = Me2, (2), and Rx = (OEt)2 (3)). All the compounds had similar two-dimensional fishnet-type structures, where the two [Ru2] units were fully coordinated with the four cyano groups of TCNQRx. The compounds 1-3 were categorized as a one-electron transferred ionic state (1e-I) with D+-A--D formulation (D+[triple bond, length as m-dash][RuII,III2]+; A-[triple bond, length as m-dash]TCNQRx˙-). This subunit state formally derived a ferrimagnetically ordered state composed of up-spins with S = 1 for [RuII,II2] and S = 3/2 for [RuII,III2]+ and a down-spin of S = 1/2 for TCNQRx˙-, with antiferromagnetic superexchange interactions in each layer. Eventually, 1-3 became three-dimensional ferrimagnets with Curie temperatures TC = 93, 93, and 92 K, respectively, owing to the presence of interlayer ferromagnetic interactions. The interlayer translational distances (l2) for the three compounds were 10.56, 10.54, and 10.84 Å, respectively, which agreed with the empirical prediction based on the threshold value of l2 > 10.3 Å for a valid ferromagnetic interaction.
使用桨轮型双钌(II,II)配合物[Ru2(3,5-F2PhCO2)4(THF)2](3,5-F2PhCO2-=3,5-二氟苯甲酸根;简称[Ru2])作为 D 和 7,7,8,8-四氰基对醌二甲烷衍生物(TCNQRx;2,5-R-取代 TCNQ)作为 A 在 DCM/TCE 或 DCE 溶剂体系(DCM=二氯甲烷,TCE=1,1,2,2-四氯乙烷,DCE=1,2-二氯乙烷)中进行施主(D)/受主(A)组装反应,得到 D2A 型二维层状化合物 [{Ru2(3,5-F2PhCO2)4}2{TCNQRx}]·nsolv(Rx=H2(1),Rx=Me2(2),和 Rx=(OEt)2(3))。所有化合物都具有相似的二维鱼网型结构,其中两个[Ru2]单元完全与 TCNQRx 的四个氰基配位。化合物 1-3 被归类为单电子转移离子态(1e-I),具有 D+-A--D 配方(D+[三键,长度为破折号][RuII,III2]+;A-[三键,长度为破折号]TCNQRx˙-)。这种亚基态形式上产生了由[RuII,II2]的上自旋 S = 1 和[RuII,III2]+的上自旋 S = 3/2 以及 TCNQRx˙-的下自旋 S = 1/2 组成的亚铁磁有序态,每个层中存在反铁磁超交换相互作用。最终,由于层间铁磁相互作用的存在,1-3 分别成为具有居里温度 TC = 93、93 和 92 K 的三维亚铁磁体。三种化合物的层间平移距离(l2)分别为 10.56、10.54 和 10.84 Å,这与基于 l2>10.3 Å 的有效铁磁相互作用的阈值的经验预测一致。