Department of Chemistry, Faculty of Science, Hokkaido University, North-10 West-8, Kita-ku, Sapporo, Hokkaido 060-0810, Japan.
Department of Applied Chemistry for Environment, School of Biological and Environmental Sciences, Kwansei Gakuin University, 1 Gakuen-Uegahara, Sanda, Hyogo 669-1330, Japan.
Dalton Trans. 2023 Jul 4;52(26):8864-8872. doi: 10.1039/d3dt00192j.
Molecular crystals of Pt(II) complexes with metallophilic interactions can provide bright assembly-induced luminescence with colour tunability. However, the brittleness of many of these crystals makes their application in flexible optical materials difficult. Herein, we have achieved the elastic deformation of crystals of polyhalogenated Pt(II) complexes exhibiting bright assembly-induced luminescence. A crystal of [Pt(bpic)(dFppy)] (Hbpic = 5-bromopicolinic acid, HdFppy = 2-(2,4-difluorophenyl)pyridine) and a co-crystal of [Pt(bpic)(dFppy)] and [Pt(bpic)(ppy)] (Hppy = 2-phenylpyridine) were found to exhibit significant elastic deformation due to their highly anisotropic interaction topologies. While the crystal of [Pt(bpic)(dFppy)] exhibited monomer-based ligand-centred ππ* emission with an emission quantum yield of 0.40, the co-crystal exhibited bright, triplet metal-metal-to-ligand charge transfer (MMLCT) emission owing to Pt⋯Pt interactions, thereby achieving a significantly higher emission quantum yield of 0.94.
具有金属键相互作用的 Pt(II) 配合物的分子晶体可以提供具有颜色可调性的明亮组装诱导发光。然而,这些晶体中的许多晶体都很脆,使得它们难以应用于柔性光学材料。在此,我们实现了具有明亮组装诱导发光的多卤化 Pt(II) 配合物晶体的弹性变形。[Pt(bpic)(dFppy)](Hbpic = 5-溴吡啶酸,HdFppy = 2-(2,4-二氟苯基)吡啶)的晶体和[Pt(bpic)(dFppy)]和[Pt(bpic)(ppy)](Hppy = 2-苯基吡啶)的共晶体由于其各向异性的相互作用拓扑结构而表现出显著的弹性变形。虽然[Pt(bpic)(dFppy)]的晶体表现出基于单体的配体中心ππ*发射,发射量子产率为 0.40,但共晶体由于 Pt⋯Pt 相互作用表现出明亮的三重态金属-金属到配体电荷转移(MMLCT)发射,从而实现了显著更高的发射量子产率 0.94。