Theiss Tobias, Buss Stefan, Maisuls Iván, López-Arteaga Rafael, Brünink Dana, Kösters Jutta, Hepp Alexander, Doltsinis Nikos L, Weiss Emily A, Strassert Cristian A
Institut für Anorganische und Analytische Chemie, Westfälische Wilhelms-Universität Münster, Corrensstraße 28/30, 48149 Münster, Germany.
CiMIC, SoN, CeNTech, Westfälische Wilhelms-Universität Münster, Heisenbergstraße 11, 48149 Münster, Germany.
J Am Chem Soc. 2023 Feb 13. doi: 10.1021/jacs.2c09775.
The synthesis as well as the structural and photophysical characterization of two isoleptic bis-cyclometalated Pt(II) and Pd(II) complexes, namely [] and [], bearing a tailored dianionic tetradentate ligand () are reported. The isostructural character and intermolecular interactions of [] and [] were assessed by NMR spectroscopy and X-ray diffraction analysis. Both complexes show fully ligand-controlled aggregation, demonstrating that a judicious molecular design can tune the photophysical properties. In fact, by introduction of fluorine atoms on defined positions and methoxy groups on complementary sites, metal-metal interactions can be forced by a head-to-tail stacking. Hence, [] shows luminescence from metal-perturbed ligand-centered or from metal-metal-to-ligand charge-transfer triplet states in diluted solutions, in frozen glasses and in crystals, with high photoluminescence quantum yields and long lifetimes in the microsecond range. At room temperature (RT) in concentrated fluid solutions, the palladium analogue [] surprisingly emits luminescence from aggregated species involving supramolecular interactions. Time-resolved photoluminescence and transient absorption spectroscopies demonstrated that ultrafast intersystem crossing occurs for both metals, which outruns any competitive relaxation pathway from the photoexcited singlet state. Furthermore, we demonstrate that the radiationless deactivation can be suppressed in frozen glassy matrices at 77 K and by intermolecular interactions in fluid solutions at RT. In both cases and as indicated by density functional theory calculations, the lowest emissive state acts as an energy trap from which the thermal population of dissociative states with formal occupation of an antibonding Pd-centered 4d orbital is suppressed. This occurs as the energy gap between the emissive and the dark states surpasses .
报道了两种具有定制双阴离子四齿配体()的同配双环金属化Pt(II)和Pd(II)配合物,即[]和[]的合成以及结构和光物理表征。通过核磁共振光谱和X射线衍射分析评估了[]和[]的同构特征和分子间相互作用。两种配合物均表现出完全由配体控制的聚集,表明合理的分子设计可以调节光物理性质。事实上,通过在特定位置引入氟原子和在互补位点引入甲氧基,可以通过头对头堆积强制形成金属-金属相互作用。因此,[]在稀释溶液、冷冻玻璃和晶体中表现出源于金属扰动的配体中心或金属-金属到配体电荷转移三重态的发光,具有高光致发光量子产率和微秒级的长寿命。在室温(RT)下的浓流体溶液中,钯类似物[]令人惊讶地从涉及超分子相互作用的聚集物种中发射发光。时间分辨光致发光和瞬态吸收光谱表明,两种金属都发生超快系间窜越,这超过了光激发单重态的任何竞争弛豫途径。此外,我们证明在77 K的冷冻玻璃基质中以及在室温下的流体溶液中通过分子间相互作用可以抑制无辐射失活。在这两种情况下,正如密度泛函理论计算所示,最低发射态充当能量陷阱,抑制了具有形式上占据以钯为中心的反键4d轨道的解离态的热布居。当发射态和暗态之间的能隙超过时会发生这种情况。