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具有环金属配体的过渡金属荧光粉:基础与应用。

Transition-metal phosphors with cyclometalating ligands: fundamentals and applications.

机构信息

Department of Chemistry, National Tsing Hua University, Hsinchu 30013, Taiwan.

出版信息

Chem Soc Rev. 2010 Feb;39(2):638-55. doi: 10.1039/b916237b. Epub 2009 Dec 7.

Abstract

One goal of this critical review is to provide advanced methodologies for systematic preparation of transition-metal based phosphors that show latent applications in the field of organic light emitting diodes (OLEDs). We are therefore reviewing various types of cyclometalating chelates for which the favorable metal-chelate bonding interaction, on the one hand, makes the resulting phosphorescent complexes highly emissive in both fluid and solid states at room temperature. On the other hand, fine adjustment of ligand-centered pi-pi* electronic transitions allows tuning of emission wavelength across the whole visible spectrum. The cyclometalating chelates are then classified according to types of cyclometalating groups, i.e. either aromatic C-H or azolic N-H fragment, and the adjacent donor fragment involved in the formation of metallacycles; the latter is an N-containing heterocycle, N-heterocyclic (NHC) carbene fragment or even diphenylphosphino group. These cyclometalating ligands are capable to react with heavy transition-metal elements, namely: Ru(II), Os(II), Ir(III) and Pt(II), to afford a variety of highly emissive phosphors, for which the photophysical properties as a function of chelate or metal characteristics are systematically discussed. Using Ir(III) complexes as examples, the C--N chelates possessing both C-H site and N-heterocyclic donor group are essential for obtaining phosphors with emission ranging from sky-blue to saturated red, while the N--N chelates such as 2-pyridyl-C-linked azolates are found useful for serving as true-blue chromophores due to their increased ligand-centered pi-pi* energy gap. Lastly, the remaining NHC carbene and benzyl phosphine chelates are highly desirable to serve as ancillary chelates in localizing the electronic transition between the metal and remaining lower energy chromophoric chelates. As for the potential opto-electronic applications, many of them exhibit remarkable performance data, which are convincing to pave a broad avenue for further development of all types of phosphorescent displays and illumination devices (94 references).

摘要

本次综述的一个目标是提供用于制备过渡金属基荧光粉的先进方法,这些荧光粉在有机发光二极管(OLED)领域具有潜在应用。因此,我们正在回顾各种类型的环金属螯合物,一方面,这些螯合物有利于金属-螯合物键合相互作用,使得所得磷光配合物在室温下在液体和固体状态下都具有高度发光性。另一方面,配体中心的π-π电子跃迁的精细调整允许在整个可见光谱范围内调谐发射波长。然后根据环金属螯合基团的类型,将环金属螯合物分类,即芳族 C-H 或唑啉 N-H 片段,以及形成金属环的相邻供体片段;后者是含 N 的杂环、N-杂环(NHC)碳烯片段甚至二苯基膦基团。这些环金属螯合配体能够与重过渡金属元素反应,即:Ru(II)、Os(II)、Ir(III)和 Pt(II),以提供各种高度发光的荧光粉,系统地讨论了这些荧光粉的光物理性质作为螯合物或金属特性的函数。以 Ir(III) 配合物为例,具有 C-H 位点和 N-杂环供体基团的 C-N 螯合物对于获得发射范围从天蓝色到饱和红色的磷光粉是必不可少的,而 N-N 螯合物,如 2-吡啶-C 连接的唑啉,则由于其增加的配体中心π-π能量间隙,被发现对于作为真正的蓝色发色团很有用。最后,剩余的 NHC 碳烯和苄基膦螯合物非常适合作为辅助螯合物,用于定位金属和剩余的低能量发色团螯合物之间的电子跃迁。对于潜在的光电应用,其中许多都表现出显著的性能数据,这令人信服地为进一步开发各种类型的磷光显示器和照明设备铺平了广阔的道路(94 篇参考文献)。

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