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多官能基二噻二唑基自由基:并 1' 吡咯基二噻二唑基中的荧光、电致发光和光电导性能。

Multifunctional Dithiadiazolyl Radicals: Fluorescence, Electroluminescence, and Photoconducting Behavior in Pyren-1'-yl-dithiadiazolyl.

机构信息

Department of Chemistry & Biochemistry , University of Windsor , 401 Sunset Avenue , Windsor , ON N9B 3P4 , Canada.

Department of Electrical & Computer Engineering, Waterloo Institute of Nanotechnology , University of Waterloo , 200 University Avenue West , Waterloo , ON N2L 3G1 , Canada.

出版信息

J Am Chem Soc. 2018 May 23;140(20):6260-6270. doi: 10.1021/jacs.7b12592. Epub 2018 May 8.

Abstract

The pyren-1'-yl-functionalized dithiadiazolyl (DTDA) radical, CHCNSSN (1), is monomeric in solution and exhibits fluorescence in the deep-blue region of the visible spectrum (440 nm) upon excitation at 241 nm. The salt [1][GaCl] exhibits similar emission, reflecting the largely spectator nature of the radical in the fluorescence process, although the presence of the radical leads to a modest quenching of emission (Φ = 98% for 1 and 50% for 1) through enhancement of non-radiative decay processes. Time-dependent density functional theory studies on 1 coupled with the similar emission profiles of both 1 and 1 are consistent with the initial excitation being of predominantly pyrene π-π* character. Spectroscopic studies indicate stabilization of the excited state in polar media, with the fluorescence lifetime for 1 (τ = 5 ns) indicative of a short-lived excited state. Comparative studies between the energies of the frontier orbitals of pyren-1'-yl nitronyl nitroxide (2, which is not fluorescent) and 1 reveal that the energy mismatch and poor spatial overlap between the DTDA radical SOMO and the pyrene π manifold in 1 efficiently inhibit the non-radiative electron-electron exchange relaxation pathway previously described for 2. Solid-state films of both 1 and [1][GaCl] exhibit broad emission bands at 509 and 545 nm, respectively. Incorporation of 1 within a host matrix for OLED fabrication revealed electroluminescence, with CIE coordinates of (0.205, 0.280) corresponding to a sky-blue emission. The brightness of the device reached 1934 cd/m at an applied voltage of 16 V. The crystal structure of 1 reveals a distorted π-stacked motif with almost regular distances between the pyrene rings but alternating long-short contacts between DTDA radicals. Solid state measurements on a thin film of 1 reveal emission occurs at shorter wavelengths (375 nm) whereas conductivity measurements on a single crystal of 1 show a photoconducting response at longer wavelength excitation (455 nm).

摘要

吡喃-1'-基二噻二唑基(DTDA)自由基 CHCNSSN(1)在溶液中为单体,在 241nm 激发下于可见光谱的深蓝色区域(440nm)显示荧光。盐 [1][GaCl] 表现出相似的发射,反映了荧光过程中自由基的主要旁观者性质,尽管自由基的存在通过增强非辐射衰减过程导致发射适度猝灭(1 的Φ=98%,1 的Φ=50%)。对 1 的时间相关密度泛函理论研究以及 1 和 1 的相似发射谱一致表明,初始激发主要是芘的 π-π*特征。光谱研究表明,在极性介质中稳定激发态,1 的荧光寿命(τ=5ns)表明激发态寿命短。对吡喃-1'-基硝酮氮氧化物(2,不发荧光)和 1 的前线轨道能量的比较研究表明,DTDA 自由基 SOMO 与 1 中芘 π 丛之间的能量不匹配和空间重叠不良有效地抑制了先前描述的 2 的非辐射电子-电子交换弛豫途径。1 和 [1][GaCl] 的固态薄膜分别在 509nm 和 545nm 处显示出宽发射带。将 1 掺入用于 OLED 制造的主体基质中,显示出电致发光,CIE 坐标为(0.205,0.280),对应于天蓝色发射。在 16V 的应用电压下,器件的亮度达到 1934cd/m。1 的晶体结构显示出扭曲的π堆积基序,芘环之间的距离几乎规则,但 DTDA 自由基之间存在交替的长-短接触。1 的薄膜的固态测量显示发射发生在较短的波长(375nm),而 1 的单晶的电导率测量显示在较长波长激发(455nm)下显示出光电导响应。

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