我們藉由合環反應合成了含不同氮數的芳香雜環,並搭配上含未共軛之輔助 配位基合成了一系列的鉑二價錯合物,並且利用輔助配位基磷原子上的苯環來提 供立體障礙,使得這一系列化合物都沒有Pt-Pt作用力的存在。這一系列的化合 物除了dfPPyPtP^O在室溫溶液下可放出極弱的磷光外,其他的在溶液下均不放 光。其放光波段隨著含氮雜環上的氮數增加有藍位移(blue shift)的趨勢;從465 nm到474 nm,但是因為其半高寬太寬(50~75 nm),而使得放出之光色為藍綠光。 以dfppyPtP^O以及TriazoPyPtP^O這兩個化合物當作磷光摻雜物分別做了元件A 以及元件B,以下是所做出來的元件結果: 元件A:NPB(30 nm)/mCP:dfPPyPtPO(10%,30 nm)/BCP(10 nm)/Alq(30 nm)/LiF/Al ,元件外部量子效率(ηext)為2.13 %,電流效率(ηc)為5.84 cd/A,最大亮度(Lmax) 為6596 cd/m2,CIE座標為(0.17,0.45)。 元件B: NPB(30 nm)/mCP:TriazoPyPtP^O(10%,30 nm)/BCP(10 nm)/Alq(30 nm)/LiF/Al,元件外部量子效率(ηext)為2.17 %,電流效率(ηc)為6.10 cd/A, 最大亮度(Lmax)為4951 cd/m2,CIE座標為(0.21,0.49)。
We used cyclolization to synthesize heteroaromatics that contain different numbers of N to combine with non-conjugated ancillary ligand to synthesize a series of Pt(II) complex. The phenyl group on the P atom of ancillary ligand created steric hindrance which inhibits the Pt-Pt interaction in this series of compound. This series of compound did not emit phosphoresence in solvents besides compound dfppyPtP^O; yet, its emittance was rather weak. As the number of N in the heteroaromatics increased the emitting λmax blue shifted from 465 nm to 474 nm. However, the width of the full-width-half-maximum (FWHM) was too wide which resulted in the emittance of blue-green light. We take dfPPyPtP^O and TriazoPyPtP^O as dophants to construct devices A and B, and the followings are the results. Device A: NPB(30 nm)/mCP:dfPPyPtPO(10%,30 nm)/BCP(10 nm)/Alq(30 nm)/LiF/Al; this device can achieve an external quantum efficiency(ηext) of 2.13%, current efficiency(ηc) of 5.84 cd/A, maximum brightness(Lmax) of 6596 cd/m2, and CIE coordinates of (0.17,0.45). Device B: NPB(30 nm)/mCP:TriazoPyPtP^O(10%,30 nm)/BCP(10 nm)/Alq(30 nm)/LiF/Al; this device can achieve an external quantum efficiency(ηext) of 2.17%, current efficiency(ηc) of 6.10 cd/A, maximum brightness(Lmax) of 4951 cd/m2, and CIE coordinates of(0.21,0.49).