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1. 南京师范大学化学系, 江苏, 南京, 210097
2. 江苏省重点光电技术实验室, 江苏, 南京, 210097
收稿日期:2003-04-28,
修回日期:2003-06-05,
纸质出版日期:2004-07-20
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王崇侠, 余忠清, 李邨, 王炳祥, 黄晓华. 二(2-苯基-8-羟基喹啉)锌和喹啉锌的合成和荧光性质[J]. 发光学报, 2004,25(4): 414-418
WANG Chong-xia, YU Zhong-qing, LI Chun, WANG Bing-xiang, HUANG Xiao-hua. Synthesis and Fluorescence Properties of Bis(2-phenyl-8-hydroxyquinolato)zinc and Bis(8-hydroxyquinolato)zinc[J]. Chinese Journal of Luminescence, 2004,25(4): 414-418
王崇侠, 余忠清, 李邨, 王炳祥, 黄晓华. 二(2-苯基-8-羟基喹啉)锌和喹啉锌的合成和荧光性质[J]. 发光学报, 2004,25(4): 414-418 DOI:
WANG Chong-xia, YU Zhong-qing, LI Chun, WANG Bing-xiang, HUANG Xiao-hua. Synthesis and Fluorescence Properties of Bis(2-phenyl-8-hydroxyquinolato)zinc and Bis(8-hydroxyquinolato)zinc[J]. Chinese Journal of Luminescence, 2004,25(4): 414-418 DOI:
合成了一种新型二(2-苯基8-羟基喹啉)锌配合物。利用元素分析、红外吸收光谱等方法表征了结构
并对比研究了二(2-苯基8-羟基喹啉)锌和喹啉锌的荧光性质
前者的激发光谱在465nm处出现了较强的吸收
并且发射峰位置发生了明显的红移
由喹啉锌的495nm移至2-苯基8-羟基喹啉锌和喹啉锌的521nm处。对有关的吸收峰的归属进行了讨论
初步认为苯环的取代增加了有机配体π-π键的共轭程度
使HOMO-LUMO之间能隙变小
引起发射峰红移。
Since the first reports of efficient electroluminescence from an organic thin film device using the metal chelate tris(8-hydroxyquinoline)aluminum(Alq
3
) as the emissive layer materials
some efforts have been devoted not only to tailor emission wavelength by a functional group introduced onto the quinolinolato ligand
but also to synthesize the new metal chelating compound.However
there is no report on the relationship between the substituent of phenyl moiety in the 2-position of 8-quinolinol and an emission property.Therefore
a systematic study to clarify a relationship between a molecular structure and emission property is evidently necessary for developing a more useful emissive compound.Bis(2-phenyl-8-hydroxyquinolato)zinc and bis(8-hydroxyquinolato)zinc were synthesized firstly according to the relating reference.The melting point
composition and structure were also determined by a series test methods.The substituent of phenyl group dependence of luminescence band of the 8-quinolinolato anions was systematically investigated with excitation spectra and emission spectra of prepared samples.The luminescence band at 495nm for bis(8-hydroxyquinolato)zinc is presented under 225
283
348
395nm excitations
respectively.The luminescence band at 521nm for bis(2-phenyl-8-hydroxyquinolato)zinc is presented under 225
283
348
395
465nm excitation
respectively
which showed to exhibit strong photoluminescence efficiency.It is suggested that the assignment of absorption bands at 225
283
348nm of the above mentioned two samples could be ascribed to the β
ρ and α band of π
→
π
*
transition in the quinolinolato ring.The absorption bands at 395nm existing in the above mentioned two samples have been probably attributed to the charge transfer between the d orbital on zinc ion and vacant π orbital on the ligand.The new absorption band of 465nm presented in bis(2-phenyl-8-hydroxyquinolato)zinc chelate is a new energy level ascribed to the intramolecular charge transfer between the different conjugating π systems existed in the quinolinolato ring and in the substituent of phenyl moiety in the 2-position of 8-quinolinol
which also means that this new chelate exhibits photostimulated luminescence not only with ultraviolet radiation
but also visible light at room temperature.It is suggested that introducing the substituent of phenyl moiety in the 2-position of 8-quinolinol is an effective way for red shifted emission
which changes the energy level of the highest occupied molecular orbital(HOMO) through π orbital interactions.Further
insight into the detailed mechanism of photostimulated luminescence from bis(2-phenyl-8-hydroxyquinolato)zinc chelate requires additional experimental and theoretical studies.Industrially the photostimulated luminescence phenomenon of the detailed mechanism of photostimulated luminescence from bis(2-phenyl-8-hydroxyquinolato)zinc could have use as a new type fluorescent material for optical memories and organic light emission devices.
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