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woshibadchen金虫 (正式写手)
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[求助]
50金币求英译汉 有机二极管专业
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The synthesis and structural, photophysical, electrochemical, and electroluminescent properties of a class of platinum(II) complexes bearing ó-alkynyl ancillary ligands, namely [(C^N^N)Pt(C≡C)nR] [H(C^N^N)═ 6-aryl-2,2′-bipyridine; n= 1- 4; R= aryl, alkyl, or trimethylsilyl], have been studied. Substituents with different steric and electronic properties were introduced into the tridentate cyclometalating and arylacetylide ligands, and the π-conjugation length of the oligoynyl moiety was homologously extended from ethynyl to octatetraynyl. The X-ray crystal structures of several derivatives confirm the Pt (C≡C) ligation and reveal various intermolecular interactions, such as π-π,Pt… Pt, and C- H …F- C. The complexes display good thermal stability and intense phosphorescence in fluid and glassy solutions with high quantum yields and microsecond lifetimes. Their emission energies are sensitive to solvent polarity, the electronic affinities of the substituents on both the cyclometalating and arylacetylide groups, and the length of the oligoynyl ligand. By choosing appropriate cyclometalating and ó-alkynyl ligands, the emission color of this class of platinum(II) complexes can be tuned from green-yellow to saturated red. In addition to 3MLCT [Pt(5d)→π*(C^N^N)] and 3IL(C^N^N), intriguing 3IL(alkynyl) excited states localized on -(C≡C)4 and (C≡Cpyrenyl-1) moieties that afford narrow-bandwidth emissions have been observed. Selected Pt(II) complexes were doped into the emissive region of multilayer, vapor-deposited organic light-emitting diodes. The tunable electrophosphorescence energy resembles that recorded in fluid solutions for these emitters, and the devices exhibit high luminance and efficiencies (up to 4.2 cd A- 1). 谢绝软件翻译，谢谢 [ Last edited by woshibadchen on 2011-6-27 at 08:44 ] |
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liubencai
木虫之王 (文坛精英)
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5楼2011-06-27 09:42:56
liubencai
木虫之王 (文坛精英)
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2楼2011-06-27 09:08:43
liubencai
木虫之王 (文坛精英)
- 翻译EPI: 37
- 应助: 84 (初中生)
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- 金币: 100902
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- 注册: 2006-08-20
- 性别: GG
- 专业: 配位化学
4楼2011-06-27 09:27:43