化学
卡宾
发光
铂金
亚甲基
激发态
配体(生物化学)
晶体结构
结晶学
金属
光化学
立体化学
药物化学
催化作用
有机化学
核物理学
受体
物理
生物化学
光电子学
作者
Yuzhen Zhang,Jai Anand Garg,Clément Michelin,Thomas Fox,Olivier Blacque,Koushik Venkatesan
出处
期刊:Inorganic Chemistry
[American Chemical Society]
日期:2011-01-18
卷期号:50 (4): 1220-1228
被引量:50
摘要
A series of luminescent N-heterocyclic carbene platinum(II) complexes, [(pmim)Pt(C≡C-R)(2)] (R = C(6)H(5) (2), C(6)H(4)OMe (3), C(6)H(2)(OMe)(3) (4), C(6)H(4)NMe(2) (5), C(4)H(3)S (6), C(6)H(4)C≡CC(6)H(5) (7), 1-pyrenyl (8), and C(6)H(4)F (9)), were successfully synthesized using the precursor (pmim)PtI(2), 1 (pmim = 1,1'-dipentyl-3,3'-methylene-diimidazoline-2,2'-diylidene). The X-ray crystal structures of 1, 4, 5, and 7 have been determined. These complexes showed long-lived emission in solution at room temperature. The emission origin of the complexes is tentatively assigned to be from triplet states of predominantly intraligand (IL) character with some mixing of metal-to-ligand charge-transfer (MLCT) character. TD-DFT and DFT calculations have been performed on most of the complexes to ascertain the nature of the excited state. Changes in the alkynyl ligands lead to a change in the absorption and emission maxima seen for these complexes in a potentially predictable way.
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