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A trimetallic mixed Ru(II)/Fe(II) terpyridyl complex with a long-lived excited state in solution at room temperature
被引:79
作者
:
Baitalik, S
论文数:
0
引用数:
0
h-index:
0
机构:
Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
Baitalik, S
[
1
]
Wang, XY
论文数:
0
引用数:
0
h-index:
0
机构:
Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
Wang, XY
[
1
]
Schmehl, RH
论文数:
0
引用数:
0
h-index:
0
机构:
Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
Schmehl, RH
[
1
]
机构
:
[1]
Tulane Univ, Dept Chem, New Orleans, LA 70118 USA
来源
:
JOURNAL OF THE AMERICAN CHEMICAL SOCIETY
|
2004年
/ 126卷
/ 50期
关键词
:
D O I
:
10.1021/ja044561s
中图分类号
:
O6 [化学];
学科分类号
:
0703 ;
摘要
:
The photophysical behavior of a series of mono- and trimetallic Ru(II) and mixed Ru(II)/Fe(II) bis-terpyridyl complexes was examined. The complexes have bridging terpyridyl ligands linked by phenylene-vinylene substituents on the terpyridyl. For the complexes bridged by a single phenylene-vinylene, the lowest-energy excited state is metal-to-ligand charge transfer (MLCT), and excited-state decay is on the 1-10 ns time scale. The complexes with two phenylene-vinylene groups have thermally equilibrated excited states that are localized on the phenylene-vinylene bridge and have much longer lifetimes (>200 ns). Remarkably, the trimetallic complex having an Fe(II) terpyridyl center also has a long-lived excited state, despite the fact that low-energy iron-localized excited states exist on the complex. Copyright © 2004 American Chemical Society.
引用
收藏
页码:16304 / 16305
页数:2
相关论文
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