Baitalik Sujoy, Wang Xian-yong, Schmehl Russell H
Department of Chemistry, Tulane University, New Orleans, Louisiana 70118, USA.
J Am Chem Soc. 2004 Dec 22;126(50):16304-5. doi: 10.1021/ja044561s.
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.
研究了一系列单金属和三金属钌(II)以及混合钌(II)/铁(II)双吡啶配合物的光物理行为。这些配合物具有通过吡啶基上的亚苯基 - 亚乙烯基取代基连接的桥连吡啶基配体。对于由单个亚苯基 - 亚乙烯基桥连的配合物,能量最低的激发态是金属到配体的电荷转移(MLCT),激发态衰减时间在1 - 10纳秒范围内。具有两个亚苯基 - 亚乙烯基基团的配合物具有热平衡的激发态,该激发态定域在亚苯基 - 亚乙烯基桥上,并且具有长得多的寿命(>200纳秒)。值得注意的是,具有铁(II)吡啶基中心的三金属配合物也具有长寿命的激发态,尽管该配合物上存在低能量的铁定域激发态。