Luminescence that lasts from Pt(trpy)Cl+ derivatives (trpy=2,2′;6′,2″-terpyridine)
Luminescence that lasts from Pt(trpy)Cl+ derivatives (trpy=2,2′;6′,2″-terpyridine)
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DOI:
10.1016/s0010-8545(02)00041-3
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发表时间:
2002-07
影响因子:
20.6
通讯作者:
D. McMillin;Jeffrey J. Moore
中科院分区:
文献类型:
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作者:
D. McMillin;Jeffrey J. Moore
This report outlines progress to date in preparing Pt(trpy)Cl+derivatives that exhibit long-lived photoluminescence in solution (trpy=2,2′;6′,2″-terpyridine). The trpy complex itself is a versatile binding agent/reporter probe for biological macromolecules but is non-emissive, except in solids or low-temperature glasses. Derivatives investigated are of the type Pt(4′-R-T)Y+, where 4′-R-T denotes a 4′-substituted form of the trpy ligand and Y is a pseudohalide co-ligand. Simple halide replacement yields the Pt(trpy)OH+derivative which has facilitated luminescence-based DNA-binding studies. Other complexes with long-lived excited states in fluid solution include Pt(4′-NMe2-T)Cl+and Pt(4′-Pyre1-T)Cl+, where Pyre1 designates a 1-pyrenyl substituent. Due to intra-ligand charge-transfer character, Pt(4′-NMe2-T)Cl+and Pt(4′-Pyre1-T)Cl+each exhibit relatively low energy absorption maxima. Open coordination sites support quenching by Lewis bases, however, the effect is less evident with increased intra-ligand orbital parentage in the excited state.