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Synthesis and photophysical characterization of luminescent lanthanide complexes of nucleotide-functionalized cyclen-and dipicolinate-based ligands
被引:9
|作者:
Vithanarachchi, Sashiprabha M.
[1
]
Kovacs, Daniel
[1
]
Borbas, K. Eszter
[1
]
机构:
[1] Uppsala Univ, Dept Chem, Angstrom Lab, Lagerhyddsvagen 1, S-75120 Uppsala, Sweden
基金:
瑞典研究理事会;
关键词:
Lanthanide;
Luminescence;
Cyclen;
Dipicolinic acid;
Nucleic acid;
EXCITED-STATES;
NOBEL LECTURE;
DNA;
BINDING;
PROBES;
SENSITIZATION;
IONS;
COORDINATION;
POLYMORPHISM;
PROTECTION;
D O I:
10.1016/j.ica.2016.07.047
中图分类号:
O61 [无机化学];
学科分类号:
070301 ;
081704 ;
摘要:
Luminescent Eu(III)-and Tb(III)-complexes based on functionalized tetraazamacrocycle (cyclen) or dipicolinic acid (dpa) metal binding sites, and carrying 20-or 50-linked uridine moieties were prepared. The light-harvesting antennae were either a coumarin (in the cyclen-based architectures) or the dpa-moiety itself. Antenna excitation resulted in metal-centered emission for all complexes. The presence of the uridine resulted in less intense lanthanide emission compared to non-nucleotide-modified reference compounds. Nd(III)-complexes of cyclen ligands carrying a uridine but without a sensitizing antenna were also synthesized; these are envisioned as energy transfer acceptors to the Eu(III)-complexes. The possibility for Eu-to-Nd energy transfer was probed. The reported complexes are models for oligonucleotide- attached lanthanide probes. (C) 2016 The Author(s). Published by Elsevier B.V.
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页码:148 / 158
页数:11
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