Novel Molecular Building Blocks Based on the Boradiazaindacene Chromophore: Applications in Fluorescent Metallosupramolecular Coordination Polymers

被引:57
作者
Bozdemir, Oe. Altan [1 ,2 ]
Buyukcakir, Onur [1 ,2 ,3 ]
Akkaya, Engin U. [1 ,2 ]
机构
[1] Bilkent Univ, Dept Chem, TR-06800 Ankara, Turkey
[2] Bilkent Univ, UNAM, Inst Mat Sci & Nanotechnol, TR-06800 Ankara, Turkey
[3] Middle E Tech Univ, Dept Chem, TR-06531 Ankara, Turkey
关键词
coordination polymers; dyes/pigments; polymerization; self-assembly; Sonogashira coupling; RESONANCE ENERGY-TRANSFER; SUPRAMOLECULAR POLYMERS; BODIPY DYES; PHOTODYNAMIC THERAPY; TERPYRIDINE; CHEMISTRY; EFFICIENT; BORON; ION; ARCHITECTURES;
D O I
10.1002/chem.200802538
中图分类号
O6 [化学];
学科分类号
070301 [无机化学];
摘要
We designed and synthesized novel boradiazaindacene (Bodipy) derivatives that are appropriately functionalized for metal-ion-mediated supramolecular polymerization. Thus, ligands for 2-terpyridyl-, 2,6-terpyridyl-. and bipyridyl-functionalized Bodipy dyes were synthesized through Sonogashira couplings. These fluorescent building blocks are responsive to metal ions in a stoichiometry-dependent manner. Octahedral coordinating metal ions such as Zn-II result in polymerization at a stoichiometry corresponding to two terpyridyl ligands to one Zn-II ion. However, at increased metal ion concentrations, the dynamic equilibria are re-established in such a way that the monomeric metal complex dominates. The position of equilibria can easily be monitored by H-1 NMR and fluorescence spectroscopies. As expected, although open-shell Fe-II ions form similar complex structures, these cations quench the fluorescence emission of all four functionalized Bodipy ligands.
引用
收藏
页码:3830 / 3838
页数:9
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