Amine-Responsive Adaptable Nanospaces: Fluorescent Porous Coordination Polymer for Molecular Recognition

被引:195
作者
Haldar, Ritesh [1 ]
Matsuda, Ryotaro [2 ]
Kitagawa, Susumu [2 ,3 ]
George, Subi J. [1 ]
Maji, Tapas Kumar [1 ,4 ]
机构
[1] Jawaharlal Nehru Ctr Adv Sci Res, New Chem Unit, Bangalore 560064, Karnataka, India
[2] Kyoto Univ, Inst Integrated Cell Mat Sci, Sakyo Ku, Kyoto 6068501, Japan
[3] Kyoto Univ, Dept Synthet Chem & Biol Chem, Grad Sch Engn, Kyoto 6158510, Japan
[4] Jawaharlal Nehru Ctr Adv Sci Res, Chem & Phys Mat Unit, Bangalore 560064, Karnataka, India
关键词
charge transfer; energy transfer; molecular recognition; supramolecular encapsulation; X-ray diffraction; METAL-ORGANIC FRAMEWORKS; SELECTIVE CO2 CAPTURE; CHARGE-TRANSFER; ENERGY-TRANSFER; MICROPOROUS METAL; ADSORPTION; SEPARATION; TRANSFORMATION; LUMINESCENCE; ELECTRON;
D O I
10.1002/anie.201405619
中图分类号
O6 [化学];
学科分类号
0703 ;
摘要
Flexible and dynamic porous coordination polymers (PCPs) with well-defined nanospaces composed of chromophoric organic linkers provide a scaffold for encapsulation of versatile guest molecules through noncovalent interactions. PCPs thus provide a potential platform for molecular recognition. Herein, we report a flexible 3D supramolecular framework {[Zn(ndc)(o-phen)]center dot DMF}(n) (o-phen= 1,10-phenanthroline, ndc=2,6-napthalenedicarboxylate) with confined nanospaces that can accommodate different electron-donating aromatic amine guests with selective turn-on emission signaling. This system serves as a molecular recognition platform through an emission-readout process. Such unprecedented tunable emission with different amines is attributed to its emissive charge-transfer (CT) complexation with o-phen linkers. In certain cases this CT emission is further amplified by energy transfer from the chromophoric linker unit ndc, as evidenced by single-crystal X-ray structural characterization.
引用
收藏
页码:11772 / 11777
页数:6
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