| Literature DB >> 25213865 |
Ritesh Haldar1, Ryotaro Matsuda, Susumu Kitagawa, Subi J George, Tapas Kumar Maji.
Abstract
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)]⋅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.Entities:
Keywords: X-ray diffraction; charge transfer; energy transfer; molecular recognition; supramolecular encapsulation
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Year: 2014 PMID: 25213865 DOI: 10.1002/anie.201405619
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336