Journal
JOURNAL OF PHYSICAL CHEMISTRY C
Volume 120, Issue 14, Pages 7757-7766Publisher
AMER CHEMICAL SOC
DOI: 10.1021/acs.jpcc.6b01118
Keywords
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Funding
- NSFC
- PCSIRT [IRT1205]
- Beijing Engineering Center for Hierarchical Catalysts
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Integrating polyoxometalates into porphyrin moieties via covalent bond is expected to be a new approach to tune and enhance the nonlinear optical responses of porphyrins. The effectiveness and efficiency of this proposal has been examined and witnessed by studying two new hybrid compounds as a prototype, namely, (Bu4N)(4)K-2[{C52H32N5O2Zn}HNC(CH2O)(3)P2V3W15O59]center dot 2(C4H9NO) (1) and (Bu4N)(4)K-2 [{C52H34N5O2}HNC (CH2O)(3)P2V3W15O59]center dot 3(C4H9NO] (2) in which porphyrins acting as electron donor and Dawson type polyoxometalate acting as electron acceptor are connected via short tether through covalent bond. The new compounds are systematically characterized by means of elemental analyses, FT-IR, H-1 NMR, ESI-MS, TG/DTA, UV-vis, fluorescence emission spectra, and cyclic voltammetry measurement. Remarkably, great enhancement in reverse saturation absorption is achieved in 1 and 2 which is ca. 1 order of magnitude greater than their individual reactants. Additionally, optical-limiting thresholds are obtained being 0.484 J/cm(2) for 1 and 0.501 J/cm(2) for 2, respectively, implying their high potential as low-power optical-limiting materials.
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