2016
DOI: 10.1039/c5nj02874d
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Design, synthesis, linear and nonlinear photophysical properties of novel pyrimidine-based imidazole derivatives

Abstract: Novel pyrimidine imidazole derivatives with flexible ether chains have been synthesised and evaluated for their cell imaging performanceviaphotophysical investigations and theoretical calculations.

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Cited by 35 publications
(20 citation statements)
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“…On the other hand, comparison of the 2PA properties reveals the relative efficiency of the cores. The values of Fs for 6P are smaller than L1, 16 understandably due to the acceptors linked to the cores. Fs decreases by ten times when the core is changed from imidazolyl to imidazolyl-hexauorophosphate.…”
Section: Two-photon Excited Uorescence (2pef)mentioning
confidence: 87%
See 3 more Smart Citations
“…On the other hand, comparison of the 2PA properties reveals the relative efficiency of the cores. The values of Fs for 6P are smaller than L1, 16 understandably due to the acceptors linked to the cores. Fs decreases by ten times when the core is changed from imidazolyl to imidazolyl-hexauorophosphate.…”
Section: Two-photon Excited Uorescence (2pef)mentioning
confidence: 87%
“…Clearly, the polarity of the solvent and the excitation wavelength has a signicant inuence on the action two-photon absorption cross section. Compared to the previous chromophores derived from pyrimidine, 15,16,24,25 small changes in the structure may have important implications in terms of molecular engineering for specic applications because the 2PA properties (in terms of cross sections, position of the maximum, and bandwidth), as well as the one photon and the photoluminescence characteristics can be affected considerably. Increasing the branch number results in a pronounced enhancement of the 2PA cross sections in the NIR region, which may imply that extending the p-conjugation domain is accomplished by increasing the number of branches.…”
Section: Two-photon Excited Uorescence (2pef)mentioning
confidence: 99%
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“…Organic molecules with donor‐acceptor (D–A) architect find uses in the area of organic solar cells (OSCs), organic light‐emitting diodes (OLEDs), organic photovoltaics (OPVs), organic thin‐film transistors (OTFTs), two‐photon absorption (2PA), photodynamic therapy, ion‐sensing, cell imaging, fluorescent molecular rotors (FMR's) and non‐linear optical (NLO) materials . Efforts are made to diversify the D–A materials by designing and synthesizing a wide spectrum of dipolar, quadrupolar, octupolar and multi‐branched chromophores .…”
Section: Introductionmentioning
confidence: 99%