2021
DOI: 10.1016/j.cej.2021.128984
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Temperature triggered high-performance carbon dots with robust solvatochromic effect and self-quenching-resistant deep red solid state fluorescence for specific lipid droplet imaging

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Cited by 70 publications
(39 citation statements)
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“…Several CDs have been reported for imaging lipid droplets. [112][113][114][115][116][117][118][119] Gao et al prepared CDs (R-CDs210) with a high PLQY (73% for yellow fluorescence) from thiourea and o-phenylenediamine through a solvothermal method (Figure 3C). [112] In particular, R-CDs210 exhibited deep-red solid-state fluorescence, as the polymer chains on their surface impeded the direct contact between their subfluorophores and carbonized core.…”
Section: Lipid Dropletmentioning
confidence: 99%
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“…Several CDs have been reported for imaging lipid droplets. [112][113][114][115][116][117][118][119] Gao et al prepared CDs (R-CDs210) with a high PLQY (73% for yellow fluorescence) from thiourea and o-phenylenediamine through a solvothermal method (Figure 3C). [112] In particular, R-CDs210 exhibited deep-red solid-state fluorescence, as the polymer chains on their surface impeded the direct contact between their subfluorophores and carbonized core.…”
Section: Lipid Dropletmentioning
confidence: 99%
“…[112][113][114][115][116][117][118][119] Gao et al prepared CDs (R-CDs210) with a high PLQY (73% for yellow fluorescence) from thiourea and o-phenylenediamine through a solvothermal method (Figure 3C). [112] In particular, R-CDs210 exhibited deep-red solid-state fluorescence, as the polymer chains on their surface impeded the direct contact between their subfluorophores and carbonized core. Moreover, R-CDs210 possessed an evident solvatochromic effect with an emission shift (up to %132 nm) from green to far-red region when the solvent polarity was elevated, which was accompanied with the decrease in the PLQY from 73% to 1%.…”
Section: Lipid Dropletmentioning
confidence: 99%
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“…Carbon dots (CDs), a novel type of fluorescent nanomaterial, are being increasingly used in sensing, bioimaging, catalysis, and light-emitting diodes, given their attractive features such as tunable photoluminescence, biocompatibility, readily available raw materials, and simple preparation. Although CDs have been successfully applied to target various organelles, such as the lysosomes, mitochondria, endoplasmic reticulum, and nucleolus, research on LD-targeting CDs is limited. To the best of our knowledge, only two LD-targeting CD reports have been published. , Fan and co-workers reported LD-targeting CDs based on the control of the temperature during synthesis, while Yu and co-workers described a room-temperature oxidative polymerization method. A primary reason for this deficiency is the lack of effective LD-targeting groups that can be readily incorporated in the design of probes, unlike other organelles such as the lysosome (targetable by the morpholine group), mitochondria (high affinity for the triphenylphosphonium group), and the endoplasmic reticulum (sulfonamide group). , In addition, the synthesis of CDs is akin to a “black box” type of reaction, making it challenging to design CDs with the desired optical and binding properties.…”
Section: Introductionmentioning
confidence: 99%
“…To the best of our knowledge, only two LD-targeting CD reports have been published. 28,29 Fan and co-workers reported LD-targeting CDs based on the control of the temperature during synthesis, while Yu and co-workers described a room-temperature oxidative polymerization method. A primary reason for this deficiency is the lack of effective LD-targeting groups that can be readily incorporated in the design of probes, unlike other organelles such as the lysosome (targetable by the morpholine group), mitochondria (high affinity for the triphenylphosphonium group), and the endoplasmic reticulum (sulfonamide group).…”
Section: Introductionmentioning
confidence: 99%