Abstract:Supramolecular host-guest chemistry has provided many opportunities for the design and construction of new fluorescent systems in various applications, particularly in the field of sensing. Owing to the special structure and fascinating utilities, cucurbit[n]urils (CB[n]s) existing themselves as a young family of molecular vessels, it construction a stable host-guest supramolecular complex with a variety of fluorescent dyes and indicators, that has been used as a powerful fluorescent probe and is widely used i… Show more
“…1 (top) The reaction between glycoluril and formaldehyde. (bottom) Space-filling models of CB [5,6,7,8] demonstrating the increasing size yet constant height of the CB[n] macrocycles. Copyright 2015, American Chemical Society.…”
Section: Functionalization and Fabrication Of Gold Nanoparticles And ...mentioning
confidence: 99%
“…2.1.1 In situ synthesis method. In 2007, Corma et al synthesized CB [5,6,7] capped Au NPs with variable sizes from 1.2 to 10 nm for the first time, by adding NaBH 4 to CB [5,6,7] and a HAuCl 4 mixture in water/ethanol solution. 33 Interestingly, CB [7] has a larger cavity with an inner diameter of 0.73 nm, and a small (B0.7 nm) gold nanocluster (Au NC) could be fabricated in situ inside the cavity.…”
Section: Preparation Of Cucurbituril Functionalized Gold Nanoparticlesmentioning
confidence: 99%
“…33 Interestingly, CB [7] has a larger cavity with an inner diameter of 0.73 nm, and a small (B0.7 nm) gold nanocluster (Au NC) could be fabricated in situ inside the cavity. 33 After this pioneering work, Scherman and co-workers reported the preparation of CB [5] capped Au NPs and investigated their dynamic aggregation in water, 10 which started a new era in the synthesis and application of CB[n]-Au NPs.…”
Section: Preparation Of Cucurbituril Functionalized Gold Nanoparticlesmentioning
confidence: 99%
“…28 Notably, this process eliminates the need for traditional reductants or external energy sources, in which CB [7] plays a dual role of both the reductant and stabilizer. Moreover, our group extended this green in situ synthesis method to produce CB [5,6,7,8] functionalized Au NPs. 42 The diameter of the prepared particle was strongly dependent on the ring sizes of CB[n]s, which increased from 4.6 nm to 15.5 nm with increasing portal diameters of CB[n], resulting in decreased catalytic activity for 4-nitrophenol (4-NP) reduction (Fig.…”
Section: Preparation Of Cucurbituril Functionalized Gold Nanoparticlesmentioning
confidence: 99%
“…2,3 In recent years, robust CB[n]-based sensing platforms at different scales, ranging from biomacromolecular (such as, protein or DNA) assemblies to one or a few small molecules, have been developed. [4][5][6][7] Although lots of CB[n] based sensors have been developed, most of them are performed using an associative binding assay (ABA) or indicator displacement assay (IDA) with the known limitations of low signal-to-noise ratios and sensitivity. 8 Direct signal generation is highly desirable for inherently a The State Key Laboratory of Refractories and Metallurgy, Coal Conversion and…”
Cucurbit[n]urils (CB[n]s, n=5–8, 10, and 14), one of the synthetic macrocycles with unique host-guest properties, have triggered increasing research interest in recent years. Gold nanoparticles (Au NPs) and electrodes stand...
“…1 (top) The reaction between glycoluril and formaldehyde. (bottom) Space-filling models of CB [5,6,7,8] demonstrating the increasing size yet constant height of the CB[n] macrocycles. Copyright 2015, American Chemical Society.…”
Section: Functionalization and Fabrication Of Gold Nanoparticles And ...mentioning
confidence: 99%
“…2.1.1 In situ synthesis method. In 2007, Corma et al synthesized CB [5,6,7] capped Au NPs with variable sizes from 1.2 to 10 nm for the first time, by adding NaBH 4 to CB [5,6,7] and a HAuCl 4 mixture in water/ethanol solution. 33 Interestingly, CB [7] has a larger cavity with an inner diameter of 0.73 nm, and a small (B0.7 nm) gold nanocluster (Au NC) could be fabricated in situ inside the cavity.…”
Section: Preparation Of Cucurbituril Functionalized Gold Nanoparticlesmentioning
confidence: 99%
“…33 Interestingly, CB [7] has a larger cavity with an inner diameter of 0.73 nm, and a small (B0.7 nm) gold nanocluster (Au NC) could be fabricated in situ inside the cavity. 33 After this pioneering work, Scherman and co-workers reported the preparation of CB [5] capped Au NPs and investigated their dynamic aggregation in water, 10 which started a new era in the synthesis and application of CB[n]-Au NPs.…”
Section: Preparation Of Cucurbituril Functionalized Gold Nanoparticlesmentioning
confidence: 99%
“…28 Notably, this process eliminates the need for traditional reductants or external energy sources, in which CB [7] plays a dual role of both the reductant and stabilizer. Moreover, our group extended this green in situ synthesis method to produce CB [5,6,7,8] functionalized Au NPs. 42 The diameter of the prepared particle was strongly dependent on the ring sizes of CB[n]s, which increased from 4.6 nm to 15.5 nm with increasing portal diameters of CB[n], resulting in decreased catalytic activity for 4-nitrophenol (4-NP) reduction (Fig.…”
Section: Preparation Of Cucurbituril Functionalized Gold Nanoparticlesmentioning
confidence: 99%
“…2,3 In recent years, robust CB[n]-based sensing platforms at different scales, ranging from biomacromolecular (such as, protein or DNA) assemblies to one or a few small molecules, have been developed. [4][5][6][7] Although lots of CB[n] based sensors have been developed, most of them are performed using an associative binding assay (ABA) or indicator displacement assay (IDA) with the known limitations of low signal-to-noise ratios and sensitivity. 8 Direct signal generation is highly desirable for inherently a The State Key Laboratory of Refractories and Metallurgy, Coal Conversion and…”
Cucurbit[n]urils (CB[n]s, n=5–8, 10, and 14), one of the synthetic macrocycles with unique host-guest properties, have triggered increasing research interest in recent years. Gold nanoparticles (Au NPs) and electrodes stand...
The constant need for high‐performance aniline‐ or phenol‐based fluorophores suitable for the construction of activity‐based fluorescent probes, led us to study both synthesis and photophysics of C3‐N‐methylpyridinium‐4‐yl substituted 7‐(dialkylamino)/7‐hydroxycoumarins. Indeed, in the field of photoactive organic molecules, the positively charged N‐alkylpyridinium‐4‐yl groups are often used as acceptor units to dramatically impact spectral features through promoting intramolecular charge transfer (ICT) processes. They are also known as effective water‐solubilizing and mitochondria targeting moieties. The poor fluorescence efficiency of cationic 7‐hydroxycoumarin derivatives in aqueous physiological conditions was highlighted and rationalized by the predominance of a neutral quinonoid form in such buffer medium. The ability of the excited singlet state (S1) of this neutral species to undergo intersystem crossing (ISC) to triplet state (T1) was partly supported by phosphorescence measurements of singlet oxygen. We also took advantage of green‐emissive properties of 7‐(diethylamino)‐3‐(N‐methylpyridinium‐4‐yl)coumarin to successfully design and validate a novel small‐molecule fluorescent probe for the detection of alkaline phosphatase (ALP), based on the "covalent‐assembly" principle. A practical use of ortho‐formylated 7‐hydroxy‐3‐(N‐methylpyridinium‐4‐yl)coumarin was next considered with the synthesis of a Fe(III)‐salen complex whose the potential as a "molecular disassembly" probe for fluorogenic sensing of pyrophosphate (PPi) anion was assessed.
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