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Carbon dots

The photolysis of arenediazonium salts has been widely used for intramolecular cyclizations in the synthesis of 1-phenylethylisoquinoline alkaloids by Kametani and Fukumoto (review 1972). An example is the photolysis of the diazonium ion 10.73, which resulted in the formation of O-benzylandrocymbine (10.74) (Kametani et al., 1971). The mechanism of this cyclization is obviously quite complex, since the carbon (as cation or radical ) to which the diazonio group is attached in 10.73 does not react with the aromatic CH group, but with the tertiary carbon (dot in 10.73), forming a quinone-like ring (10.74). In our opinion the methyl cation released is likely to react with the counter-ion X- or the solvent. [Pg.282]

The carbons dotted in the product derive from the cyclopropyl conjunctive reagent. [Pg.16]

Sun YP et al (2006) Quantum-sized carbon dots for bright and colorful photoluminescence. J Am Chem Soc 128 7756-7757... [Pg.34]

Fig. 16.3 A carbon nanoparticle with surface defects (left), and emission color variations in carbon dots depending on size and type of defects. Adapted from Cao et at. [53] and Sun et at. [54] with kind permission from American Chemical Society (2006 and 2013). Fig. 16.3 A carbon nanoparticle with surface defects (left), and emission color variations in carbon dots depending on size and type of defects. Adapted from Cao et at. [53] and Sun et at. [54] with kind permission from American Chemical Society (2006 and 2013).
Fig. 3.14. Ranges of one-bond carbon-13-proton coupling constants for sp3, sp2, and sp carbons (dotted rectangles) and linear correlation between JCH and carbon s character of comparable compounds (coupling constants from Ref. [115]). The empirical relation is. /CH 500 s (Hz). Fig. 3.14. Ranges of one-bond carbon-13-proton coupling constants for sp3, sp2, and sp carbons (dotted rectangles) and linear correlation between JCH and carbon s character of comparable compounds (coupling constants from Ref. [115]). The empirical relation is. /CH 500 s (Hz).
Figure 17. Plots of the reduced current density against the applied potential obtained from the as-activated carbon (dotted line) and as-reactivated carbon (dashed line) electrode specimens. Solid line represents the ideal double layer capacitor where the time constant is zero. Reprinted from C.-H. Kim, S.-I. Pyun, and H.-C. Shin, J. Electrochem. Soc. 149 (2002) A93. Copyright 2001, with permission from The Electrochemical Society. Figure 17. Plots of the reduced current density against the applied potential obtained from the as-activated carbon (dotted line) and as-reactivated carbon (dashed line) electrode specimens. Solid line represents the ideal double layer capacitor where the time constant is zero. Reprinted from C.-H. Kim, S.-I. Pyun, and H.-C. Shin, J. Electrochem. Soc. 149 (2002) A93. Copyright 2001, with permission from The Electrochemical Society.
N, N-DIETHYLCARBANILIDE see DJC400 DIETHYL CARBINOL see IHPOlO DIETHYLCARBINOL see IHPOlO DIETHYL CARBITOL see DIW800 DIETHYL CARBONATE see DIX200 DIETHYL CARBONATE (DOT) see DIX200 DIETHYL CELLOSOL /E (DOT) see EJE500 DIETHYLCETONE (FRENCH) see DJN750... [Pg.1625]

Soft Materials (CP, functionalized Graphene or -Fullerene derivatives, Graphene-Quantum/Carbon dots) (Electron acceptor)... [Pg.31]

Keywords Quantum confinement, quantum-confined nanomaterials (QCNs), quantum dots (QDs), tetrapods, nanocrystals, nanorods, carbon dots (C-dots), graphene quantum dots (GQDs), CdSe, CdS, CdTe, PbS, PbSe, blends, nanocomposites, in-situ polymerization, organic photovoltaics (OPVs), organic light-emitting diodes (OLEDs), dye-sensitized solar cells (DSSCs)... [Pg.163]

Poiymers, Carbon dots materials Shapes Needies... [Pg.457]

X., Shi, J., and Hao, A. (2014) Reduced graphene oxide-carbon dots composite as an enhanced material for electrochemical determination of dopamine. Electrochim. Acta, 130, 805 -809. [Pg.160]

For C-based QDs, nanodiamond and carbon dots are most extensively reported. Synthesis techniques include surface modification, oxidation with concentrated acid, electrochemistry, laser ablation, organic carbonization, and template methods. ... [Pg.65]


See other pages where Carbon dots is mentioned: [Pg.165]    [Pg.59]    [Pg.267]    [Pg.451]    [Pg.12]    [Pg.55]    [Pg.271]    [Pg.225]    [Pg.744]    [Pg.121]    [Pg.137]    [Pg.76]    [Pg.167]    [Pg.214]    [Pg.798]    [Pg.282]    [Pg.8]    [Pg.86]    [Pg.86]    [Pg.87]    [Pg.89]    [Pg.91]    [Pg.93]    [Pg.95]    [Pg.97]    [Pg.99]    [Pg.101]    [Pg.103]    [Pg.105]    [Pg.107]    [Pg.109]    [Pg.111]    [Pg.113]    [Pg.115]    [Pg.177]   
See also in sourсe #XX -- [ Pg.167 ]

See also in sourсe #XX -- [ Pg.165 ]




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Carbon dots absorption

Carbon dots photoluminescence

Carbon dots property

Carbon dots synthesis

Carbon dots toxicity

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