Abstract:Carbon Dots (CDs) are carbon nanoparticles which were discovered in 2004. Despite two decades of intensive work from the scientific community and a colossal amount of gathered experimental data, no definitive consensus exists to date on several key aspects such as the actual definition of CDs and the origin of their emissive properties. This review proposes a critical evaluation of these fundamental questions. Lay persons will also find here an alternative introduction to the CDs domain, including synthetic st… Show more
“…Moreover, if we compare the value of the acid/base sites in the initial mixture of precursors, it is possible to quantify retained sites on NCDs surfaces. In fact, some of the initial starting material acid/base moieties are lost during the synthesis due to decarboxylation reactions, dehydration, formation of amide bonds and appearance of molecular side‐products that are removed from NCDs during the purification step [5,38,39] . Specifically, up to 50 %±4% of sites are retained for NCDs‐ 2 compared to just 20 %±4% for NCDs‐ 1 , showing a steep increase in the bi‐component synthesis with respect to the mono‐component approach (Figure 3f).…”
Section: Resultsmentioning
confidence: 99%
“…In fact, some of the initial starting material acid/base moieties are lost during the synthesis due to decarboxylation reactions, dehydration, formation of amide bonds and appearance of molecular side-products that are removed from NCDs during the purification step. [5,38,39] Specifically, up to 50 % � 4% of sites are retained for NCDs-2 compared to just 20 % � 4% for NCDs-1, showing a steep increase in the bicomponent synthesis with respect to the mono-component approach (Figure 3f). Interestingly, a clear correlation can be observed between the total number of acid/base sites, the percentage of retained sites, and the length of the DA used (see Section B.2.3 of the Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…Carbon dots (CDs) are an emerging class of quasi‐spherical carbon‐based nanoparticles with dimensions below 10 nm [1–4] . In recent years, these nanomaterials have gained popularity thanks to their excellent luminescence and optical features, considerable solubility in aqueous and polar solvents, high chemical and photostability, as well as their low toxicity and excellent biocompatibility [3,5,6] . Moreover, CDs can be readily produced from inexpensive and abundant molecular precursors through straightforward and robust bottom‐up synthetic protocols [7,8] .…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4] In recent years, these nanomaterials have gained popularity thanks to their excellent luminescence and optical features, considerable solubility in aqueous and polar solvents, high chemical and photostability, as well as their low toxicity and excellent biocompatibility. [3,5,6] Moreover, CDs can be readily produced from inexpensive and abundant molecular precursors through straightforward and robust bottom-up synthetic protocols. [7,8] Interestingly, when molecules are used as precursors, the structure of the resulting CDs may reflect the molecular features of the starting materials.…”
Amine‐rich carbon dots (NCDs) have become promising nano‐aminocatalytic platforms in organic synthesis. These nanomaterials can be effectively produced through straightforward bottom‐up approaches using inexpensive nitrogen‐containing molecular precursors as a starting material. However, to date, there is still a limited understanding of how the molecular features of these precursors affect the catalytic activity of the resulting nanoparticles. This study concerns the production of a new family of NCDs, which use l‐arginine and different alkyl diamines as starting materials. The surface amines of all these NCDs were comprehensively characterized, thus allowing us to provide a correlation between the structural features of the nanoparticles and their catalytic performance with a selected amino‐catalyzed organic transformation. Importantly, the most active nano‐aminocatalysts, namely, NCDs‐3, were then used as a basis for the formation of a wide variety of functionalized organic compounds in water under mild reaction conditions.
“…Moreover, if we compare the value of the acid/base sites in the initial mixture of precursors, it is possible to quantify retained sites on NCDs surfaces. In fact, some of the initial starting material acid/base moieties are lost during the synthesis due to decarboxylation reactions, dehydration, formation of amide bonds and appearance of molecular side‐products that are removed from NCDs during the purification step [5,38,39] . Specifically, up to 50 %±4% of sites are retained for NCDs‐ 2 compared to just 20 %±4% for NCDs‐ 1 , showing a steep increase in the bi‐component synthesis with respect to the mono‐component approach (Figure 3f).…”
Section: Resultsmentioning
confidence: 99%
“…In fact, some of the initial starting material acid/base moieties are lost during the synthesis due to decarboxylation reactions, dehydration, formation of amide bonds and appearance of molecular side-products that are removed from NCDs during the purification step. [5,38,39] Specifically, up to 50 % � 4% of sites are retained for NCDs-2 compared to just 20 % � 4% for NCDs-1, showing a steep increase in the bicomponent synthesis with respect to the mono-component approach (Figure 3f). Interestingly, a clear correlation can be observed between the total number of acid/base sites, the percentage of retained sites, and the length of the DA used (see Section B.2.3 of the Supporting Information).…”
Section: Resultsmentioning
confidence: 99%
“…Carbon dots (CDs) are an emerging class of quasi‐spherical carbon‐based nanoparticles with dimensions below 10 nm [1–4] . In recent years, these nanomaterials have gained popularity thanks to their excellent luminescence and optical features, considerable solubility in aqueous and polar solvents, high chemical and photostability, as well as their low toxicity and excellent biocompatibility [3,5,6] . Moreover, CDs can be readily produced from inexpensive and abundant molecular precursors through straightforward and robust bottom‐up synthetic protocols [7,8] .…”
Section: Introductionmentioning
confidence: 99%
“…[1][2][3][4] In recent years, these nanomaterials have gained popularity thanks to their excellent luminescence and optical features, considerable solubility in aqueous and polar solvents, high chemical and photostability, as well as their low toxicity and excellent biocompatibility. [3,5,6] Moreover, CDs can be readily produced from inexpensive and abundant molecular precursors through straightforward and robust bottom-up synthetic protocols. [7,8] Interestingly, when molecules are used as precursors, the structure of the resulting CDs may reflect the molecular features of the starting materials.…”
Amine‐rich carbon dots (NCDs) have become promising nano‐aminocatalytic platforms in organic synthesis. These nanomaterials can be effectively produced through straightforward bottom‐up approaches using inexpensive nitrogen‐containing molecular precursors as a starting material. However, to date, there is still a limited understanding of how the molecular features of these precursors affect the catalytic activity of the resulting nanoparticles. This study concerns the production of a new family of NCDs, which use l‐arginine and different alkyl diamines as starting materials. The surface amines of all these NCDs were comprehensively characterized, thus allowing us to provide a correlation between the structural features of the nanoparticles and their catalytic performance with a selected amino‐catalyzed organic transformation. Importantly, the most active nano‐aminocatalysts, namely, NCDs‐3, were then used as a basis for the formation of a wide variety of functionalized organic compounds in water under mild reaction conditions.
“…In recent times, the commonly employed synthetic strategy for the preparation of these materials has relied on the solvothermal treatment of small organic molecules. Indeed, the appropriate selection of starting materials, doping agents, and synthetic conditions affords CNDs with tailored structural and optical properties [3–5] . Among other possible applications, CNDs can be considered as a new generation of nano‐catalysts.…”
In this work, a microwave synthesis followed by a simple purification process produces a new type of chiral Carbon Nanodots (CNDs). These CNDs are soluble in organic solvents, exhibit amino groups on their surface and display interesting absorption and emission properties along with mirror image profiles in the electronic circular dichroism spectrum. All these features set the stage for CNDs to act as multifunctional catalytic platforms, able to promote diverse chemical transformations. In particular, the outer shell composition of CNDs was instrumental to carry out organocatalytic reactions in an enantioselective fashion. In addition, the redox and light‐absorbing properties of the material are suitable to drive photochemical processes. Finally, the photoredox and organocatalytic activations of CNDs were exploited at the same time to promote a cross‐dehydrogenative coupling. This work demonstrates that CNDs can be used as catalysts to promote multiple reactivities, previously considered exclusive domain of molecular catalysts.
Carbonized polymer dots (CPDs) have shown exceptional potential across a wide range of applications. However, their practical utilization is significantly greatly impeded by the lack of precise control over their structures and functionalities. Consequently, the development of controlled synthesis strategies for CPDs with well‐defined structures and tailored functionalities remains a critical challenge in the field. Here, the controlled synthesis of functional CPDs with reversible assembly properties via airflow‐assisted melt polymerization, followed by a one‐step post‐synthetic doping strategy, is reported. This synthetic approach achieves high product yield, uniform and tunable structures, as well as customized functionalities including solid‐state emission, enhanced catalytic performance (3.5–45 times higher than conventional methods), and selective gas storage in the resulting CPDs. The ability to tailor the properties of CPDs through controlled synthesis opens up new opportunities for their practical application in photocatalysis and gas storage.
scite is a Brooklyn-based organization that helps researchers better discover and understand research articles through Smart Citations–citations that display the context of the citation and describe whether the article provides supporting or contrasting evidence. scite is used by students and researchers from around the world and is funded in part by the National Science Foundation and the National Institute on Drug Abuse of the National Institutes of Health.