Carbon nanoparticles (CNPs) represent a recent class of nanomaterials, based on carbon sp² atoms in the inner core. These new nano-dots cover a wide range of application fields: analytical, sensing and biosensing, bioimaging, theranostic, and molecular communication. However, their use as nanocatalysts is relatively new. Although CNPs can be easily synthesized and obtained in good amounts, few reports on their catalytic applications have been reported. This minireview collects the use of these nanoparticles as catalysts highlighting the improvements with respect to the classic catalytic systems. In particular, due to their unique optical and electrical properties, and due to the possibility to cover the external shell with a wide variety of functional groups, CNPs have found catalytic applications in three main classes of reactions: (i) photocatalysis, (ii) acid–base catalysis and (iii) electro catalysis.

Nerve agents (NAs) are a group of highly toxic organophosphorus compounds developed before World War II. They are related to organophosphorus pesticides, although they have much higher human acute toxicity than commonly used pesticides. After the detection of the presence of NAs, the critical step is the fast decontamination of the environment in order to avoid the lethal effect of these organophosphorus compounds on exposed humans. This review collects the catalytic degradation reactions of NAs, in particular focusing our attention on chemical hydrolysis. These reactions are catalyzed by different catalyst categories (metal-based, polymeric, heterogeneous, enzymatic and MOFs), all of them described in this review.

A new protocol to obtain carbon nanoparticles (CNPs) covalently functionalized with a chiral Mn-Salen catalyst is described here. The new nanocatalyst (CNPs-Mn-Salen) was tested in the enantioselective epoxidation of some representative alkenes (CN-chromene, 1,2-dihydronaphthalene and cis-β-ethyl styrene), obtaining better enantiomeric excess values than that of the catalyst single molecule, highlighting the role of the nanostructure in the enantioselectivity.

Herein, supramolecular carbon nanoparticle aggregates were obtained via covalent functionalization of the shell of nanoparticles with triazine and subsequent hydrogen bonding reticulation upon the addition of naphthalene diimide. The resulting reticulated nanoparticles maintained the optical properties required for artificial chemical communication but exhibited a reduced diffusion coefficient, enabling sharper and more intense molecular bit capabilities when employed as chemical messengers. As a result, they are ideal candidates for the transport of information along extended fluid paths. We believe that our results represent a further step towards the understanding and optimization of all the experimental parameters affecting the information transfer efficiency in artificial chemical communication.

Precision medicine requests accurate serological inspections to precisely stratify patients for targeted treatment. Intact transition epitope mapping analysis proved surrogate seroconversion of a model organism’s serum when spiked with a monoclonal murine anti-Ovalbumin antibody (mAb) with epitope resolution. Isolation of the IgG fraction from blood serum applied two consecutive protein precipitation steps followed by ultrafiltration and resulted in an ESI-MS analysis-ready IgG preparation. For epitope mapping by epitope extraction, the Ovalbumin antigen was digested with trypsin. After desalting, the peptide mixture was added to the ESI-MS-ready IgG preparation from mAb-spiked serum and the solution was incubated to form an immune complex between the Ovalbumin-derived epitope peptide and the anti-Ovalbumin mAb. Then, the entire mixture of proteins and peptides was directly electrosprayed. Sorting of ions in the mass spectrometer’s gas phase, dissociation of the immune complex ions by collision-induced dissociation, and recording of the epitope peptide ion that had been released from the immune complex proved the presence of the anti-Ovalbumin mAb in serum. Mass determination of the complex-released epitope peptide ion with isotope resolution is highly accurate, guaranteeing high specificity of this novel analysis approach, which is termed Intact Transition Epitope Mapping—Serological Inspections by Epitope EXtraction (ITEM—SIX).