Role of Oxygen Defects in Eliciting a Divergent Fluorescence Response of Single-Walled Carbon Nanotubes to Dopamine and Serotonin.

Modulating the optical response of fluorescent nanoparticles through rational modification of their surface chemistry can yield distinct optical signatures upon the interaction with structurally related molecules. Herein, we present a method for tuning the fluorescence response of single-walled carbon nanotubes (SWCNTs) toward dopamine (DA) and serotonin, two structurally related monoamine-hydroxylated aromatic neurotransmitters, by introducing oxygen defects into (6,5) chirality-enriched SWCNTs suspended by sodium cholate (SC). This modification facilitated opposite optical responses toward these neurotransmitters, where DA distinctly increased the fluorescence of the defect-induced emission of SWCNTs (D-SWCNTs) 6-fold, while serotonin notably decreased it.

Dynamic Tracking of Biological Processes Using Near-Infrared Fluorescent Single-Walled Carbon Nanotubes.

Biological processes are characterized by dynamic and elaborate temporal patterns driven by the interplay of genes, proteins, and cellular components that are crucial for adaptation to changing environments. This complexity spans from molecular to organismal scales, necessitating their real-time monitoring and tracking to unravel the active processes that fuel living systems and enable early disease detection, personalized medicine, and drug development. Single-walled carbon nanotubes (SWCNTs), with their unique physicochemical and optical properties, have emerged as promising tools for real-time tracking of such processes.

Monitoring Enzyme Activity Using Near-Infrared Fluorescent Single-Walled Carbon Nanotubes.

Enzymes serve as pivotal biological catalysts that accelerate essential chemical reactions, thereby influencing a variety of physiological processes. Consequently, the monitoring of enzyme activity and inhibition not only yields crucial insights into health and disease conditions but also forms the basis of research in drug discovery, toxicology, and the understanding of disease mechanisms. In this context, near-infrared (NIR) fluorescent single-walled carbon nanotubes (SWCNTs) have emerged as effective tools for tracking enzyme activity and inhibition through diverse strategies.

Rationally Designed Functionalization of Single-Walled Carbon Nanotubes for Real-Time Monitoring of Cholinesterase Activity and Inhibition in Plasma.

Enzymes play a pivotal role in regulating numerous bodily functions. Thus, there is a growing need for developing sensors enabling real-time monitoring of enzymatic activity and inhibition. The activity and inhibition of cholinesterase (CHE) enzymes in blood plasma are fluorometrically monitored using near-infrared (NIR) fluorescent single-walled carbon nanotubes (SWCNTs) as probes, strategically functionalized with myristoylcholine (MC)- the substrate of CHE.

Excitation-Dependent Fluorescence with Excitation-Selective Circularly Polarized Luminescence from Hierarchically Organized Atomic Nanoclusters.

Nanometer-scaled objects are known to have dimension-related properties, but sometimes the assembly of such objects can lead to the emergence of other properties. Here, we show the assembly of atomically precise gold nanoclusters into large fibrillar structures that are featuring excitation-dependent luminescence with an excitation-selective circularly polarized luminescence (CPL), even though all components are achiral. The origin of CPL in the assembly of atomic clusters has been attributed to the hierarchical organization of atomic clusters into fibrillar structures, mediated via a hydrogen bonding interaction with a surfactant.

The Role of Surface Groups in Dictating the Chiral-Solvent-Induced Assembly of Carbon Dots into Structures Exhibiting Circularly Polarized Luminescence.

Here, the use of achiral nanoparticles and solvent-induced chirality transfer is combined for the making of large structures exhibiting chiroptical properties in the form of circularly polarized luminescence (CPL). The nanoparticles that the authors use are carbon dots (C-Dots) that are known for their bright luminescence and the ability to tune their surface moieties by using different precursors in their synthesis. Here, the result of adding the chiral solvent limonene into an aqueous solution of various C-Dots is explored, differentiated by their surface group.

Controlling the Chemistry of Nanoclusters: From Atomic Precision to Controlled Assembly.

Metal nanoclusters have gained prominence in nanomaterials sciences, owing to their atomic precision, structural regularity, and unique chemical composition. Additionally, the ligands stabilizing the clusters provide great opportunities for linking the clusters in higher order dimensions, eventually leading to the formation of a repertoire of nanoarchitectures. This makes the chemistry of atomic clusters worth exploring.

Functionalized Au nanoclusters as luminescent probes for protein carbonylation detection.

Atomically precise, ligand-protected gold nanoclusters (AuNCs) attract considerable attention as contrast agents in the biosensing field. However, the control of their optical properties and functionalization of surface ligands remain challenging. Here we report a strategy to tailor AuNCs for the precise detection of protein carbonylation-a causal biomarker of ageing.

An ambient complexation reaction of zinc acetate and ascorbic acid leads to a new form of nanoscale particles with emergent optical properties.

We report the formation of nanoscale particles from the complexation reaction between zinc acetate and ascorbic acid under ambient conditions and in an aqueous medium. The reaction led to the formation of a molecular complex with the formula Zn (AA) (OAc) (, , and = possible smallest positive integer) with AA meaning ascorbate, based on the mass spectrometry results. Following this, the formation of luminescent nanoscale particles - the size of which increased with time - was observed.

Four orders-of-magnitude enhancement in the two-photon excited photoluminescence of homoleptic gold thiolate nanoclusters following zinc ion-induced aggregation.

Herein we report unprecedented determination of the molar mass of zinc mediated assemblies of homoleptic gold nanoclusters, based on charge detection mass spectrometry measurements. The accurate determination of the molar mass of zinc coordinated assemblies of gold clusters has further allowed unambiguous determination of the two-photon excited photoluminescence cross section of the same. Furthermore, in line with one-photon excited photoluminescence measurements, four orders-of-magnitude enhancement in two-photon excited photoluminescence of gold nanoclusters has been observed following complexation with zinc ions.

Second harmonic scattering from mass characterized 2D graphene oxide sheets.

In this communication, we report the second harmonic scattering from mass characterized 2D graphene oxide sheets dispersed in an aqueous suspension, in the femtosecond regime at 800 nm laser excitation. Charge-detection mass-spectrometry, performing at the single sheet level, allows for an exhaustive molar mass distribution and thus concentration for these 2D nanomaterials samples. The orientation-averaged hyperpolarizability value is (1.

Tailoring the luminescence of atomic clusters via ligand exchange reaction mediated post synthetic modification.

The growing prominence of atomic nanoclusters in fields of practical relevance has made modulation of their luminescent characteristics an important challenge for their future applications. Herein we report chemical reaction assisted modulation of luminescence of histidine stabilized gold nanoclusters via a ligand exchange reaction with cysteine. Upon addition of 3.

Zinc-Ion-Induced Aggregation of Gold Clusters for Visible-Light-Excitation-Based Fluorimetric Discrimination of Geometrical Isomers.

Herein, we report discrimination of dicarboxylic acids - fumaric acid (FA) and maleic acid (MA) - exhibiting geometrical isomerism, using nanoclusters based luminescent probe having excitation under broad day light. The luminescent probe was designed via complexation reaction between zinc ions and ligands (mercaptopropioinc acid; MPA) stabilizing the gold nanoclusters. This resulted in formation of nanoaggregates exhibiting bright green luminescence upon excitation at 450 nm capable of discriminating between FA and MA upto nanomolar level.

Complexation Reaction-Based Two-Dimensional Luminescent Crystalline Assembly of Atomic Clusters for Recyclable Storage of Oxygen.

In this work, we report storage of oxygen in two-dimensional (2D) crystalline nanosheets comprising luminescent gold nanoclusters (Au NCs). Complexation reaction between Au NCs (stabilized by l-phenylalanine and mercaptopropionic acid) and zinc ions led to the formation of crystalline assembly of Au NCs. The crystalline nature of the assembly of Au NCs was confirmed through transmission electron microscopy (TEM), high-resolution TEM, and selected area electron diffraction (SAED) analysis.

Photo induced chemical modification of surface ligands for aggregation and luminescence modulation of copper nanoclusters in the presence of oxygen.

Surface modification of nanoparticles has been a popular approach to tailor the properties of nanoparticles. Herein we report the unprecedented photo oxidation of cysteine moeties on the surface of copper nanoclusters (Cu NCs) leading to aggregation of Cu NCs, which further led to quenching of luminescence of the latter. Upon illumination of a dispersion of Cu NCs at 365 nm wavelength light, the luminescence of Cu NCs was completely quenched.

Visible Light Excitation-Induced Luminescence from Gold Nanoclusters Following Surface Ligand Complexation with Zn for Daylight Sensing and Cellular Imaging.

Herein, we report a complexation reaction-mediated extended aggregation of gold nanoclusters exhibiting luminescence under visible light excitation. The complexation reaction between the carboxylate groups of mercaptopropionic acid and zinc ions induced the aggregation of gold nanoclusters, which featured bright green luminescence upon excitation with visible light of wavelength 450 nm and beyond. This luminescence of aggregated Au NCs, easily discernible with bare eyes (under broad daylight excitation), was used as a probe for luminescence-based detection of molecules based on the p K values of the latter.

Room-Temperature Delayed Fluorescence of Gold Nanoclusters in Zinc-Mediated Two-Dimensional Crystalline Assembly.

We report that complexation-reaction-mediated two-dimensional crystalline assembly of gold (Au) nanoclusters (NCs) exhibits room-temperature delayed fluorescence at 605 nm, with an unprecedented long lifetime of 0.5 ms and an exceptionally high quantum yield of 19.1 ± 0.

Crystallization-Induced Emission Enhancement of Nanoclusters and One-Step Conversion of "Nanoclusters to Nanoparticles" as the Basis for Intracellular Logic Operations.

Herein, we report the construction of intracellular logic operations using luminescent histidine stabilized gold nanoclusters (His Au NCs). The luminescence intensity of His Au NCs was found to be significantly enhanced following interaction with zinc ions, owing to "Crystallization induced emission enhancement". Further, the luminescence intensity of His Au NCs was found to be effectively quenched in presence of sulphide ions, owing to transformation of emissive His Au NCs to non-emissive gold nanoparticles.

Crystalline assembly of gold nanoclusters for mitochondria targeted cancer theranostics.

Herein, we report the formation of a crystalline assembly of gold (Au) nanoclusters for cancer theranostics via active targeting of mitochondria. To the best of our knowledge, this is the first report of the target specific activity of an "assembly of gold nanoclusters". Au nanoclusters were stabilized with mercaptopropionic acid and l-tyrosine.

Zinc-Coordinated Hierarchical Organization of Ligand-Stabilized Gold Nanoclusters for Chiral Recognition and Separation.

Three-dimensional organization of d- or l-tryptophan and mercaptopropionic acid-stabilized gold nanoclusters has been achieved by complexation of ligands using zinc ions. Powder X-ray diffraction and transmission electron microscopy analyses substantiated the crystalline nature of the assembly of atomic nanoclusters. The hierarchical arrangement of the nanoclusters exhibited superior optical properties (namely, enhanced photoluminescence and excited-state lifetime) as compared to the non-assembled nanoclusters.

Thumb Imprint Based Detection of Hyperbilirubinemia Using Luminescent Gold Nanoclusters.

Early and easy detection of diseases, using point-of-care and inexpensive devices, not only provides option for early treatment but also reduces the risk of propagation. Herein we report the fabrication of a robust film based luminescence indicator of bilirubin, which can indicate hyperbilirubinemia through the thumb imprint of the patient. The UV-light induced luminescence intensity of the film, made out of chitosan stabilised gold (Au) nanoclusters, which was effectively quenched in the presence of Cu ions, recovered in the presence of bilirubin from skin or blood serum.