Synthesis and characterization of a new water-soluble non-cytotoxic mito-tracker capped silicon quantum dot

19-25Allyl triphenylphosphonium bromide based mito-tracker capped silicon quantum dot (Mito-SiQDs) has been synthesized through an inverse micelle process. It was then fully characterized by transmission electron microscopy, energy-dispersive X-ray spectroscopy, dynamic light scattering techniques and X-ray photoelectron spectroscopic method. Energy dispersive X-ray spectroscopy analyses of the quantum dots confirm the presence of carbon, silicon, phosphorous and bromine atoms in Mito-SiQDs. Morphological study by transmission electron microscopy experiment showed the formation of the particles of size 11-12 nm of quantum dot dimension. The high negative zeta potential value of –23.7 mV calculated from dynamic light scattering study indicates the high stability of the circumvent agglomeration of Mito-SiQDs. The mito-tracker capped silicon quantum dot has blue emission at 400 nm wavelength upon excitation at 327 nm. Mito-SiQDs has not shown any significant cytotoxic effect with 10 to 50 μL/mL concentration on HeLa cell line for at least up to 12 h of its treatment. The Mito-SiQDs would be useful a possible fluorescent marker to visualize mitochondrial subcellular compartment in living cell through fluorescence imaging study

Insight on the presence of dimethylammonium cation within anionic metal-organic supramolecular host: structural, Hirshfeld surface, optical and theoretical analysis

A new supramolecular metal-organic complex, [(DMA)+{Fe(IDA)2}-] (where H2IDA = iminodiacetic acid and DMA = dimethylammonium cation) (1), has been synthesized solvothermally at 90 °C from reaction of ferric(III) chloride hexahydrate with nitrilotriacetic acid (H3NTA) in stoichiometric ratio. The complex was characterized by single crystal X-ray diffraction (SCXRD) along with spectroscopic analyses. During the reaction process, H3NTA is degraded into IDA2- ligand. Structural analysis reveals that 1 is mononuclear and crystallizes in the monoclinic space group C2/c. Within the [Fe(IDA)2]- unit, Fe3+ shows six-coordinate distorted octahedral geometry. The [Fe(IDA)2]- units are connected by strong N1-H1···O4 hydrogen bonds to form anionic 2D supramolecular layers which are further connected by weak C-H···O hydrogen bonds to form a 3D metal-organic supramolecular host (MOSH) structure having 1D supramolecular channels along the crystallographic c-axis. DMA cations are present within the supramolecular channels through N2-H2···O2 hydrogen bonding interactions. Hirshfeld surface analysis and corresponding 2D fingerprint plots indicate that O···H interactions are the major supramolecular interactions present between MOSH and guest DMA cation. DFT calculations reveal that the HOMO and LUMO of the [Fe(IDA)2]- unit are composed of mixed metal-ligand orbitals. Both the absorption and emission spectra of the complex were studied in aqueous phase and the result was correlated with the TDDFT study.</p

A New Lysosome-Targetable Turn-On Fluorogenic Probe for Carbon Monoxide Imaging in Living Cells

A lysosome-targetable fluorogenic probe, LysoFP-NO₂, was designed and synthesized based on a naphthalimide fluorophore that can detect selectively carbon monoxide (CO) in HEPES buffer (pH 7.4, 37 °C) through the transformation of the nitro group into an amino-functionalized system in the presence of CO. LysoFP-NO₂ triggered a “turn-on” fluorescence response to CO with a simultaneous increase of fluorescence intensity by more than 75 times. The response is selective over a variety of relevant reactive nitrogen, oxygen, and sulfur species. Also, the probe is an efficient candidate for monitoring changes in intracellular CO in living cells (MCF7), and the fluorescence signals specifically localize in the lysosome compartment