Environmentally Benign Carbon Nanodots Prepared from Lemon for the Sensitive and Selective Fluorescence Detection of Fe(III) and Tannic Acid.

Photoluminescent carbon nanodots (CNDs) were prepared using a biocarbon source of lemon extract. The obtained CNDs are of spherical shape and are enriched with the carboxylic acid fucntionalities. CNDs exhibited a fluorescence emission at 445 nm and unveiled blue luminescence in ultraviolet excitation. The influences of pH and ionic strength toward the stability of CNDs were investigated in detail and the obtained stability authenticates their applicability in different environmental conditions. The competitive binding of Fe3+ with CNDs quenches the fluorescence behavior of CNDs and was further quenched with the selective complex formation of Fe3+ with tannic acid (TA). The interference experiments specified that CNDs-Fe3+ assembly selectively detected TA and the co-existing molecules have not influenced the quenching effect of TA with CNDs-Fe3+. The analytical reliability of constructed sensor was validated from the recovery obtained in the range of 91.66-107.02% in real samples. Thus the low cost and environmentally benign CNDs prepared from natural biomass provide new avenues in the fluorescence detection of biologically significant metal ions and biomolecules, facilitating their competency in on-site applications of real environmental samples.

Crystal structure of 2-amino-5-nitro-pyridinium sulfamate.

The title mol-ecular salt, C5H6N3O2 (+) ·H2NO3S(-), was obtained from the reaction of sulfamic acid with 2-amino-5-nitro-pyridine. A proton transfer from sulfamic acid to the pyridine N atom occurred, resulting in the formation of a salt. As expected, this protonation leads to the widening of the C-N-C angle of the pyridine ring, to 122.9 (3)°, with the pyridinium ring being essentially planar (r.m.s. deviation = 0.025 Å). In the crystal, the ion pairs are joined by three N-H⋯O and one N-H⋯N hydrogen bonds in which the pyridinium N atom and the amino N atom act as donors, and are hydrogen bonded to the carboxyl-ate O atoms and the N atom of the sulfamate anion, thus generating an R (3) 3(22) ring motif. These motifs are linked by further N-H⋯O hydrogen bonds enclosing R (3) 3(8) loops, forming sheets parallel to (100). The sheets are linked via weak C-H⋯O hydrogen bonds, forming a three-dimensional structure. The O atoms of the nitro group are disordered over two sets of sites with a refined occupancy ratio of 0.737 (19):0.263 (19).

2-Amino-5-nitro-pyridinium hydrogen oxalate.

In the cation of the title mol-ecular salt, C5H6N3O2 (+)·C2HO4 (-), the dihedral angle between the aromatic ring and the nitro group is 3.5 (3)°; in the anion, the dihedral angle between the CO2 and CO2H planes is 10.5 (2)°. In the crystal, the anions are linked into [100] chains by O-H⋯O hydrogen bonds. The cations cross-link the chains by way of N-H⋯O hydrogen bonds and the structure is consolidated by C-H⋯O inter-actions.