Sub 1 nm Poly(acrylic acid)-Capped Copper Nanoparticles for the Synthesis of 1,2,3-Triazole Compounds.

The stable, water-soluble, and fluorescent sub 1 nm sized poly(acrylic acid)-capped copper nanoparticles (PAACC NPs) were synthesized using a high-intensity ultrasound sonication (30 KHz) method. The reduction of copper NPs from copper(II) salt by mild reducing agent l-ascorbic acid in an aqueous medium was achieved in the presence of poly(acrylic acid). The PAACC NPs were characterized by DRS UV-visible, XPS, PL, FESEM, and HRTEM techniques. The resulting PAACC NPs show orange fluorescence with a peaking center at 560 nm. The PAACC NPs serve as effective catalysts for the synthesis of 1,2,3-triazoles via click reaction in good yields under mild reaction conditions.

Crystal structures and Hirshfeld surface analyses of 4,4'-{[1,3-phenyl-enebis(methyl-ene)]bis-(-oxy)}bis-(3-meth-oxy-benzaldehyde) and 4,4'-{[(1,4-phenyl-ene-bis(methyl-ene)]bis-(-oxy)}bis-(3-meth-oxy-benzalde-hyde).

The title compounds, C24H22O6 (I) and C24H22O6 (II), each crystallize with half a mol-ecule in the asymmetric unit. The whole mol-ecule of compound (I) is generated by twofold rotation symmetry, the twofold axis bis-ecting the central benzene ring. The whole mol-ecule of compound (II) is generated by inversion symmetry, the central benzene ring being located on an inversion center. In (I), the outer benzene rings are inclined to each other by 59.96 (10)° and by 36.74 (9)° to the central benzene ring. The corresponding dihedral angles in (II) are 0.0 and 89.87 (12)°. In the crystal of (I), mol-ecules are linked by C-H⋯O hydrogen bonds and C-H⋯π inter-actions, forming ribbons propagating along the [10] direction. In the crystal of (II), mol-ecules are linked by C-H⋯O hydrogen bonds, forming a supra-molecular framework. The Hirshfeld surface analyses indicate that for both compounds the H⋯H contacts are the most significant, followed by O⋯H/H⋯O and C⋯H/H⋯C contacts.

The crystal structures and Hirshfeld surface analysis of N',N'''-((1E,1'E)-{[methyl-enebis(-oxy)]bis-(6-bromo-3,1-phenyl-ene)}bis-(methan-ylyl-idene))bis-(isonicotinohydrazide) dihydrate and N',N'''-((1E,1'E)-{[butane-1,4-diylbis(-oxy)]bis-(2,1-phenyl-ene)}bis-(methan-ylyl-idene))bis-(isonicotino-hydrazide) [+ solvent].

The title compounds, C27H20Br2N6O4·2H2O, (I), and C30H28N6O4·[+ solvent], (II), both crystallize with one half-mol-ecule in the asymmetric unit. The whole mol-ecule of (I) is generated by twofold rotation symmetry, with the twofold rotation axis bis-ecting the C atom of the -O-CH2-O- bridge. This results in a folded or U-shaped conformation of the mol-ecule. The whole mol-ecule of (II) is generated by inversion symmetry, with the central CH2-CH2 bond of the -O-(CH2)4-O- bridge being located about a center of inversion. This results in a step-like conformation of the mol-ecule. The central C(=O)N-N=C regions of the isonicotinohydrazide moieties in both compounds are planar and the configuration about the imine C=N bonds is E. In compound (I), the benzene and pyridine rings are inclined to each other by 37.60 (6)°. The two symmetry-related pyridine rings are inclined to each other by 74.24 (6)°, and the two symmetry-related benzene rings by 7.69 (6)°. In compound (II), the benzene and pyridine rings are inclined to each other by 25.56 (11)°. The symmetry-related pyridine rings are parallel, as are the two symmetry-related benzene rings. In the crystal of (I), a pair of water mol-ecules link the organic mol-ecules via Owater-H⋯O and Owater-H⋯N hydrogen bonds, forming chains along [001], and enclosing an R 4 2(8) and two R 1 2(5) ring motifs. The chains are linked by N-H⋯Npyridine hydrogen bonds, forming a supra-molecular framework. There are also a number of C-H⋯O hydrogen bonds, and C-H⋯π and offset π-π inter-actions [inter-planar distance = 3.294 (1) Å] present reinforcing the framework. In the crystal of (II), mol-ecules are linked by N-H⋯Npyridine hydrogen bonds, forming a supra-molecular framework. Here too there are also a number of C-H⋯O hydrogen bonds present, and a C-H⋯π inter-action, reinforcing the framework. For compound (II), a region of disordered electron density was corrected for using the SQUEEZE [Spek (2015 ▸). Acta Cryst. C71, 9-18] routine in PLATON. Their formula mass and unit-cell characteristics were not taken into account during refinement.

Synthesis of chitosan capped copper oxide nanoleaves using high intensity (30kHz) ultrasound sonication and their application in antifouling coatings.

The synthesis of chitosan capped copper oxide nanoleaves (CCCO NLs) was carried out under three different reaction conditions viz. 1) room temperature, 2) 70°C and 3) high intensity ultrasound (30kHz) sonication method and it has been found that the high intensity ultrasound (30kHz) sonication is the best method when compared to other two methods. The advantages of the present synthetic method are: i) easy one step process, ii) lesser reaction time, iii) good yield, iv) reproducible and v) calcination is not required. The resulting chitosan capped copper oxide nanoleaves were characterized by Diffuse Reflectance UV-Visible Spectroscopy (DRS), Fourier Transform Infra-Red Spectroscopy (FT-IR), X-ray Diffraction (XRD), X-ray Photoelectron Spectroscopy (XPS), Field Emission Scanning Electron Microscopy (FESEM), High Resolution Transmission Electron Microscopy (HRTEM) and Thermo gravimetric analysis (TGA). The CCCO NLs were blended with commercial paints such as polyurethane clear, polyurethane white and acrylic emulsion and applied on to three different surfaces (wood, mild steel and cement slab panels). The hydrophilicity of CCCONP coated panels was analyzed by water contact angle measurement and their antifouling behavior was investigated against three different green and marine algae viz. Arthrospira, Chlorella and Amphora. The antifouling efficiency of the CCCO NLs against the algae was found to be 78-92%.

One pot green synthesis of Ag, Au and Au-Ag alloy nanoparticles using isonicotinic acid hydrazide and starch.

Gold-silver alloy nanoparticles were synthesized via chemical reduction of varying mole fractions of chloroauric acid (HAuCl4) and silver nitrate (AgNO3) by environmentally benign isonicotinic acid hydrazide (INH) in the presence of starch as a capping agent in aqueous medium. The absorption spectra of Au-Ag nanoparticles show blue shift with increasing silver content indicating the formation of alloy nanoparticles. When the Ag content in the alloy decreases the size of the nanoparticles increases and as a result of which the oxidation potential also increases. The emission maximum undergoes a red shift from 443 to 614 nm. The nanoparticles are monodisperse and spherical with an average particle size of 3-18 nm. The catalytic behavior of alloy nanoparticles indicate that the rate constant for the reduction of 4-nitro phenol to 4-amino phenol increases exponentially from metallic Ag to metallic Au as Au content increases in the Au-Ag alloy nanoparticles.