Mesoporous cadmium sulfide nanoparticles derived from a new cadmium anthranilato complex: Characterization and induction of morphological abnormalities in pathogenic fungi

A cadmium complex of the general formula Cd(C13H9O2NCl)2(H2O)2 {C13H9O2NCl = 2‐(4‐chlorophenylamino)benzoate} was synthesized and characterized regarding its CHN data, solution molar conductivity and spectroscopic (UV–Vis. and IR) properties. Cadmium sulfide nanoparticles (CdS NPs) were grown form the microcrystalline complex and thiourea via a hydrothermal route. The as‐prepared NPs were assigned based on X‐ray powder diffraction (PXRD), transmission electron microscopy (TEM), field emission scanning electron microscopy (FE‐SEM) and Brunauer – Emmett – Teller (BET) surface area measurements. The CdS absorption and emission spectra were also recorded that revealed an energy gap of 2.47 eV and large Stokes shift of 130 nm. For the as‐prepared NPs, the measurements have also indicated a mesoporous structure and an average particle size of 20–28 nm associated with an average pore diameter of 11.21 nm. The as‐synthesized CdS NPs acted as antifungal controlling agent against human and plant pathogenic fungi of serious environmental and health concerns. The NPs at concentration of 200 ppm inhibited several fungi with inhibition efficiency of 100% against Aspergillus ustus Au‐28. The nanoparticles induced morphological abnormalities in fungal mycelia, conidia and vesicle. Additionally, they inhibited the conidia septum formation, accelerated the chlamydospores generation and enlarged the yeast cells. Wurtzite CdS nanoparticles (NPs) were prepared via a new hydrothermal route and fully characterized. The NPs at concentration of 200 ppm inhibited several pathogenic fungi with inhibition efficiency of 100% against Aspergillus ustus. Moreover, the nanoparticles induced morphological abnormalities including mycelia, conidia and vesicle deformations, inhibiting conidia septum formation, acceleration of chlamydospores generation and formation of enlarged yeast cells.