In recent years, titanium(iv) dioxide nanoparticles (TiO2NPs) have shown promising potential in various biological applications such as antimicrobials, drug delivery, photodynamic therapy, biosensors, and tissue engineering.
Rod‐like organometallic dithiol containing square‐planar Pt(II) centers, i. e., trans,trans‐[(H3COCS)Pt(PBu3)2(C≡C−C6H4−C6H4−C≡C)(PBu3)2Pt(SCOCH3)] was used as bifunctional stabilizing agent for the synthesis of Pd‐, Au‐, and AgNPs (MNPs). All the MNPs showed diameters of about 4 nm, which can be controlled by carefully modulating the synthesis parameters. Covalent MNPs stabilization occurred through a single S bridge between Pt(II) and the noble metal nanocluster surfaces, leading to a network of regularly spaced NPs with the formation of dyads, as supported by SR‐XPS data and by TEM imaging analysis. The chemical nature of NPs systems was also confirmed by EDS and NMR. Comparison between SR‐XPS data of MNPs and self‐assembled monolayers and multilayers of pristine rod‐like dithiols deposited onto polycrystalline gold surfaces revealed an electronic interaction between Pt(II) centers and biphenyl moieties of adjacent ligands, stabilizing the organic structure of the network. The possibility to obtain networks of regularly spaced MNPs opens outstanding perspectives in optoelectronics.
The preparation of three different functionalized palladium nanoparticles (PdNPs) systems for room temperature BTX (benzene, toluene, p‐xylene) sensing detection and their morphostructural characterization is described. PdNPs are prepared through a two‐phase water/toluene wet chemical reduction method in the presence of bifunctional organic thiols as stabilizing agents suitable for the formation of covalently linked PdNPs networks: p‐terphenyl‐4,4″‐dithiol (PdNPs‐TR), biphenyl‐4,4′‐dithiol (PdNPs‐BP), or with 9,9‐didodecyl‐2,7‐bis(acetylthio)fluorene (PdNPs‐FL). Comparing the hydrodynamic diameter values, TR and BP ligands help to obtain networks consisting of spherical NPs of about 2 nm, in which each bifunctional ligand act as a bridge between PdNPs. In contrast, PdNPs‐FL show a population centered at <2RH> = 45 ± 5 nm. To perform preliminary gas sensing measurements, PdNPs networks are cast deposited on interdigitated electrodes to study their resistive response toward volatile organic compounds (VOCs) such as benzene (0–5%), toluene (0–1.7%), and p‐xylene (0–0.4%) (BTX) and common interfering gases (H2S, NH3, SO2, and relative humidity, RH). PdNPs‐FL show enhanced response to BTX with an appreciable response also toward H2S and RH. PdNPs‐TR exhibit a better ability to discriminate benzene gas with a negligible response after H2S exposure. Moreover, all the PdNPs systems show little to no response to NH3 and SO2 gases, offering an interesting perspective in practical sensing applications.
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