Laser synthesis of nanoparticles in organic solvents – products, reactions, and perspectives

• Theo Fromme,
• Sven Reichenberger,
• Katharine M. Tibbetts and
• Stephan Barcikowski

Beilstein J. Nanotechnol. 2024, 15, 638–663, doi:10.3762/bjnano.15.54

• the ablation of Pb, Zn, and Cu was performed by Niu et al. in thiols to gain the respective sulfides [157]. In contrast to the change of the nanoparticle core, Choi et al. elegantly obtained N-doped carbon shells or nitrides when they ablated in acetonitrile [104][105]. A change of solvent to

Nanomedicines against Chagas disease: a critical review

• Maria Jose Morilla,
• Kajal Ghosal and
• Eder Lilia Romero

Beilstein J. Nanotechnol. 2024, 15, 333–349, doi:10.3762/bjnano.15.30

• , resulting in its fast killing. Lately, it was suggested that the major metabolic impact of BNZ is on the glutathione (and trypanothione) pathway so that covalent binding of BNZ with low-molecular-weight thiols and with protein thiols is the drug’s primary mode of action against T. cruzi [15]. In mammalian

Spatial variations of conductivity of self-assembled monolayers of dodecanethiol on Au/mica and Au/Si substrates

• Julian Skolaut,
• Jędrzej Tepper,
• Federica Galli,
• Wulf Wulfhekel and
• Jan M. van Ruitenbeek

Beilstein J. Nanotechnol. 2023, 14, 1169–1177, doi:10.3762/bjnano.14.97

• of current characteristics strongly depends on the substrate chosen to deposit the SAM onto. For this study, we employ alkane thiols, which are allowed to form a SAM on different types of Au substrates. We have chosen dodecanethiol (DDT) molecules and study them on commercially available Au

Antibody-conjugated nanoparticles for target-specific drug delivery of chemotherapeutics

• Mamta Kumari,
• Amitabha Acharya and
• Praveen Thaggikuppe Krishnamurthy

Beilstein J. Nanotechnol. 2023, 14, 912–926, doi:10.3762/bjnano.14.75

• the reduction of disulfide bonds. Thiols, also called sulfhydryls, in the cysteine side chain are slightly less abundant than primary amines; therefore, the coupling by thiol groups is more selective [52]. Thiols in cysteines are linked by disulfide bonds (–S–S–) through an oxidation process where the

• thiols groups are oxidized into disulfides. The disulfide bonds stabilize tertiary and quaternary protein structures and play a crucial role in protein folding [53][54]. For conjugation, free thiol and reduced thiol groups are required. Many proteins contain cysteine moieties linked with thiol. In

N-Heterocyclic carbene-based gold etchants

• Robert B. Chevalier,
• Justin Pantano,
• Matthew K. Kiesewetter and
• Jason R. Dwyer

Beilstein J. Nanotechnol. 2023, 14, 865–871, doi:10.3762/bjnano.14.71

• Robert B. Chevalier Justin Pantano Matthew K. Kiesewetter Jason R. Dwyer Department of Chemistry, University of Rhode Island, 140 Flagg Road, Kingston, RI, 02881, USA 10.3762/bjnano.14.71 Abstract N-Heterocyclic carbenes (NHCs) are an emerging alternative to thiols for the formation of stable

• a fixture of materials science. Thiols continue to dominate as the most prevalent choice of SAM constituents on gold [1][2][3][4][5][6][7][8][9][10][11]. They benefit from a long history of widespread use and general ease of adoption. Unfortunately, the gold–sulfur bond can limit the range of

• , an NHC-based monolayer has even been shown to protect against thiol displacement on gold surfaces [13]. Thus, in spite of the challenges that can be presented by NHC synthesis [17], they offer appeal even in light of the more general commercial availability of a wide range of thiols. The covalent

Detection and imaging of Hg(II) in vivo using glutathione-functionalized gold nanoparticles

• Gufeng Li,
• Shaoqing Li,
• Rui Wang,
• Min Yang,
• Lizhu Zhang,
• Yanli Zhang,
• Wenrong Yang and
• Hongbin Wang

Beilstein J. Nanotechnol. 2022, 13, 549–559, doi:10.3762/bjnano.13.46

• University, Waurn Ponds, Victoria 3216, Australia 10.3762/bjnano.13.46 Abstract The optical and biological properties of functionalized gold nanoparticles (GNPs) have been widely used in sensing applications. GNPs have a strong binding ability to thiol groups. Furthermore, thiols are used to bind functional

Investigation of electron-induced cross-linking of self-assembled monolayers by scanning tunneling microscopy

• Patrick Stohmann,
• Sascha Koch,
• Yang Yang,
• Christopher David Kaiser,
• Julian Ehrens,
• Jürgen Schnack,
• Niklas Biere,
• Dario Anselmetti,
• Armin Gölzhäuser and
• Xianghui Zhang

Beilstein J. Nanotechnol. 2022, 13, 462–471, doi:10.3762/bjnano.13.39

• K and the substrate was held at room temperature. The chamber pressure during the evaporation process was ≈10−8 mbar and the evaporation time was ≈30 min. X-ray photoelectron spectroscopy was employed to monitor the existence of thiolates as well as physisorbed thiols. To remove physisorbed

Sputtering onto liquids: a critical review

• Anastasiya Sergievskaya,
• Adrien Chauvin and
• Stephanos Konstantinidis

Beilstein J. Nanotechnol. 2022, 13, 10–53, doi:10.3762/bjnano.13.2

• metal precursor, usually a salt such as HAuCl4, is chemically reduced by a (ii) reagent (e.g., sodium citrate, sodium borohydrate, ascorbic acid, glucose, hydrazine, or various amines) in the presence of a (iii) stabilizing agent (e.g., organic thiols, amines, acids, or various surfactants, i.e

Modification of a SERS-active Ag surface to promote adsorption of charged analytes: effect of Cu²⁺ ions

• Bahdan V. Ranishenka,
• Andrei Yu. Panarin,
• Irina A. Chelnokova,
• Sergei N. Terekhov,
• Peter Mojzes and
• Vadim V. Shmanai

Beilstein J. Nanotechnol. 2021, 12, 902–912, doi:10.3762/bjnano.12.67

• charged hydrophilic thiols (sodium 2-mercaptoethyl sulfonate, mercaptopropionic acid, 2-mercaptoethanol, 2-(dimethylamino)ethanethiol hydrochloride, and thiocholine) to vary the surface charge of the SERS substrate. We used two oppositely charged porphyrins, cationic copper(II) tetrakis(4-N-methylpyridyl

• study the electrostatic interaction with an analyte and exclude factors caused by complex specific interactions with the Ag surface, we used a set of organic thiols with differently charged functional groups and similar linker length. Additionally, we checked previously reported approaches on the

• with the Ag surface, we used a set of organic thiols with the same linker length but differently charged hydrophilic functional groups. Thiol functionality guarantees a strong binding to the surface and a sufficiently dense molecule packing to make the surface properties determined by the introduced

Fate and transformation of silver nanoparticles in different biological conditions

• Barbara Pem,
• Marija Ćurlin,
• Darija Domazet Jurašin,
• Valerije Vrček,
• Rinea Barbir,
• Vedran Micek,
• Raluca M. Fratila,
• Jesus M. de la Fuente and
• Ivana Vinković Vrček

Beilstein J. Nanotechnol. 2021, 12, 665–679, doi:10.3762/bjnano.12.53

• are created by several pathways, including partial AgNPs dissolution in the gastric fluid, uptake and systemic transport of ionic and nanoparticulate Ag as thiol and selenium complexes, and final deposition in the near-skin regions [15]. Especially important is the process of interaction with thiols

• owing to their many physiological roles and evidences for thiol-containing proteins as major targets for toxic effects of ionic Ag [25]. In the presence of biothiols the soluble complexes are formed. Thiols possess a high affinity for soft Lewis acid metals and may easily coordinate Ag+ [9][26][27]. The

Ultrasensitive detection of cadmium ions using a microcantilever-based piezoresistive sensor for groundwater

• Dinesh Rotake,
• Anand Darji and
• Nitin Kale

Beilstein J. Nanotechnol. 2020, 11, 1242–1253, doi:10.3762/bjnano.11.108

• cadmium. Verification of performed experiment results using EDX In general, the thiol groups can bind to all types of HMIs. Thus, to selectively bind and detect Cd(II) the thiols goups need to be modified or functionalized with materials that are selective for Cd(II). The experimental results show that

Silver-decorated gel-shell nanobeads: physicochemical characterization and evaluation of antibacterial properties

• Marta Bartel,
• Katarzyna Markowska,
• Marcin Strawski,
• Krystyna Wolska and
• Maciej Mazur

Beilstein J. Nanotechnol. 2020, 11, 620–630, doi:10.3762/bjnano.11.49

• layer producing silver nanoparticles but also transforms a fraction of sulfonic groups in the polymer to moieties with sulfur in a lower oxidation state, likely thiols. It is hypothesized that the generated thiol groups are anchoring the nanoparticles in the gel shell of the nanobeads stabilizing the

• have been partially reduced to thiol moieties. In consequence, the thiols interact with the silver nanoparticles anchoring them in the gel layer on the nanobeads. Moreover, it has been shown that the nanocomposite exhibits considerable antibacterial activity, comparable or superior to that of non

• reduced to a thiol moiety [37]. If this is the case, it may be hypothesized that the generated thiols adsorb on the surface of the silver nanoparticles (the adsorption of thiols on silver surfaces is a well-known phenomenon). It should be noted, however, that the binding energy of sulfur in aromatic

Luminescent gold nanoclusters for bioimaging applications

• Nonappa

Beilstein J. Nanotechnol. 2020, 11, 533–546, doi:10.3762/bjnano.11.42

• of gold nanoclusters. A) Nanoclusters provide a link between molecular complexes and plasmonic nanoparticles. B) X-ray structure of [Au25(PET)18], from CSD entry JACVOB. C) Chemical structure of some of the organic thiols discussed in this review (PET: phenylethane thiol; LA: lipoic acid; GSH

Preparation and in vivo evaluation of glyco-gold nanoparticles carrying synthetic mycobacterial hexaarabinofuranoside

• Gennady L. Burygin,
• Polina I. Abronina,
• Nikita M. Podvalnyy,
• Sergey A. Staroverov,
• Leonid O. Kononov and
• Lev A. Dykman

Beilstein J. Nanotechnol. 2020, 11, 480–493, doi:10.3762/bjnano.11.39

• and 4 might be exchanged with various thiols present in vivo, immunization with the prepared Ara6-GNPs 3 and 4 was successful, which indicates that such glyco-GNPs preparations are indeed capable of inducing antibody response. Clarification of these complex issues clearly requires further studies. The

• uptake of glycans incorporated in glyco-GNPs since free glycans (haptens) cannot be phagocytosed per se due to their small size. Probably, the substitution of glycans on the surface of glyco-GNPs with endogenous cellular thiols and amines facilitates the subsequent translocation of glycans to the surface

Multiwalled carbon nanotube based aromatic volatile organic compound sensor: sensitivity enhancement through 1-hexadecanethiol functionalisation

• Nadra Bohli,
• Meryem Belkilani,
• Juan Casanova-Chafer,
• Eduard Llobet and
• Adnane Abdelghani

Beilstein J. Nanotechnol. 2019, 10, 2364–2373, doi:10.3762/bjnano.10.227

• -mercaptohexadecanoic acid (MHDA) showed no response to aromatic vapours [22]. As presented in Table 1, the vapours tested are nonpolar in nature and therefore have a high affinity with the hydrophobic CH3 group of the HDT. On the contrary, MHDA molecules are carboxylic acid terminated thiols, which are hydrophilic

• the sensor response was studied in a previous work [32]. The response to vapours remains basically unchanged for sensors employing hydrophobic thiols due to their hydrophobicity [31]. Such long-chain alkanethiol functionalised and decorated MWCNTs showed a high contact angle with water, which remains

Toxicity and safety study of silver and gold nanoparticles functionalized with cysteine and glutathione

• Barbara Pem,
• Igor M. Pongrac,
• Lea Ulm,
• Ivan Pavičić,
• Valerije Vrček,
• Darija Domazet Jurašin,
• Marija Ljubojević,
• Adela Krivohlavek and
• Ivana Vinković Vrček

Beilstein J. Nanotechnol. 2019, 10, 1802–1817, doi:10.3762/bjnano.10.175

• lead to the formation of thiol-coated AgNPs [48]. New clusters consisting of Ag2S can be created from free Ag+ [47]. This process, known as sulfidation, affects AgNP behavior in the biological system [49], most notably by reducing their toxicity [47][50]. The binding of thiols to AuNP surfaces has been

Alloyed Pt₃M (M = Co, Ni) nanoparticles supported on S- and N-doped carbon nanotubes for the oxygen reduction reaction

• Stéphane Louisia,
• Yohann R. J. Thomas,
• Pierre Lecante,
• Marie Heitzmann,
• M. Rosa Axet,
• Pierre-André Jacques and
• Philippe Serp

Beilstein J. Nanotechnol. 2019, 10, 1251–1269, doi:10.3762/bjnano.10.125

• matrix, while the oxidation of surface thiols should produce S–O bonds (peak at 168 eV). The presence of pyrite could arise from the significant amount of remaining iron catalyst in this sample. Different nitrogen groups are present in N-CNT, and the proportion of these groups was determined by

Scavenging of reactive oxygen species by phenolic compound-modified maghemite nanoparticles

• Małgorzata Świętek,
• Yi-Chin Lu,
• Rafał Konefał,
• Liliana P. Ferreira,
• M. Margarida Cruz,
• Yunn-Hwa Ma and
• Daniel Horák

Beilstein J. Nanotechnol. 2019, 10, 1073–1088, doi:10.3762/bjnano.10.108

• wavelength of 765 nm [22]. The FC reagent measures the total antioxidant capacity of not only phenolic compounds but also carbohydrates, thiols, vitamins, amines, unsaturated fatty acids, and various complex specimens [23]. The antioxidant properties of the modified chitosans increased in the following

Enhanced inhibition of influenza virus infection by peptide–noble-metal nanoparticle conjugates

• Zaid K. Alghrair,
• David G. Fernig and
• Bahram Ebrahimi

Beilstein J. Nanotechnol. 2019, 10, 1038–1047, doi:10.3762/bjnano.10.104

• nanoparticles (Figure 1A). This indicates that the FluPep sequence did not reduce the stability of the gold nanoparticles under these standard conditions. A more stressful test is ligand exchange with small thiols [26][27][28][29]. The ligand exchange results in a ligand shell that is unable to prevent

Structural and optical properties of penicillamine-protected gold nanocluster fractions separated by sequential size-selective fractionation

• Xiupei Yang,
• Zhengli Yang,
• Fenglin Tang,
• Jing Xu,
• Maoxue Zhang and
• Martin M. F. Choi

Beilstein J. Nanotechnol. 2019, 10, 955–966, doi:10.3762/bjnano.10.96

• ]. Unbound thiols (164 eV) cannot be found in the XPS spectra of the five fractions nor can the oxidized sulfur species (S 2p > 166 eV) be observed [35]. The observation confirms the stability of the NCs. The sulfur S 2p3/2 binding energy values (Figure 8) are 162.08, 162.14, 162.36 and 162.50 eV for

Hydrophilicity and carbon chain length effects on the gas sensing properties of chemoresistive, self-assembled monolayer carbon nanotube sensors

• Juan Casanova-Cháfer,
• Carla Bittencourt and
• Eduard Llobet

Beilstein J. Nanotechnol. 2019, 10, 565–577, doi:10.3762/bjnano.10.58

• , Belgium 10.3762/bjnano.10.58 Abstract Here we describe the development of chemoresistive sensors employing oxygen-plasma-treated, Au-decorated multiwall carbon nanotubes (MWCNTs) functionalized with self-assembled monolayers (SAMs) of thiols. For the first time, the effects of the length of the carbon

• chain and its hydrophilicity on the gas sensing properties of SAMs formed on carbon nanotubes are studied, and additionally, the gas sensing mechanisms are discussed. Four thiols differing in the length of the carbon chain and in the hydrophobic or hydrophilic nature of the head functional group are

• studied. Transmission electron microscopy, Raman spectroscopy and X-ray photoelectron spectroscopy are used to analyze the resulting gas-sensitive hybrid films. Among the different nanomaterials tested, short-chain thiols having a hydrophilic head group, self-assembled onto Au-decorated carbon nanotubes

Fabrication of photothermally active poly(vinyl alcohol) films with gold nanostars for antibacterial applications

• Mykola Borzenkov,
• Maria Moros,
• Claudia Tortiglione,
• Serena Bertoldi,
• Nicola Contessi,
• Silvia Faré,
• Angelo Taglietti,
• Agnese D’Agostino,
• Piersandro Pallavicini,
• Maddalena Collini and
• Giuseppe Chirico

Beilstein J. Nanotechnol. 2018, 9, 2040–2048, doi:10.3762/bjnano.9.193

• ) were commercially available from Fluka. Poly(ethylene glycol) thiols ( = 5000 g/mol; SH-PEG5000–OCH3 and SH-PEG5000–COOH), polyethylene glycol tert-octylphenyl ether (Triton X-100), chloroauric acid, ascorbic acid, silver nitrate, and sodium borohydride were purchased from Sigma-Aldrich and used as

Tuning adhesion forces between functionalized gold colloidal nanoparticles and silicon AFM tips: role of ligands and capillary forces

• Sven Oras,
• Sergei Vlassov,
• Marta Berholts,
• Rünno Lõhmus and
• Karine Mougin

Beilstein J. Nanotechnol. 2018, 9, 660–670, doi:10.3762/bjnano.9.61

• ) equipped with PeakForce QNM (Quantitative Nanoscale Mechanics) module. Au NPs were synthesized by a seed-mediated process and then functionalized with thiols containing different functional groups: amino, hydroxy, methoxy, carboxy, methyl, and thiol. Adhesion measurements showed strong differences between

• NPs and silicon tip depending on the nature of the tail functional group. The dependence of the adhesion on ligand density for different thiols with identical functional tail-group was also demonstrated. The calculated contribution of the van der Waals (vdW) forces between particles was in good

• force microscopy in ambient conditions. Au NPs were synthesized by chemical reduction of metal salts and functionalized with thiols presenting different tail groups varying from a very hydrophobic to a highly hydrophilic behavior. The tail groups were either an amino (–NH2), hydroxy (–OH), carboxyl

Facile phase transfer of gold nanorods and nanospheres stabilized with block copolymers

• Yaroslav I. Derikov,
• Georgiy A. Shandryuk,
• Raisa V. Talroze,
• Alexander A. Ezhov and
• Yaroslav V. Kudryavtsev

Beilstein J. Nanotechnol. 2018, 9, 616–627, doi:10.3762/bjnano.9.58

• or cetyl trimethylammonium bromide-stabilized Au nanorods with a solution of thiol- [18] or amine-terminated [19] surfactants in organic solvent. With a strong affinity to gold, thiols and amines replace nanoparticle shells via ligand exchange, while the tails of these molecules provide miscibility

Patterning of supported gold monolayers via chemical lift-off lithography

• Liane S. Slaughter,
• Kevin M. Cheung,
• Sami Kaappa,
• Huan H. Cao,
• Qing Yang,
• Thomas D. Young,
• Andrew C. Serino,
• Sami Malola,
• Jana M. Olson,
• Stephan Link,
• Hannu Häkkinen,
• Anne M. Andrews and
• Paul S. Weiss

Beilstein J. Nanotechnol. 2017, 8, 2648–2661, doi:10.3762/bjnano.8.265

• chemically similar to bulk Au since they are amenable to self-assembly of thiols, and thus, to forming Au–S bonds. The chemical ability to modify the supported Au monolayers resulting from CLL implies opportunities for large-scale, transparent, sensor technologies, which could be straightforwardly fabricated

• , in place of thiols [64][65]. Theorists have investigated the influence of collective interactions among alkanethiol backbones on the removal of clusters of SAM molecules from Au surfaces [66][67]. For example, less nanomechanical force is required to pull a monolayer of heptanethiolates and Au atoms