Synthesis of nickel/gallium nanoalloys using a dual-source approach in 1-alkyl-3-methylimidazole ionic liquids

• Ilka Simon,
• Julius Hornung,
• Juri Barthel,
• Jörg Thomas,
• Maik Finze,
• Roland A. Fischer and
• Christoph Janiak

Beilstein J. Nanotechnol. 2019, 10, 1754–1767, doi:10.3762/bjnano.10.171

• carbene ligands (NHC) stabilize metal clusters and nanoparticles [44]. By insertion of the transition-metal center into the C2–H bond of imidazolium salts, transition-metal hydride complexes are formed [45]. Finally, H transfer reactions from the transition metal to GaCp* lead to the release of Cp*H

The impact of crystal size and temperature on the adsorption-induced flexibility of the Zr-based metal–organic framework DUT-98

• Simon Krause,
• Volodymyr Bon,
• Hongchu Du,
• Rafal E. Dunin-Borkowski,
• Ulrich Stoeck,
• Irena Senkovska and
• Stefan Kaskel

Beilstein J. Nanotechnol. 2019, 10, 1737–1744, doi:10.3762/bjnano.10.169

• supramolecular building blocks (SBBs), which consist of Zr6 clusters interconnected by 3,6-carbazole dicarboxylate ligands [20]. An additional benzoate functionality of the ligand connects the SBB into a 3D framework with a structure (Figure 1) similar to MIL-53 [21][22]. Upon removal of the solvent molecules

Tailoring the magnetic properties of cobalt ferrite nanoparticles using the polyol process

• Malek Bibani,
• Romain Breitwieser,
• Alex Aubert,
• Vincent Loyau,
• Silvana Mercone,
• Souad Ammar and
• Fayna Mammeri

Beilstein J. Nanotechnol. 2019, 10, 1166–1176, doi:10.3762/bjnano.10.116

• emerged as promising and versatile chemical route for the preparation of highly crystalline, monodisperse particles that are isotropic in shape [20][21]. Polyols act not only of solvents, but also as complexing ligands, avoiding the presence of any surfactant. Hydrolysis ratio, nature of polyol, synthesis

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 will possess just one single FluPep ligand [30]. At higher molar fractions the number of FluPep ligands per nanoparticle will increase. It is interesting to note that not all gold nanoparticles were observed to bind to the CM-Sepharose column at higher molar fractions of FluPep ligand, something

• -Sepharose. As the percentage of FluPep incorporated into the ligand shell increased, so did the percentage of nanoparticles bound to CM-Sepharose (Figure 6). This suggests that the molar fraction of FluPep ligand in the initial mixture of ligands added to the nanoparticles reflects its incorporation into

• , Wokingham, UK) and 384-well plates from Corning (Lowell, US) and the concentration of gold nanoparticles and of silver nanoparticles was determined at 450 nm [18] and 392 nm [49], respectively. Synthesis of FluPep functionalised nanoparticles Mixed-matrix ligands 70:30 (mol/mol) CVVVT-ol/ HS(CH2)11(OC2H4

Serum type and concentration both affect the protein-corona composition of PLGA nanoparticles

• Katrin Partikel,
• Robin Korte,
• Dennis Mulac,
• Hans-Ulrich Humpf and
• Klaus Langer

Beilstein J. Nanotechnol. 2019, 10, 1002–1015, doi:10.3762/bjnano.10.101

• serum; nanoparticles; poly(lactide-co-glycolic acid); protein corona; proteomics; Introduction Nanoparticle (NP)-based drug carrier systems offer outstanding opportunities in the treatment of many serious diseases. The unique physicochemical properties and the ability to bind a library of ligands make

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

• sequentially. High-resolution transmission electron microscopy (HRTEM) shows that the four fractions are well-dispersed spherical particles of diameter 3.0 ± 0.6, 2.3 ± 0.5, 1.7 ± 0.4, and 1.2 ± 0.4 nm. Proton nuclear magnetic resonance spectroscopy suggests that disulfide, excess ligands and gold(I) complexes

• size and the ratio of Au atoms to ligands of AuNCs. X-ray photoelectron spectroscopy (XPS) has also been applied to observe the molecular dependence on the gold and sulfur chemical state of organosulfur monolayers of the fractions. The photoluminescence spectra of these AuNCs in the range of 900–790 nm

• eV). These shifts are due to free ligands, disulfides and gold(I) complexes in this fraction. Additionally, a weak shoulder peak at around 168 eV is observed as shown in Figure 8F, which is assignable to sulfur oxide generated from the fractionation procedure. Upon exposure to atmospheric oxygen, two

Tungsten disulfide-based nanocomposites for photothermal therapy

• Tzuriel Levin,
• Hagit Sade,
• Rina Ben-Shabbat Binyamini,
• Maayan Pour,
• Iftach Nachman and
• Jean-Paul Lellouche

Beilstein J. Nanotechnol. 2019, 10, 811–822, doi:10.3762/bjnano.10.81

• , they reported a method based on a nickel–nitrotriacetic acid (Ni-NTA) complex as an anchoring group for different chemical functionalities [48][49][50]. Another study of the Tremel group involves terpyridine (TerPy) ligands [51]. NTA and TerPy are multi-dentate ligands, forming complexes with

• chemistry, thanks to an available valence electron in its 4f orbital. In our group, cerium was utilized in the complex form of ceric ammonium nitrate [(NH4)2Ce(IV)(NO3)6, or CAN]. In CAN the cerium ion is coordinated with six nitrate ligands through their oxygen atoms. CAN is a strong oxidizer, turning

• effect, other ligands on the cerium ion can be replaced by different polymers and linkers. The resulting nanocomposites can be used for biomedical applications, such as gene silencing [52], magnetic imaging, and drug delivery. Here we present a new and simple-to-fabricate WS2-NT-CAN-mag (WS2-NT-CM

Polydopamine-coated Au nanorods for targeted fluorescent cell imaging and photothermal therapy

• Boris N. Khlebtsov,
• Andrey M. Burov,
• Timofey E. Pylaev and
• Nikolai G. Khlebtsov

Beilstein J. Nanotechnol. 2019, 10, 794–803, doi:10.3762/bjnano.10.79

• . Meanwhile different imaging and therapeutic agents can be loaded into the shell of multifunctional nanocomposites. Various AuNR-based nanocomposites loaded with anticancer drugs [17][18][19], photodynamic dyes [20][21], MRI contrast agents [22] and many others ligands [23][24] have already been reported for

On the transformation of “zincone”-like into porous ZnO thin films from sub-saturated plasma enhanced atomic layer deposition

• Alberto Perrotta,
• Julian Pilz,
• Stefan Pachmajer,
• Antonella Milella and
• Anna Maria Coclite

Beilstein J. Nanotechnol. 2019, 10, 746–759, doi:10.3762/bjnano.10.74

• substrates and devices. By combining the metalorganic precursors adopted in ALD with the organic ligands used in MLD, hybrid organic–inorganic materials can be synthesized [2][3][4]. These materials possess properties in between their pure organic and inorganic counterparts, yet differing from the pristine

• expected, down to values of 1.0 Å/cycle for the plasma doses explored. The lower GPC resulted from the partial removal of the organic ligands of the metalorganic precursor (DEZ) and the formation of a limited number of active groups able to react with the next metalorganic precursor exposure. In order to

• justified with the formation of more Zn–OH groups due to the removal of the organic ligands. Furthermore, room-temperature PE-ALD processes have often shown in the literature the inclusion of chain-terminating –OH groups in the inorganic matrix, due to the low energy provided during the growth [47][57]. The

Deposition of metal particles onto semiconductor nanorods using an ionic liquid

• Michael D. Ballentine,
• Elizabeth G. Embry,
• Marco A. Garcia and
• Lawrence J. Hill

Beilstein J. Nanotechnol. 2019, 10, 718–724, doi:10.3762/bjnano.10.71

• agents. Photocatalytic dye degradation experiments showed that catalysts with platinum particles deposited using the ionic liquid out-performed similar materials synthesized using organic solvents and ligands. We concluded that metal particles can be deposited onto well-defined semiconductor nanorods

• synthesis conditions [5]. Well-defined nanorod substrates are synthesized using organic ligands to direct crystal growth [6], and these surface-bound ligands often play an important role in charge transfer at the particle/solvent interface [7][8][9][10][11]. However, these stabilizing ligands also insulate

• ][15][16][17]. The low surface tension of ionic liquids causes high nucleation rates and allows for the synthesis of small nanoparticles with minimal Ostwald ripening [17]. Further, many ionic liquids consist of a large anion with diffuse negative charge; this lack of strongly binding anionic ligands

Ultrasonication-assisted synthesis of CsPbBr₃ and Cs₄PbBr₆ perovskite nanocrystals and their reversible transformation

• Longshi Rao,
• Xinrui Ding,
• Xuewei Du,
• Guanwei Liang,
• Yong Tang,
• Kairui Tang and
• Jin Z. Zhang

Beilstein J. Nanotechnol. 2019, 10, 666–676, doi:10.3762/bjnano.10.66

• transformation into Cs4PbBr6 PNCs. This process is related to Ostwald ripening that was found during the nucleation and growth of PNCs [42]. Therefore, the formation of Cs4PbBr6 PNCs is promoted by the capacity of the organic ligands to dissolve PbBr2 and by the dissociation of CsPbBr3 PNCs. A series of TEM

• images (Figure 4c–h) clearly confirm that the morphology of these PNCs can be tuned easily by changing the amount of OAm in the precursor solution, while keeping the amount of OA unchanged. We attribute this morphology change to the crystal anisotropy induced by the growth kinetics. The capping ligands

• be proven by the reduction of crystal size from 65 to 11.7 nm (Figure 1 and Figure 4). This is consistent with the findings reported by Wu and co-workers [20]. As the solubility of liquid paraffin or capping ligands in water is very low, further dissolution of CsPbBr3 PNCs is inhibited, which is

Ultrathin hydrophobic films based on the metal organic framework UiO-66-COOH(Zr)

• Miguel A. Andrés,
• Clemence Sicard,
• Christian Serre,
• Olivier Roubeau and
• Ignacio Gascón

Beilstein J. Nanotechnol. 2019, 10, 654–665, doi:10.3762/bjnano.10.65

• . Keywords: hydrophobic coating; Langmuir–Blodgett (LB) films; metal organic framework (MOF); surface modification; UiO-66-COOH(Zr); Introduction Metal organic frameworks (MOFs) are well-known, crystalline, porous materials formed by metal ions (or metallic clusters) and organic ligands coordinated in a pre

Biocompatible organic–inorganic hybrid materials based on nucleobases and titanium developed by molecular layer deposition

• Leva Momtazi,
• Henrik H. Sønsteby and
• Ola Nilsen

Beilstein J. Nanotechnol. 2019, 10, 399–411, doi:10.3762/bjnano.10.39

• , indicating that the film is converted towards TiO2 and either excess TIP-ligands and/or nucleobases is lost from the film. All of these observations point towards the fact that the adenine system produces a relatively stable complex containing both TIP ligands and adenine. This complex is sufficiently stable

• , while the primary amine group in adenine takes part. Neither of the systems shows dominant Ti–N bonding schemes, but rather Ti–O bonds. This is particularly informative for the adenine system as it indicates that a significant portion of the TIP ligands are intact in the film during growth (the adenine

One-step nonhydrolytic sol–gel synthesis of mesoporous TiO₂ phosphonate hybrid materials

• Yanhui Wang,
• P. Hubert Mutin and
• Johan G. Alauzun

Beilstein J. Nanotechnol. 2019, 10, 356–362, doi:10.3762/bjnano.10.35

• case of metals, as M–C bonds are (in most cases) quite unstable, the organic groups can be linked to the metal oxide network via carboxylate or β-diketonate ligands [5][10][11]. Organophosphorus ligands such as phosphonates appear quite promising as they form strong ionocovalent M–O–P bonds with many

Removal of toxic heavy metals from river water samples using a porous silica surface modified with a new β-ketoenolic host

• Said Tighadouini,
• Smaail Radi,
• Abderrahman Elidrissi,
• Khadija Haboubi,
• Maryse Bacquet,
• Stéphanie Degoutin,
• Mustapha Zaghrioui and
• Yann Garcia

Beilstein J. Nanotechnol. 2019, 10, 262–273, doi:10.3762/bjnano.10.25

• cycles of adsorption/desorption. Compared to literature results, this material can be considered a high-performing remediation adsorbent for the extraction of Zn(II) from natural real water solution. Keywords: heavy metals; hybrid materials; β-ketoenol–pyridine–furan ligands; polluted media; porous

Thermal control of the defunctionalization of supported Au₂₅(glutathione)₁₈ catalysts for benzyl alcohol oxidation

• Zahraa Shahin,
• Hyewon Ji,
• Rodica Chiriac,
• Nadine Essayem,
• Franck Rataboul and
• Aude Demessence

Beilstein J. Nanotechnol. 2019, 10, 228–237, doi:10.3762/bjnano.10.21

• ][14][15]. The Au25(SR)18 gold thiolate cluster, the captain of the gold nanoclusters ship, is a thermodynamically stable cluster consisting of 25 gold atoms and protected by 18 thiolate ligands [16]. This gold thiolate cluster has been widely studied for its high potential in different domains of

• 4 h and showed full conversion of benzyl alcohol into mostly benzoic acid, under 1 atm of O2 at 30 °C using a base [17]. In a previous study by our group, Au25(SPhNH2)17@SBA-15, calcined at 400 °C to fully remove the ligands, induced the full conversion of benzyl alcohol after a couple of hours in

• nm, by applying Bragg’s law (Figure S3, Supporting Information File 1) [36]. This distance is in good agreement with the expected size of Au25(SG)18 including the ligands. In addition, the broad peak at 37° corresponds to the ultra-small Au25 gold core and confirms the absence of large gold

Raman study of flash-lamp annealed aqueous Cu₂ZnSnS₄ nanocrystals

• Yevhenii Havryliuk,
• Oleksandr Selyshchev,
• Mykhailo Valakh,
• Alexandra Raevskaya,
• Oleksandr Stroyuk,
• Constance Schmidt,
• Volodymyr Dzhagan and
• Dietrich R. T. Zahn

Beilstein J. Nanotechnol. 2019, 10, 222–227, doi:10.3762/bjnano.10.20

• -treated films, broad Raman features in the range of carbon-related D- and G-bands were detected (Figure 2b). These bands are related to the decomposition of ligands into amorphous carbon phases [45]. No relation between the intensity if these bands and the quality of the CZTS spectrum was observed. The

Targeting strategies for improving the efficacy of nanomedicine in oncology

• Gonzalo Villaverde and
• Alejandro Baeza

Beilstein J. Nanotechnol. 2019, 10, 168–181, doi:10.3762/bjnano.10.16

• systematic evolution of ligands by exponential enrichment (SELEX) [37]. Through this technique it is possible to obtain oligonucleotide sequences selective for many different membrane proteins. These macromolecules have been widely employed both alone and conjugated with drugs or nanoparticles [38]. Aptamers

• in the treatment efficacy compared to the passive vectorization effect provided by EPR [57]. Physical and also biological barriers disrupt, to a high extent, the desired selective interactions between the targeting ligands and their receptors. Effects such as off-targeting towards common cell

• cancers and depending on the location of the malignant tissue, the EPR is not effective at all. Combining tissular and celluar agents is a powerful tool in such cases making that active tissular targeting ligands even more important. In 2014, Yang et al. [62] described a peptide dual targeting system with

Electrolyte tuning in dye-sensitized solar cells with N-heterocyclic carbene (NHC) iron(II) sensitizers

• Mariia Karpacheva,
• Catherine E. Housecroft and
• Edwin C. Constable

Beilstein J. Nanotechnol. 2018, 9, 3069–3078, doi:10.3762/bjnano.9.285

• ) ligands. Replacing polypyridyl ligands by NHCs leads to a remarkable increase in the lifetime of the 3MLCT excited state (1000× longer), considerably enhancing electron injection [27][28][29][30][31][32][33]. The homoleptic complex 1 (Scheme 2) is currently the best-performing iron(II) NHC sensitizer

Hybrid Au@alendronate nanoparticles as dual chemo-photothermal agent for combined cancer treatment

• Anouchka Plan Sangnier,
• Romain Aufaure,
• Laurence Motte,
• Claire Wilhelm,
• Erwann Guenin and
• Yoann Lalatonne

Beilstein J. Nanotechnol. 2018, 9, 2947–2952, doi:10.3762/bjnano.9.273

• internalized by the cells and accumulates preferentially into bone tissue. Benyettou et al. showed that alendronate-coated magnetic NPs favour the intratumoral uptake and inhibit tumor growth [10]. HMBPs are also effective ligands to stabilize nanoparticles under biological conditions [11][12][13][14][15

Magnetic and luminescent coordination networks based on imidazolium salts and lanthanides for sensitive ratiometric thermometry

• Pierre Farger,
• Cédric Leuvrey,
• Mathieu Gallart,
• Pierre Gilliot,
• Guillaume Rogez,
• João Rocha,
• Duarte Ananias,
• Pierre Rabu and
• Emilie Delahaye

Beilstein J. Nanotechnol. 2018, 9, 2775–2787, doi:10.3762/bjnano.9.259

• coordination networks can be obtained either by the use of specific luminescent organic ligands or by the use of main-group elements, d10 transition metals or of trivalent lanthanide ions for the inorganic moiety [13][14]. The luminescent properties of the trivalent lanthanide ions are particularly interesting

• applications of lanthanide-based networks in information storage, quantum computing and spintronics [19][20][21][22][23]. Most of these lanthanide-based networks are obtained with neutral organic ligands such as benzene-1,4-dicarboxylate (1,4-bdc) [24], benzene-1,3,5-tricarboxylate (TMA) [25], pyridine-2,5

• -dicarboxylate (2,5-H2pdc) [24] or 1H-2-propyl-4,5-imidazoledicarboxylate (pimda) [26]. Only few examples of lanthanide-based networks obtained with charged ligands are reported in the literature [27][28][29][30]. Following this last point, we have chosen to synthesize lanthanide-based networks from positively

SERS active Ag–SiO₂ nanoparticles obtained by laser ablation of silver in colloidal silica

• Cristina Gellini,
• Francesco Muniz-Miranda,
• Alfonso Pedone and
• Maurizio Muniz-Miranda

Beilstein J. Nanotechnol. 2018, 9, 2396–2404, doi:10.3762/bjnano.9.224

• adhere to silica can be stabilized in colloidal suspensions far better than in pure metal colloids, providing improved reproducibility of the SERS data. The second motivation is to exploit the adsorption capability of the colloidal silica for various organic ligands, for example glucose, formaldehyde

• silver, but that can undergo SERS enhancement thanks to the vicinal presence of silver nanoparticles. The Ag–SiO2 colloidal nanoparticles also show an efficient SERS response for organic ligands such as 2,2'-bipyridine at a laser excitation wavelength of 1064 nm. The possibility to observe FT-SERS

High-throughput micro-nanostructuring by microdroplet inkjet printing

• Hendrikje R. Neumann and
• Christine Selhuber-Unkel

Beilstein J. Nanotechnol. 2018, 9, 2372–2380, doi:10.3762/bjnano.9.222

• BCML can intrinsically only coat surfaces with nanoparticle arrays, many biosensor applications also require well-defined structures and concentrations of ligands in microarrays [17]. Particularly the generation of cell arrays is a highly challenging task [18][19]. A feasible strategy would therefore

Block copolymers for designing nanostructured porous coatings

• Roberto Nisticò

Beilstein J. Nanotechnol. 2018, 9, 2332–2344, doi:10.3762/bjnano.9.218

• moieties. In this study, the metallo-complex selected is Ru(II)-terpyridine bis-complex. By washing the film with a Ce(IV)-containing acid solution, the Ru(II) complex between the blocks is oxidized into Ru(III) that is able to form only a monocomplex with the terpyridine ligands, thus breaking one metallo

Lead-free hybrid perovskites for photovoltaics

• Oleksandr Stroyuk

Beilstein J. Nanotechnol. 2018, 9, 2209–2235, doi:10.3762/bjnano.9.207

• -dependent bandgap, decreasing from 1.47 nm for the smallest NCs to 1.36 eV to the largest ones. The NCs are free from any surface ligands and stable long enough for the preparation of solar cell electrodes [130]. The Cs2SnI6 HPs can be formed by in situ oxidizing unstable CsSnI3 with air oxygen [112] or