Suppression of low-energy dissociative electron attachment in Fe(CO)₅ upon clustering

• Jozef Lengyel,
• Peter Papp,
• Štefan Matejčík,
• Jaroslav Kočišek,
• Michal Fárník and
• Juraj Fedor

Beilstein J. Nanotechnol. 2017, 8, 2200–2207, doi:10.3762/bjnano.8.219

• , isotope distributions and high-energy resolution ion yields can be obtained. Results The mass spectrometry analysis of anions resulting from electron interactions with Fe(CO)5 clusters is complicated by the fact that two CO ligands have the same mass as one iron atom (56 amu). We have used the fact that

• intact monomer units attached to it. The CLUB data for pure Fe(CO)5 clusters and for Fe(CO)5 aggregates adsorbed on large Ar nanoparticles are very similar, with one notable difference: with the decreasing number of ligands in the fragment anion, the band between 5 and 10 eV disappears when the

• forces difficult to asses. For aggregates on argon nanoparticles, the band between 5 and 10 eV is clearly disappearing with the increasing number of removed ligands. It is thus most probably linked with the number of ligands removed in the step (Equation 6). The origin of the ligand stabilization by

Systematic control of α-Fe₂O₃ crystal growth direction for improved electrochemical performance of lithium-ion battery anodes

• Nan Shen,
• Miriam Keppeler,
• Barbara Stiaszny,
• Holger Hain,
• Filippo Maglia and
• Madhavi Srinivasan

Beilstein J. Nanotechnol. 2017, 8, 2032–2044, doi:10.3762/bjnano.8.204

• verified by results of our test series. Diamines are typical chelate ligands that interact with appropriate coordination centers. First, octahedral-shaped complexes are formed [29], formally described as (Fe[C2H2N2R1R2]3)3+. Diamine derivatives, in which the two amine groups are located at adjacent C atoms

• −. This will result in the gradual loss of diamine ligands, leading to complexes with two OH− groups and two diamines that form a quasi-square-plane perpendicular to the OH− direction [29]. Therefore, the following hydrolysis process is inhibited in the planar direction, but favored in the normal

Synthesis and functionalization of NaGdF₄:Yb,Er@NaGdF₄ core–shell nanoparticles for possible application as multimodal contrast agents

• Dovile Baziulyte-Paulaviciene,
• Vitalijus Karabanovas,
• Marius Stasys,
• Greta Jarockyte,
• Vilius Poderys,
• Simas Sakirzanovas and
• Ricardas Rotomskis

Beilstein J. Nanotechnol. 2017, 8, 1815–1824, doi:10.3762/bjnano.8.183

• structure, where the nonactive shell protects the luminescent rare earth ions in the core from quenching caused by surface defects and organic ligands [10]. A wide variety of studies were performed to synthesize dual functional core–shell UCNPs [11][12][13]. However, it remains difficult to obtain hexagonal

• phase and stabilized with hydrophobic ligands, such as oleic acid. Consequently, they can only be dispersed in nonpolar solvents (e.g., toluene, cyclohexane). In the past few years, several methods including surface silanization [14], ligand exchange [15], ligand oxidation [16], ligand removal [17], and

• 80. The presence of the Tween 80 coating was verified by comparing its FTIR spectra to that of pure oleic acid, oleate ligands coated particles, pure Tween 80, and the final coated nanoparticles (Figure 3). NaGdF4:Yb,Er UCNPs prepared in the presence of oleic acid shows characteristic absorption

Methionine-mediated synthesis of magnetic nanoparticles and functionalization with gold quantum dots for theranostic applications

• Arūnas Jagminas,
• Agnė Mikalauskaitė,
• Vitalijus Karabanovas and
• Jūrate Vaičiūnienė

Beilstein J. Nanotechnol. 2017, 8, 1734–1741, doi:10.3762/bjnano.8.174

• specific targeting ligands, such as aptamers and antibodies. This synthesis way may also be explored in future to design superparamagnetic, methionine-stabilized plasmonic magnetite NPs decorated with Au0/Au+1 QDs. Experimental Chemicals: All chemicals, including Co(II) and Fe(III) chlorides, and HAuCl4

Group-13 and group-15 doping of germanane

• Nicholas D. Cultrara,
• Maxx Q. Arguilla,
• Shishi Jiang,
• Chuanchuan Sun,
• Michael R. Scudder,
• R. Dominic Ross and
• Joshua E. Goldberger

Beilstein J. Nanotechnol. 2017, 8, 1642–1648, doi:10.3762/bjnano.8.164

• optoelectronic properties via covalent modification with surface ligands [3][24][25][26][27][28]. While the electron mobility of germanane at room temperature has been predicted to be greater than 18,000 cm2·V−1·s−1, transport measurements on non-extrinsically doped crystals were highly resistive, indicating the

Deposition of exchange-coupled dinickel complexes on gold substrates utilizing ambidentate mercapto-carboxylato ligands

• Martin Börner,
• Laura Blömer,
• Marcus Kischel,
• Peter Richter,
• Georgeta Salvan,
• Dietrich R. T. Zahn,
• Pablo F. Siles,
• Maria E. N. Fuentes,
• Carlos C. B. Bufon,
• Daniel Grimm,
• Oliver G. Schmidt,
• Daniel Breite,
• Bernd Abel and
• Berthold Kersting

Beilstein J. Nanotechnol. 2017, 8, 1375–1387, doi:10.3762/bjnano.8.139

• ) and 8 (J = +20.8 cm−1; H = −2JS1S2). The reactivity of complexes 6–8 is reminiscent of that of pure thiolato ligands, which readily chemisorb on Au surfaces as verified by contact angle, atomic force microscopy (AFM) and spectroscopic ellipsometry measurements. The large [Ni2L] tail groups, however

• , prevent the packing and self-assembly of the hydrocarbon chains. The smaller film thickness of 7 is attributed to the specific coordination mode of the coligand. Results of preliminary transport measurements utilizing rolled-up devices are also reported. Keywords: ambidentate ligands; chemisorption; gold

• macrocyclic complexes have not been anchored to gold via ambidentate mercaptobenzoate ligands. However, polynuclear Mn12 complexes have been fixed to gold via perfluorinated mercaptobenzoate linkers [42]. Results and Discussion Synthesis and characterization of complexes The investigated compounds and their

Synthesis of [Fe(L_eq)(L_ax)]_n coordination polymer nanoparticles using blockcopolymer micelles

• Christoph Göbel,
• Ottokar Klimm,
• Florian Puchtler,
• Sabine Rosenfeldt,
• Stephan Förster and
• Birgit Weber

Beilstein J. Nanotechnol. 2017, 8, 1318–1327, doi:10.3762/bjnano.8.133

• composite nanoparticles where the BCP micelle is filled with the CP, as in the case of the [FeLeq(bpey)]n@BCP. Otherwise, in the case of more flexible ligands or ligands that lead to high spin complexes, the formation of microcrystals next to the CP–BCP nanoparticles is observed above a certain

• strategy. This allows us to investigate the influence of the coordination polymer on the formation and the SCO activity of the final nanocompound. The CPs differ in the axial ligands (Lax), namely 1,2-di(pyridin-4-yl)ethane (bpea), trans-1,2-di(pyridin-4-yl)ethene (bpee) and 1,2-di(pyridin-4-yl)ethyne

• (bpey) (Scheme 1). The ligands were chosen because of their different flexibility. From the synthesis of the bulk complexes it is known, that an increasing flexibility of the ligand leads to an increase in solubility of the obtained CP [44][45]. This way we can investigate the impact of the solubility

Carbon nanomaterials sensitize prostate cancer cells to docetaxel and mitomycin C via induction of apoptosis and inhibition of proliferation

• Kati Erdmann,
• Jessica Ringel,
• Silke Hampel,
• Manfred P. Wirth and
• Susanne Fuessel

Beilstein J. Nanotechnol. 2017, 8, 1307–1317, doi:10.3762/bjnano.8.132

• various therapeutic drugs and to be internalized by cells. Furthermore, the functionalization with targeting ligands against cancer cell-specific molecules such as antibodies, peptides or aptamers represents another advantage of carbon nanomaterials [9][10][11][12]. We and others have previously shown

Evaluation of quantum dot conjugated antibodies for immunofluorescent labelling of cellular targets

• Jennifer E. Francis,
• David Mason and
• Raphaël Lévy

Beilstein J. Nanotechnol. 2017, 8, 1238–1249, doi:10.3762/bjnano.8.125

• ligands (such as poly(ethylene glycol) (PEG) [3][4]) or they are encapsulated in amphiphilic polymers [5]. Antibodies that recognise specific biological targets can then be conjugated to these Qdots for use in immunofluorescence. Conventional immunocytochemistry (ICC) protocols involve the chemical

Nano-engineered skin mesenchymal stem cells: potential vehicles for tumour-targeted quantum-dot delivery

• Liga Saulite,
• Dominyka Dapkute,
• Karlis Pleiko,
• Ineta Popena,
• Simona Steponkiene,
• Ricardas Rotomskis and
• Una Riekstina

Beilstein J. Nanotechnol. 2017, 8, 1218–1230, doi:10.3762/bjnano.8.123

• modifications of various NPs. These modifications increase the solubility of QDs to make QDs unnoticeable by the immune system, increase the QD half-life in the blood stream and target QDs to specific ligands or antigens [12]. Different therapeutic and recognition molecules can be attached to the surfaces of

Tuning the spin coherence time of Cu(II)−(bis)oxamato and Cu(II)−(bis)oxamidato complexes by advanced ESR pulse protocols

• Ruslan Zaripov,
• Evgeniya Vavilova,
• Iskander Khairuzhdinov,
• Kev Salikhov,
• Violeta Voronkova,
• Mohammad A. Abdulmalic,
• Francois E. Meva,
• Saddam Weheabby,
• Tobias Rüffer,
• Bernd Büchner and
• Vladislav Kataev

Beilstein J. Nanotechnol. 2017, 8, 943–955, doi:10.3762/bjnano.8.96

• nuclear spins. We argue that this method can be used as a test for the relevance of the spectral diffusion for the electron spin decoherence. Our results have revealed a prominent role of the opba4– and opbon-Pr24– ligands for the dephasing of the Cu spins. The presence of additional 14N nuclei and

• protons in [Cu(opbon-Pr2)]2– as compared to [Cu(opba)]2– yields significantly shorter Tm times. Such a detrimental effect of the opbon-Pr24− ligands has to be considered when discussing a potential application of the Cu(II)−(bis)oxamato and Cu(II)−(bis)oxamidato complexes as building blocks of more

• which in their turn have been investigated with regard to the magnetic superexchange interactions between the Cu spins mediated by the O and N ligands [1][2][3][4][5][6][7][8]. In this context, the transfer of the spin density from the central metal ion to the ligands and next via the oxamato or

The role of 2D/3D spin-polarization interactions in hybrid copper hydroxide acetate: new insights from first-principles molecular dynamics

• Ziyad Chaker,
• Guido Ori,
• Mauro Boero and
• Carlo Massobrio

Beilstein J. Nanotechnol. 2017, 8, 857–860, doi:10.3762/bjnano.8.86

• fluorene phosphonates) [1][2][3]. The interest in Cu2(OH)3X systems stems from their tunable magnetic properties, strongly dependent on the nature of the organic ligands. Based on experimental evidence, CuOHAc exhibits (when seen as a bulk material) 3D antiferromagnetic (AF) interlayer character and

Probing the magnetic superexchange couplings between terminal Cu^II ions in heterotrinuclear bis(oxamidato) type complexes

• Mohammad A. Abdulmalic,
• Saddam Weheabby,
• Francois E. Meva,
• Azar Aliabadi,
• Vladislav Kataev,
• Bernd Büchner,
• Frederik Schleife,
• Berthold Kersting and
• Tobias Rüffer

Beilstein J. Nanotechnol. 2017, 8, 789–800, doi:10.3762/bjnano.8.82

• CuIINiIICuII type IV complexes. Their central [NiII(opboR2)]2– fragments were anticipated to be free of any further co-ligands. That would make these central fragments purely diamagnetic and thus these heterotrinuclear CuIINiIICuII type IV complexes, possessing terminal paramagnetic CuII ions, appear as ideal

• complexes as described in [15]. Thus, the terminal CuII ions of 1A–3A are each coordinated by two O donor atoms of the oxamidato groups as well as three N donor atoms of the pmdta ligands to form CuN3O2 coordination units closer to the ideal square-pyramidal compared to the ideal trigonal-bipyramidal

• coordination geometry with respect to their τ parameters [26], cf. Table 2. One feature, commonly observed for all CuN3O2 units, deserves specific attention. The largest bond angle of all CuN3O2 units always involves the O donor atom of the function and the middle N donor atom of the pmdta ligands, cf. Figure

Dispersion of single-wall carbon nanotubes with supramolecular Congo red – properties of the complexes and mechanism of the interaction

• Anna Jagusiak,
• Barbara Piekarska,
• Tomasz Pańczyk,
• Małgorzata Jemioła-Rzemińska,
• Elżbieta Bielańska,
• Barbara Stopa,
• Grzegorz Zemanek,
• Janina Rybarska,
• Irena Roterman and
• Leszek Konieczny

Beilstein J. Nanotechnol. 2017, 8, 636–648, doi:10.3762/bjnano.8.68

• ]. Functionalization also allows for the attachment of biologically active molecules – e.g., drugs, nucleic acids, antibodies or ligands for cell-surface receptors. This is especially important for targeted drug delivery systems based on CNT [13][15][18][19][20][21]. Noncovalent functionalization of CNTs is usually

Investigation of the photocatalytic efficiency of tantalum alkoxy carboxylate-derived Ta₂O₅ nanoparticles in rhodamine B removal

• Subia Ambreen,
• Mohammad Danish,
• Narendra D. Pandey and
• Ashutosh Pandey

Beilstein J. Nanotechnol. 2017, 8, 604–613, doi:10.3762/bjnano.8.65

• down their replacement by –OH groups. This can be achieved by the longer or more branched alkyl groups of –OR, or by replacing alkoxo ligands with chelating groups. As a result, a homogenous gel is obtained with a lesser extent of cross-linking. Bidentate complexing ligands (BL) are usually employed in

• order to lower the nucleophilicity of the tantalum alkoxides. This is achieved by the incorporation of ligands such as β-diketones, β-ketoesters, carboxylic acids [15][16][17][18]. The reaction can be schematized as: This modification in the parent alkoxide results in several alterations in the new

• atmosphere. The schematic representations of the reactions are as follows: where R′ = CH2Cl, CHCl2, CCl3. The 1H NMR spectrum of compound 3 (Figure S1, Supporting Information File 1) comprises of two triplets at δ 1.09 and 1.21, which are attributed to the methyl protons of ethoxy ligands. The methylene

Methods for preparing polymer-decorated single exchange-biased magnetic nanoparticles for application in flexible polymer-based films

• Laurence Ourry,
• Delphine Toulemon,
• Souad Ammar and
• Fayna Mammeri

Beilstein J. Nanotechnol. 2017, 8, 408–417, doi:10.3762/bjnano.8.43

• consists of a direct grafting of bromopropionyl ester molecules ob the surface of ENPs that were previously recovered and redispersed in a suitable solvent. The second uses an “all in solution” process, based on a prior decoration of ENPs by oleic acid ligands, which were subsequently exchanged by the

Comparison of four methods for the biofunctionalization of gold nanorods by the introduction of sulfhydryl groups to antibodies

• Xuefeng Wang,
• Zhong Mei,
• Yanyan Wang and
• Liang Tang

Beilstein J. Nanotechnol. 2017, 8, 372–380, doi:10.3762/bjnano.8.39

• solution and the CTAB bilayer density [15]. The common ligand exchange is the replacement of the CTAB of GNR with thiol-terminated ligands, such as thiolated poly(ethylene glycol) and mercaptoundecanoic acid [10][11]. These agents can link the amino groups of biomolecules with the carboxylic group from

Tailoring bifunctional hybrid organic–inorganic nanoadsorbents by the choice of functional layer composition probed by adsorption of Cu²⁺ ions

• Veronika V. Tomina,
• Inna V. Melnyk,
• Yuriy L. Zub,
• Aivaras Kareiva,
• Miroslava Vaclavikova,
• Gulaim A. Seisenbaeva and
• Vadim G. Kessler

Beilstein J. Nanotechnol. 2017, 8, 334–347, doi:10.3762/bjnano.8.36

• nm). The moment when the second silane is added plays an important role. It was demonstrated that the availability of ligands on the surface could be affected by the time of addition for such functions as amino, monocarboxylate, ethylenediaminetriacetic acid, and dihydroimidazole-terminated ones [32

• ]. The best surface availability of organofunctional groups was achieved for the amino-terminated ligands when the organosilane was added 30 min after start of the particle growth, and for the carboxylate-terminated ones the optimal addition time was 5.5 h after particle growth initialization. No

• arrangement of the ligands. The kinetic studies were performed first to estimate the equilibrium time (see kinetic sorption parameters obtained using pseudo-first and pseudo-second-order models for metal ions sorption in Table S5, Supporting Information File 1). According to the presented data, the kinetic

Streptavidin-coated gold nanoparticles: critical role of oligonucleotides on stability and fractal aggregation

• Roberta D'Agata,
• Pasquale Palladino and
• Giuseppe Spoto

Beilstein J. Nanotechnol. 2017, 8, 1–11, doi:10.3762/bjnano.8.1

• relevant ligands has led to dramatic progresses in both living cells as well as biomolecular diagnostic assays [3][4][5]. In particular, optical sensing exploiting the surface plasmon resonance (SPR) effect has been widely investigated and plays a significant role in biomolecular detection [6][7]. In this

From iron coordination compounds to metal oxide nanoparticles

• Mihail Iacob,
• Carmen Racles,
• Codrin Tugui,
• George Stiubianu,
• Adrian Bele,
• Liviu Sacarescu,
• Daniel Timpu and
• Maria Cazacu

Beilstein J. Nanotechnol. 2016, 7, 2074–2087, doi:10.3762/bjnano.7.198

• control of formed micro- or nanostructures [19]. Most studies in this area relate to the thermal decomposition of metal complexes with ligands such as acetylacetonates, acetates and oleates. Good results in terms of narrow size distribution of nanoparticles are correlated with nucleation and growth stages

• general, the procedure leading to metal oxide materials consists of the thermal decomposition of adequate precursors under different conditions: by classical heating at high temperature in air (calcination) or in solution, in presence of changing ligands or surfactants. Nonconventional energy sources such

Solvent-mediated conductance increase of dodecanethiol-stabilized gold nanoparticle monolayers

• Patrick A. Reissner,
• Jean-Nicolas Tisserant,
• Antoni Sánchez-Ferrer,
• Raffaele Mezzenga and
• Andreas Stemmer

Beilstein J. Nanotechnol. 2016, 7, 2057–2064, doi:10.3762/bjnano.7.196

• further depends on the percolation of charge carriers [11][12]. Initially, gold nanoparticles are typically stabilized by alkanethiol ligands, which are poor conductors. As reported, the conductivity of nanoparticle networks can be increased by immersing the substrate with the nanoparticle monolayer in a

• dependence can be expected if the decrease in lattice constant is driven by an energy minimization process. Attractive van-der-Waals forces between adjacent nanoparticles can cause agglomeration of nanoparticles, which we observed after removing the alkane ligands by UV/ozone treatment. However, van-der

• exchange of molecular ligands [3][5][6]. Our data showing a conductance increase by immersion in a pure solvent alone raise the question to what extent an exchange with more conductive molecules contributes to the overall increase in conductance. To this end, we immersed the samples for 20 h in a solvent

Functionalized platinum nanoparticles with surface charge trigged by pH: synthesis, characterization and stability studies

• Giovanna Testa,
• Laura Fontana,
• Iole Venditti and
• Ilaria Fratoddi

Beilstein J. Nanotechnol. 2016, 7, 1822–1828, doi:10.3762/bjnano.7.175

• colloidal stability; hydrophobic or hydrophilic thiol-based ligands have been deeply exploited [14][15]. Among others, 2-diethylaminoethanethiol hydrochloride (DEA) has been used as a stabilizing thiol for gold nanoparticles used for the immobilization of lipase [16]. Among others, hydrothermal and

• reducing agents such as nanocrystalline cellulose from cotton or bacterial cellulose matrixes are currently being studied [23][24]. Thiol ligands have been thoroughly investigated [25][26][27] and particular attention has been devoted to hydrophilic ligands that confer to the PtNP stability in water

Scanning probe microscopy studies on the adsorption of selected molecular dyes on titania

• Jakub S. Prauzner-Bechcicki,
• Lukasz Zajac,
• Piotr Olszowski,
• Res Jöhr,
• Antoine Hinaut,
• Thilo Glatzel,
• Bartosz Such,
• Ernst Meyer and
• Marek Szymonski

Beilstein J. Nanotechnol. 2016, 7, 1642–1653, doi:10.3762/bjnano.7.156

• the molecules to the formation of a chemical bond via the dehydrogenation of the eight H atoms of the isoindole ligands, as a result of the increased substrate temperature during the deposition. Next, Ishida and Fujita investigated the electronic properties of individual molecules. The immobilized

• different ligands. Empty-state STM images of the densely packed molecular structures. (a) and (b): the closed layer PTCDA structure obtained when the molecules are adsorbed on a sample kept at elevated to 100 °C temperature; (c) 0.6 ML of PTCDA molecules adsorbed on the sample kept at 100 °C. All STM images

Nano- and microstructured materials for in vitro studies of the physiology of vascular cells

• Alexandra M. Greiner,
• Adria Sales,
• Hao Chen,
• Sarah A. Biela,
• Dieter Kaufmann and
• Ralf Kemkemer

Beilstein J. Nanotechnol. 2016, 7, 1620–1641, doi:10.3762/bjnano.7.155

• size of adhesion proteins and their ligands, or on the size of cells, the effective structuring of surfaces with nanometer to micrometer precision is required. In this section, we review the currently available most common techniques and materials applied for the fabrication of appropriate micro

• through electrostatic interactions [149][150]. A more native coating of artificial surfaces can be achieved by absorbing molecules from the extracellular matrix (ECM). Commonly used cell ligands enabling a specific cell adhesion are either the full molecules or peptides with motifs from ECM molecules such

Antitumor magnetic hyperthermia induced by RGD-functionalized Fe₃O₄ nanoparticles, in an experimental model of colorectal liver metastases

• Oihane K. Arriortua,
• Eneko Garaio,
• Borja Herrero de la Parte,
• Maite Insausti,
• Luis Lezama,
• Fernando Plazaola,
• Jose Angel García,
• Jesús M. Aizpurua,
• Maialen Sagartzazu,
• Mireia Irazola,
• Nestor Etxebarria,
• Ignacio García-Alonso,
• Alberto Saiz-López and
• José Javier Echevarria-Uraga

Beilstein J. Nanotechnol. 2016, 7, 1532–1542, doi:10.3762/bjnano.7.147

• . These values do not agree with the concept that 19 nm diameter NPs are surrounded by one layer of oleic acid or PMAO [37], indicating rather the presence of some kind of aggregation that increases with the complexity of the recovering ligands. In the process of incorporation of the RGD peptides, the

• to the NPs. Infrared spectra of the magnetic nanoparticles have been performed in order to determine the type of ligands surrounding the magnetic nuclei (see Supporting Information File 1, Figure S2). In the case of oleic acid-coated Fe3O4@OA NPs, the –CH2 symmetric and asymmetric stretching

• between 200 °C and 500 °C, which may account for the mass evolution of oleic acid and/or other organic ligands on the sample surface. Above 700 °C, a weight loss around 10% is observed, which could be ascribed to decomposition of generated carbonates. It can be observed that the increasing weight loss for