Exploring internal structures and properties of terpolymer fibers via real-space characterizations

• Michael R. Roenbeck and
• Kenneth E. Strawhecker

Beilstein J. Nanotechnol. 2023, 14, 1004–1017, doi:10.3762/bjnano.14.83

• , this distinction in fundamental chemistry has significant implications for the structures and properties of the resulting fibers. To date, structure–property characterizations of Technora® in the literature have primarily focused on (i) X-ray diffraction (XRD), (ii) nuclear magnetic resonance (NMR

Facile preparation of Au- and BODIPY-grafted lipid nanoparticles for synergized photothermal therapy

• Yuran Wang,
• Xudong Li,
• Haijun Chen and
• Yu Gao

Beilstein J. Nanotechnol. 2022, 13, 1432–1444, doi:10.3762/bjnano.13.118

• etherate (BF3·OEt2) and 2,4-dimethylpyrrole were freshly purified by distillation under reduced pressure. Synthesis and characterization of BDP All chemical reagents were obtained from commercial suppliers and used without further purification. 1H nuclear magnetic resonance (NMR) and 13C NMR spectra were

Design of surface nanostructures for chirality sensing based on quartz crystal microbalance

• Yinglin Ma,
• Xiangyun Xiao and
• Qingmin Ji

Beilstein J. Nanotechnol. 2022, 13, 1201–1219, doi:10.3762/bjnano.13.100

• industry, detection and separation of enantiomers are essential for their safe usage. With appropriate detectors and transduction signals, various analysis instruments and techniques have been used for chirality detection or chiral separation. They include circular dichroism (CD) [9], nuclear magnetic

• resonance [10], Fourier transform infrared spectrometry (FTIR) [11], UV–vis absorption spectrometry [12], mass spectrometry (MS) [13], titration microcalorimetry [14], high-performance liquid chromatography (HPLC) [15], gas chromatography (GC), capillary electrophoresis (CE) [16], and electrochemical chiral

Surfactant-free syntheses and pair distribution function analysis of osmium nanoparticles

• Mikkel Juelsholt,
• Jonathan Quinson,
• Emil T. S. Kjær,
• Baiyu Wang,
• Rebecca Pittkowski,
• Susan R. Cooper,
• Tiffany L. Kinnibrugh,
• Søren B. Simonsen,
• Luise Theil Kuhn,
• María Escudero-Escribano and
• Kirsten M. Ø. Jensen

Beilstein J. Nanotechnol. 2022, 13, 230–235, doi:10.3762/bjnano.13.17

• reaction at 85 °C in nuclear magnetic resonance (NMR) tubes (volume approx. 0.2 mL). The size analysis suggests that the NPs are (a) 1.6 ± 0.4 nm and (b) 1.7 ± 0.3 nm. The size distribution is presented in (c) from the analysis of 103 and 106 NPs, respectively. PDFs obtained from three different syntheses

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

• implementing light scattering (dynamic and electrophoretic) techniques, spectroscopy (UV–vis, atomic absorption, nuclear magnetic resonance) and transmission electron microscopy. The obtained results demonstrated that AgNPs may transform very quickly during their journey through different biological conditions

• absorption spectroscopy (GF-AAS), nuclear magnetic resonance (NMR) spectroscopy, and transmission electron microscopy (TEM) experiments. Physicochemical characteristics of freshly prepared AgNPs Freshly prepared AgNPs coated with PVP, sodium bis(2-ethylhexyl)sulfosuccinate (AOT), and poly(ʟ-lysine) (PLL

Cu₂O nanoparticles for the degradation of methyl parathion

• Juan Rizo,
• David Díaz,
• Benito Reyes-Trejo and
• M. Josefina Arellano-Jiménez

Beilstein J. Nanotechnol. 2020, 11, 1546–1555, doi:10.3762/bjnano.11.137

• different NPs sizes (16, 29 and 45 nm), determined with X-ray diffraction (XRD) and high-resolution transmission electron microscopy (HRTEM), were synthesized using a modified Benedict’s reagent. 1H nuclear magnetic resonance (NMR) results show that the hydrolytic degradation of MP leads to the formation of

Straightforward synthesis of gold nanoparticles by adding water to an engineered small dendrimer

• Sébastien Gottis,
• Régis Laurent,
• Vincent Collière and
• Anne-Marie Caminade

Beilstein J. Nanotechnol. 2020, 11, 1110–1118, doi:10.3762/bjnano.11.95

• to the P=S group in the 31P nuclear magnetic resonance (NMR) spectra (Figure 1 and Table 1). Indeed, this signal shifted from 52.1 ppm in 1 to 33.7 ppm in 2 (Δδ = −18.4 ppm). The attempts to generate the gold nanoparticles from compound 2 were carried out by adding water. This compound was not very

Rational design of block copolymer self-assemblies in photodynamic therapy

• Maxime Demazeau,
• Laure Gibot,
• Anne-Françoise Mingotaud,
• Patricia Vicendo,
• Clément Roux and
• Barbara Lonetti

Beilstein J. Nanotechnol. 2020, 11, 180–212, doi:10.3762/bjnano.11.15

Nitrogen-vacancy centers in diamond for nanoscale magnetic resonance imaging applications

• Alberto Boretti,
• Lorenzo Rosa,
• Jonathan Blackledge and
• Stefania Castelletto

Beilstein J. Nanotechnol. 2019, 10, 2128–2151, doi:10.3762/bjnano.10.207

• 1950 [1] and the first nuclear magnetic resonance (NMR) spectrum was reported in 1952 [2]. The first NMR image followed about two decades later, in 1973 [3]. It was not until 1977 that the first human magnetic resonance (MR) images were published [4]. The last few decades have seen the consolidation of

Synthesis of highly active ETS-10-based titanosilicate for heterogeneously catalyzed transesterification of triglycerides

• Muhammad A. Zaheer,
• David Poppitz,
• Khavar Feyzullayeva,
• Marianne Wenzel,
• Jörg Matysik,
• Radomir Ljupkovic,
• Aleksandra Zarubica,
• Alexander A. Karavaev,
• Andreas Pöppl,
• Roger Gläser and
• Muslim Dvoyashkin

Beilstein J. Nanotechnol. 2019, 10, 2039–2061, doi:10.3762/bjnano.10.200

• size (scanning electron microscopy, laser diffraction), textural properties (N2 sorption, Hg porosimetry), presence of hydroxyl groups and active sites (temperature-programmed desorption of NH3 and CO2, 29Si magic angle spinning nuclear magnetic resonance (NMR)), mesopore accessibility and diffusion

• impact of the post-synthetic treatment applied to the ETS-10 titanosilicate with respect to the catalytic activity in the heterogeneously catalyzed transesterification of triglycerides. Keywords: CaO; diffusion; ETS-10; nuclear magnetic resonance (NMR); transesterification; Introduction One of the

• intrusion, acid and basic site density by NH3 and CO2 temperature-programmed desorption (TPD), presence of hydroxyl groups by 29Si magic angle spinning nuclear magnetic resonance (MAS NMR), pore interconnectivity by hyperpolarized (HP) 129Xe NMR, pore accessibility for triolein by 1H pulsed field gradient

Magnetic properties of biofunctionalized iron oxide nanoparticles as magnetic resonance imaging contrast agents

• Natalia E. Gervits,
• Andrey A. Gippius,
• Alexey V. Tkachev,
• Evgeniy I. Demikhov,
• Sergey S. Starchikov,
• Igor S. Lyubutin,
• Alexander L. Vasiliev,
• Vladimir P. Chekhonin,
• Maxim A. Abakumov,
• Alevtina S. Semkina and
• Alexander G. Mazhuga

Beilstein J. Nanotechnol. 2019, 10, 1964–1972, doi:10.3762/bjnano.10.193

• nanoparticles designed for use as MRI contrast media are precisely examined by a variety of methods: powder X-ray diffraction (XRD), transmission electron microscopy (TEM), Raman spectroscopy, Mössbauer spectroscopy and zero-field nuclear magnetic resonance (ZF-NMR) spectroscopy. TEM and XRD measurements reveal

• nanoparticles, has been repeatedly emphasized, and the exact composition of the MNPs is usually determined using X-ray diffraction (XRD) or Mössbauer spectroscopy with and without magnetic field [12][13][14]. In this work, we show other options for solving this problem using Raman and nuclear magnetic resonance

Synthesis and potent cytotoxic activity of a novel diosgenin derivative and its phytosomes against lung cancer cells

• Liang Xu,
• Dekang Xu,
• Ziying Li,
• Yu Gao and
• Haijun Chen

Beilstein J. Nanotechnol. 2019, 10, 1933–1942, doi:10.3762/bjnano.10.189

• used without further purification. Preparative column chromatography was performed using silica gel 60 with particle size 0.063–0.200 mm (70–230 mesh, Flash). Analytical thin-layer chromatography (TLC) was carried out employing silica gel 60 F254 plates (Merck, Darmstadt). Nuclear magnetic resonance

Long-term entrapment and temperature-controlled-release of SF₆ gas in metal–organic frameworks (MOFs)

• Hana Bunzen,
• Andreas Kalytta-Mewes,
• Leo van Wüllen and
• Dirk Volkmer

Beilstein J. Nanotechnol. 2019, 10, 1851–1859, doi:10.3762/bjnano.10.180

• included powder X-ray diffraction measurements, thermogravimetric analysis, Fourier-transform infrared spectroscopy, scanning electron microscopy, 19F nuclear magnetic resonance spectroscopy and computational simulations. In addition, the possibility to release the gas guest by applying elevated

• infrared (FTIR) and 19F nuclear magnetic resonance (NMR) spectroscopy. SF6 is an inert, nonflammable and nontoxic gas, which is known to be an excellent dielectric gas for high-voltage applications [15][16]. At the same time, it is also known as one of the most severe greenhouse gases [17][18]. Therefore

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

• stable NPs. Finally, we selected a molar ratio of [metallic salts]/[NaBH4]/[biothiol] = 1:10:1 for further work as it resulted in a favorable NP size (≈10 nm) and long term stability. Nuclear magnetic resonance (NMR), as an excellent tool to determine the interactions of small organic molecules with

Chiral nanostructures self-assembled from nitrocinnamic amide amphiphiles: substituent and solvent effects

• Hejin Jiang,
• Huahua Fan,
• Yuqian Jiang,
• Li Zhang and
• Minghua Liu

Beilstein J. Nanotechnol. 2019, 10, 1608–1617, doi:10.3762/bjnano.10.156

• –7.62 (m, 2H), 7.76–7.85 (d, 2H), 7.95–8.07 (d, 1H), 8.17–8.28 (d, 2H); (MALDI–TOF–MS) m/z: [M]+ calcd. for C50H88N4O5, 825.26; found, [M + Li]+ 833.5, [M + Na]+ 847.5. General characterization MALDI–TOF–MS was recorded on a Bruker Autoflex III instrument. Nuclear magnetic resonance (NMR) was

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

• modification, the nanoparticles were denoted as γ-Fe2O3@Hep-CS-G, γ-Fe2O3@Hep-CS-H, and γ-Fe2O3@Hep-CS-P, respectively. The typical particle concentration was 4.4 mg/mL. Characterization methods Attenuated total reflection Fourier transform infrared spectroscopy (ATR-FTIR) and proton nuclear magnetic resonance

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

• fractionation, the crude AuNCs and fractions obtained from SSSP have been investigated by transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), nuclear magnetic resonance (NMR), and UV–vis absorption together with photoluminescence (PL) spectroscopy. Experimental Chemicals and

• accelerating voltage of 200 kV. Proton nuclear magnetic resonance (1H NMR) spectra were performed on a Bruker AC 400 NMR spectrometer (Rheinstetten, Karlsruhe, Germany) in concentrated D2O solutions. At the same time, the fractions were investigated by a matrix-assisted laser desorption ionization time-of

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

• a nonhydrolytic sol–gel method involving the reaction of Ti(OiPr)4, acetophenone (2 equiv) and diethyl octylphosphonate (from 0 to 0.2 equiv) at 200 °C for 12 hours, in toluene. The different samples were characterized by 31P magic angle spinning nuclear magnetic resonance, Fourier transform

New micro/mesoporous nanocomposite material from low-cost sources for the efficient removal of aromatic and pathogenic pollutants from water

• Emmanuel I. Unuabonah,
• Robert Nöske,
• Jens Weber,
• Christina Günter and
• Andreas Taubert

Beilstein J. Nanotechnol. 2019, 10, 119–131, doi:10.3762/bjnano.10.11

• nuclear magnetic resonance spectroscopy suggest the formation of several new bonds in the materials upon reaction of the precursors, thus confirming the formation of a new hybrid material. Thermogravimetric analysis/differential thermal analysis and elemental analysis confirm the presence of carbonaceous

• of 4-nitrophenol. Cross-polarized magic angle spinning nuclear magnetic resonance 27Al (104.1 MHz), 13C (100.5 MHz), and 29Si (79.4 MHz) spectra of the 2Z-HYCA@650 °C nanocomposite were recorded on a Bruker DRX-400 spectrometer with a magic angle spin probe and 4 mm ZrO2 rotor 27Al signals were

• because a standard solution of NaOH used in the previous preparation of the materials (which, when reacted with ZnCl2, will yield ZnO) was omitted in the preparation of the nanocomposites in this study. Nuclear magnetic resonance spectroscopy analysis To further evaluate the composition and structure of

Characterization of the microscopic tribological properties of sandfish (Scincus scincus) scales by atomic force microscopy

• Weibin Wu,
• Christian Lutz,
• Simon Mersch,
• Richard Thelen,
• Christian Greiner,
• Guillaume Gomard and
• Hendrik Hölscher

Beilstein J. Nanotechnol. 2018, 9, 2618–2627, doi:10.3762/bjnano.9.243

• analysing the locomotion of sandfish in granular media via nuclear magnetic resonance (NMR) imaging [2] or high-speed X-ray imaging [4] indeed show that the movement of a sandfish resembles that of swimming fishes. It is surprising that sandfishes manage to bury and swim in sand without visible wear on

Formation and development of nanometer-sized cybotactic clusters in bent-core nematic liquid crystalline compounds

• Yuri P. Panarin,
• Sithara P. Sreenilayam,
• Jagdish K. Vij,
• Anne Lehmann and
• Carsten Tschierske

Beilstein J. Nanotechnol. 2018, 9, 1288–1296, doi:10.3762/bjnano.9.121

• community. A number of bent-core systems in their nematic phase were studied during the last decade and some of these were shown to exhibit biaxiality on a macroscopic scale using X-ray diffraction (XRD) [12][13] and nuclear magnetic resonance (NMR) [14]. In most studies, however, the long axes of the

Kinetics of solvent supported tubule formation of Lotus (Nelumbo nucifera) wax on highly oriented pyrolytic graphite (HOPG) investigated by atomic force microscopy

• Sujit Kumar Dora,
• Kerstin Koch,
• Wilhelm Barthlott and
• Klaus Wandelt

Beilstein J. Nanotechnol. 2018, 9, 468–481, doi:10.3762/bjnano.9.45

• by a number of experimental techniques, e.g., X-ray powder diffraction (XRD), electron diffraction (ED) and nuclear magnetic resonance (NMR) techniques [16][17][18][19]. Out of the vast variety of wax morphologies, tubules constitute one of the most prominent types and can be distinguished into three

The interplay between spin densities and magnetic superexchange interactions: case studies of mono- and trinuclear bis(oxamato)-type complexes

• Azar Aliabadi,
• Bernd Büchner,
• Vladislav Kataev and
• Tobias Rüffer

Beilstein J. Nanotechnol. 2017, 8, 2245–2256, doi:10.3762/bjnano.8.224

• ] has a long history of applications in this research field. By now ESR has become an established method along with neutron diffraction (ND) and nuclear magnetic resonance (NMR) spectroscopies since it does not require large amounts of a sample as is the case for ND, and often offers a better

Spin-chemistry concepts for spintronics scientists

• Konstantin L. Ivanov,
• Alexander Wagenpfahl,
• Carsten Deibel and
• Jörg Matysik

Beilstein J. Nanotechnol. 2017, 8, 1427–1445, doi:10.3762/bjnano.8.143

• electron paramagnetic resonance (EPR) intensities in CH4 gas under irradiation by Fessenden and Schuler in 1963 [4]. Soon later, Bargon and Fischer observed anomalous nuclear magnetic resonance (NMR) intensities upon thermal radical-pair formation [5]. Such anomalous intensity patterns are nowadays

Recombinant DNA technology and click chemistry: a powerful combination for generating a hybrid elastin-like-statherin hydrogel to control calcium phosphate mineralization

• Mohamed Hamed Misbah,
• Mercedes Santos,
• Luis Quintanilla,
• Christina Günter,
• Matilde Alonso,
• Andreas Taubert and
• José Carlos Rodríguez-Cabello

Beilstein J. Nanotechnol. 2017, 8, 772–783, doi:10.3762/bjnano.8.80

• purification, ELRs were characterized using matrix-assisted laser deposition ionization time of flight mass spectrometry (MALDI-TOF-MS), attenuated total reflection infrared spectroscopy (ATR-IR) and nuclear magnetic resonance spectroscopy (1H NMR). 3 Preparation of ELR hydrogels ELR hydrogels were made by

• dispensed onto the MALDI plate along with 1 μL of aqueous ELR solution. The plate was dried in air and mass spectra were recorded using a Bruker autoflex speed instrument with a nitrogen laser (337 nm) operating in positive ion mode with delayed extraction. 6.2 Nuclear magnetic resonance (NMR) spectroscopy