Identifying diverse metal oxide nanomaterials with lethal effects on embryonic zebrafish using machine learning

• Richard Liam Marchese Robinson,
• Haralambos Sarimveis,
• Philip Doganis,
• Xiaodong Jia,
• Marianna Kotzabasaki,
• Christiana Gousiadou,
• Stacey Lynn Harper and
• Terry Wilkins

Beilstein J. Nanotechnol. 2021, 12, 1297–1325, doi:10.3762/bjnano.12.97

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

• 4-nitrophenol (4-NPh) as the main product. While the P=S bond of MP becomes P=O, confirmed by 31P NMR. Although Cu2O is a widely known photocatalyst, the degradation of methyl parathion was associated to the surface basicity of Cu2O NPs. Indirect evidence for the basicity of Cu2O NPs was achieved

• through UV–vis absorption of 4-NPh. Likewise, it was shown that the surface basicity increases with decreasing nanoparticle size. The presence of CuCO3 on the surface of Cu2O, identified using X-ray photoelectron spectroscopy (XPS), passivates its surface and consequently diminishes the degradation of MP

• . Keywords: copper(I) oxide (Cu2O); Cu2O nanoparticles; degradation; methyl parathion; surface basicity; Introduction Organophosphorus pesticides (OPPs) are one of many kinds of pesticides that have attracted some attention mainly due to their neurotoxic effect [1][2][3]. The primary mechanism of action of

Adsorptive removal of bulky dye molecules from water with mesoporous polyaniline-derived carbon

• Hyung Jun An,
• Jong Min Park,
• Nazmul Abedin Khan and
• Sung Hwa Jhung

Beilstein J. Nanotechnol. 2020, 11, 597–605, doi:10.3762/bjnano.11.47

• functional group (for example, via protonation or deprotonation) under different conditions of acidity/basicity. In this study, the q6h values were checked over KOH-900 for AR1 and JBG under pH 2–12. As shown in Figure 7, the q6h for AR1 decreased monotonously with increasing pH of the solution; however, the

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

• ]. The high activity of ETS-10 in the transesterification reactions compared to zeolites and other molecular sieves originates presumably from its pronounced Brønsted basicity of the shared oxygen atoms [20]. For example, it has been reported that the parent ETS-10 catalyst is approximately four times

• -ETS-10/60, and 24.2 m2 g−1 for P-ETS-10/60. In the conducted Hg porosimetry experiments, in contrast to the N2 sorption, the micropores were not reachable for Hg, while the macropores did contribute to the measured surface area. Characterization of acidity and basicity of the ETS-10-based

• “effective” basicity seen by the reactants might differ from the measured values. In addition to this, as is evident from the results of DTA and 29Si NMR, calcination leads to the partial surface dehydroxylation. This might improve the accessibility of mesopores for triolein via the increased surface

Biocatalytic oligomerization-induced self-assembly of crystalline cellulose oligomers into nanoribbon networks assisted by organic solvents

• Yuuki Hata,
• Yuka Fukaya,
• Toshiki Sawada,
• Masahito Nishiura and
• Takeshi Serizawa

Beilstein J. Nanotechnol. 2019, 10, 1778–1788, doi:10.3762/bjnano.10.173

• ability (acidity) α, the hydrogen bond acceptor ability (basicity) β, and the dipolarity/polarizability π*, β was found to be correlated. The organic solvents with relatively high β-values were found to induce the nanoribbon network formation (Table 2). This finding suggests that the precipitation of the

Playing with covalent triazine framework tiles for improved CO₂ adsorption properties and catalytic performance

• Giulia Tuci,
• Andree Iemhoff,
• Housseinou Ba,
• Lapo Luconi,
• Andrea Rossin,
• Vasiliki Papaefthimiou,
• Regina Palkovits,
• Jens Artz,
• Cuong Pham-Huu and
• Giuliano Giambastiani

Beilstein J. Nanotechnol. 2019, 10, 1217–1227, doi:10.3762/bjnano.10.121

• basicity of its surface generates preferential interactions with Lewis acids such as CO2 [33]. The rational selection of monomers featured by Lewis-basic sites, eventually combined with structural directing co-monomers can be used to tune the surface basicity and morphology of the materials and

• , consequently, optimize their gas-adsorption capacity. In addition, the control of the chemico-physical properties (i.e., pore-size distribution, specific surface area (SSA) and surface basicity) of the target samples is known to play a fundamental role in the control of their performance (activity and

• ][40][41][42][43][44]. Most importantly, the rational balance between morphological and basic material surface properties has been claimed to control the catalyst stability on stream: the higher the “chemically accessible” surface basicity, the lower the sample deactivation/passivation due to the

Metal-free catalysis based on nitrogen-doped carbon nanomaterials: a photoelectron spectroscopy point of view

• Mattia Scardamaglia and
• Carla Bittencourt

Beilstein J. Nanotechnol. 2018, 9, 2015–2031, doi:10.3762/bjnano.9.191

• pyridonic configuration. This is consistent with the adsorption of an O atom on the C atom next to the pyridinic N, as sketched in Figure 13c. Similar results were previously obtained on multilayer graphene by performing XPS measurements after the ORR [116]. This behavior was ascribed to the Lewis basicity

Understanding the performance and mechanism of Mg-containing oxides as support catalysts in the thermal dry reforming of methane

• Nor Fazila Khairudin,
• Mohd Farid Fahmi Sukri,
• Mehrnoush Khavarian and
• Abdul Rahman Mohamed

Beilstein J. Nanotechnol. 2018, 9, 1162–1183, doi:10.3762/bjnano.9.108

• developments on the use of Mg as a support or promoter for DRM catalysts. Its high basicity and high thermal stability make Mg suitable for introduction into the highly endothermic reaction of DRM. The introduction of Mg as a support or promoter for Ni-based catalysts allows for good metal dispersion on the

• and catalytic characteristics as a catalyst support combined with a high dispersion of small active particles for suppressing carbon formation [55]. The decreased carbon formation in DRM is due to the high basicity of MgO to capture CO2, thereby accelerating the overall reaction [34][49][51

• decreasing the rate of methane decomposition. Meanwhile, Theofanidis et al. [28] stated that carbon deposition could be solved with a higher distribution of active metal on the support surface, high basicity of catalyst surface to capture acidic CO2, and the addition of resources that offer an oxygen atom

Two-dimensional carbon-based nanocomposites for photocatalytic energy generation and environmental remediation applications

• Suneel Kumar,
• Ashish Kumar,
• Ashish Bahuguna,
• Vipul Sharma and
• Venkata Krishnan

Beilstein J. Nanotechnol. 2017, 8, 1571–1600, doi:10.3762/bjnano.8.159

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

• basicity of the Naryl vs the Nalkyl donor atoms [24]. In the following the geometries of the terminal [Cu(pmdta)]2+ fragments will be briefly described. It should be emphasized that the findings described in the following have been made analogously for our previously reported homotrinuclear CuIICuIICuII

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

• was optimized controlling the synthesis conditions, such as concentrations of reactants, basicity of the medium, and the process temperature. Keywords: copper(II) ions; methyl groups; N- and F-containing functional groups; silica nanospheres; sol–gel processes; sorption; surface chemistry

Surfactant-controlled composition and crystal structure of manganese(II) sulfide nanocrystals prepared by solvothermal synthesis

• Elena Capetti,
• Anna M. Ferretti,
• Vladimiro Dal Santo and
• Alessandro Ponti

Beilstein J. Nanotechnol. 2015, 6, 2319–2329, doi:10.3762/bjnano.6.238

• precursor. When we used a single surfactant (carboxylic acid, alcohol, thiol, amine), α-MnS nanocrystals were obtained. The peculiar role of the amine seems to be related to its basicity. The nanocrystals were characterized by TEM and electron diffraction; ATR-FTIR spectroscopy provided information about

• , alcohol, and thiol surfactants. This set allowed us to understand how basicity, nucleophilicity and ability to undergo condensation reaction with stearic acid affect the structure directing ability of the surfactant. The crystal structure of the resulting NCs was determined by analyzing the electron

• morphological parameters. It is clear from Table 1 that amines direct the reaction toward γ-MnS NCs while all other free surfactants (or the absence thereof) lead to α-MnS NCs. This γ-directing effect, independent of the amine chain length and degree of saturation, seems to be related to the basicity of amines

From lithium to sodium: cell chemistry of room temperature sodium–air and sodium–sulfur batteries

• Philipp Adelhelm,
• Pascal Hartmann,
• Conrad L. Bender,
• Martin Busche,
• Christine Eufinger and
• Juergen Janek

Beilstein J. Nanotechnol. 2015, 6, 1016–1055, doi:10.3762/bjnano.6.105

Non-covalent and reversible functionalization of carbon nanotubes

• Antonello Di Crescenzo,
• Valeria Ettorre and
• Antonella Fontana

Beilstein J. Nanotechnol. 2014, 5, 1675–1690, doi:10.3762/bjnano.5.178

• with N,N-dimethylformamide (DMF) [40], highlighting that a high value of β (the hydrogen bond acceptance basicity), a negligible value of R (the hydrogen bond donation parameter of Taft and Kamlet) and a high value for π* (solvochromic parameter) [41] are necessary, although not sufficient conditions

Controlled synthesis and tunable properties of ultrathin silica nanotubes through spontaneous polycondensation on polyamine fibrils

• Jian-Jun Yuan,
• Pei-Xin Zhu,
• Daisuke Noda and
• Ren-Hua Jin

Beilstein J. Nanotechnol. 2013, 4, 793–804, doi:10.3762/bjnano.4.90

• of [OH]/[CH2CH2NH] during the neutralization as well as on the basicity of the alkali compound and on the concentration of the silica source. The synthesis of silica nanotubes established here could be easily applied to a fabrication on the kilogram scale. Silica nanotubes that were obtained from the

• -concentration of oligomer methoxysilane also accelerates the collapse of the LPEI crystallites. Effect of the alkali basicity. We also tried to use different alkalies to induce the room-temperature self-assembly of LPEI from the protonated state. The synthesis conditions are similar to that used for the silica

• the LPEI crystallization was delayed due to weak basicity of the ammonia solution and a low degree of deprotonation of LPEI–H+. This is consistent with the formation of silica nanofilms by using NaOH with low molar ratios [OH]/[EI]. Furthermore, when increasing the molar ratio [OH]/[EI] to 0.8, the

Nanostructure-directed chemical sensing: The IHSAB principle and the dynamics of acid/base-interface interaction

• James L. Gole and
• William Laminack

Beilstein J. Nanotechnol. 2013, 4, 20–31, doi:10.3762/bjnano.4.3

• basicity of the decorated interface. This process changes the interaction of the interface with the analyte. The observed change to the more basic oxinitrides does not represent a simple increase in surface basicity but appears to involve a change in molecular electronic structure, which is well explained

• corresponding oxinitrides, with a greatly increased basicity. Using a defined procedure, based on established molecular and semiconductor properties, the IHSAB model dictates the coupling of analyte/interface acid/base interactions with the properties of the majority charge carriers in an extrinsic

• oxinitrides [9][10], as it introduces basicity, also facilitates the change of sensor response through optical pumping [11]. The extrinsic semiconductor is, however, independently variable with a distinctly different band structure and electron dynamics associated with n- or p-type doping. Although these two

Twofold role of calcined hydrotalcites in the degradation of methyl parathion pesticide

• Alvaro Sampieri,
• Geolar Fetter,
• María Elena Villafuerte-Castrejon,
• Adriana Tejeda-Cruz and
• Pedro Bosch

Beilstein J. Nanotechnol. 2011, 2, 99–103, doi:10.3762/bjnano.2.11

• have correlated the degradation of an aqueous solution of MP at room temperature, with the basicity of the adsorbing materials. It was found that the metal composition of hydrotalcites determines both the surface electronic properties (basic or acidic) and the sorption capacity. Depending on the basic

• strength, some calcined hydrotalcites can catalyze the transformation of MP to p-nitrophenol (p-NP) and retain its by-products. Such a process has the advantage of being able to be carried out at room temperature and at the pH of the pesticide solution. Keywords: basicity; hydrotalcite; methyl parathion