“…In the experiment, six anionic species were detected: C(6)H(5)N(2)O(−), C(5)H(4)N(−), NCO(−), O(−)/NH(2)(−), and CN(−), with NCO(−) being the most prominent anion. …”
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“…The higher catalytic activity of AC-Mt might be attributed to the larger reactive surface area of well-dispersed magnetite for ˙OH production and the recharge of the magnetite surface by the AC support via Fe–O–C bonds. However, the removal rate of MB by GO-Mt was one order of magnitude slower than that of bare magnetite nanoparticles under the same experimental conditions, presumably due to the wrapping of GO around magnetite nanoparticles or extensive aggregation of GO-Mt composites. …”
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“…When YX = OC, a secondary minimum is observed corresponding to lengthened and shortened distances r(ClF) and r(CCl), respectively, relative to the primary minimum, suggesting a significant contribution from the Mulliken inner complex structure [O=C–Cl](+)···F(–). A conventional weak, halogen-bond complex OC···ClF occurs at the primary minimum. …”
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“…Metal induced molecular level changes of root and leaf samples indicate the presence of OH, NH(2), and CH(3) deformation as well as C-O-H and C-O-C stretch. A prominent band corresponding to CH(3) deformation, pointing hemicellulose fortification, occurs in the cell walls of the xylem, aiding in Zn localization. …”
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“…In the title compound, C(16)H(11)BrN(6)O·2C(2)H(6)OS, the 1,2,3,7-tetra­hydro­imid­azo[1,2-a]pyridine ring system and the oxindole moiety are both nearly planar [maximum deviations = 0.042 (2) and 0.115 (2) Å, respectively] and their planes form a dihedral angle of 86.04 (5)° with each other. Inter­molecular N—H⋯O, C—H⋯O and C—H⋯N hydrogen bonds link mol­ecules in the crystal through the O atoms of the solvent mol­ecules, generating a three-dimensional network. …”
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“…The samples were fixed in Zamboni solution (4% phosphate-buffered paraformaldehyde and 0.4% picric acid), snap-frozen and stored at -70ºC. 14 µm sections were then obtained. Immunofluorescence staining for VIP (Peninsula Laboratories) was performed and its images documented by conventional photography. …”
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“…The side-on end-on dinitrogen hydride complex [{Na(dme)}(2){(O(3))Nb}(2)(μ-η(1):η(2)-N(2))(μ-H)(2)] (3-Na, [O(3)](3−) = [(3,5-(t)Bu(2)-2-O-C(6)H(2))(3)CH](3−)) was observed to undergo facile elimination of H(2) and cleavage of the N–N bond in the presence of 9-borabicyclo[3.3.1]nonane (9-BBN), AlMe(3), and ZnMe(2). …”
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“…·O and N—H⋯Cl hydrogen bonds, together with C—H⋯O, C—H⋯Cl and C—H⋯π inter­actions, links the complex mol­ecules and the water mol­ecules to form a supra­molecular three-dimensional framework. …”
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“…The mol­ecular structure of the title complex, [Ni(C(13)H(8)F(2)N(2)O)(C(14)H(32)P(2))] or Ni(oFPU)(dippe), where oFPU is the dianion of bis­(2-fluoro­phen­yl)urea and dippe is 1,2-bis­(di-iso­propyl­phosphino)ethane, comprises an Ni(II) atom with a distorted square-planar coordination environment (geometry index τ(4) = 0.195). …”
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“…The covalently bound inorganic-organic hybrid coagulant (CBHyC) used in this work had a complementary relationship with biodegradation for the organics removal: this coagulant reduced toxicity and enhanced the biodegradation by preferentially removing refractory substances such as lignin with a high degree of oxidation (O/C > 0.3). This study provides molecular insight into the organics of tire pyrolysis wastewater removed by a combined treatment process, supporting the advancement and application of waste rubber recycling technology. …”
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“…C–H, C–C and C–O bonds were gradually oxidized to C[double bond, length as m-dash]C, C–O, C[double bond, length as m-dash]O and O–H bonds by hydrogen abstraction reaction during the reaction of reactive species with organic contaminants. …”
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“…Besides, the opening band gap was observed for several derivatives, and the relationship between the band gap and O/C ratio was found to be nonmonotonic. Analysis of the density of states showed that bands around the Fermi levels of derivatives between graphene and hydroxyl groups are mainly composed of 2p(z) orbitals of carbon and oxygen atoms.…”
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“…The optimal catalyst, V-pg-C(3)N(4)-0.46, achieves 60% benzene conversion and 99.7% phenol selectivity at 60 (o)C with H(2)O(2) as the oxidant.…”
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“…HPH caused a decrease in the surface hydrophobicity of the glycated protein, an increase in the abundance of free sulfhydryl groups, unfolding of the protein molecular structure, and the formation of new covalent bonds (C=O, C=N). Additionally, the particle size of emulsions created with SPI-GOS conjugates was reduced under HPH, thus improving the emulsifying properties of SPI. …”
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“…The complex formed between carbon xerogel and TiO(2) phase was investigated through FTIR, proving the presence of a Ti-O–C chemical linkage. The physicochemical properties of the synthesised adsorbent–photocatalyst were probed using FESEM, BET analysis and UV–Vis analysis. …”
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“…The energies of the O−H∙∙∙O=C intramolecular hydrogen bonds were compared quantitatively for the series of ortho-disubstituted benzenes and Z-isomers of olefins via a molecular tailoring approach. …”
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“…Compared with Sp, Ms held more surface O–H, aliphatic and aromatic groups, while Sa had more phenolic, C–O (or C–O–C), and Si–O groups, and Sb held more C–O (or C–O–C) and Si–O groups; besides, Sa, Sb, and Ms had larger SSA than Sp. …”
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“…Second, a network of circulating canals connected to a water bath provides temperature control to within ± 0.1 ºC under variable irradiance, humidity, and air flow conditions. …”
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“…Due to the high variability of the expected particle rates, ranging from several kHz/cm^2 in the external regions up to several MHz/cm2 in the inner ones, different sub-detector technologies that could replace or simply complement the old ones are under investigation, with the aim to choose the best option in terms of granularity, radiation hardness and effective spark quenching up to integrated charges of O(C/cm^2). An overview of the state of the art of the muon detector design for the LHCb Upgrade II will be here presented.…”
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“…Analysis of the surface chemical states suggested that the hydrophilic behavior of DLC:SiO(x) treated with oxygen plasma is attributed to surface enrichment with C–O–C, SiO(2), and Si–Si chemical bonds as well as significant removal of hydrophobic Si–CH(x) functional groups. …”
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