Academic literature on the topic 'Sulfonate based ligands'

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Journal articles on the topic "Sulfonate based ligands"

1

Yon, Marjorie, Claire Pibourret, Jean-Daniel Marty, and Diana Ciuculescu-Pradines. "Easy colorimetric detection of gadolinium ions based on gold nanoparticles: key role of phosphine-sulfonate ligands." Nanoscale Advances 2, no. 10 (2020): 4671–81. http://dx.doi.org/10.1039/d0na00374c.

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Specific interactions between sulfonate groups of phosphine-sulfonate ligands on the surface of Au nanoparticles and Gd<sup>3+</sup> ions allow the colorimetric detection of Gd<sup>3+</sup> ions at the μM level.
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2

Meng, Xing, Shu-Yan Song, Xue-Zhi Song, et al. "A tetranuclear copper cluster-based MOF with sulfonate–carboxylate ligands exhibiting high proton conduction properties." Chemical Communications 51, no. 38 (2015): 8150–52. http://dx.doi.org/10.1039/c5cc01732g.

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A tetranuclear copper cluster-based MOF with sulfonate–carboxylate ligands has been synthesized. It possesses 1D irregular channels lined with sulfonate, carboxylate, and DMF molecules, which show a high proton conductivity of 7.4 × 10<sup>−4</sup> S cm<sup>−1</sup> at 95 °C and 95% relative humidity.
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3

Shankar, Ravi, Archana Jain, Gabriele Kociok-Köhn, and Kieran C. Molloy. "Diorganotin-Based Coordination Polymers Derived from Sulfonate/Phosphonate/Phosphonocarboxylate Ligands." Inorganic Chemistry 50, no. 4 (2011): 1339–50. http://dx.doi.org/10.1021/ic1018423.

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4

Sun, Daofeng, Rong Cao, Wenhua Bi, Xiaoju Li, Yanqin Wang, and Maochun Hong. "Self-Assembly of Novel Silver Polymers Based on Flexible Sulfonate Ligands." European Journal of Inorganic Chemistry 2004, no. 10 (2004): 2144–50. http://dx.doi.org/10.1002/ejic.200300813.

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5

D'Vries, Richard F., German E. Gomez, Diego F. Lionello, M. Cecilia Fuertes, Galo J. A. A. Soler-Illia, and Javier Ellena. "Luminescence, chemical sensing and mechanical properties of crystalline materials based on lanthanide–sulfonate coordination polymers." RSC Advances 6, no. 111 (2016): 110171–81. http://dx.doi.org/10.1039/c6ra23516f.

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The relationship between the structural features with the mechanical, luminescent and sensing properties were studied in the compounds formed from lanthanide metals, 3-hydroxinaphthalene-2,7-disulfonate and 1,10-phenanthroline ligands.
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6

Wang, Qiu-Ya, Xue-Ling Zhang, Qing-Hua Meng, Dong Xue, Yun He, and Zun-Ting Zhang. "Metal–organic coordination polymers based on Cs(I), Rb(I) and isoflavone-3′-sulfonate ligands." Polyhedron 85 (January 2015): 953–61. http://dx.doi.org/10.1016/j.poly.2014.10.017.

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7

Shankar, Ravi, Archana Jain, Gabriele Kociok-Köhn, and Kieran C. Molloy. "Synthesis and characterization of diethyltin-based three dimensional self-assemblies derived from sulfonate–phosphonate ligands." Inorganica Chimica Acta 372, no. 1 (2011): 108–14. http://dx.doi.org/10.1016/j.ica.2011.01.084.

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8

Ahoulou, Samuel, Clara Richart, Cédric Carteret, Sébastien Pillet, Neus Vilà, and Alain Walcarius. "Weak Coordinating Character of Organosulfonates in Oriented Silica Films: An Efficient Approach for Immobilizing Cationic Metal-Transition Complexes." Molecules 27, no. 17 (2022): 5444. http://dx.doi.org/10.3390/molecules27175444.

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Iron (II) tris(2,2′-bipyridine) complexes, [Fe(bpy)3]2+, have been synthesized and immobilized in organosulfonate-functionalized nanostructured silica thin films taking advantage of the stabilization of [Fe(H2O)6]2+ species by hydrogen bonds to the anionic sulfonate moieties grafted to the silica nanopores. In a first step, thiol-based silica films have been electrochemically generated on indium tin oxide (ITO) substrates by co-condensation of 3-mercaptopropyltrimethoxysilane (MPTMS) and tetraethoxysilane (TEOS). Secondly, the thiol function has been modified to sulfonate by chemical oxidation using hydrogen peroxide in acidic medium as an oxidizing agent. The immobilization of [Fe(bpy)3]2+ complexes has been performed in situ in two consecutive steps: (i) impregnation of the sulfonate functionalized silica films in an aqueous solution of iron (II) sulfate heptahydrate; (ii) dipping of the iron-containing mesostructures in a solution of bipyridine ligands in acetonitrile. The in situ formation of the [Fe(bpy)3]2+ complex is evidenced by its characteristic optical absorption spectrum, and elemental composition analysis using X-ray photoelectron spectroscopy. The measured optical and electrochemical properties of immobilized [Fe(bpy)3]2+ complexes are not altered by confinement in the nanostructured silica thin film.
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9

Zemke, Jennifer M., Thomas E. Novet, and David R. Tyler. "Investigation of ligand effects on exciton recombination in PbS nanoparticles." Canadian Journal of Chemistry 89, no. 3 (2011): 339–46. http://dx.doi.org/10.1139/v10-169.

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Multiple exciton generation (MEG) and exciton recombination were studied by femtosecond transient absorption spectroscopy in PbS nanoparticles (NPs) capped with oleic acid (PbS–OLA) and 2,3-dimercaptopropane sulfonate (PbS–DMPS) ligands. Analysis of the transient absorption data showed that the PbS–DMPS nanoparticles exhibit increased rates of multi- and single-exciton recombination compared with the PbS–OLA nanoparticles; however, the MEG yield for both sets of particles was the same within experimental error. The origin of the differences in the exciton recombination decay rates is unknown, but it is speculated that it may be due to the ionic functionality of DMPS or to the different ligating atoms of the OLA and DMPS ligands. The PbS–DMPS nanoparticles were highly sensitive to the presence of oxygen, which caused a dramatic increase in nonradiative decay pathways, which can be mistaken for multiexciton absorbance and decay. Removal of oxygen eliminated the nonradiative decay pathways. Overall, this study showed that the dynamics of MEG can be modified by changing the NP ligand shell, a result that may be useful in the development of NP-based thin-film solar devices.
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10

Wu, Hua, Xian-Wu Dong, Hai-Yan Liu, et al. "Construction of a series of inorganic–organic hybrid coordination polymers based on hexamethylenetetramine and sulfonate ligands." Inorganica Chimica Acta 373, no. 1 (2011): 19–26. http://dx.doi.org/10.1016/j.ica.2011.03.041.

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