Academic literature on the topic 'Phosphine-sulfonate'

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Journal articles on the topic "Phosphine-sulfonate"

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Römbke, Patric, Annette Schier, and Hubert Schmidbaur. "(Phosphine)Silver(I) Sulfonate Complexes." Zeitschrift für Naturforschung B 58, no. 1 (2003): 168–72. http://dx.doi.org/10.1515/znb-2003-0126.

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Abstract Phosphine)silver(I) organosulfonate complexes of the type (R3P)AgOS(O)2R’ have been prepared in good yields from the corresponding silver sulfonates and tertiary phosphines in dichloromethane solution [R3 = Ph3, Ph2(2-Py), Me2Ph, with R’ = 4-Me-C6H4; R = Ph, R’ = Et and 2,5-Me2-C6H4]. If ethanol is present in the reaction mixture, the products contain one equivalent of ethanol. The crystal structures of (Ph3P)AgOS(O)2(C6H4-4-Me)(EtOH) (1), and (Me2PhP)AgOS(O)2(C6H4-4- Me) (5) have been determined. Complex 1 is present as a dimer in which the monomeric units feature intermolecular Ag-O
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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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Xia, Jian, Yixin Zhang, Xiaoqiang Hu, et al. "Sterically very bulky aliphatic/aromatic phosphine-sulfonate palladium catalysts for ethylene polymerization and copolymerization with polar monomers." Polymer Chemistry 10, no. 4 (2019): 546–54. http://dx.doi.org/10.1039/c8py01568f.

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Song, Guangzhi, Wenmin Pang, Weimin Li, Min Chen, and Changle Chen. "Phosphine-sulfonate-based nickel catalysts: ethylene polymerization and copolymerization with polar-functionalized norbornenes." Polymer Chemistry 8, no. 47 (2017): 7400–7405. http://dx.doi.org/10.1039/c7py01661a.

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Na, Yinna, Dan Zhang, and Changle Chen. "Modulating polyolefin properties through the incorporation of nitrogen-containing polar monomers." Polymer Chemistry 8, no. 15 (2017): 2405–9. http://dx.doi.org/10.1039/c7py00127d.

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Chen, Min, Wenping Zou, Zhengguo Cai, and Changle Chen. "Norbornene homopolymerization and copolymerization with ethylene by phosphine-sulfonate nickel catalysts." Polymer Chemistry 6, no. 14 (2015): 2669–76. http://dx.doi.org/10.1039/c5py00010f.

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Leonard, Nadia G., Grace V. Parker, Paul G. Williard, and Wesley H. Bernskoetter. "Coordination Chemistry of Iridium Phosphine–Sulfonate Complexes." Journal of Inorganic and Organometallic Polymers and Materials 24, no. 1 (2013): 157–63. http://dx.doi.org/10.1007/s10904-013-9966-y.

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Zhou, Xiaoyuan, Sébastien Bontemps, and Richard F. Jordan. "Base-Free Phosphine−Sulfonate Nickel Benzyl Complexes." Organometallics 27, no. 19 (2008): 4821–24. http://dx.doi.org/10.1021/om800741w.

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Rezabal, E., J. M. Ugalde, and G. Frenking. "The trans Effect in Palladium Phosphine Sulfonate Complexes." Journal of Physical Chemistry A 121, no. 40 (2017): 7709–16. http://dx.doi.org/10.1021/acs.jpca.7b06856.

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10

Zhu, Ling, Shuang Li, Xiaohui Kang, Wenzhen Zhang та Yi Luo. "A DFT Study of the Copolymerization of Methyl Vinyl Sulfone and Ethylene Catalyzed by Phosphine–Sulfonate and α-Diimine Palladium Complexes". Catalysts 13, № 6 (2023): 1026. http://dx.doi.org/10.3390/catal13061026.

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Density functional theory (DFT) calculations were comparatively carried out to reveal the origins of different catalytic performances from phosphine–benzene sulfonate (A, [{P^O}PdMe(L)] (P^O = Κ2-P,O-Ar2PC6H4SO3 with Ar = 2-MeOC6H4)) and α-diimine (B, [{N^N}PdMe(Cl)] (N^N = (ArN=C(Me)-C(Me)=NAr) with Ar = 2,6-iPr2C6H3)) palladium complexes toward the copolymerization of ethylene and methyl vinyl sulfone (MVS). Having achieved agreement between theory and experiment, it was found that the favorable 2,1-selective insertion of MVS into phosphine–sulfonate palladium complex A was due to there bein
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Dissertations / Theses on the topic "Phosphine-sulfonate"

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Gaikwad, S. "Late transition metal catalyzed insertion copolymerization of 1,1-disubstituted difunctional polar monomers with ethylene: synthesis, reactivity and Implications." Thesis(Ph.D.), CSIR-National Chemical Laboratory, Pune, 2019. http://dspace.ncl.res.in:8080/xmlui/handle/20.500.12252/5835.

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Among various polymers produced worldwide, polyolefins (i.e. polyethylene and polypropene) stand out as the largest volume polymers and due to their outstanding properties, such as solvent resistance, thermal stability and found applications in various commodities. However, due to the absence of functional groups in these polymers, they perform poorly when functional surfaces are required. Incorporation of only a small amount of functionalized monomers, randomly distributed in the polymer backbone, would most likely produce functional surfaces, without deteriorating the beneficial properties o
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