Статті в журналах з теми "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 (January 1, 2003): 168–72. http://dx.doi.org/10.1515/znb-2003-0126.
Повний текст джерелаYon, 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.
Повний текст джерелаXia, Jian, Yixin Zhang, Xiaoqiang Hu, Xin Ma, Lei Cui, Jianfu Zhang, and Zhongbao Jian. "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.
Повний текст джерелаSong, 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.
Повний текст джерелаNa, 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.
Повний текст джерелаChen, 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.
Повний текст джерелаLeonard, 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 (October 2, 2013): 157–63. http://dx.doi.org/10.1007/s10904-013-9966-y.
Повний текст джерелаZhou, Xiaoyuan, Sébastien Bontemps, and Richard F. Jordan. "Base-Free Phosphine−Sulfonate Nickel Benzyl Complexes." Organometallics 27, no. 19 (October 13, 2008): 4821–24. http://dx.doi.org/10.1021/om800741w.
Повний текст джерелаRezabal, E., J. M. Ugalde, and G. Frenking. "The trans Effect in Palladium Phosphine Sulfonate Complexes." Journal of Physical Chemistry A 121, no. 40 (October 2, 2017): 7709–16. http://dx.doi.org/10.1021/acs.jpca.7b06856.
Повний текст джерелаZhu, 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 (20 червня 2023): 1026. http://dx.doi.org/10.3390/catal13061026.
Повний текст джерелаBashir, Oumar, Laurence Piche, and Jerome P. Claverie. "18-Electron Ruthenium Phosphine Sulfonate Catalysts for Olefin Metathesis." Organometallics 33, no. 14 (July 9, 2014): 3695–701. http://dx.doi.org/10.1021/om500212x.
Повний текст джерелаIto, Shingo, Yusuke Ota, and Kyoko Nozaki. "Ethylene/allyl monomer cooligomerization by nickel/phosphine–sulfonate catalysts." Dalton Transactions 41, no. 45 (2012): 13807. http://dx.doi.org/10.1039/c2dt31771k.
Повний текст джерелаDu, Qing, Liping Zhao, Lihua Guo, Xingxing Ge, Shumiao Zhang, Zhishan Xu, and Zhe Liu. "Lysosome-targeted Cyclometalated Iridium (III) Anticancer Complexes Bearing Phosphine-Sulfonate Ligands." Applied Organometallic Chemistry 33, no. 2 (December 7, 2018): e4746. http://dx.doi.org/10.1002/aoc.4746.
Повний текст джерелаBlaskó, Andrei, Clifford A. Bunton, Eduardo A. Toledo, Paul M. Holland, and Faruk Nome. "SN2 reactions of a sulfonate ester in mixed cationic/phosphine oxide micelles." J. Chem. Soc., Perkin Trans. 2, no. 12 (1995): 2367–73. http://dx.doi.org/10.1039/p29950002367.
Повний текст джерелаAnselment, Timo M. J., Christian Wichmann, Carly E. Anderson, Eberhardt Herdtweck, and Bernhard Rieger. "Structural Modification of Functionalized Phosphine Sulfonate-Based Palladium(II) Olefin Polymerization Catalysts." Organometallics 30, no. 24 (December 26, 2011): 6602–11. http://dx.doi.org/10.1021/om200734x.
Повний текст джерелаRavasio, Andrea, Laura Boggioni, and Incoronata Tritto. "Copolymerization of Ethylene with Norbornene by Neutral Aryl Phosphine Sulfonate Palladium Catalyst." Macromolecules 44, no. 11 (June 14, 2011): 4180–86. http://dx.doi.org/10.1021/ma2006427.
Повний текст джерелаSkupov, Kirill M., Pooja R. Marella, Michel Simard, Glenn P. A. Yap, Nathan Allen, David Conner, Brian L. Goodall, and Jerome P. Claverie. "Palladium Aryl Sulfonate Phosphine Catalysts for the Copolymerization of Acrylates with Ethene." Macromolecular Rapid Communications 28, no. 20 (October 15, 2007): 2033–38. http://dx.doi.org/10.1002/marc.200700370.
Повний текст джерелаWeng, Wei, Zhongliang Shen, and Richard F. Jordan. "Copolymerization of Ethylene and Vinyl Fluoride by (Phosphine-Sulfonate)Pd(Me)(py) Catalysts." Journal of the American Chemical Society 129, no. 50 (December 2007): 15450–51. http://dx.doi.org/10.1021/ja0774717.
Повний текст джерелаLuo, Shuji, Javier Vela, Graham R. Lief, and Richard F. Jordan. "Copolymerization of Ethylene and Alkyl Vinyl Ethers by a (Phosphine- sulfonate)PdMe Catalyst." Journal of the American Chemical Society 129, no. 29 (July 2007): 8946–47. http://dx.doi.org/10.1021/ja072562p.
Повний текст джерелаZou, Chen, Wenmin Pang, and Changle Chen. "Influence of chelate ring size on the properties of phosphine-sulfonate palladium catalysts." Science China Chemistry 61, no. 9 (April 25, 2018): 1175–78. http://dx.doi.org/10.1007/s11426-018-9237-6.
Повний текст джерелаYang, Bangpei, Wenmin Pang, and Min Chen. "Redox Control in Olefin Polymerization Catalysis by Phosphine-Sulfonate Palladium and Nickel Complexes." European Journal of Inorganic Chemistry 2017, no. 18 (May 10, 2017): 2510–14. http://dx.doi.org/10.1002/ejic.201700214.
Повний текст джерелаChen, Min, Bangpei Yang, and Changle Chen. "Redox-Controlled Olefin (Co)Polymerization Catalyzed by Ferrocene-Bridged Phosphine-Sulfonate Palladium Complexes." Angewandte Chemie International Edition 54, no. 51 (November 2, 2015): 15520–24. http://dx.doi.org/10.1002/anie.201507274.
Повний текст джерелаChen, Min, Bangpei Yang, and Changle Chen. "Redox-Controlled Olefin (Co)Polymerization Catalyzed by Ferrocene-Bridged Phosphine-Sulfonate Palladium Complexes." Angewandte Chemie 127, no. 51 (November 2, 2015): 15740–44. http://dx.doi.org/10.1002/ange.201507274.
Повний текст джерелаTan, Chen, Muhammad Qasim, Wenmin Pang, and Changle Chen. "Ligand–metal secondary interactions in phosphine–sulfonate palladium and nickel catalyzed ethylene (co)polymerization." Polymer Chemistry 11, no. 2 (2020): 411–16. http://dx.doi.org/10.1039/c9py00904c.
Повний текст джерелаLiang, Tao, and Changle Chen. "Side-Arm Control in Phosphine-Sulfonate Palladium- and Nickel-Catalyzed Ethylene Polymerization and Copolymerization." Organometallics 36, no. 12 (June 15, 2017): 2338–44. http://dx.doi.org/10.1021/acs.organomet.7b00294.
Повний текст джерелаKochi, Takuya, Shusuke Noda, Kenji Yoshimura, and Kyoko Nozaki. "Formation of Linear Copolymers of Ethylene and Acrylonitrile Catalyzed by Phosphine Sulfonate Palladium Complexes." Journal of the American Chemical Society 129, no. 29 (July 2007): 8948–49. http://dx.doi.org/10.1021/ja0725504.
Повний текст джерелаNakamura, Akifumi, Takeharu Kageyama, Hiroki Goto, Brad P. Carrow, Shingo Ito, and Kyoko Nozaki. "P-Chiral Phosphine–Sulfonate/Palladium-Catalyzed Asymmetric Copolymerization of Vinyl Acetate with Carbon Monoxide." Journal of the American Chemical Society 134, no. 30 (July 23, 2012): 12366–69. http://dx.doi.org/10.1021/ja3044344.
Повний текст джерелаLanzinger, Dominik, Marco M. Giuman, Timo M. J. Anselment, and Bernhard Rieger. "Copolymerization of Ethylene and 3,3,3-Trifluoropropene Using (Phosphine-sulfonate)Pd(Me)(DMSO) as Catalyst." ACS Macro Letters 3, no. 9 (September 4, 2014): 931–34. http://dx.doi.org/10.1021/mz5004344.
Повний текст джерелаYang, Bangpei, Shuoyan Xiong, and Changle Chen. "Manipulation of polymer branching density in phosphine-sulfonate palladium and nickel catalyzed ethylene polymerization." Polym. Chem. 8, no. 40 (2017): 6272–76. http://dx.doi.org/10.1039/c7py01281k.
Повний текст джерелаKochi, Takuya, Kenji Yoshimura, and Kyoko Nozaki. "Synthesis of anionic methylpalladium complexes with phosphine–sulfonate ligands and their activities for olefin polymerization." Dalton Trans., no. 1 (2006): 25–27. http://dx.doi.org/10.1039/b512452m.
Повний текст джерелаRezabal, Elixabete, José M. Asua, and Jesus M. Ugalde. "Homopolymerization of Ethylene by Palladium Phosphine Sulfonate Catalysts: The Role of Structural and Environmental Factors." Organometallics 34, no. 1 (December 31, 2014): 373–80. http://dx.doi.org/10.1021/om5011947.
Повний текст джерелаSun, Jiajie, Min Chen, Gen Luo, Changle Chen, and Yi Luo. "Diphosphazane-monoxide and Phosphine-sulfonate Palladium Catalyzed Ethylene Copolymerization with Polar Monomers: A Computational Study." Organometallics 38, no. 3 (January 30, 2019): 638–46. http://dx.doi.org/10.1021/acs.organomet.8b00796.
Повний текст джерелаWu, Zixia, Min Chen, and Changle Chen. "Ethylene Polymerization and Copolymerization by Palladium and Nickel Catalysts Containing Naphthalene-Bridged Phosphine–Sulfonate Ligands." Organometallics 35, no. 10 (March 16, 2016): 1472–79. http://dx.doi.org/10.1021/acs.organomet.6b00076.
Повний текст джерелаKageyama, Takeharu, Shingo Ito, and Kyoko Nozaki. "Vinylarene/CO Copolymerization and Vinylarene/Polar Vinyl Monomer/CO Terpolymerization Using Palladium/Phosphine-Sulfonate Catalysts." Chemistry - An Asian Journal 6, no. 2 (January 20, 2011): 690–97. http://dx.doi.org/10.1002/asia.201000668.
Повний текст джерелаZhang, Randi, Rong Gao, Qingqiang Gou, Jingjing Lai, and Xinyang Li. "Recent Advances in the Copolymerization of Ethylene with Polar Comonomers by Nickel Catalysts." Polymers 14, no. 18 (September 12, 2022): 3809. http://dx.doi.org/10.3390/polym14183809.
Повний текст джерелаKapdi, Anant R., Shatrughn Bhilare, Santosh Kori, Harshita Shet, Gundapally Balaram, Koosam Mahendar, and Yogesh S. Sanghvi. "Scale-Up of a Heck Alkenylation Reaction: Application to the Synthesis of an Amino-Modifier Nucleoside ‘Ruth Linker’." Synthesis 52, no. 23 (September 8, 2020): 3595–603. http://dx.doi.org/10.1055/s-0040-1707260.
Повний текст джерелаBurke, Nichola J., Andrew D. Burrows, Mary F. Mahon, and John E. Warren. "Hydrogen bond network structures based on sulfonated phosphine ligands: The effects of complex geometry, cation substituents and phosphine oxidation on guanidinium sulfonate sheet formation." Inorganica Chimica Acta 359, no. 11 (August 2006): 3497–506. http://dx.doi.org/10.1016/j.ica.2006.01.008.
Повний текст джерелаNoda, Shusuke, Takuya Kochi, and Kyoko Nozaki. "Synthesis of Allylnickel Complexes with Phosphine Sulfonate Ligands and Their Application for Olefin Polymerization without Activators." Organometallics 28, no. 2 (January 26, 2009): 656–58. http://dx.doi.org/10.1021/om800781b.
Повний текст джерелаNoda, Shusuke, Takuya Kochi, and Kyoko Nozaki. "Synthesis of Allylnickel Complexes with Phosphine Sulfonate Ligands and Their Application for Olefin Polymerization without Activators." Organometallics 28, no. 21 (November 9, 2009): 6378. http://dx.doi.org/10.1021/om900860v.
Повний текст джерелаChang, Chun-Fang, Kenji Hamase та Makoto Tsunoda. "Analysis of Total Thiols in the Urine of a Cystathionine β-Synthase-Deficient Mouse Model of Homocystinuria Using Hydrophilic Interaction Chromatography". Molecules 25, № 7 (9 квітня 2020): 1735. http://dx.doi.org/10.3390/molecules25071735.
Повний текст джерелаCai, Zhengguo, Zhongliang Shen, Xiaoyuan Zhou, and Richard F. Jordan. "Enhancement of Chain Growth and Chain Transfer Rates in Ethylene Polymerization by (Phosphine-sulfonate)PdMe Catalysts by Binding of B(C6F5)3 to the Sulfonate Group." ACS Catalysis 2, no. 6 (May 15, 2012): 1187–95. http://dx.doi.org/10.1021/cs300147c.
Повний текст джерелаFeng, Ge, Matthew P. Conley, and Richard F. Jordan. "Differentiation between Chelate Ring Inversion and Aryl Rotation in a CF3-Substituted Phosphine-Sulfonate Palladium Methyl Complex." Organometallics 33, no. 17 (August 21, 2014): 4486–96. http://dx.doi.org/10.1021/om500699t.
Повний текст джерелаVacher, Antoine, Anissa Amar, Franck Camerel, Yann Molard, Camille Latouche, Thierry Roisnel, Vincent Dorcet, Abdou Boucekkine, Huriye Akdas-Kiliç, and Mathieu Achard. "Modulation of emission properties of phosphine-sulfonate ligand containing copper complexes: playing with solvato-, thermo-, and mechanochromism." Dalton Transactions 48, no. 6 (2019): 2128–34. http://dx.doi.org/10.1039/c8dt04502j.
Повний текст джерелаXia, Jian, Yixin Zhang, Jianfu Zhang, and Zhongbao Jian. "High-Performance Neutral Phosphine-Sulfonate Nickel(II) Catalysts for Efficient Ethylene Polymerization and Copolymerization with Polar Monomers." Organometallics 38, no. 5 (February 22, 2019): 1118–26. http://dx.doi.org/10.1021/acs.organomet.8b00916.
Повний текст джерелаMehmood, Andleeb, Xiaowei Xu, Xiaohui Kang, and Yi Luo. "Origin of different chain-end microstructures in ethylene/vinyl halide copolymerization catalysed by phosphine–sulfonate palladium complexes." New Journal of Chemistry 44, no. 39 (2020): 16941–47. http://dx.doi.org/10.1039/d0nj03350b.
Повний текст джерелаChen, Min, and Changle Chen. "Rational Design of High-Performance Phosphine Sulfonate Nickel Catalysts for Ethylene Polymerization and Copolymerization with Polar Monomers." ACS Catalysis 7, no. 2 (January 18, 2017): 1308–12. http://dx.doi.org/10.1021/acscatal.6b03394.
Повний текст джерелаDu, Qing, Yuliang Yang, Lihua Guo, Meng Tian, Xingxing Ge, Zhenzhen Tian, Liping Zhao, Zhishan Xu, Juanjuan Li, and Zhe Liu. "Fluorescent half-sandwich phosphine-sulfonate iridium(III) and ruthenium(II) complexes as potential lysosome-targeted anticancer agents." Dyes and Pigments 162 (March 2019): 821–30. http://dx.doi.org/10.1016/j.dyepig.2018.11.009.
Повний текст джерелаPfeiffer, Christine M., Dan L. Huff, S. Jay Smith, Dayton T. Miller, and Elaine W. Gunter. "Comparison of Plasma Total Homocysteine Measurements in 14 Laboratories: An International Study." Clinical Chemistry 45, no. 8 (August 1, 1999): 1261–68. http://dx.doi.org/10.1093/clinchem/45.8.1261.
Повний текст джерелаGarcía Suárez, Eduardo J., Aurora Ruiz, Sergio Castillón, Werner Oberhauser, Claudio Bianchini, and Carmen Claver. "New alkyl derivatives phosphine sulfonate (P–O) ligands. Catalytic activity in Pd-catalysed Suzuki–Miyaura reactions in water." Dalton Trans., no. 27 (2007): 2859–61. http://dx.doi.org/10.1039/b707590c.
Повний текст джерелаZong, Yanlin, Chaoqun Wang, Yixin Zhang, and Zhongbao Jian. "Polar-Functionalized Polyethylenes Enabled by Palladium-Catalyzed Copolymerization of Ethylene and Butadiene/Bio-Based Alcohol-Derived Monomers." Polymers 15, no. 4 (February 19, 2023): 1044. http://dx.doi.org/10.3390/polym15041044.
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