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Journal articles on the topic 'Suzuki polymerization'

Author: Grafiati

Published: 29 June 2021

Last updated: 8 February 2022

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1

Bautista, Michael V., Anthony J. Varni, Josué Ayuso-Carrillo, Matthew C. Carson, and Kevin J. T. Noonan. "Pairing Suzuki–Miyaura cross-coupling and catalyst transfer polymerization." Polymer Chemistry 12, no. 10 (2021): 1404–14. http://dx.doi.org/10.1039/d0py01507e.

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2

Namgung, Ho, Jeong Jun Lee, Young Jin Gwon, and Taek Seung Lee. "Synthesis of tetraphenylethylene-based conjugated microporous polymers for detection of nitroaromatic explosive compounds." RSC Advances 8, no. 60 (2018): 34291–96. http://dx.doi.org/10.1039/c8ra06463f.

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3

Guo, Ting, Wenkai Zhong, Jianhua Zou, Lei Ying, Wei Yang, and Junbiao Peng. "Efficient binary white light-emitting polymers grafted with iridium complexes as side groups." RSC Advances 5, no. 109 (2015): 89888–94. http://dx.doi.org/10.1039/c5ra16717e.

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4

Wang, Ziyu, Cheng Wang, Yayun Fang, Hong Yuan, Yiwu Quan, and Yixiang Cheng. "Color-tunable AIE-active conjugated polymer nanoparticles as drug carriers for self-indicating cancer therapy via intramolecular FRET mechanism." Polymer Chemistry 9, no. 23 (2018): 3205–14. http://dx.doi.org/10.1039/c8py00329g.

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5

Dai, Chunhui, Dongliang Yang, Xiao Fu, Qingmin Chen, Chengjian Zhu, Yixiang Cheng, and Lianhui Wang. "A study on tunable AIE (AIEE) of boron ketoiminate-based conjugated polymers for live cell imaging." Polymer Chemistry 6, no. 28 (2015): 5070–76. http://dx.doi.org/10.1039/c5py00733j.

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6

Yokozawa, Tsutomu, Yutaka Nanashima, Haruhiko Kohno, Ryosuke Suzuki, Masataka Nojima, and Yoshihiro Ohta. "Catalyst-transfer condensation polymerization for precision synthesis of π-conjugated polymers." Pure and Applied Chemistry 85, no. 3 (August 12, 2012): 573–87. http://dx.doi.org/10.1351/pac-con-12-03-13.

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Catalyst-transfer condensation polymerization, in which the catalyst activates the polymer end-group, followed by reaction with the monomer and transfer of the catalyst to the elongated polymer end-group, has made it feasible to control the molecular weight, polydispersity, and end-groups of π-conjugated polymers. In this paper, our recent progress of Kumada–Tamao Ni catalyst-transfer coupling polymerization and Suzuki–Miyaura Pd catalyst-transfer coupling polymerization is described. In the former polymerization method, the polymerization of Grignard pyridine monomers was investigated for the synthesis of well-defined n-type π-conjugated polymers. Para-type pyridine monomer, 3-alkoxy-2-bromo-5-chloromagnesiopyridine, afforded poly(pyridine-2,5-diyl) with low solubility in the reaction solvent, whereas meta-type pyridine monomer, 2-alkoxy-5-bromo-3-chloromagnesio-pyridine, yielded soluble poly(pyridine-3,5-diyl) with controlled molecular weight and low polydispersity. In Suzuki–Miyaura catalyst-transfer coupling polymerization, t-Bu3PPd(Ph)Br was an effective catalyst, and well-defined poly(p-phenylene) and poly(3-hexylthiophene) (P3HT) were obtained by concomitant use of CsF/18-crown-6 as a base in tetrahydrofuran (THF) and a small amount of water.

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7

Sugita, Hajime, Masataka Nojima, Yoshihiro Ohta, and Tsutomu Yokozawa. "Unstoichiometric Suzuki–Miyaura cyclic polymerization of extensively conjugated monomers." Polymer Chemistry 10, no. 10 (2019): 1182–85. http://dx.doi.org/10.1039/c8py01741g.

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Suzuki–Miyaura polycondensation of an excess of extensively conjugated aromatic dibromide with 1.0 equivalent of phenylenediboronate in the presence of ^tBu₃PPd(0) precatalyst afforded cyclic polymers.

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8

Wang, Yunshu, Shuangshuang Zhang, Laibing Wang, Wei Zhang, Nianchen Zhou, Zhengbiao Zhang, and Xiulin Zhu. "The Suzuki coupling reaction as a post-polymerization modification: a promising protocol for construction of cyclic-brush and more complex polymers." Polymer Chemistry 6, no. 25 (2015): 4669–77. http://dx.doi.org/10.1039/c5py00551e.

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9

Sugita, Hajime, Masataka Nojima, Yoshihiro Ohta, and Tsutomu Yokozawa. "Unusual cyclic polymerization through Suzuki–Miyaura coupling of polyphenylene bearing diboronate at both ends with excess dibromophenylene." Chemical Communications 53, no. 2 (2017): 396–99. http://dx.doi.org/10.1039/c6cc08333a.

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10

Wang, Haiqing, Dehui Sun, Qichen Lu, Fulei Wang, Lili Zhao, Zengfu Zhang, Xun Wang, and Hong Liu. "Bio-inspired synthesis of mesoporous HfO2 nanoframes as reactors for piezotronic polymerization and Suzuki coupling reactions." Nanoscale 11, no. 12 (2019): 5240–46. http://dx.doi.org/10.1039/c9nr00707e.

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Mesoporous HfO₂ nanoframes were elaborately fabricated, inspired by the flexible assembly principles in the biomolecules, and were demonstrated as nanoreactors for piezotronic polymerization and Suzuki coupling reactions.

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11

Huang, Cheng-Wei, Wen-Yu Ji, and Shiao-Wei Kuo. "Stimuli-responsive supramolecular conjugated polymer with phototunable surface relief grating." Polymer Chemistry 9, no. 20 (2018): 2813–20. http://dx.doi.org/10.1039/c8py00439k.

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A facile method to synthesize azobenzene- and thymine (T)-functionalized conjugated copolymers through Suzuki coupling polymerization and click reactions and used in surface relief gratings displaying long-range-ordered interference patterns.

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12

Yang, Po-Chih, Hua-Wen Wen, Chih-Wei Huang, and Yi-Ning Zhu. "Synthesis and chemosensory properties of two-arm truxene-functionalized conjugated polyfluorene containing terpyridine moiety." RSC Advances 6, no. 90 (2016): 87680–89. http://dx.doi.org/10.1039/c6ra15965f.

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We report the responsive fluorescence chemosensory phenomena of a truxene-functionalized conjugated polymer (P1) with pendant terminal terpyridine (tpy) groups as receptors for metal ions synthesized via a Suzuki polymerization reaction.

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13

Page, Zachariah A., Feng Liu, Thomas P. Russell, and Todd Emrick. "Rapid, facile synthesis of conjugated polymer zwitterions in ionic liquids." Chem. Sci. 5, no. 6 (2014): 2368–73. http://dx.doi.org/10.1039/c4sc00475b.

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Ionic liquids (ILs) were utilized for the rapid air-stable Suzuki polymerization of polar zwitterionic thiophene monomers, precluding the need for volatile organic solvents, phosphine ligands and phase transfer catalysts typically used in conjugated polymer synthesis.

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14

Elmalem, Einat, Anton Kiriy, and Wilhelm T. S. Huck. "Chain-Growth Suzuki Polymerization of n-Type Fluorene Copolymers." Macromolecules 44, no. 22 (November 22, 2011): 9057–61. http://dx.doi.org/10.1021/ma201934q.

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15

Zhang, Hong-Hai, Yu-Xing Zhu, Weiyu Wang, Jiahua Zhu, Peter V. Bonnesen, and Kunlun Hong. "Controlled synthesis of ortho, para-alternating linked polyarenes via catalyst-transfer Suzuki coupling polymerization." Polymer Chemistry 9, no. 24 (2018): 3342–46. http://dx.doi.org/10.1039/c8py00070k.

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A novel class of ortho, para-alternating linked polyarenes is synthesized via catalyst-transfer Suzuki coupling polymerization with Pd₂(dba)₃/t-Bu₃P/p-BrC₆H₄COPh as initiator.

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16

Nau, Jennifer, and Thomas J. J. Müller. "Dithienothiazine Copolymers – Synthesis and Electronic Properties of Novel Redox-Active Fluorescent Polymers." Organic Materials 03, no. 02 (April 2021): 293–301. http://dx.doi.org/10.1055/a-1528-6301.

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Dithienothiazine copolymers are efficiently obtained by Suzuki polymerization or in situ lithiation–Negishi polymerization in good to excellent yields. Gel permeation chromatography was applied to characterize the dispersities and degrees of polymerization of these novel materials. Thermogravimetric analysis shows that the copolymers are stable towards side-chain cleavage up to 200 °C. The materials are deep red to black amorphous solids or resins and their absorption and emission spectra in solution reveal broad absorption bands in the visible and orange to deep red luminescence upon UV excitation. According to the optical band gaps these novel copolymers qualify as a new class of low band gap organic semiconductors.

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17

Seto, Hirokazu, Takumi Tono, Akiko Nagaoka, Mai Yamamoto, Yumiko Hirohashi, and Hiroyuki Shinto. "Preparation and characterization of glycopolymers with biphenyl spacers via Suzuki coupling reaction." Organic & Biomolecular Chemistry 19, no. 20 (2021): 4474–77. http://dx.doi.org/10.1039/d1ob00617g.

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18

Lee, Junghoon, A.-Reum Han, Sang Myeon Lee, Dohyuk Yoo, Joon Hak Oh, and Changduk Yang. "Siloxane-Based Hybrid Semiconducting Polymers Prepared by Fluoride-Mediated Suzuki Polymerization." Angewandte Chemie 127, no. 15 (February 12, 2015): 4740–43. http://dx.doi.org/10.1002/ange.201411557.

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19

Lee, Junghoon, A.-Reum Han, Sang Myeon Lee, Dohyuk Yoo, Joon Hak Oh, and Changduk Yang. "Siloxane-Based Hybrid Semiconducting Polymers Prepared by Fluoride-Mediated Suzuki Polymerization." Angewandte Chemie International Edition 54, no. 15 (February 12, 2015): 4657–60. http://dx.doi.org/10.1002/anie.201411557.

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20

Akbayrak, Merve, and Ahmet M. Önal. "Synthesis and electrochemical polymerization of diketopyrrolopyrrole based donor–acceptor–donor monomers containing 3,6- and 2,7-linked carbazoles." Polymer Chemistry 7, no. 39 (2016): 6110–19. http://dx.doi.org/10.1039/c6py01489e.

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Three new donor–acceptor–donor type monomers bearing 2,7- or 3,6-linked carbazoles as the donor unit and diketopyrrolopyrrole as the acceptor unit were synthesized via a Suzuki cross coupling reaction.

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21

Ramaotsoa, G. Valerie, Ian Strydom, Jenny-Lee Panayides, and Darren Riley. "Immobilized tetrakis(triphenylphosphine)palladium(0) for Suzuki–Miyaura coupling reactions under flow conditions." Reaction Chemistry & Engineering 4, no. 2 (2019): 372–82. http://dx.doi.org/10.1039/c8re00235e.

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An immobilized triphenylphosphine scaffold was prepared by precipitation polymerization and functionalized to afford a cost-effective source of solid-supported tetrakis(triphenylphosphine)palladium(0).

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22

Gobalasingham, Nemal S., Seyma Ekiz, Robert M. Pankow, Francesco Livi, Eva Bundgaard, and Barry C. Thompson. "Carbazole-based copolymers via direct arylation polymerization (DArP) for Suzuki-convergent polymer solar cell performance." Polymer Chemistry 8, no. 30 (2017): 4393–402. http://dx.doi.org/10.1039/c7py00859g.

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23

ten Hove, Jan Bart, Jeroen Appel, Johanna M. van den Broek, Alexander J. C. Kuehne, and Joris Sprakel. "Conjugated Polymer Shells on Colloidal Templates by Seeded Suzuki-Miyaura Dispersion Polymerization." Small 10, no. 5 (November 13, 2013): 957–63. http://dx.doi.org/10.1002/smll.201302039.

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24

Fischer, Christoph S., Christian Jenewein, and Stefan Mecking. "Conjugated Star Polymers from Multidirectional Suzuki–Miyaura Polymerization for Live Cell Imaging." Macromolecules 48, no. 3 (January 29, 2015): 483–91. http://dx.doi.org/10.1021/ma502294n.

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25

Yokozawa, Tsutomu, Ryosuke Suzuki, Masataka Nojima, Yoshihiro Ohta, and Akihiro Yokoyama. "Precision Synthesis of Poly(3-hexylthiophene) from Catalyst-Transfer Suzuki−Miyaura Coupling Polymerization." Macromolecular Rapid Communications 32, no. 11 (April 20, 2011): 801–6. http://dx.doi.org/10.1002/marc.201100037.

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26

Vogt, Christian G., Sven Grätz, Stipe Lukin, Ivan Halasz, Martin Etter, Jack D. Evans, and Lars Borchardt. "Direct Mechanocatalysis: Palladium as Milling Media and Catalyst in the Mechanochemical Suzuki Polymerization." Angewandte Chemie International Edition 58, no. 52 (December 19, 2019): 18942–47. http://dx.doi.org/10.1002/anie.201911356.

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27

Brookins, Robert N., Kirk S. Schanze, and John R. Reynolds. "Base-Free Suzuki Polymerization for the Synthesis of Polyfluorenes Functionalized with Carboxylic Acids." Macromolecules 40, no. 10 (May 2007): 3524–26. http://dx.doi.org/10.1021/ma070070r.

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28

Yokozawa, Tsutomu, Haruhiko Kohno, Yoshihiro Ohta, and Akihiro Yokoyama. "Catalyst-Transfer Suzuki−Miyaura Coupling Polymerization for Precision Synthesis of Poly(p-phenylene)." Macromolecules 43, no. 17 (September 14, 2010): 7095–100. http://dx.doi.org/10.1021/ma101073x.

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29

Carrillo, Josué Ayuso, Michael J. Ingleson, and Michael L. Turner. "Thienyl MIDA Boronate Esters as Highly Effective Monomers for Suzuki–Miyaura Polymerization Reactions." Macromolecules 48, no. 4 (February 10, 2015): 979–86. http://dx.doi.org/10.1021/ma502542g.

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30

Kosaka, Kentaro, Tatsuya Uchida, Koichiro Mikami, Yoshihiro Ohta, and Tsutomu Yokozawa. "AmPhos Pd-Catalyzed Suzuki–Miyaura Catalyst-Transfer Condensation Polymerization: Narrower Dispersity by Mixing the Catalyst and Base Prior to Polymerization." Macromolecules 51, no. 2 (January 2, 2018): 364–69. http://dx.doi.org/10.1021/acs.macromol.7b01990.

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31

Bautista, Michael V., Anthony J. Varni, Josué Ayuso-Carrillo, Chia-Hua Tsai, and Kevin J. T. Noonan. "Chain-Growth Polymerization of Benzotriazole Using Suzuki–Miyaura Cross-Coupling and Dialkylbiarylphosphine Palladium Catalysts." ACS Macro Letters 9, no. 9 (August 28, 2020): 1357–62. http://dx.doi.org/10.1021/acsmacrolett.0c00580.

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32

Parrenin, Laurie, Cyril Brochon, Georges Hadziioannou, and Eric Cloutet. "Low Bandgap Semiconducting Copolymer Nanoparticles by Suzuki Cross-Coupling Polymerization in Alcoholic Dispersed Media." Macromolecular Rapid Communications 36, no. 20 (August 21, 2015): 1816–21. http://dx.doi.org/10.1002/marc.201500324.

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33

Kosaka, Kentaro, Yoshihiro Ohta, and Tsutomu Yokozawa. "Influence of the Boron Moiety and Water on Suzuki-Miyaura Catalyst-Transfer Condensation Polymerization." Macromolecular Rapid Communications 36, no. 4 (December 12, 2014): 373–77. http://dx.doi.org/10.1002/marc.201400530.

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34

Sun, Huiliang, Shuren Zhang, Yike Yang, Xiao Li, Hongmei Zhan, and Yanxiang Cheng. "Excellent Control of Perylene Diimide End Group in Polyfluorene via Suzuki Catalyst Transfer Polymerization." Macromolecular Chemistry and Physics 217, no. 24 (November 9, 2016): 2726–35. http://dx.doi.org/10.1002/macp.201600412.

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35

Yang, Yun Xian, Ji Ping Yang, Bing Zhou, and Jing Yu Zhang. "Synthesis and Characterization of Novel Polymer of Vinyl Carbazole Bearing Thiophene Groups." Advanced Materials Research 562-564 (August 2012): 512–15. http://dx.doi.org/10.4028/www.scientific.net/amr.562-564.512.

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Combination of vinyl carbazole and thiophene groups’ excellent thermal properties and optical properties, a novel polymer named poly(2,7-bi-2-thienyl-9-vinyl-9-H-carbazole) was synthesized via radical polymerization and Suzuki reaction. The polymer was characterized using Fourier transform infrared spectrometer(FT-IR), gel permeation chromatography(GPC), differential scanning calorimetry(DSC), and X-Ray fluorescence spectrometer(XRF). It was found that this π-conjugated polymer containing vinyl carbazole and thiophene groups gave a high glass transition temperature (Tg=251°C). This feature made poly(2,7-bi-2-thienyl-9-vinyl-9-H-carbazole) possessing an excellent thermal performance.

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36

Soo Choi, Moon, Hyung Jun Kim, Taek Seung Lee, and Won Seok Lyoo. "Newly Synthesized Branch-type Aromatic Oxadiazole Polymer and Binary Fluorescence Patterning on its Film." High Performance Polymers 19, no. 5-6 (October 2007): 531–40. http://dx.doi.org/10.1177/0954008306081195.

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Aromatic side-chain oxadiazole polymer linked with 9,9'-dioctylfluorene was successfully synthesized via Suzuki coupling reaction. Hydroxyphenyl group was attached in the 2-position of the oxadiazole unit in the polymer side chain to control the optical properties of the polymer. We confirmed the presence of the t-butoxycarbonyl group on the hydroxyl group using thermogravimetric analysis, which was incorporated to avoid side reaction during polymerization. We also performed the simple and easy fabrication method for the dual fluorescence image using photochemical cleavage of the t-butoxycarbonyl group from the polymer to induce fluorescence color changes before and after UV irradiation.

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37

Schroot, Robert, Ulrich S. Schubert, and Michael Jäger. "Poly(N-alkyl-3,6-carbazole)s via Suzuki–Miyaura Polymerization: From Macrocyclization toward End Functionalization." Macromolecules 50, no. 4 (February 8, 2017): 1319–30. http://dx.doi.org/10.1021/acs.macromol.7b00144.

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38

Li, Haibo, Xiaofu Wu, Bowei Xu, Hui Tong, and Lixiang Wang. "Solution-processible hyperbranched conjugated polymer nanoparticles with tunable particle sizes by Suzuki polymerization in miniemulsion." RSC Advances 3, no. 23 (2013): 8645. http://dx.doi.org/10.1039/c3ra40901e.

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39

Maeyama, Katsuya, Kenji Yamashita, Hiromu Saito, Shunichi Aikawa, and Yasuhiko Yoshida. "Synthesis of aromatic poly(ether ketone)s bearing optically active macrocycles through Suzuki coupling polymerization." Polymer Journal 44, no. 4 (January 11, 2012): 315–20. http://dx.doi.org/10.1038/pj.2011.134.

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40

Maeyama, Katsuya, Tadashi Tsukamoto, Masanori Suzuki, Shuhei Higashibayashi, and Hidehiro Sakurai. "Nanosized palladium-catalyzed Suzuki–Miyaura coupling polymerization: synthesis of soluble aromatic poly(ether ketone)s." Polymer Journal 45, no. 4 (August 29, 2012): 401–5. http://dx.doi.org/10.1038/pj.2012.158.

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41

Maeyama, Katsuya, Tadashi Tsukamoto, Masanori Suzuki, Shuhei Higashibayashi, and Hidehiro Sakurai. "Synthesis of Aromatic Polyketones Bearing 1,1′-Binaphthyl-2,2′-dioxy Units through Suzuki–Miyaura Coupling Polymerization." Chemistry Letters 40, no. 12 (December 5, 2011): 1445–46. http://dx.doi.org/10.1246/cl.2011.1445.

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42

Reddy, Lavanya, Suja T. Dharmabalan, Kanakaraju Manupati, Ragini Yeeravalli, Lakshmi D. Vijay, Kavitha Donthiboina, Vadithe Lakshma Naik, and Amitava Das. "Concise Synthesis of 1,1-Diarylvinyl Sulfones and Investigations on their Antiproliferative Activity via Tubulin Inhibition." Anti-Cancer Agents in Medicinal Chemistry 20, no. 12 (September 7, 2020): 1469–74. http://dx.doi.org/10.2174/1871520620666200423075630.

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Background: Discovery of small molecules that inhibit tubulin polymerization is an attractive strategy for the development of new and improved anti-proliferative agents. Objective: A series of novel 2-sulfonyl-1,1-diarylethenes were designed towards this end keeping in view the favorable chemical and pharmacological virtues of unsaturated sulfones. Methods: Rapid, convenient and efficient two-step assembly of the designed molecules was achieved by the vicinal iodo-sulfonylation-Suzuki coupling sequence. Results: As hypothesized, these compounds showed good anti-proliferative activity against different tissuespecific cancer cell lines: MCF-7, DU-145, A-549, HepG2, and HeLa. The most active compound, pnitrophenyl ring-bearing analog, exhibited an IC50 value of 0.90μM against A-549 cells. Flow cytometry studies on this derivative revealed that it arrests the cell cycle of A-549 cells at the G2/M phase. This compound exhibited molecular binding to tubulin as well as tubulin polymerization inhibition comparable to that of colchicine. Conclusion: A new class of potent, tubulin binding anticancer agents based on 1,1,-diarylvinyl sulfone scaffold has been designed and synthesized.

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43

Otaki, Masashi, Reiji Kumai, Hajime Sagayama, and Hiromasa Goto. "Synthesis of Polyazobenzenes Exhibiting Photoisomerization and Liquid Crystallinity." Polymers 11, no. 2 (February 17, 2019): 348. http://dx.doi.org/10.3390/polym11020348.

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While only a few studies have investigated the synthesis of main chain-type polyazobenzenes, they continue to draw an increasing amount of attention owing to their industrial applications in holography, dyes, and functional adhesives. In this study, dibromoazobenzene was prepared as a monomer for constructing azo-based π-conjugated polymers. Miyaura–Suzuki cross-coupling polymerization was conducted to develop copolymers containing an azobenzene unit as a photoisomerization block and a pyrimidine-based liquid crystal generator block. The prepared polymers exhibited thermotropic liquid crystallinity and underwent cis and trans photoisomerization upon irradiation with ultraviolet and visible light. Furthermore, the photoisomerization behavior was examined using optical absorption spectroscopy and synchrotron X-ray diffraction spectrometry.

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44

Lim, Eunhee. "Synthesis and Characterization of Carbazole-Benzothiadiazole-Based Conjugated Polymers for Organic Photovoltaic Cells with Triazole in the Main Chain." International Journal of Photoenergy 2013 (2013): 1–7. http://dx.doi.org/10.1155/2013/607826.

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We have synthesized a series of carbazole-benzothiadiazole-triazole based copolymers, poly[(N-9′-heptadecanyl-2,7-carbazole)-co-(5,5-(4′,7′-di-2-thienyl-2′,1′,3′-benzothiadiazole))-co-((4-(4-butylphenyl)-3,5-diphenyl-4H-1,2,4]triazole))] (PCz3TBTz) by Suzuki coupling polymerization. The optical and electrochemical properties of the copolymers could be tuned by changing the comonomer unit of triazole from 0% to 80%. Organic photovoltaic (OPV) cells were fabricated by blending the synthesized polymers as a donor and PCBM as an acceptor. The material solubility and film morphology were improved by introducing the triazole unit in the main chain. Improved OPV device performance of 1.74% was achieved in the presence of an optimal amount of triazole moieties.

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45

Nojima, Masataka, Takeru Kamigawara, Yoshihiro Ohta, and Tsutomu Yokozawa. "Catalyst‐Transfer Suzuki–Miyaura Condensation Polymerization of Stilbene Monomer: Different Polymerization Behavior Depending on Halide and Aryl Group of ArPd(tBu3P)X Initiator." Journal of Polymer Science Part A: Polymer Chemistry 57, no. 3 (August 7, 2018): 297–304. http://dx.doi.org/10.1002/pola.29169.

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46

Huber, Steffen, and Stefan Mecking. "Straightforward Synthesis of Conjugated Block Copolymers by Controlled Suzuki–Miyaura Cross-Coupling Polymerization Combined with ATRP." Macromolecules 52, no. 15 (July 31, 2019): 5917–24. http://dx.doi.org/10.1021/acs.macromol.9b01165.

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47

Li, Gang, Ki-Young Yoon, Xinjue Zhong, Xiaoyang Zhu, and Guangbin Dong. "Efficient Bottom-Up Preparation of Graphene Nanoribbons by Mild Suzuki-Miyaura Polymerization of Simple Triaryl Monomers." Chemistry - A European Journal 22, no. 27 (May 31, 2016): 9116–20. http://dx.doi.org/10.1002/chem.201602007.

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48

Xing, Zeyong, Jian Zhang, Xiaohong Li, Wei Zhang, Laibing Wang, Nianchen Zhou, and Xiulin Zhu. "Design and property of thermoresponsive core-shell fluorescent nanoparticles via RAFT polymerization and suzuki coupling reaction." Journal of Polymer Science Part A: Polymer Chemistry 51, no. 19 (June 26, 2013): 4021–30. http://dx.doi.org/10.1002/pola.26822.

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49

Maeyama, Katsuya, Tadashi Tsukamoto, Hiroaki Kumagai, Shuhei Higashibayashi, and Hidehiro Sakurai. "Synthesis of organosoluble and fluorescent aromatic polyketones bearing 1,1′-binaphthyl units through Suzuki–Miyaura coupling polymerization." Polymer Bulletin 72, no. 11 (June 29, 2015): 2903–16. http://dx.doi.org/10.1007/s00289-015-1443-z.

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50

Lienkamp, Karen, Ingo Schnell, Franziska Groehn, and Gerhard Wegner. "Polymerization of Styrene Sulfonate Ethyl Ester by ATRP: Synthesis and Characterization of Macromonomers for Suzuki Polycondensation." Macromolecular Chemistry and Physics 207, no. 22 (November 24, 2006): 2066–73. http://dx.doi.org/10.1002/macp.200600322.

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