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Journal articles on the topic 'Polycyclotrimerization'

Author: Grafiati

Published: 4 June 2021

Last updated: 1 February 2022

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1

Wang, Zhe, Yang Shi, Jian Wang, et al. "Indium-catalyzed polycyclotrimerization of diynes: a facile route to prepare regioregular hyperbranched polyarylenes." Polym. Chem. 5, no. 20 (2014): 5890–94. http://dx.doi.org/10.1039/c4py00859f.

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2

Lin, R. "Kinetics of polycyclotrimerization of 4,4′-thiodiphenylcyanate." Polymer 36, no. 17 (1995): 3349–54. http://dx.doi.org/10.1016/0032-3861(95)99435-w.

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3

Lin, R. H., A. C. Su, and J. L. Hong. "Kinetics of polycyclotrimerization of aromatic dicyanates." Journal of Polymer Research 4, no. 4 (1997): 191–202. http://dx.doi.org/10.1007/s10965-006-0025-z.

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4

Xu, Kaitian, Han Peng, Qunhui Sun, et al. "Polycyclotrimerization of Diynes: Synthesis and Properties of Hyperbranched Polyphenylenes." Macromolecules 35, no. 15 (2002): 5821–34. http://dx.doi.org/10.1021/ma020365z.

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5

Zhou, Haitao, Jianzhao Liu, Shixuan Du, et al. "Direct Visualization of Surface-Assisted Two-Dimensional Diyne Polycyclotrimerization." Journal of the American Chemical Society 136, no. 15 (2014): 5567–70. http://dx.doi.org/10.1021/ja501308s.

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6

Stahlová, Sabina, Jan Sedlácek, Jan Svoboda, Miroslav Polášek, and Jirí Zedník. "Aromatic Schiff Bases Multiply Substituted with Terminal Ethynyl Groups: Potential Building Blocks for Conjugated Polymers and Oligomers." Australian Journal of Chemistry 68, no. 8 (2015): 1237. http://dx.doi.org/10.1071/ch14639.

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Nine mostly novel aromatic Schiff bases containing from two-to-four terminal ethynyl groups and one or two methanimine groups per one molecule are reported. The spectral and density functional theory characteristics and the extent of conjugation are discussed in connection with the structure and architecture of the prepared compounds. The applicability of compounds as building blocks for conjugated polymers is shown in TaCl5-catalyzed polycyclotrimerization (proceeding in ethynyl groups) yielding either soluble luminescent or insoluble microporous polymers.

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7

Fainleib, A., O. Grigoryeva, O. Starostenko, A. Vashchuk, S. Rogalsky, and D. Grande. "Acceleration effect of ionic liquids on polycyclotrimerization of dicyanate esters." Express Polymer Letters 10, no. 9 (2016): 722–29. http://dx.doi.org/10.3144/expresspolymlett.2016.66.

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8

Shi, Jianbing, Bin Tong, Wei Zhao, et al. "Acetylene Polycyclotrimerization: Synthesis and Characterization of Ferrocene-Containing Hyperbranched Polyarylenes." Macromolecules 40, no. 15 (2007): 5612–17. http://dx.doi.org/10.1021/ma062899w.

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9

Li, Zhen, Jacky W. Y. Lam, Yongqiang Dong, et al. "Construction of Hyperbranched Polyphenylenes Containing Ferrocenyl Units by Alkyne Polycyclotrimerization." Macromolecules 39, no. 19 (2006): 6458–66. http://dx.doi.org/10.1021/ma0601823.

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10

Lin, Rong-Hsien, An-Chung Su, and Jin-Long Hong. "Effect of intramolecular cycles on the polycyclotrimerization of aromatic dicyanates." Journal of Applied Polymer Science 73, no. 10 (1999): 1927–38. http://dx.doi.org/10.1002/(sici)1097-4628(19990906)73:10<1927::aid-app12>3.0.co;2-o.

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11

Lin, R. H., A. C. Su, and J. L. Hong. "Glass-transition temperature: Conversion relationship in the polycyclotrimerization of 4,4?-thiodiphenylcyanate." Journal of Polymer Science Part B: Polymer Physics 38, no. 5 (2000): 726–38. http://dx.doi.org/10.1002/(sici)1099-0488(20000301)38:5<726::aid-polb10>3.0.co;2-u.

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12

Lin, Rong-Hsien, An-Chung Su, and Jinn-Lung Hong. "Glass transition temperatureversus conversion relationship in the polycyclotrimerization of aromatic dicyanates." Polymer International 49, no. 4 (2000): 345–57. http://dx.doi.org/10.1002/(sici)1097-0126(200004)49:4<345::aid-pi374>3.0.co;2-d.

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13

Mukhametov, R. R., Yu I. Merkulova, E. V. Dolgova, and M. I. Dushin. "Synthesis of heat-resistant polymer matrices via polycyclotrimerization of cyanate esters." Polymer Science Series D 8, no. 1 (2015): 22–26. http://dx.doi.org/10.1134/s1995421215010104.

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14

Sergeyev, V. A., V. K. Shitikov, A. S. Kurapov, and I. P. Antonova-Antipova. "Polycyclotrimerization of dipropargyl ethers and mixtures of them with monopropargyl ethers." Polymer Science U.S.S.R. 31, no. 6 (1989): 1300–1306. http://dx.doi.org/10.1016/0032-3950(89)90156-1.

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15

Gu, Kai, and Xiao Di Xu. "Synthesis of Hyperbranched Polyphenylacetylene Resins and the Influence of their Molecular Architecture on their Properties." Advanced Materials Research 1095 (March 2015): 385–92. http://dx.doi.org/10.4028/www.scientific.net/amr.1095.385.

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Hyperbranched polyphenylacetylene resins were obtained by the homo-and copolycyclotrimerizations of diynes and monoynes initiated by tantalum-based catalysts, with the aim of exploring new synthetic routes to hyperbranched polyphenylacetylene resins. A group of hyperbranched poly (alkylenephenylenes) (hb-PAPs) were synthesized by TaBr5-Ph4Sn catalyzed polycyclotrimerization of 1,7-octadiyne. To improve the solubility of the homopolymers,the diyne monomers were copolymerized with phenylacetylene. IR,and 1H NMR Spectrum confirmed that the target polymers had formed via a [2+2+2] cyclotrimerizati

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16

Häußler, Matthias, Jianzhao Liu, Jacky Wing Yip Lam, Anjun Qin, Ronghua Zheng, and Ben Zhong Tang. "Polycyclotrimerization of aromatic diynes: Synthesis, thermal stability, and light-emitting properties of hyperbranched polyarylenes." Journal of Polymer Science Part A: Polymer Chemistry 45, no. 18 (2007): 4249–63. http://dx.doi.org/10.1002/pola.22246.

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17

Jim, Cathy K. W., AnJun Qin, Jacky W. Y. Lam, JianZhao Liu, Matthias Haeussler, and Ben Zhong Tang. "Amine-catalyzed polycyclotrimerization of arylene bipropiolate: A metal-free and regioselective route to hyperbranched polymer." Science in China Series B: Chemistry 51, no. 8 (2008): 705–8. http://dx.doi.org/10.1007/s11426-008-0086-4.

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18

Radamshina, E. R., V. A. Grigor'eva, V. V. Komratova, A. I. Kuzaev, and S. M. Baturin. "Study of the polycyclotrimerization of 1,6-hexamethylenediisocyanate and gel permeation chromatographic analysis of the products." Polymer Science U.S.S.R. 32, no. 6 (1990): 1237–41. http://dx.doi.org/10.1016/0032-3950(90)90183-7.

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19

Sergeyev, V. A., V. K. Shitikov, S. S. A. Pavlova, G. I. Timofeyeva, N. V. Chizhova, and N. N. Kudryavtseva. "Features of the structure and molecular-mass distribution of the products of the polycyclotrimerization of isocyanates." Polymer Science U.S.S.R. 30, no. 7 (1988): 1602–8. http://dx.doi.org/10.1016/0032-3950(88)90452-2.

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20

Rogovina, L. Z., V. G. Vasil'ev, L. I. Makarova, et al. "The formation, structure and properties of network polymers synthesized by polycyclotrimerization of carbo-functional organosilicon macrodiisocyanates in solution." Polymer Science U.S.S.R. 30, no. 1 (1988): 122–30. http://dx.doi.org/10.1016/0032-3950(88)90264-x.

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21

Qin, An-jun, Cathy, K. W. Jim, Jacky, W. Y. Lam, Jing-zhi Sun, and Ben Zhong Tang. "SYNTHESIS OF A HYPERBRANCHED POLY(AROYLARYLENE) CONTAINING TRIAZOLE AND FLUORENE FUNCTIONALITIES BY CLICK CHEMISTRY AND METAL-FREE, REGIOSELECTIVE POLYCYCLOTRIMERIZATION." Chinese Journal of Polymer Science 27, no. 02 (2009): 145. http://dx.doi.org/10.1142/s0256767909003765.

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22

Qin, Anjun, Jacky W. Y. Lam, Hongchen Dong, et al. "Metal-Free, Regioselective Diyne Polycyclotrimerization: Synthesis, Photoluminescence, Solvatochromism, and Two-Photon Absorption of a Triphenylamine-Containing Hyperbranched Poly(aroylarylene)." Macromolecules 40, no. 14 (2007): 4879–86. http://dx.doi.org/10.1021/ma070200w.

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23

Liu, Jianzhao, Ronghua Zheng, Youhong Tang, et al. "Hyperbranched Poly(silylenephenylenes) from Polycyclotrimerization of A2-Type Diyne Monomers: Synthesis, Characterization, Structural Modeling, Thermal Stability, and Fluorescent Patterning." Macromolecules 40, no. 21 (2007): 7473–86. http://dx.doi.org/10.1021/ma071062d.

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24

Kovalins’ka, T. V., V. I. Sakhno, Yu V. Ivanov, et al. "Study of functionality of polymer films by dense electron beams." Polymer journal 42, no. 4 (2020): 254–61. http://dx.doi.org/10.15407/polymerj.42.04.254.

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Methodology of using megavolt electrons for investigation of the functionality of thin polymer films of polycyanurates (PCN) is described. The relevance of research is determined by the prospects of using films as a functional basis for improvement of track-etched technologies of nanoporous nuclear filters, where ionizing radiation is used in most of technological stages of their production. Functionality control is the main criterion for the qualification of films on the suitability for production of nuclear filters on their base. Development of megavolt electrons radiation methods is promisi

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25

Dong, Hongchen, Ronghua Zheng, Jacky W. Y. Lam, Matthias Häussler, Anjun Qin, and Ben Zhong Tang. "A New Route to Hyperbranched Macromolecules: Syntheses of Photosensitive Poly(aroylarylene)s via 1,3,5-Regioselective Polycyclotrimerization of Bis(aroylacetylene)s." Macromolecules 38, no. 15 (2005): 6382–91. http://dx.doi.org/10.1021/ma050342v.

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26

Chan, Carrie Y. K., Jacky W. Y. Lam, Cathy K. W. Jim, Herman H. Y. Sung, Ian D. Williams, and Ben Zhong Tang. "Polycyclotrimerization of Dinitriles: A New Polymerization Route for the Construction of Soluble Nitrogen-Rich Polytriazines with Hyperbranched Structures and Functional Properties." Macromolecules 46, no. 24 (2013): 9494–506. http://dx.doi.org/10.1021/ma402066k.

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27

Fainleib, A., O. Grigoryeva, A. Vashchuk, et al. "Effect of ionic liquids on kinetic parameters of dicyanate ester polycyclotrimerization and on thermal and viscoelastic properties of resulting cyanate ester resins." Express Polymer Letters 13, no. 5 (2019): 469–83. http://dx.doi.org/10.3144/expresspolymlett.2019.39.

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28

Zheng, Ronghua, Hongchen Dong, Han Peng, Jacky W. Y. Lam, and Ben Zhong Tang. "Construction of Hyperbranched Poly(alkenephenylene)s by Diyne Polycyclotrimerization: Single-Component Catalyst, Glycogen-like Macromolecular Structure, Facile Thermal Curing, and Strong Thermolysis Resistance." Macromolecules 37, no. 14 (2004): 5196–210. http://dx.doi.org/10.1021/ma049871+.

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29

Jim, Cathy K. W., Anjun Qin, Jacky W. Y. Lam, et al. "Facile Polycyclotrimerization of “Simple” Arylene Bipropiolates: A Metal-Free, Regioselective Route to Functional Hyperbranched Polymers with High Optical Transparency, Tunable Refractive Index, Low Chromatic Aberration, and Photoresponsive Patternability." Macromolecules 42, no. 12 (2009): 4099–109. http://dx.doi.org/10.1021/ma900076z.

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30

Liu, Jianzhao, Li Zhang, Jacky W. Y. Lam, et al. "Exploration of Effective Catalysts for Diyne Polycyclotrimerization, Synthesis of an Ester-Functionalized Hyperbranched Polyphenylene, and Demonstration of Its Utility as a Molecular Container with Implication for Controlled Drug Delivery." Macromolecules 42, no. 19 (2009): 7367–78. http://dx.doi.org/10.1021/ma901247q.

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31

Lebedev, B. V., T. A. Bykova, Ye G. Kiparisova, V. A. Pankratov, Ts M. Frenkel', and V. V. Korshak. "A calorimetric study of 1,6-hexamethylene diisocyanate, its polycyclotrimerizatinn and the resulting polycyclotrimer in the 13·8–370 K region." Polymer Science U.S.S.R. 27, no. 7 (1985): 1581–87. http://dx.doi.org/10.1016/0032-3950(85)90348-x.

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