Relevant bibliographies by topics / Polycyclotrimerization

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  1. Journal articles
  2. Dissertations / Theses

Academic literature on the topic 'Polycyclotrimerization'

Author: Grafiati
Published: 4 June 2021
Last updated: 1 February 2022

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Journal articles on the topic "Polycyclotrimerization"

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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Dissertations / Theses on the topic "Polycyclotrimerization"

1

Dong, Hongchen. "Synthesis of hyperbranched polyarylenes and poly(aroylarylene)s by polycyclotrimerization of alkynes and their applications as photoresist and precursors for magnetic ceramics /." View abstract or full-text, 2005. http://library.ust.hk/cgi/db/thesis.pl?CHEM%202005%20DONG.

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2

Stahlová, Sabina. "Funkcionalizované mikroporézní polymerní sítě připravené z ethynylarenů." Doctoral thesis, 2016. http://www.nusl.cz/ntk/nusl-353418.

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The preparation of a new group of functionalized conjugated polymer networks has been described based on spontaneous quaternization polymerization of ethynylpyridines with bis(bromomethyl)arenes. The networks consisted of polyacetylene chains with pyridyl and pyridiniumyl pendants cross-linked with -CH2(arylene)CH2- links. The variation of the ratio of monomer and quaternization agent in the feed modified the ratio of pyridyl and pyridiniumyl groups in the networks (pyridyl/pyridiniumyl ratios from 0 to 1.32). The networks did not exhibit a permanent microporosity that could be confirmed by ni
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