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Journal articles on the topic 'Poly(p-phenylenes)'

Author: Grafiati
Published: 5 June 2025
Last updated: 1 August 2025

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1

Riehn, R., J. Morgado, R. Iqbal, et al. "Fluorine-substituted poly(p-phenylenes vinylenes) copolymers." Synthetic Metals 124, no. 1 (2001): 67–69. http://dx.doi.org/10.1016/s0379-6779(01)00424-6.

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2

Somitsch, Dieter, Franz P. Wenzl, Emil J. W. List, et al. "The Raman spectra of different ladder type poly(p-phenylenes) and ladder type oligo(p-phenylenes)." Macromolecular Symposia 181, no. 1 (2002): 383–88. http://dx.doi.org/10.1002/1521-3900(200205)181:1<383::aid-masy383>3.0.co;2-f.

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3

Vanhee, S., R. Rulkens, U. Lehmann, et al. "Synthesis and Characterization of Rigid Rod Poly(p-phenylenes)." Macromolecules 29, no. 15 (1996): 5136–42. http://dx.doi.org/10.1021/ma960124p.

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4

Cianga, Ioan, Yesim Hepuzer, and Yusuf Yagci. "Poly(p-phenylenes) with well-defined side chain polymers." Macromolecular Symposia 183, no. 1 (2002): 145–58. http://dx.doi.org/10.1002/1521-3900(200207)183:1<145::aid-masy145>3.0.co;2-r.

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5

Somitsch, D., F. P. Wenzl, G. Leising, et al. "Temperature dependent structural stability of ladder type poly(p-phenylenes)." Synthetic Metals 119, no. 1-3 (2001): 349–50. http://dx.doi.org/10.1016/s0379-6779(00)01389-8.

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6

Connolly, Michael, Frank Karasz, and Mark Trimmer. "Viscoelastic and Dielectric Relaxation Behavior of Substituted Poly(p-phenylenes)." Macromolecules 28, no. 6 (1995): 1872–81. http://dx.doi.org/10.1021/ma00110a022.

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7

Durgaryan, A. H., R. H. Arakelyan, N. A. Durgaran, and E. E. Matinyan. "Synthesis, Characterization, and Electrical Properties of Poly(azophenyleneazo-2,4-diamino-1,5-phenylenes)." Journal of Polymers 2014 (February 23, 2014): 1–6. http://dx.doi.org/10.1155/2014/594841.

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Poly(azophenyleneazo-2,4-diamino-1,5-phenylenes) were synthesized via diazotization of m- and p-phenylenediamine and azocoupling with m-phenylenediamine. It is found that, simultaneously, dihydrobenztriazolic units were formed as a result of cyclization reaction between amino and azo groups located in ortho position to each other. Oxidation of poly(azo-p-phenyleneazo-2,4-diamino-1,5-phenylene) was carried out and new polymer with benzotriazolic units in the main polymer chain was obtained. The conductivities of obtained polymers doped with iodine were increased with doping levels increase from
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8

Grem, G., C. Paar, J. Stampfl, G. Leising, J. Huber, and U. Scherf. "Soluble Segmented Stepladder poly(p-phenylenes) for Blue-Light-Emitting Diodes." Chemistry of Materials 7, no. 1 (1995): 2–4. http://dx.doi.org/10.1021/cm00049a001.

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9

Ravindranath, Renu, Parayil Kumaran Ajikumar, Sheeja Bahulayan, et al. "Ultrathin Conjugated Polymer Network Films of Carbazole Functionalized Poly(p-Phenylenes) via Electropolymerization." Journal of Physical Chemistry B 111, no. 23 (2007): 6336–43. http://dx.doi.org/10.1021/jp070127b.

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10

Yoshida, Yuji, Jing Ping Ni, Nobutaka Tanigaki, and Kiyoshi Yase. "Polarized Electroluminescence of Oligophenyl Thin Films Prepared on Friction Transferred Poly(p-Phenylenes)." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 370, no. 1 (2001): 69–72. http://dx.doi.org/10.1080/10587250108030041.

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11

Henrique S. Paulino, Paulo, Camilla F. Silva, Wagner B. De Almeida, Luciana Guimarães, and Clebio S. Nascimento. "A theoretical study of poly(p-phenylenes) and their cyclodextrin-based insulated molecular wires." Computational and Theoretical Chemistry 1197 (March 2021): 113157. http://dx.doi.org/10.1016/j.comptc.2021.113157.

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12

Kim, Seungho, Jennifer Jackiw, Edward Robinson, et al. "Water Soluble Photo- and Electroluminescent Alkoxy-Sulfonated Poly(p-phenylenes) Synthesized via Palladium Catalysis." Macromolecules 31, no. 4 (1998): 964–74. http://dx.doi.org/10.1021/ma970781x.

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13

Papamokos, George, Jakob Wudarczyk, Robert Graf, et al. "Dipolar Relaxation in Functionalized Poly-p-phenylenes Bearing Ultrastrong Dipoles Perpendicular to the Backbone." Macromolecules 51, no. 9 (2018): 3330–39. http://dx.doi.org/10.1021/acs.macromol.8b00215.

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14

Yokoyama, Toshihiko, Kazuhiko Seki, Ikuo Morisada, Kunishige Edamatsu та Toshiaki Ohta. "X-ray absorption spectra of poly-p-phenylenes and polyacenes: localization of π orbitals". Physica Scripta 41, № 1 (1990): 189–92. http://dx.doi.org/10.1088/0031-8949/41/1/046.

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15

Havinga, E. E., and L. W. Van Horssen. "Dependence of the electrical conductivity of heavily-doped poly-p-phenylenes on the chain length." Synthetic Metals 16, no. 1 (1986): 55–70. http://dx.doi.org/10.1016/0379-6779(86)90153-0.

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16

Chen, Yulan, Weiguo Huang, Cuihong Li, and Zhishan Bo. "Synthesis of Fully Soluble Azomethine-Bridged Ladder-Type Poly(p-phenylenes) by Bischler−Napieralski Reaction." Macromolecules 43, no. 24 (2010): 10216–20. http://dx.doi.org/10.1021/ma1021117.

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17

Simon, G. P., M. Safari Ardi, A. A. Goodwin, et al. "Molecular mobility of substituted poly(p-phenylenes) characterized by a range of polymer relaxation techniques." Journal of Polymer Science Part B: Polymer Physics 36, no. 9 (1998): 1465–81. http://dx.doi.org/10.1002/(sici)1099-0488(19980715)36:9<1465::aid-polb5>3.0.co;2-j.

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18

Lee, Hyo Joong, Sheng-Yun Cui, and Su-Moon Park. "Electrochemistry of Conductive Polymers: XXV. Electrochemical Preparation and Characterization of Poly(p-phenylenes) from Biphenyl and p-Terphenyl." Journal of The Electrochemical Society 148, no. 10 (2001): D139. http://dx.doi.org/10.1149/1.1401080.

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19

Goodson, Felix E., Thomas I. Wallow, and Bruce M. Novak. "Application of “Transfer-Free” Suzuki Coupling Protocols toward the Synthesis of “Unambiguously Linear” Poly(p-phenylenes)." Macromolecules 31, no. 7 (1998): 2047–56. http://dx.doi.org/10.1021/ma9717294.

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20

Wright, Michael E., Kimberly M. Lott, Mark A. McHugh, and Zhihao Shen. "Synthesis of Fluorinated and Hydrocarbon Ester Functionalized Poly(p-phenylenes) and Their Solubility in Supercritical Fluids." Macromolecules 36, no. 7 (2003): 2242–47. http://dx.doi.org/10.1021/ma021615e.

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21

Li, Hairong, and Suresh Valiyaveettil. "Water-Soluble Multifunctional Cross-Conjugated Poly(p-phenylenes) as Stimuli-Responsive Materials: Design, Synthesis, and Characterization." Macromolecules 40, no. 17 (2007): 6057–66. http://dx.doi.org/10.1021/ma0708500.

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22

Lauter, Ulrich, Wolfgang H. Meyer, Volker Enkelmann, and Gerhard Wegner. "Supramolecular structures of poly(p-phenylenes) with oxyethylene side chains and their mixtures with lithium salts." Macromolecular Chemistry and Physics 199, no. 10 (1998): 2129–40. http://dx.doi.org/10.1002/(sici)1521-3935(19981001)199:10<2129::aid-macp2129>3.0.co;2-s.

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23

Li, Meng-Hu, Yu-Long Hai, Ning Lu, et al. "Poly-p-phenylenes as Novel Bulk-type Anode Materials for Potassium-Ion Batteries: A First-Principles Study." Journal of Physical Chemistry C 124, no. 42 (2020): 23045–51. http://dx.doi.org/10.1021/acs.jpcc.0c07415.

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24

Verma, Amita, Kanchan Saxena, Chanderkant, et al. "Soluble Substituted Poly-p-phenylenes - A New Material for Application in Light-Emitting Diodes: Synthesis and Characterization." Applied Biochemistry and Biotechnology 96, no. 1-3 (2001): 215–24. http://dx.doi.org/10.1385/abab:96:1-3:215.

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25

Piyali, Ghosh, Karmakar Somnath, and Mandal Bholanath. "Matrix product forms for the characteristic polynomial coefficients of poly(p-phenylene) graphs." Journal of Indian Chemical Society Vol. 91, Dec 2014 (2014): 2197–210. https://doi.org/10.5281/zenodo.5744943.

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Department of Chemistry, The University of Burdwan, Burdwan-713 104, West Bengal, India <em>E-mail</em> : piyali1979@gmail.com, skarmakarbu@rediffmail.com, bmandal_05@yahoo.com <em>Fax </em>: 91-342-2567938 <em>Manuscript received online 16 August 2013, accepted 04 July 2014</em> The expressions for the characteristic polynomial (CP) coefficients both in matrix product and analytical forms for linear poly(<em>p</em>-phenylenes) (PPP) with different end groups (<em>R<sub>s</sub></em> , <em>s</em> = 1, 2 ) such as hydrogen, methylene, allyl, pentadienyl and of their various combinations have bee
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26

Zhang, Di, Liming Tao, Junping Ju, Yanming Wang, Qihua Wang, and Tingmei Wang. "Postmodification of linear poly- p -phenylenes to prepare hyper-crosslinked polymers: Tuning the surface areas by the molecular weight." Polymer 60 (March 2015): 234–40. http://dx.doi.org/10.1016/j.polymer.2015.01.053.

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27

Havinga, E. E., and L. W. Van Horssen. "Influence of chain length and structural order on the electrical conductivity of poly-p-phenylenes heavily doped with potassium." Synthetic Metals 17, no. 1-3 (1987): 623–28. http://dx.doi.org/10.1016/0379-6779(87)90809-5.

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28

Liu, Song Qiu, Baoling Wang, et al. "Study on the Formation of the Ketonic Defects in the Thermal Degradation of Ladder-Type Poly(p-phenylenes) by Vibrational Spectroscopy." Journal of Physical Chemistry B 109, no. 49 (2005): 23366–70. http://dx.doi.org/10.1021/jp0547818.

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29

Mierzwa, M., G. Floudas, M. Neidhöfer, et al. "Constrained dynamics in supramolecular structures of poly(p-phenylenes) with ethylene oxide side chains: A combined dielectric and nuclear magnetic resonance investigation." Journal of Chemical Physics 117, no. 13 (2002): 6289–99. http://dx.doi.org/10.1063/1.1504437.

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30

Mondal, Swapnadeep, та Bholanath Mandal. "Degree-based topological indices and total π-electron energies of some benzenoid hydrocarbons: correlations of strain energies and bulk modulus with such indices". Zeitschrift für Naturforschung A, 17 червня 2025. https://doi.org/10.1515/zna-2025-0134.

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Abstract Degree-based and neighbourhood degree-sum-based (or hybrid degree-based) topological indices (TIs) for some benzenoid hydrocarbons viz. linear polyacences, methylene substituated linear polyacences, cyclacenes, linear poly (p-phenylenes), methylene substituated linear poly (p-phenylenes), and cylindrical poly (p-phenylenes) with r hexagonal rings are expressed as linear functions of r. For a given system the variation of degree-based Randić and harmonic indices or that of their hybrid indices with r is quite similar while that differs with their corresponding hybrid degree-based indic
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31

Paulino, Paulo Henrique S., Luciana Guimarães, and Clebio S. Nascimento. "Chemical modification and doping of poly(p-phenylenes): A theoretical study." Journal of Molecular Modeling 30, no. 4 (2024). http://dx.doi.org/10.1007/s00894-024-05920-5.

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32

Prins, P., F. C. Grozema, J. M. Schins, S. Patil, U. Scherf, and L. D. A. Siebbeles. "High Intrachain Hole Mobility on Molecular Wires of Ladder-Type Poly(p-Phenylenes)." Physical Review Letters 96, no. 14 (2006). http://dx.doi.org/10.1103/physrevlett.96.146601.

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33

Bag, Kingshuk, and Narayanaswamy Jayaraman. "Synthesis of Controlled Chain Length Formyl Oligo‐p‐Phenylenes, Studies of Physical and Cellular Imaging Behavior." Journal of Polymer Science, December 29, 2024. https://doi.org/10.1002/pol.20240648.

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ABSTRACTSynthesis of chain length‐controlled oligo‐p‐phenylenes, formylation through post‐functionalization, photophysical and biochemical properties are described herein. Synthesis of oligo‐p‐phenylene oligomers with controlled chain length is facilitated by using multivalent dendritic PdII catalysts. Suzuki–Miyaura oligomerization of bromo/iodophenylboronic acids in H2O:THF (3:1) solutions, mediated by one to three generations of poly(propyl ether imine) (PETIM) dendritic catalysts, leads to oligomers with degree of polymerization (DP) 14–26. Upon synthesis, the oligomers are subjected to fo
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34

Reynolds, John R., Andrew D. Child, Jose P. Ruiz, et al. "Optical Absorption, Luminescence, And Redox Switching Properties Of Polyphenylene Derivatives." MRS Proceedings 328 (1993). http://dx.doi.org/10.1557/proc-328-191.

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ABSTRACTA series of polyphenylene derivative polymers with a variety of heterocyclic units along the main chain, and various pendant groups, have been synthesized and their optoelectrochemical properties examined. Polyphenylenes containing electronically isolated emitter centers have optical absorption and luminescence characteristics which are a function of the length of the conjugated unit. A water soluble electroactive rigid-rod poly (p-phenylene), specifically Poly[2,5-bis (propoxy-3-sulfonate)-1,4-phenylene-alt,4-phenylene], has been prepared. Solution cast films of this polymer exhibit o
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35

Prins, P., F. C. Grozema, J. M. Schins, et al. "Effect of intermolecular disorder on the intrachain charge transport in ladder-type poly(p-phenylenes)." Physical Review B 73, no. 4 (2006). http://dx.doi.org/10.1103/physrevb.73.045204.

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36

Gitsas, A., G. Floudas, and G. Wegner. "Effects of temperature and pressure on the stability and mobility of phases in rigid rod poly(p-phenylenes)." Physical Review E 69, no. 4 (2004). http://dx.doi.org/10.1103/physreve.69.041802.

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