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Journal articles on the topic 'Telechelic polymers'

Author: Grafiati

Published: 4 June 2021

Last updated: 6 September 2023

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1

Farah, Abdiaziz A., and William J. Pietro. "Telechelic poly(ε-caprolactones) with tethered mixed ligand ruthenium(II) chromophores." Canadian Journal of Chemistry 82, no. 5 (May 1, 2004): 595–607. http://dx.doi.org/10.1139/v03-215.

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Well-characterized templates of polymer-forming ligands and their ruthenium tris(α,α′-diimine) initiators were utilized to divergently ring open an ε-caprolactone monomer. The same polymers were also obtained through the synthesis of quinoline and bipyridine diimine ligands incorporating poly(ε-caprolactone) (PCL) chains. These polymers contain vacant molecular recognition sites, enabling subsequent chelation of these macroligands to metal precursors. Both methods provided telechelic (ε-caprolactone) ruthenium(II)-centered polyesters of various hierarchy. Solution properties and thermal behaviour of such polyesters are described.Key words: redox polymers, poly(ε-caprolactone), telechelics, metalpolymer complexes, macroligands, ring-opening polymerization (ROP).

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2

Tezuka, Yasuyuki. "Telechelic polymers." Progress in Polymer Science 17, no. 3 (January 1992): 471–514. http://dx.doi.org/10.1016/0079-6700(92)90022-q.

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3

Li, Song Tao, Dan Li, and Chun Ju He. "Synthesis of Allyl Functionalized Telechelic PVP by Reversible Addition-Fragmentation Chain Transfer (RAFT) Polymerization." Materials Science Forum 789 (April 2014): 235–39. http://dx.doi.org/10.4028/www.scientific.net/msf.789.235.

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Telechelic polymers have been explored widely because they are precursors for preparing multi-block copolymers, grafted polymers, star polymers, and polymer networks [1-2]. A variety of telechelic polymers with terminals like hydroxy, carboxylic, epoxy groups and carbon–carbon double bond have been prepared by controlled radical polymerization (CRP) techniques including nitroxide-mediated polymerization (NMP), atom transfer radical polymerization (ATRP) and reversible addition-fragmentation chain transfer polymerization (RAFT)[3-5].The CRP techniques can not only control the molecular weight but also can be carried out in the presence of many functional groups from monomers, initiators, or chain transfer agents (CTA).

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4

Adrian Figg, C., Ashton N. Bartley, Tomohiro Kubo, Bryan S. Tucker, Ronald K. Castellano, and Brent S. Sumerlin. "Mild and efficient synthesis of ω,ω-heterodifunctionalized polymers and polymer bioconjugates." Polymer Chemistry 8, no. 16 (2017): 2457–61. http://dx.doi.org/10.1039/c7py00225d.

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5

Tasic, Aleksandra, Marija Pergal, Malisa Antic, and Vesna Antic. "Synthesis, structure and thermogravimetric analysis of α,ω-telechelic polydimethylsiloxanes of low molecular weight." Journal of the Serbian Chemical Society 82, no. 12 (2017): 1395–416. http://dx.doi.org/10.2298/jsc170427082t.

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A series of ?,?-telechelic polydimethylsiloxanes (PDMS), with predetermined molecular weights of about 2500 g mol-1, was synthesized by siloxane equilibration reaction. Syntheses were performed using octamethylcyclotetrasiloxane (D4) and various disiloxanes: hexamethyldisiloxane (HMDS), 1,1,3,3-tetramethyldisiloxane (TMDS), 1,3-divinyltetramethyldisiloxane (DVTMDS), 1,3-bis(3-carboxypropyl)tetramethyldisiloxane (DCPTMDS) and 1,3-bis(3-aminopropyl)tetramethyldisiloxane (DAPTMDS). The role of the disiloxane was to introduce terminal functional groups at the end of the polymer chains and to control the molecular weight of the polymers. Polymers with trimethyl, hydrido, vinyl, carboxypropyl and aminopropyl end-groups were obtained in this way. The structure of the ?,?-telechelic PDMSs was confirmed by NMR and IR spectroscopy. The molecular weights of the polymers were determined by 1H-NMR, gel permeation chromatography (GPC) and dilute solution viscometry. Thermogravimetric analysis (TGA) under nitrogen and air showed that the type of the terminal groups significantly influenced the thermal and thermo-oxidative stability, as well as the degradation mechanism of the ?,?-telechelic PDMSs.

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6

Buss, Bonnie L., Logan R. Beck, and Garret M. Miyake. "Synthesis of star polymers using organocatalyzed atom transfer radical polymerization through a core-first approach." Polymer Chemistry 9, no. 13 (2018): 1658–65. http://dx.doi.org/10.1039/c7py01833a.

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7

Kumar, Aatish, Christopher P. Lowe, Martien A. Cohen Stuart, and Peter G. Bolhuis. "Trigger sequence can influence final morphology in the self-assembly of asymmetric telechelic polymers." Soft Matter 12, no. 7 (2016): 2095–107. http://dx.doi.org/10.1039/c5sm01453k.

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We report on a numerical study of polymer network formation of asymmetric biomimetic telechelic polymers with two reactive ends based on a self-assembling collagen, elastin or silk-like polypeptide sequence.

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8

Baudis, Stefan, Andreas Lendlein, and Marc Behl. "Robot Assisted Synthesis and Characterization of Polyester-based Polyurethanes." MRS Proceedings 1718 (2015): 109–15. http://dx.doi.org/10.1557/opl.2015.493.

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ABSTRACTDihydroxy telechelics are precursors for the synthesis of multiblock copolymers. In order to synthesize high molecular weight polymers with good elastic properties it is necessary to gain detailed knowledge of the reaction behavior of these precursors. Therefore it was explored whether the polyaddition reaction of polyester-diols can be established in a robotic synthesizer platform to facilitate the elucidation of reaction characteristics. A series of 16 reactions was performed using a telechelic polyester and trimethylhexamethylene diisocyanate. The chain extension behavior of the building block was compared with respect to the Carothers equation. It was found, that the chain extension behavior follows the expected trend. The molecular weight of the polymers increased when the optimal ratio of reactive groups was approached.

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9

Volianiuk, Kateryna, Nataliya Mitina, Nataliya Kinash, Khrystyna Harhay, Larysa Dolynska, Zoriana Nadashkevich, Orest Hevus, and Alexander Zaichenko. "Telechelic Oligo(N-Vinylpyrolydone)swith Cumene Based Terminal Groups for Block-Copolymer and Nanoparticle Obtaining." Chemistry & Chemical Technology 16, no. 1 (February 20, 2022): 34–41. http://dx.doi.org/10.23939/chcht16.01.034.

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Polymers with terminal epoxy, phosphate, fluoroalkyl groups were obtained by radical polymerization in the presence of chain transfer agents derived from isopropylbenzene. The structure of polymers was confirmed by NMR spectra and functional analysis. Polymers with functional fragment were used for synthesis of polymer-inorganic particles and copolymers with poly(2-ethyl-2-oxazoline) fragment.

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10

Milner, Scott T., and Thomas A. Witten. "Bridging attraction by telechelic polymers." Macromolecules 25, no. 20 (September 1992): 5495–503. http://dx.doi.org/10.1021/ma00046a057.

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11

Paterson, Marion, and John F. Kennedy. "Telechelic polymers: Synthesis and applications." Carbohydrate Polymers 12, no. 1 (January 1990): 122–23. http://dx.doi.org/10.1016/0144-8617(90)90110-e.

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12

Vandenbergh, Joke, Gijs Ramakers, Luk van Lokeren, Guy van Assche, and Thomas Junkers. "Synthesis of degradable multi-segmented polymers via Michael-addition thiol–ene step-growth polymerization." RSC Advances 5, no. 100 (2015): 81920–32. http://dx.doi.org/10.1039/c5ra18861j.

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Degradable multi-segmented poly(β-thioester) linear polymers and networks are synthesized via step-growth thiol–ene polymerization of diacrylates with telechelic dithiol polystyrene and poly(isobornylacrylate) precursor polymers.

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13

Dasmahapatra, Ashok Kumar, and G. Diwakar Reddy. "Conformational transition of telechelic star polymers." Polymer 54, no. 9 (April 2013): 2392–400. http://dx.doi.org/10.1016/j.polymer.2013.02.048.

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14

GARCÍA-CUÉLLAR, ALEJANDRO J., and WALTER G. CHAPMAN. "Solvent effects on model telechelic polymers." Molecular Physics 96, no. 7 (April 10, 1999): 1063–74. http://dx.doi.org/10.1080/00268979909483049.

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15

Billen, Joris, Mark Wilson, and Arlette R. C. Baljon. "Shear banding in simulated telechelic polymers." Chemical Physics 446 (January 2015): 7–12. http://dx.doi.org/10.1016/j.chemphys.2014.11.001.

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16

Jerome, R., M. Henrioulle-Granville, B. Boutevin, and J. J. Robin. "Telechelic polymers: Synthesis, characterization and applications." Progress in Polymer Science 16, no. 5 (October 1991): 837–906. http://dx.doi.org/10.1016/0079-6700(91)90012-a.

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17

Su, Jiahui, Hong Huang, Yanyan Cui, Yingyin Chen, and Xiaoxuan Liu. "A photo-induced nitroxide trapping method to prepare α,ω-heterotelechelic polymers." Polymer Chemistry 7, no. 14 (2016): 2511–20. http://dx.doi.org/10.1039/c6py00104a.

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18

Katoh, Takayoshi, Tomoya Suzuki, Yoshihiro Ohta, and Tsutomu Yokozawa. "Importance of a reversible reaction for the synthesis of telechelic polymers by means of polycondensation using an excess of one monomer." Polymer Chemistry 13, no. 6 (2022): 794–800. http://dx.doi.org/10.1039/d1py01498f.

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Reversible unstoichiometric polycondensation of a diol formate and dicarboxylic acid ester through an ester–ester exchange reaction is an effective strategy for the synthesis of telechelic polymers free from contamination with cyclic polymers.

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19

Schmolke, Willi, Mostafa Ahmadi, and Sebastian Seiffert. "Enhancement of metallo-supramolecular dissociation kinetics in telechelic terpyridine-capped poly(ethylene glycol) assemblies in the semi-dilute regime." Physical Chemistry Chemical Physics 21, no. 35 (2019): 19623–38. http://dx.doi.org/10.1039/c9cp03911b.

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20

Liu, Peng, Zhenghao Dong, and Andreas F. M. Kilbinger. "Mono-telechelic polymers by catalytic living ring-opening metathesis polymerization with second-generation Hoveyda–Grubbs catalyst." Materials Chemistry Frontiers 4, no. 9 (2020): 2791–96. http://dx.doi.org/10.1039/d0qm00417k.

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21

Vinciguerra, Daniele, Johanna Tran, and Julien Nicolas. "Telechelic polymers from reversible-deactivation radical polymerization for biomedical applications." Chemical Communications 54, no. 3 (2018): 228–40. http://dx.doi.org/10.1039/c7cc08544c.

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Strategies for the synthesis of telechelic polymers by reversible-activation radical polymerization for biomedical applications are covered spanning from drug delivery and targeting to theranostics and sensing.

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22

Illés, Gergely, Csaba Németh, Karina Ilona Hidas, József Surányi, Adrienn Tóth, Ferenc Pajor, and Péter Póti. "Synthesis of New Type Polymers by Quasi-Living Atom Transfer Radical Polymerization." Polymers 14, no. 14 (July 8, 2022): 2795. http://dx.doi.org/10.3390/polym14142795.

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Thanks to the polymer revolution of the 20th century, plastics are now part of our everyday lives. We use plastics as naturally as if they had always been an integral part of our lives. However, in the recent past, we were still predominantly using wood, metal, and glass objects, which were replaced by plastic products at an explosive rate. In many cases, this replacement has resulted in products with better physical, chemical, or biological properties. The changeover was too rapid, and the consequences were not recognized in time. This is evidenced by the huge scale of plastic pollution worldwide today. It is therefore in the interests of the future of both humans and animals that we must pay particular attention to the direct and indirect environmental impact of plastics introduced in animal husbandry. Starting from the tetrafunctional initiator produced as the first step of my work, poly(n-butyll acrylate) star polymers of different molecular weights were synthesized by atom transfer radical polymerization, using the so-called “core first” method. The bromine chain end of the produced star polymers was replaced by an azide group using a substitution reaction. Propalgyl telechelic PEGs were synthesized as a result of lattice end modification of poly(ethylene glycol) with different molecular weights. The azidated star polymers were connected with propalgyl telechelic PEGs using Huisgen’s “click” chemical process, and as a result of the “click” connection, amphiphilic polymer networks with several different structures were obtained.

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23

Li, Boyu, Joey Kim, and Julie Kornfield. "A Molecular Picture for the Thermo-Reversibility of Gels Formed by Isophthalic Acid-Ended Telechelic Polymers." MRS Proceedings 1794 (2015): 9–14. http://dx.doi.org/10.1557/opl.2015.638.

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ABSTRACTWe demonstrate that isophthalic acid-ended telechelic poly(1,5-cyclooctadiene)s (A-PCODs) form thermo-reversible gels in non-polar solvent with a unique molecular mechanism for their thermo-reversibility. Like other associative telechelic polymers, A-PCODs form “flower-like” micelles at low concentration and form gels through bridging at higher concentration which exhibit linear viscoelasticity. However, unlike the widely studied hydrophobically end-capped PEOs, A-PCODs show clear thermo-reversibility in viscosity and dynamic modulus around 30 °C due to the hydrogen-bonding end groups. In addition, they differ from other reported thermo-reversible gelators (eg. Pluronics, PNIPAm containing block copolymers, etc.): neither the end group nor the backbone in the present system has a critical solution temperature within the measured temperature range (0 °C to 60 °C), indicating that the present system has a unique mechanism for its thermo-reversibility. To obtain a molecular picture of the mechanism, rheology and small angle neutron scattering (SANS) studies were implemented. Topological changes above the transition temperature (30 °C) were observed in both oscillatory rheology and SANS. SANS reveals that the size of clusters, which are formed by interacting micelles, depends highly on temperature (T) but independent of polymer concentration. These results cannot be explained by current theories on associative telechelic polymers which assume constant and large aggregation number of end groups at all temperatures and concentrations. We hypothesize that the temperature-sensitive sol-gel transition is due to a decrease in aggregation number for T above the critical temperature in our system, and this temperature-dependence of aggregation number is further determined by the chemical structure and hydrogen-bonding property of isophthalic acid ends.

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24

Chung, T. C., and M. Chasmawala. "A new synthetic route to telechelic polymers." Macromolecules 24, no. 12 (June 1991): 3718–20. http://dx.doi.org/10.1021/ma00012a041.

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25

Misra, Sanjay, and Wayne L. Mattice. "Telechelic Polymers between Two Impenetrable Adsorbing Surfaces." Macromolecules 27, no. 8 (April 1994): 2058–65. http://dx.doi.org/10.1021/ma00086a013.

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26

Goethals, Eric J. "Telechelic polymers by cationic ring-opening polymerization." Makromolekulare Chemie. Macromolecular Symposia 6, no. 1 (December 1986): 53–66. http://dx.doi.org/10.1002/masy.19860060109.

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27

Wei, Ming-Hsin, Boyu Li, R. L. Ameri David, Simon C. Jones, Virendra Sarohia, Joel A. Schmitigal, and Julia A. Kornfield. "Megasupramolecules for safer, cleaner fuel by end association of long telechelic polymers." Science 350, no. 6256 (October 1, 2015): 72–75. http://dx.doi.org/10.1126/science.aab0642.

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We used statistical mechanics to design polymers that defy conventional wisdom by self-assembling into “megasupramolecules” (≥5000 kg/mol) at low concentration (≤0.3 weight percent). Theoretical treatment of the distribution of individual subunits—end-functional polymers—among cyclic and linear supramolecules (ring-chain equilibrium) predicts that megasupramolecules can form at low total polymer concentration if, and only if, the backbones are long (>400 kg/mol) and end-association strength is optimal. Viscometry and scattering measurements of long telechelic polymers having polycyclooctadiene backbones and acid or amine end groups verify the formation of megasupramolecules. They control misting and reduce drag in the same manner as ultralong covalent polymers. With individual building blocks short enough to avoid hydrodynamic chain scission (weight-average molecular weights of 400 to 1000 kg/mol) and reversible linkages that protect covalent bonds, these megasupramolecules overcome the obstacles of shear degradation and engine incompatibility.

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28

Schumaker, Mark F., and Irving R. Epstein. "Simulation of a simple model for aggregating telechelic ionomers." Canadian Journal of Physics 68, no. 9 (September 1, 1990): 1099–104. http://dx.doi.org/10.1139/p90-154.

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We develop a simple model for the aggregation of telechelic ionomers by extending the well-known algorithm for particle diffusion-limited aggregation (DLA). The distribution of sticky and nonsticky regions of the polymer and specific rules for binding are incorporated. Thirteen aggregates are grown to a final size of 2441 polymers each. The distribution of accessible binding sites modifies the growth of these clusters as compared with DLA. The dynamical dimension estimated from the growth of the radius of gyration is found to have a value of 1.81 ± 0.04, significantly larger than values reported for particle DLA. However, a careful analysis of our data suggests that the dimension is nonstationary and decreasing at the largest cluster sizes attained. We have also investigated the scaling of the average mass of the cluster interface with the number of polymers and the radius of gyration. Our results suggest that the fractal dimension of the cluster interface is close to one, in agreement with previously reported findings for particle DLA.

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29

Zaichenko, Alexander, Natalya Mitina, Kateryna Rayevska, Taras Skorohoda, Jan Zawadiak, Danuta Gilner, Volodymyr Lobaz, and Volodymyr Novikov. "Design of polymers of block, comb-like and highly branched structures with peroxide-containing chains." Chemistry & Chemical Technology 1, no. 2 (June 15, 2007): 71–78. http://dx.doi.org/10.23939/chcht01.02.71.

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The tailored synthesis of telechelic oligoperoxides (TO), oligoperoxide metal complexes (OMC) as well as the development of controlled radical polymerization in aqueous and hydrocarbon media initiated by them provides prospective approaches for the obtaining block, comb-like and highly branched polymers with the backbone and branches of various nature, polarity, length and reactivity. The polymer-precursors and final products were investigated by chemical, spectral and rheological techniques. The novel peroxide-containing copolymers were studied in the reactions of radical polymerization in heterogeneous and homogeneous media.

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30

Zhou, Huaxing, and Jeremiah A. Johnson. "Photo-controlled Growth of Telechelic Polymers and End-linked Polymer Gels." Angewandte Chemie 125, no. 8 (January 17, 2013): 2291–94. http://dx.doi.org/10.1002/ange.201207966.

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31

Zhou, Huaxing, and Jeremiah A. Johnson. "Photo-controlled Growth of Telechelic Polymers and End-linked Polymer Gels." Angewandte Chemie International Edition 52, no. 8 (January 17, 2013): 2235–38. http://dx.doi.org/10.1002/anie.201207966.

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32

Kaur, Gagan, Arthur Bertrand, Julien Bernard, Toby D. M. Bell, and Kei Saito. "UV-reversible chain extendable polymers from thymine functionalized telechelic polymer chains." Journal of Polymer Science Part A: Polymer Chemistry 52, no. 18 (June 23, 2014): 2557–61. http://dx.doi.org/10.1002/pola.27282.

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33

Horrion, J., R. Jérôme, and Ph Teyssié. "Halato-telechelic polymers. XV. Ionic cross-interactions of immiscible telechelic polymers: A reversible pathway to block copolymer-type materials." Journal of Polymer Science Part A: Polymer Chemistry 28, no. 1 (January 15, 1990): 153–71. http://dx.doi.org/10.1002/pola.1990.080280111.

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34

Rovigatti, Lorenzo, Barbara Capone, and Christos N. Likos. "Soft self-assembled nanoparticles with temperature-dependent properties." Nanoscale 8, no. 6 (2016): 3288–95. http://dx.doi.org/10.1039/c5nr04661k.

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Telechelic star polymers, i.e. star polymers made of a number f of di-block copolymers grafted on a central anchoring point, spontaneously and reliably self-assemble into soft patchy particles. The properties of the stars can be finely controlled by changing the physical and chemical parameters of the solution, providing a robust route for the generation of novel materials.

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35

Melaku, Ashenafi Zeleke, Wei-Tsung Chuang, Yeong-Tarng Shieh, Chih-Wei Chiu, Duu-Jong Lee, Juin-Yih Lai, and Chih-Chia Cheng. "Programmed exfoliation of hierarchical graphene nanosheets mediated by dynamic self-assembly of supramolecular polymers." Materials Chemistry Frontiers 5, no. 18 (2021): 6998–7011. http://dx.doi.org/10.1039/d1qm00810b.

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Programming hierarchical graphene nanosheets by two-step exfoliation of graphite combined with an adenine-functionalized telechelic polymer in o-dichlorobenzene can achieve highly stable graphene nanosheets with wide-range tunable layer thickness.

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36

Carro, Shirley, Valeria J. Gonzalez-Coronel, Jorge Castillo-Tejas, Hortensia Maldonado-Textle, and Nancy Tepale. "Rheological Properties in Aqueous Solution for Hydrophobically Modified Polyacrylamides Prepared in Inverse Emulsion Polymerization." International Journal of Polymer Science 2017 (2017): 1–13. http://dx.doi.org/10.1155/2017/8236870.

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Inverse emulsion polymerization technique was employed to synthesize hydrophobically modified polyacrylamide polymers with hydrophobe contents near to feed composition. Three different structures were obtained: multisticker, telechelic, and combined. N-Dimethyl-acrylamide (DMAM), n-dodecylacrylamide (DAM), and n-hexadecylacrylamide (HDAM) were used as hydrophobic comonomers. The effect of the hydrophobe length of comonomer, the initial monomer, and surfactant concentrations on shear viscosity was studied. Results show that the molecular weight of copolymer increases with initial monomer concentration and by increasing emulsifier concentration it remained almost constant. Shear viscosity measurements results show that the length of the hydrophobic comonomer augments the hydrophobic interactions causing an increase in viscosity and that the polymer thickening ability is higher for combined polymers.

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37

Xia, Yan, Rafael Verduzco, Robert H. Grubbs, and Julia A. Kornfield. "Well-Defined Liquid Crystal Gels from Telechelic Polymers." Journal of the American Chemical Society 130, no. 5 (February 2008): 1735–40. http://dx.doi.org/10.1021/ja077192j.

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38

Meng, Xiao-Xia, and William B. Russel. "Rheology of telechelic associative polymers in aqueous solutions." Journal of Rheology 50, no. 2 (March 2006): 189–205. http://dx.doi.org/10.1122/1.2167467.

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39

Lo Verso, Federica, Christos N. Likos, and Hartmut Löwen. "Computer Simulation of Thermally Sensitive Telechelic Star Polymers†." Journal of Physical Chemistry C 111, no. 43 (November 2007): 15803–10. http://dx.doi.org/10.1021/jp0737606.

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40

Yang, Junying, Rong Wang, and Daiqian Xie. "Self-organization in suspensions of telechelic star polymers." Polymer 205 (September 2020): 122866. http://dx.doi.org/10.1016/j.polymer.2020.122866.

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41

Pujari, N. S., J. Trivedi, G. C. Ingavle, and S. Ponrathnam. "Novel beaded polymers from telechelic methacrylic ether esters." Reactive and Functional Polymers 66, no. 10 (October 2006): 1087–96. http://dx.doi.org/10.1016/j.reactfunctpolym.2006.01.020.

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42

Wadgaonkar, Indrajit, and Apratim Chatterji. "Network formation and gelation in telechelic star polymers." Journal of Chemical Physics 146, no. 8 (February 28, 2017): 084906. http://dx.doi.org/10.1063/1.4975691.

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43

Kudo, Hiroto, Fumio Sanda, and Takeshi Endo. "Synthesis and reactions of cysteine-based telechelic polymers." Journal of Polymer Science Part A: Polymer Chemistry 39, no. 1 (2000): 23–31. http://dx.doi.org/10.1002/1099-0518(20010101)39:1<23::aid-pola30>3.0.co;2-4.

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44

Rezvantalab, Hossein, and Ronald G. Larson. "Bridging Dynamics of Telechelic Polymers between Solid Surfaces." Macromolecules 51, no. 5 (March 5, 2018): 2125–37. http://dx.doi.org/10.1021/acs.macromol.7b01517.

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45

Iskin, Birol, Gorkem Yilmaz, and Yusuf Yagci. "Telechelic Polymers by Visible-Light-Induced Radical Coupling." Macromolecular Chemistry and Physics 214, no. 1 (November 23, 2012): 94–98. http://dx.doi.org/10.1002/macp.201200491.

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46

de Jongh, Patrick A. J. M., Mechelle R. Bennett, Greg S. Sulley, Paul Wilson, Thomas P. Davis, David M. Haddleton, and Kristian Kempe. "Facile one-pot/one-step synthesis of heterotelechelic N-acylated poly(aminoester) macromonomers for carboxylic acid decorated comb polymers." Polymer Chemistry 7, no. 44 (2016): 6703–7. http://dx.doi.org/10.1039/c6py01553k.

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47

Ajaz, A. G. "Hydroxyl-Terminated Polybutadiene Telechelic Polymer (HTPB): Binder for Solid Rocket Propellants." Rubber Chemistry and Technology 68, no. 3 (July 1, 1995): 481–506. http://dx.doi.org/10.5254/1.3538752.

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Abstract This paper presents a review of hydroxyl-terminated polybutadiene telechelic polymer (HTPB) with emphasis on its preparation, properties, end group modifications, hydrogenation, role as polyurethane precursors and binders for solid rocket propellants.

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48

Kwon, Yongmoon, and Joseph P. Kennedy. "Polymerizability, copolymerizability, and properties of cyanoacrylate-telechelic polyisobutylenes I: three-arm star cyanoacrylate-telechelic polyisobutylene." Polymers for Advanced Technologies 18, no. 10 (October 2007): 800–807. http://dx.doi.org/10.1002/pat.969.

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Chassenieux, Christophe, Taco Nicolai, Dominique Durand, Jean-Fran�ois Gohy, and Robert J�r�me. "Aggregation behaviour of monosulfonated telechelic ionomers." Polymer International 49, no. 6 (2000): 561–66. http://dx.doi.org/10.1002/1097-0126(200006)49:6<561::aid-pi413>3.0.co;2-7.

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Schädler, Volker, Achim Franck, Ulrich Wiesner, and Hans W. Spiess. "EPR Studies on Telechelic Polymers: Characterization of Ion Multiplets." Macromolecules 30, no. 13 (June 1997): 3832–38. http://dx.doi.org/10.1021/ma961591+.

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