Статті в журналах з теми "Alkynes Thermal properties"
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Ознайомтеся з топ-33 статей у журналах для дослідження на тему "Alkynes Thermal properties".
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Michinobu, Tsuyoshi. "Click synthesis of donor–acceptor-type aromatic polymers." Pure and Applied Chemistry 82, no. 4 (March 13, 2010): 1001–9. http://dx.doi.org/10.1351/pac-con-09-09-09.
Повний текст джерелаCervera-Procas, Ramón, José-Luis Serrano, and Ana Omenat. "A Highly Versatile Polymer Network Based on Liquid Crystalline Dendrimers." International Journal of Molecular Sciences 22, no. 11 (May 27, 2021): 5740. http://dx.doi.org/10.3390/ijms22115740.
Повний текст джерелаHernández-Fernández, Joaquín, John R. Castro-Suarez, and Carlos A. T. Toloza. "Iron Oxide Powder as Responsible for the Generation of Industrial Polypropylene Waste and as a Co-Catalyst for the Pyrolysis of Non-Additive Resins." International Journal of Molecular Sciences 23, no. 19 (October 3, 2022): 11708. http://dx.doi.org/10.3390/ijms231911708.
Повний текст джерелаSchumann, Hans, Gert Admiraal, and Paul T. Beurskens. "Zum Koordinationsverhalten von Alkinen gegenüber dem [C5H5(P(OCH3)3)2Fe]+-Fragment: Bildung und Struktur carbonylfreier Halbsandwichkomplexe mit Alkin- und Vinylidenliganden / Coordination Properties of Alkynes towards the [C5H5Fe(P(OCH3)3)2]+ Fragment: Formation and Structure of Carbonylfree Halfsandwich Complexes with Alkyne and Vinylidene Ligands." Zeitschrift für Naturforschung B 47, no. 8 (August 1, 1992): 1125–33. http://dx.doi.org/10.1515/znb-1992-0813.
Повний текст джерелаSchock, Marvin, and Stefan Bräse. "Reactive & Efficient: Organic Azides as Cross-Linkers in Material Sciences." Molecules 25, no. 4 (February 24, 2020): 1009. http://dx.doi.org/10.3390/molecules25041009.
Повний текст джерелаJiang, Wenzhao, Hangbo Yue, Peter Shuttleworth, Pengbo Xie, Shanji Li, and Jianwei Guo. "Adamantane-Based Micro- and Ultra-Microporous Frameworks for Efficient Small Gas and Toxic Organic Vapor Adsorption." Polymers 11, no. 3 (March 13, 2019): 486. http://dx.doi.org/10.3390/polym11030486.
Повний текст джерелаRaytchev, Pascal Dimitrov, Céline Besset, Etienne Fleury, Jean-Pierre Pascault, Julien Bernard, and Eric Drockenmuller. "1,4:3,6-Dianhydrohexitols: Original platform for the design of biobased polymers using robust, efficient, and orthogonal chemistry." Pure and Applied Chemistry 85, no. 3 (August 15, 2012): 511–20. http://dx.doi.org/10.1351/pac-con-12-03-11.
Повний текст джерелаLiu, Yu, Hai-Ying Wang, Gang Chen, Xiao-Ping Xu, and Shun-Jun Ji. "Synthesis and Properties of Novel 'Ethyne-linked' Compounds Containing Carbazole and 1, 8-naphthalimide Groups." Australian Journal of Chemistry 62, no. 8 (2009): 934. http://dx.doi.org/10.1071/ch08411.
Повний текст джерелаHu, Yingxue, Joshua B. Marlow, Rajesh Ramanathan, Wenyue Zou, Hui Geok Tiew, Matthew J. Pottage, Vipul Bansal, Rico F. Tabor, and Brendan L. Wilkinson. "Synthesis and Properties of Photoswitchable Carbohydrate Fluorosurfactants." Australian Journal of Chemistry 68, no. 12 (2015): 1880. http://dx.doi.org/10.1071/ch15434.
Повний текст джерелаYu, Wen Hao, Yue Feng Bai, Yang Jing, Shi Chang Nie, Bi Qin Wang, Ping Hu, and Ke Qing Zhao. "Synthesis of Disk-Rod-Disk Liquid Crystal Trimers by Using Click Chemistry." Key Engineering Materials 428-429 (January 2010): 106–10. http://dx.doi.org/10.4028/www.scientific.net/kem.428-429.106.
Повний текст джерелаYu, Zhuoer, Jun Zhang, Bangqiang Wu, Liqiang Wan, and Farong Huang. "Polytriazole resins toughened by an azide-terminated polyhedral oligomeric silsesquioxane (OADTP)." e-Polymers 21, no. 1 (January 1, 2021): 289–98. http://dx.doi.org/10.1515/epoly-2021-0033.
Повний текст джерелаAcar, Işıl, Ayça Bal, and Gamze Güçlü. "The use of intermediates obtained from aminoglycolysis of waste poly(ethylene terephthalate) (PET) for the synthesis of water-reducible alkyd resin." Canadian Journal of Chemistry 91, no. 5 (May 2013): 357–63. http://dx.doi.org/10.1139/cjc-2012-0370.
Повний текст джерелаFloros, Michael C., Alcides Lopes Leão, and Suresh S. Narine. "Vegetable Oil Derived Solvent, and Catalyst Free “Click Chemistry” Thermoplastic Polytriazoles." BioMed Research International 2014 (2014): 1–14. http://dx.doi.org/10.1155/2014/792901.
Повний текст джерелаKashina, Anna V., Tamara K. Meleshko, Natalia N. Bogorad, Viktor K. Lavrentyev та Alexander V. Yakimansky. "Molecular Brushes with a Polyimide Backbone and Poly(ε-Caprolactone) Side Chains by the Combination of ATRP, ROP, and CuAAC". Polymers 13, № 19 (28 вересня 2021): 3312. http://dx.doi.org/10.3390/polym13193312.
Повний текст джерелаLegzdins, Peter, Kevin M. Smith, and Steven J. Rettig. "Synthesis, characterization, and properties of some cyclopentadienyl molybdenum nitrosyl benzyl complexes." Canadian Journal of Chemistry 79, no. 5-6 (May 1, 2001): 502–9. http://dx.doi.org/10.1139/v00-158.
Повний текст джерелаTomczyk, Mateusz D., Mariusz Zalewski, Per T. Jørgensen, Jesper Wengel, and Krzysztof Walczak. "Polyamine–Oligonucleotide Conjugates: 2′-OMe-Triazole-Linked 1,4,7,10-Tetraazacyclododecane and Intercalating Dyes and Their Effect on the Thermal Stability of DNA Duplexes." Pharmaceutics 14, no. 1 (December 28, 2021): 66. http://dx.doi.org/10.3390/pharmaceutics14010066.
Повний текст джерелаT. de Carvalho, Layde, Maria Luiza da S. Paula, Rodolfo M. de Moraes, Gizelda M. Alves, Talita M. Lacerda, Julio C. dos Santos, Amilton M. dos Santos, and Simone de F. Medeiros. "Chemical Modification of Pullulan Exopolysaccharide by Grafting Poly(3-hydroxybutyrate-co-3-hydroxyvalerate) (PHBHV) via Click Chemistry." Polymers 12, no. 11 (October 29, 2020): 2527. http://dx.doi.org/10.3390/polym12112527.
Повний текст джерелаTrejo-Maldonado, Melisa, Aisha Womiloju, Steffi Stumpf, Stephanie Hoeppener, Ulrich S. Schubert, Luis E. Elizalde, and Carlos Guerrero-Sanchez. "Triazole-Functionalized Mesoporous Materials Based on Poly(styrene-block-lactic acid): A Morphology Study of Thin Films." Polymers 14, no. 11 (May 31, 2022): 2231. http://dx.doi.org/10.3390/polym14112231.
Повний текст джерелаUlloa, José Antonio, Joaquín Barberá, and José Luis Serrano. "Gold Nanoparticles Modification with Liquid Crystalline Polybenzylic Dendrons via 1,3-Dipolar Cycloaddition." Nanomaterials 12, no. 22 (November 16, 2022): 4026. http://dx.doi.org/10.3390/nano12224026.
Повний текст джерелаRiccardi, Claudia, Albert Meyer, Jean-Jacques Vasseur, Domenico Cavasso, Irene Russo Krauss, Luigi Paduano, François Morvan, and Daniela Montesarchio. "Design, Synthesis and Characterization of Cyclic NU172 Analogues: A Biophysical and Biological Insight." International Journal of Molecular Sciences 21, no. 11 (May 29, 2020): 3860. http://dx.doi.org/10.3390/ijms21113860.
Повний текст джерелаNielsen, Mogens Brøndsted, Søren Lindbæk Broman, Michael Åxman Petersen, Asbjørn Sune Andersson, Tanja Skouw Jensen, Kristine Kilså, and Anders Kadziola. "New routes to functionalized dihydroazulene photoswitches." Pure and Applied Chemistry 82, no. 4 (March 9, 2010): 843–52. http://dx.doi.org/10.1351/pac-con-09-07-08.
Повний текст джерелаEl-Bindary, Ashraf, Hala Kiwaan, Abdel Ghany Shoair, Fawzia El-Ablack, and Ahmed Eessa. "Synthesis and characterization of hyperbranched silane-modified alkyd as a polymer for environmentally friendly low VOC polyurethane coatings." Pigment & Resin Technology 49, no. 2 (August 31, 2019): 102–9. http://dx.doi.org/10.1108/prt-10-2018-0108.
Повний текст джерелаSagdic, Gokhan, Emrah Cakmakci, Ozgun Daglar, Ufuk Saim Gunay, Gurkan Hizal, Umit Tunca, and Hakan Durmaz. "Thermal and mechanical properties of thiol-ene photocured thermosets containing DOPO-based liquid reactive flame retardant synthesized by metal-free azide-alkyne click reaction." Progress in Organic Coatings 167 (June 2022): 106825. http://dx.doi.org/10.1016/j.porgcoat.2022.106825.
Повний текст джерелаZafar, Fahmina, Syed Marghoob Ashraf, and Sharif Ahmad. "Self-cured polymers from non-drying oil." Chemistry & Chemical Technology 2, no. 4 (December 15, 2008): 285–93. http://dx.doi.org/10.23939/chcht02.04.285.
Повний текст джерелаSantos, Jose, Pavel Jelínek, David Ecija, and Nazario Martin. "(Invited) On-Surface Synthesis of Acene Polymers." ECS Meeting Abstracts MA2022-01, no. 11 (July 7, 2022): 811. http://dx.doi.org/10.1149/ma2022-0111811mtgabs.
Повний текст джерелаMajed Jari Mohammed, Majed Jari Mohammed, Abdul Amir H. Kadhum Abdul Amir H Kadhum, and Adnan Ibrahim Mohammed and Sameer H. Abbood Al Rekabi Adnan Ibrahim Mohammed and Sameer H Abbood Al Rekabi. "Synthesis of One New Sugar Imine Molecule." Journal of the chemical society of pakistan 42, no. 1 (2020): 103. http://dx.doi.org/10.52568/000622.
Повний текст джерелаMajed Jari Mohammed, Majed Jari Mohammed, Abdul Amir H. Kadhum Abdul Amir H Kadhum, and Adnan Ibrahim Mohammed and Sameer H. Abbood Al Rekabi Adnan Ibrahim Mohammed and Sameer H Abbood Al Rekabi. "Synthesis of One New Sugar Imine Molecule." Journal of the chemical society of pakistan 42, no. 1 (2020): 103. http://dx.doi.org/10.52568/000622/jcsp/42.01.2020.
Повний текст джерелаYang, Haicun, Zinan Cai, Haotian Liu, Zheng Cao, Yanping Xia, Wenzhong Ma, Fanghong Gong, Guoliang Tao, and Chunlin Liu. "Tailoring the surface of attapulgite by combining redox-initiated RAFT polymerization with alkynyl-thiol click reaction for polycarbonate nanocomposites:Effect of polymer brush chain length on mechanical, thermal and rheological properties." Materials Chemistry and Physics 241 (February 2020): 122334. http://dx.doi.org/10.1016/j.matchemphys.2019.122334.
Повний текст джерелаXia, Chun-Gu, Simon G. Bott, and Michael G. Richmond. "Reaction of the dicobalt alkyne compound Co2(CO)6( -dmad) with the diphosphine ligand 4,5-bis(diphenylphosphino)-4-cyclopenten-1,3-dione (bpcd). Spectroscopic properties, X-ray diffraction data, and thermal reactivity of the chelating isomer of Co2(CO)4(bpcd)( -dmad)." Journal of Chemical Crystallography 34, no. 8 (August 2004): 513–21. http://dx.doi.org/10.1023/b:jocc.0000042019.54785.9a.
Повний текст джерелаZerbib, Souad, Mostafa Khouili, Marco Catto, and Latifa Bouissane. "Sydnone: Synthesis, reactivity and biological activities." Current Medicinal Chemistry 29 (June 20, 2022). http://dx.doi.org/10.2174/0929867329666220620123050.
Повний текст джерелаFengling, Qing, Yao Rongxing, Wang Lianjun, Li Hongqi, and Meng Weidong. "Chemical modification of poly(vinylacetylene) via click reaction." e-Polymers 8, no. 1 (December 1, 2008). http://dx.doi.org/10.1515/epoly.2008.8.1.1580.
Повний текст джерелаVebr, aurélien, Magali Dallegre, Laurent Autissier, Charlotte Drappier, Karel Lejeune, Didier Gigmes, and Anthony Kermagoret. "Nitroxide mediated radical polymerization for the preparation of poly(vinyl chloride) grafted poly(acrylate) copolymers." Polymer Chemistry, 2022. http://dx.doi.org/10.1039/d2py00308b.
Повний текст джерелаOfori-Boadu, Andrea Nana, DeAndria Bryant, Christian Bock-Hyeng, Zerihun Assefa, Frederick Aryeetey, Samira Munkaila, and Elham Fini. "Physiochemical characterization of agricultural waste biochars for partial cement replacement." International Journal of Building Pathology and Adaptation ahead-of-print, ahead-of-print (March 31, 2021). http://dx.doi.org/10.1108/ijbpa-04-2020-0026.
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