Статті в журналах з теми "Perfluorés"
Оформте джерело за APA, MLA, Chicago, Harvard та іншими стилями
Ознайомтеся з топ-50 статей у журналах для дослідження на тему "Perfluorés".
Біля кожної праці в переліку літератури доступна кнопка «Додати до бібліографії». Скористайтеся нею – і ми автоматично оформимо бібліографічне посилання на обрану працю в потрібному вам стилі цитування: APA, MLA, «Гарвард», «Чикаго», «Ванкувер» тощо.
Також ви можете завантажити повний текст наукової публікації у форматі «.pdf» та прочитати онлайн анотацію до роботи, якщо відповідні параметри наявні в метаданих.
Переглядайте статті в журналах для різних дисциплін та оформлюйте правильно вашу бібліографію.
BODIN, Clara, Roxane CHÊNE, Annie MARION, Léa SOUVIGNET, Aurélie CORTÉJADE, and Mickaël NICOLAS. "Développement et validation d’une méthode de quantification de 25 composés perfluorés dans les eaux usées." TSM 12 2023, TSM 12 2023 (December 20, 2023): 143–63. http://dx.doi.org/10.36904/tsm/202312143.
Повний текст джерелаPortella, C., та J. P. Pete. "Photoréduction d'esters d'acides perfluorés dans l'hexaméthylphosphortriamide (HMPT). Elimination sélective du fluor en α du groupe carboxyle". Tetrahedron Letters 26, № 2 (січень 1985): 211–14. http://dx.doi.org/10.1016/s0040-4039(00)61882-8.
Повний текст джерелаBoutevin, B., B. Youssef, L. Abdellah, and N. M. Dinia. "Synthèse et propriétés de polysiloxanes photoré ticulables—IV. Polysiloxanes à greffons perfluorés et à greffons uréthanes vinyliques." European Polymer Journal 32, no. 6 (June 1996): 701–8. http://dx.doi.org/10.1016/0014-3057(95)00210-3.
Повний текст джерелаLéty-Sistel, Chantal, Bernard Sébille, and Claude Quivoron. "Étude Spectroscopique De La Formation De Complexes Par Liaison Hydrogène Entre La Polyvinylpyrrolidone Et Des Acides Carboxyliques Perfluorés." Journal of Polymer Science: Polymer Symposia 52, no. 1 (March 8, 2007): 311–25. http://dx.doi.org/10.1002/polc.5070520126.
Повний текст джерелаCHATELET, A., A. FOURNIER, S. JURJANZ, S. LERCH, H. TOUSSAINT, M. DELANNOY, C. FEIDT, and G. RYCHEN. "L’épandage de matières fertilisantes d’origine résiduaire sur les prairies comporte-t-il des risques en termes de transfert de polluants organiques et inorganiques vers la chaîne alimentaire ?" INRA Productions Animales 28, no. 5 (January 14, 2020): 383–98. http://dx.doi.org/10.20870/productions-animales.2015.28.5.3041.
Повний текст джерелаGiroux, Isabelle, Serge Hébert, and David Berryman. "Qualité de l’eau du Saint-Laurent de 2000 à 2014 : paramètres classiques, pesticides et contaminants émergents." Qualité de l’eau 140, no. 2 (June 2, 2016): 26–34. http://dx.doi.org/10.7202/1036500ar.
Повний текст джерелаGolokhvastova, D. S., Ya V. Zonov, V. M. Karpov, and T. V. Mezhenkova. "Interaction of polyfluorobenzocyclobutenes with oleum." Журнал органической химии 59, no. 1 (January 15, 2023): 51–61. http://dx.doi.org/10.31857/s0514749223010032.
Повний текст джерелаBillah, Md Baki. "Determination of perfluorinated compounds (PFCs) in the fine particulate matter (PM2.5) in China." Jahangirnagar University Journal of Biological Sciences 5, no. 1 (September 25, 2016): 21–27. http://dx.doi.org/10.3329/jujbs.v5i1.29740.
Повний текст джерелаHOGUE, CHERYL. "FOCUS ON PERFLUOROS." Chemical & Engineering News 81, no. 16 (April 21, 2003): 9. http://dx.doi.org/10.1021/cen-v081n016.p009.
Повний текст джерелаKovtonyuk, Vladimir N., Yuri V. Gatilov, Pavel V. Nikul’shin, and Roman A. Bredikhin. "Synthesis of Polyfluorinated Thia- and Oxathiacalixarenes Based on Perfluoro-m-xylene." Molecules 26, no. 3 (January 20, 2021): 526. http://dx.doi.org/10.3390/molecules26030526.
Повний текст джерелаYang, Ji-Cheng, Hong-Bo Ni, Jin Li, Cheng-Xue Zhao, and Yong-Ming Zhang. "Synthesis and Characterisation of P-perfluoro{-1-[2-(2-fluorosulfonylethoxy) Propoxy]}Ethylated Polystyrene." Journal of Chemical Research 2005, no. 8 (August 2005): 546–48. http://dx.doi.org/10.3184/030823405774663336.
Повний текст джерелаGolden, William G., Erin M. Brown, Sadie E. Solem, and Robert W. Zoellner. "Complete conformational analyses of perfluoro-n-pentane, perfluoro-n-hexane, and perfluoro-n-heptane." Journal of Molecular Structure: THEOCHEM 867, no. 1-3 (October 2008): 22–27. http://dx.doi.org/10.1016/j.theochem.2008.07.011.
Повний текст джерелаGimenez, Diana, Anica Dose, Nicholas L. Robson, Graham Sandford, Steven L. Cobb, and Christopher R. Coxon. "2,2,2-Trifluoroethanol as a solvent to control nucleophilic peptide arylation." Organic & Biomolecular Chemistry 15, no. 19 (2017): 4081–85. http://dx.doi.org/10.1039/c7ob00295e.
Повний текст джерелаGuzmán Almagro, Elena, Rosario Cobo Soriano, Irene Fuentes-Vega, Ana Fernández Hortelano, and Julio González Martin-Moro. "Retained subretinal perfluorocarbon in multimodal image." OphthaTherapy. Therapies in Ophthalmology 8, no. 2 (April 8, 2021): 87–91. http://dx.doi.org/10.24292/01.ot.100421.
Повний текст джерелаCaminade, Anne-Marie, Maurice Le Blanc, Fayez El Khatib, and Max Koeniga. "Ozonolyse d'olefines perfluorees." Tetrahedron Letters 26, no. 24 (January 1985): 2889–90. http://dx.doi.org/10.1016/s0040-4039(00)98863-4.
Повний текст джерелаD, Kumar. "Perfluoro Curcumin Strongly Interacts with ABC Transporter (ABCG2): A Molecular Docking Study." Journal of Embryology & Stem Cell Research 2, no. 2 (2018): 1–10. http://dx.doi.org/10.23880/jes-16000113.
Повний текст джерелаChowdhury, Tuhin, and Aditya Pradhan. "Acute Hydrops with Micro-Cornea – an Extremely Rare Condition: A Case Report." Ophthalmology @ Point of Care 1, no. 1 (January 2017): oapoc.0000003. http://dx.doi.org/10.5301/oapoc.0000003.
Повний текст джерелаBegum, Farzana, Muhammad Ikram, Brendan Twamley, and Robert J. Baker. "Perfluorinated phosphine and hybrid P–O ligands for Pd catalysed C–C bond forming reactions in solution and on Teflon supports." RSC Advances 9, no. 50 (2019): 28936–45. http://dx.doi.org/10.1039/c9ra04863d.
Повний текст джерелаRoesner, Emily K., Darya Asheghali, Alina Kirillova, Michael J. Strauss, Austin M. Evans, Matthew L. Becker, and William R. Dichtel. "Arene–perfluoroarene interactions confer enhanced mechanical properties to synthetic nanotubes." Chemical Science 13, no. 8 (2022): 2475–80. http://dx.doi.org/10.1039/d1sc05932g.
Повний текст джерелаShou, Keyun, Jun Ki Hong, Elliot S. Wood, James M. Hook, Andrew Nelson, Yanting Yin, Gunther G. Andersson, Antonio Abate, Ullrich Steiner, and Chiara Neto. "Ultralow surface energy self-assembled monolayers of iodo-perfluorinated alkanes on silica driven by halogen bonding." Nanoscale 11, no. 5 (2019): 2401–11. http://dx.doi.org/10.1039/c8nr08195f.
Повний текст джерелаWei, Han-Chao, and Richard J. Lagow. "The synthesis of the largest perfluoro macrocycles; perfluoro [60]-crown-20 and perfluoro [30]-crown-10." Chemical Communications, no. 21 (2000): 2139–40. http://dx.doi.org/10.1039/b004168h.
Повний текст джерелаColpaert, Maxime, Marta Zaton, Vincent Ladmiral, Deborah Jones, Jacques Rozière, and Bruno Ameduri. "Crosslinked terpolymers of vinylidene fluoride, perfluoro-3,6-dioxa-4-methyl-7-octene sulfonyl fluoride, and cure site monomers for membranes in PEMFC applications." Polymer Chemistry 10, no. 17 (2019): 2176–89. http://dx.doi.org/10.1039/c9py00188c.
Повний текст джерелаCrawford, Jennifer M., Kyle E. Shelton, Emily K. Reeves, Bryce K. Sadarananda, and Dipannita Kalyani. "Nickel-catalyzed decarboxylative arylation of azoles with perfluoro- and nitrobenzoates." Organic Chemistry Frontiers 2, no. 6 (2015): 726–29. http://dx.doi.org/10.1039/c5qo00040h.
Повний текст джерелаDecato, Sarah, Troy Bemis, Eric Madsen, and Sandro Mecozzi. "Synthesis and characterization of perfluoro-tert-butyl semifluorinated amphiphilic polymers and their potential application in hydrophobic drug delivery." Polym. Chem. 5, no. 22 (2014): 6461–71. http://dx.doi.org/10.1039/c4py00882k.
Повний текст джерелаHao, Jinmeng, Yanfeng Wei, and Jianxin Mu. "Ultra-low dielectric constant materials with hydrophobic property derived from polyhedral oligomeric silsequioxane (POSS) and perfluoro-aromatics." RSC Advances 6, no. 90 (2016): 87433–39. http://dx.doi.org/10.1039/c6ra17499j.
Повний текст джерелаSysoiev, Dmytro, and Thomas Huhn. "Basic enemies of photochromism: irreversible transformation of fluorinated diarylethenes to polyenic enamines and enols." Photochemical & Photobiological Sciences 19, no. 11 (2020): 1511–16. http://dx.doi.org/10.1039/d0pp00292e.
Повний текст джерелаVasiliev, N. V., Yu E. Lyashenko, A. E. Patalakha, and G. A. Sokolski. "Perfluoro 1,3,4-oxadiazoles." Journal of Fluorine Chemistry 58, no. 2-3 (August 1992): 375. http://dx.doi.org/10.1016/s0022-1139(00)80841-6.
Повний текст джерелаVasiliev, N. V., Yu E. Lyashenko, A. E. Patalakha, and G. A. Sokolski. "Perfluoro-1,3,4-oxadiazoles." Journal of Fluorine Chemistry 65, no. 3 (December 1993): 227–31. http://dx.doi.org/10.1016/s0022-1139(00)80860-x.
Повний текст джерелаWessolowski, Holger, Gerd-Volker Röschenthaler, Rolf Winter та Gary L. Gard. "(E)-1,2-Difluoro-1-(pentafluoro-λ6-sulfanyl)- 2-iodoethylene". Zeitschrift für Naturforschung B 46, № 1 (1 січня 1991): 123–25. http://dx.doi.org/10.1515/znb-1991-0122.
Повний текст джерелаYi, Hai, Markus Albrecht, Arto Valkonen та Kari Rissanen. "Perfluoro-1,1′-biphenyl and perfluoronaphthalene and their derivatives as π-acceptors for anions". New Journal of Chemistry 39, № 1 (2015): 746–49. http://dx.doi.org/10.1039/c4nj01654h.
Повний текст джерелаJi, Li, Jia-Shuai Liu, Xiao-Yan Wang, Jun-Fang Li, Zhou Chen, Saihu Liao, Xiu-Li Sun, and Yong Tang. "An efficient and mild route to highly fluorinated polyolefins via copolymerization of ethylene and 5-perfluoroalkylnorbornenes." Polymer Chemistry 10, no. 26 (2019): 3604–9. http://dx.doi.org/10.1039/c9py00009g.
Повний текст джерелаSha, Min, Ren Ming Pan, and Biao Jiang. "One-Pot Catalytic Epoxidation Reaction of Perfluoro-2-methyl-2-pentene with Tri-n-butylamine N-Oxide or N, N-Dimethylcyclohexylamine N-Oxide." Advanced Materials Research 685 (April 2013): 357–61. http://dx.doi.org/10.4028/www.scientific.net/amr.685.357.
Повний текст джерелаWoodlief, Tracey, Samuel Vance, Qing Hu, and Jamie DeWitt. "Immunotoxicity of Per- and Polyfluoroalkyl Substances: Insights into Short-Chain PFAS Exposure." Toxics 9, no. 5 (May 1, 2021): 100. http://dx.doi.org/10.3390/toxics9050100.
Повний текст джерелаBarbosa, Marta O., Nuno Ratola, Vera Homem, M. Fernando R. Pereira, Adrián M. T. Silva, Ana R. L. Ribeiro, Marta Llorca, and Marinella Farré. "Per- and Poly-Fluoroalkyl Substances in Portuguese Rivers: Spatial-Temporal Monitoring." Molecules 28, no. 3 (January 26, 2023): 1209. http://dx.doi.org/10.3390/molecules28031209.
Повний текст джерелаPereira-da-Silva, J., M. Mendes, F. Kossoski, A. I. Lozano, R. Rodrigues, N. C. Jones, S. V. Hoffmann, and F. Ferreira da Silva. "Perfluoro effect on the electronic excited states of para-benzoquinone revealed by experiment and theory." Physical Chemistry Chemical Physics 23, no. 3 (2021): 2141–53. http://dx.doi.org/10.1039/d0cp05626j.
Повний текст джерелаFarkas, Vajk, Gábor Turczel, János Deme, Attila Domján, László Trif, Anvar Mirzaei, Dang Vu Hai, et al. "Synthesis and characterization of a pH-responsive mesalazine-polynorbornene supramolecular assembly." Polymer Chemistry 12, no. 14 (2021): 2175–80. http://dx.doi.org/10.1039/d1py00194a.
Повний текст джерелаLiu, Yang, Wangchang Li, Peiying Li, Yanmin Guo, Peng Cui, and Zhuxia Zhang. "Theoretical exploration of noncovalent interactions in Sc2C2@C2n (n = 40, 41, and 42)⊂[12]CPP, PF[12]CPP." RSC Advances 13, no. 7 (2023): 4553–63. http://dx.doi.org/10.1039/d2ra08153a.
Повний текст джерелаChavan, Santosh N., Anil K. Padhan, and Debaprasad Mandal. "Self-assembly of fluorous amphiphilic copolymers with ionogels and surface switchable wettability." Polymer Chemistry 9, no. 17 (2018): 2258–70. http://dx.doi.org/10.1039/c8py00273h.
Повний текст джерелаКопылов, Павел Сергеевич. "Fire extinguishing efficiency of perfluoro-isohexenes." Pozharnaia bezopasnost`, no. 1(102) (March 24, 2021): 47–53. http://dx.doi.org/10.37657/vniipo.pb.2021.67.54.005.
Повний текст джерелаHösl, Andreas, Juriy Pachin, Alise Chachereau, Andreas Kornath, and Christian M. Franck. "Perfluoro-1,3-dioxolane and perfluoro-oxetane: promising gases for electrical insulation." Journal of Physics D: Applied Physics 52, no. 5 (November 26, 2018): 055203. http://dx.doi.org/10.1088/1361-6463/aaef5b.
Повний текст джерелаMalinowski, Marek, Agnieszka Iwan, Igor Tazbir, Bartosz Boharewicz, Andrzej Sikora, and Andrzej Stafiniak. "Polyazomethines and their acid–base interactions with Nafion and Nafion–imidazole membranes for efficient fuel cells." Sustainable Energy & Fuels 1, no. 8 (2017): 1810–19. http://dx.doi.org/10.1039/c7se00296c.
Повний текст джерелаGe, H., E. Yamazaki, N. Yamashita, S. Taniyasu, A. Ogata, and M. Furuuchi. "Particle size specific distribution of perfluoro alkyl substances in atmospheric particulate matter in Asian cities." Environmental Science: Processes & Impacts 19, no. 4 (2017): 549–60. http://dx.doi.org/10.1039/c6em00564k.
Повний текст джерелаWu, Tingjuan, Anfeng Li, Kexin Chen, Xingxing Peng, Jing Zhang, Mou Jiang, Shizhen Chen, Xing Zheng, Xin Zhou, and Zhong-Xing Jiang. "Perfluoro-tert-butanol: a cornerstone for high performance fluorine-19 magnetic resonance imaging." Chemical Communications 57, no. 63 (2021): 7743–57. http://dx.doi.org/10.1039/d1cc02133h.
Повний текст джерелаHao, Jinmeng, Yanfeng Wei, Bo Chen, and Jianxin Mu. "Polymerization of polyhedral oligomeric silsequioxane (POSS) with perfluoro-monomers and a kinetic study." RSC Advances 7, no. 18 (2017): 10700–10706. http://dx.doi.org/10.1039/c6ra26183c.
Повний текст джерелаMel’nik, O. A., М. S. Kondratenko, A. A. Tyutyunov, S. M. Igumnov, and A. R. Khokhlov. "Synthesis and hydrophobic properties of poly[(perfluoro-tret-hexyl)bytylmethacrylate]." Доклады Академии наук 485, no. 4 (May 22, 2019): 447–50. http://dx.doi.org/10.31857/s0869-56524854447-450.
Повний текст джерелаPeng, Y., J. X. Hu, H. Lu, R. M. Wilson, M. Motevalli, I. Hernández, W. P. Gillin, P. B. Wyatt, and H. Q. Ye. "Functionalisation of ligands through click chemistry: long-lived NIR emission from organic Er(iii) complexes with a perfluorinated core and a hydrogen-containing shell." RSC Advances 7, no. 1 (2017): 128–31. http://dx.doi.org/10.1039/c6ra25494b.
Повний текст джерелаArslanov, G. M., B. M. Aznabaev, T. R. Mukhamadeev, Z. R. Yanbukhtina, T. I. Dibaev, and G. R. Shakirova. "Electron Microscopic Retina Changes in Rabbit Eyes with Perfluorocarbon Liquids Intravitreal Tamponade." Ophthalmology in Russia 16, no. 1 (March 30, 2019): 81–87. http://dx.doi.org/10.18008/1816-5095-2019-1-81-87.
Повний текст джерелаIshii, I., R. McLaren, A. P. Hitchcock, K. D. Jordan, Y. Choi та M. B. Robin. "The σ* molecular orbitals of perfluoroalkanes as studied by inner-shell electron energy loss and electron transmission spectroscopies". Canadian Journal of Chemistry 66, № 8 (1 серпня 1988): 2104–21. http://dx.doi.org/10.1139/v88-336.
Повний текст джерелаChen, Wanhao, Changhao Zhu, Xinnan Xu, and Xuejun Liu. "Perfluoro-1-butanesulfonic acid etching strategy for dendrite suppression in aqueous zinc metal batteries." RSC Advances 14, no. 27 (2024): 19090–95. http://dx.doi.org/10.1039/d4ra03632h.
Повний текст джерелаJing, Naiyong, and David M. Lemal. "The perfluoro-1,3,5-hexatrienes." Journal of Organic Chemistry 59, no. 7 (April 1994): 1844–48. http://dx.doi.org/10.1021/jo00086a040.
Повний текст джерела