[{"title":"Reversible functionalization and exfoliation of graphite by a Diels–Alder reaction with furfuryl amine","date_created":"2022-06-28T11:49:14Z","publisher":"Royal Society of Chemistry (RSC)","year":"2022","issue":"27","language":[{"iso":"eng"}],"keyword":["General Chemical Engineering","General Chemistry"],"abstract":[{"text":"<jats:p>Furfuryl amine-functionalized few-layered graphene was prepared <jats:italic>via</jats:italic> a mechanochemical process by a [4 + 2] cycloaddition under solvent-free conditions.</jats:p>","lang":"eng"}],"publication":"RSC Advances","doi":"10.1039/d2ra02566c","author":[{"last_name":"Filvan Torkaman","full_name":"Filvan Torkaman, Najmeh","id":"77435","first_name":"Najmeh"},{"last_name":"Kley","full_name":"Kley, Marina","first_name":"Marina"},{"first_name":"Wolfgang","last_name":"Bremser","full_name":"Bremser, Wolfgang"},{"first_name":"René","full_name":"Wilhelm, René","last_name":"Wilhelm"}],"volume":12,"date_updated":"2022-06-28T12:13:10Z","citation":{"chicago":"Filvan Torkaman, Najmeh, Marina Kley, Wolfgang Bremser, and René Wilhelm. “Reversible Functionalization and Exfoliation of Graphite by a Diels–Alder Reaction with Furfuryl Amine.” <i>RSC Advances</i> 12, no. 27 (2022): 17249–56. <a href=\"https://doi.org/10.1039/d2ra02566c\">https://doi.org/10.1039/d2ra02566c</a>.","ieee":"N. Filvan Torkaman, M. Kley, W. Bremser, and R. Wilhelm, “Reversible functionalization and exfoliation of graphite by a Diels–Alder reaction with furfuryl amine,” <i>RSC Advances</i>, vol. 12, no. 27, pp. 17249–17256, 2022, doi: <a href=\"https://doi.org/10.1039/d2ra02566c\">10.1039/d2ra02566c</a>.","ama":"Filvan Torkaman N, Kley M, Bremser W, Wilhelm R. Reversible functionalization and exfoliation of graphite by a Diels–Alder reaction with furfuryl amine. <i>RSC Advances</i>. 2022;12(27):17249-17256. doi:<a href=\"https://doi.org/10.1039/d2ra02566c\">10.1039/d2ra02566c</a>","bibtex":"@article{Filvan Torkaman_Kley_Bremser_Wilhelm_2022, title={Reversible functionalization and exfoliation of graphite by a Diels–Alder reaction with furfuryl amine}, volume={12}, DOI={<a href=\"https://doi.org/10.1039/d2ra02566c\">10.1039/d2ra02566c</a>}, number={27}, journal={RSC Advances}, publisher={Royal Society of Chemistry (RSC)}, author={Filvan Torkaman, Najmeh and Kley, Marina and Bremser, Wolfgang and Wilhelm, René}, year={2022}, pages={17249–17256} }","short":"N. Filvan Torkaman, M. Kley, W. Bremser, R. Wilhelm, RSC Advances 12 (2022) 17249–17256.","mla":"Filvan Torkaman, Najmeh, et al. “Reversible Functionalization and Exfoliation of Graphite by a Diels–Alder Reaction with Furfuryl Amine.” <i>RSC Advances</i>, vol. 12, no. 27, Royal Society of Chemistry (RSC), 2022, pp. 17249–56, doi:<a href=\"https://doi.org/10.1039/d2ra02566c\">10.1039/d2ra02566c</a>.","apa":"Filvan Torkaman, N., Kley, M., Bremser, W., &#38; Wilhelm, R. (2022). Reversible functionalization and exfoliation of graphite by a Diels–Alder reaction with furfuryl amine. <i>RSC Advances</i>, <i>12</i>(27), 17249–17256. <a href=\"https://doi.org/10.1039/d2ra02566c\">https://doi.org/10.1039/d2ra02566c</a>"},"intvolume":"        12","page":"17249-17256","publication_status":"published","publication_identifier":{"issn":["2046-2069"]},"user_id":"77435","department":[{"_id":"35"},{"_id":"321"},{"_id":"603"}],"_id":"32263","status":"public","type":"journal_article"},{"publication":"Journal of the Serbian Chemical Society","type":"journal_article","status":"public","abstract":[{"lang":"eng","text":"<jats:p>A rapid and convenient preparation of acyclic imides by the reaction of\r\n   aliphatic and aromatic nitriles with acyclic carboxylic anhydride in the\r\n   presence of catalytic amounts of p-toluenesulfonic acid under thermal or\r\n   ultrasonic conditions is reported. The advantages of this procedure are\r\n   moderate reaction times, good to excellent yields, use of inexpensive and\r\n   ecofriendly catalyst. The reaction of nitriles with aliphatic anhydrides\r\n   proceeds in thermal conditions, while by the use of ultrasound irradiations\r\n   these reactions get accelerated.</jats:p>"}],"department":[{"_id":"163"}],"user_id":"77435","_id":"32265","language":[{"iso":"eng"}],"extern":"1","keyword":["General Chemistry"],"issue":"4","publication_identifier":{"issn":["0352-5139","1820-7421"]},"publication_status":"published","intvolume":"        77","page":"415-421","citation":{"ama":"Nasr-Esfahani M, Montazerozohori M, Filvan Torkaman N. Ultrasound-assisted catalytic synthesis of acyclic imides in the presence of p-toluenesulfonic acid under solvent free conditions. <i>Journal of the Serbian Chemical Society</i>. 2011;77(4):415-421. doi:<a href=\"https://doi.org/10.2298/jsc110511168n\">10.2298/jsc110511168n</a>","ieee":"M. Nasr-Esfahani, M. Montazerozohori, and N. Filvan Torkaman, “Ultrasound-assisted catalytic synthesis of acyclic imides in the presence of p-toluenesulfonic acid under solvent free conditions,” <i>Journal of the Serbian Chemical Society</i>, vol. 77, no. 4, pp. 415–421, 2011, doi: <a href=\"https://doi.org/10.2298/jsc110511168n\">10.2298/jsc110511168n</a>.","chicago":"Nasr-Esfahani, Masoud, Morteza Montazerozohori, and Najmeh Filvan Torkaman. “Ultrasound-Assisted Catalytic Synthesis of Acyclic Imides in the Presence of p-Toluenesulfonic Acid under Solvent Free Conditions.” <i>Journal of the Serbian Chemical Society</i> 77, no. 4 (2011): 415–21. <a href=\"https://doi.org/10.2298/jsc110511168n\">https://doi.org/10.2298/jsc110511168n</a>.","apa":"Nasr-Esfahani, M., Montazerozohori, M., &#38; Filvan Torkaman, N. (2011). Ultrasound-assisted catalytic synthesis of acyclic imides in the presence of p-toluenesulfonic acid under solvent free conditions. <i>Journal of the Serbian Chemical Society</i>, <i>77</i>(4), 415–421. <a href=\"https://doi.org/10.2298/jsc110511168n\">https://doi.org/10.2298/jsc110511168n</a>","short":"M. Nasr-Esfahani, M. Montazerozohori, N. Filvan Torkaman, Journal of the Serbian Chemical Society 77 (2011) 415–421.","mla":"Nasr-Esfahani, Masoud, et al. “Ultrasound-Assisted Catalytic Synthesis of Acyclic Imides in the Presence of p-Toluenesulfonic Acid under Solvent Free Conditions.” <i>Journal of the Serbian Chemical Society</i>, vol. 77, no. 4, National Library of Serbia, 2011, pp. 415–21, doi:<a href=\"https://doi.org/10.2298/jsc110511168n\">10.2298/jsc110511168n</a>.","bibtex":"@article{Nasr-Esfahani_Montazerozohori_Filvan Torkaman_2011, title={Ultrasound-assisted catalytic synthesis of acyclic imides in the presence of p-toluenesulfonic acid under solvent free conditions}, volume={77}, DOI={<a href=\"https://doi.org/10.2298/jsc110511168n\">10.2298/jsc110511168n</a>}, number={4}, journal={Journal of the Serbian Chemical Society}, publisher={National Library of Serbia}, author={Nasr-Esfahani, Masoud and Montazerozohori, Morteza and Filvan Torkaman, Najmeh}, year={2011}, pages={415–421} }"},"year":"2011","volume":77,"date_created":"2022-06-28T12:28:49Z","author":[{"first_name":"Masoud","full_name":"Nasr-Esfahani, Masoud","last_name":"Nasr-Esfahani"},{"full_name":"Montazerozohori, Morteza","last_name":"Montazerozohori","first_name":"Morteza"},{"last_name":"Filvan Torkaman","full_name":"Filvan Torkaman, Najmeh","id":"77435","first_name":"Najmeh"}],"date_updated":"2022-06-28T12:34:17Z","publisher":"National Library of Serbia","doi":"10.2298/jsc110511168n","title":"Ultrasound-assisted catalytic synthesis of acyclic imides in the presence of p-toluenesulfonic acid under solvent free conditions"}]