Pregled bibliografske jedinice broj: 1266580
Detecting elusive radicals using spin traps. Case study on Hofmann-Löffler-Freytag reaction
Detecting elusive radicals using spin traps. Case study on Hofmann-Löffler-Freytag reaction // 28HSKIKI : 28th Croatian Meeting of Chemists and Chemical Engineers and 6th Symposium Vladimir Prelog : Book of Abstracts / Rogošić, Marko (ur.).
Zagreb: Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2023. str. 141-141 (poster, recenziran, sažetak, znanstveni)
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Naslov
Detecting elusive radicals using spin traps.
Case study on Hofmann-Löffler-Freytag reaction
Autori
Zubčić, Gabrijel ; Kolympadi Marković, Maria ; Marković, Dean ; Portada, Tomislav ; Bešić, Erim ; Šakić, Davor
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
28HSKIKI : 28th Croatian Meeting of Chemists and Chemical Engineers and 6th Symposium Vladimir Prelog : Book of Abstracts
/ Rogošić, Marko - Zagreb : Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2023, 141-141
Skup
28th Croatian Meeting of Chemists and Chemical Engineers
Mjesto i datum
Rovinj, Hrvatska, 28.03.2023. - 31.03.2023
Vrsta sudjelovanja
Poster
Vrsta recenzije
Recenziran
Ključne riječi
radicals ; rearrangement ; reaction mechanism
Sažetak
A wide variety of systems are being researched with the goal of functionalizing distant unfunctionalized (alkane) carbons using updated versions of the Hoffmann-Löffler-Freytag (HLF) reaction. [1] The induced cleavage of sulfonamides with iodine and a co-oxidant is one of the more popular methods within the HLF reaction procedures. In such procedures, an N- radical is generated via homolytic cleavage of the N–I bond, when iodosulfonamide, an intermediate product, is photochemically activated. [2] Considering that N radicals are unstable intermediates, the stability of such radicals, which is described in the work done by Šakić and Zipse, [3] determines their concentration and thus the possibility of detection using the electron paramagnetic resonance (EPR) devices. A series of differentially N- substituted amines was prepared in good to excellent yields in order to activate the N–H bond thereby producing the coveted N-radicals which take part in rearrangement as described in the HLF reaction mechanism. The identity of these compounds was confirmed by 1H, 13C NMR and IR measurements. These N-centered radicals have already been detected via EPR measurements and described by the Muñiz group, [4] ; however, Khort [5] has done extensive theoretical calculations and therefore has raised some serious doubts regarding this work. Herein, we provide results collected from EPR experiments regarding detection of the N-centered radicals utilizing spin traps, along with theoretical calculations to serve as support and elucidation of the experiments. References [1.] L.R. Reddy, B.V.S. Reddy, E.J. Corey, Organic Letters 8 (2006) 2819-2821. [2.] T. Duhamel, C.J. Stein, C. Martínez, M. Reiher, K. Muñiz, ACS Catalysis 8 (2018) 3918-3925. [3.] D. Šakić, H. Zipse, Advanced Synthesis and Catalysis 358 (2016) 3983-3991. [4.] A.E. Bosnidou, T. Duhamel, K. Muñiz, European Journal of Organic Chemistry 2020 (2020) 6361- 6365. [5.] H. Korth, European Journal of Organic Chemistry 2020 (2020) 6366-6367.
Izvorni jezik
Engleski
Znanstvena područja
Kemija, Farmacija
POVEZANOST RADA
Projekti:
--UIP-2020-02-4857 - Svjetlošću pogonjena funkcionalizacija nereaktivnih pozicija korištenjem oksidacijske aminacije (LIGHT-N-RING) (Šakić, Davor) ( CroRIS)
Ustanove:
Farmaceutsko-biokemijski fakultet, Zagreb,
Institut "Ruđer Bošković", Zagreb,
Sveučilište u Rijeci - Odjel za biotehnologiju
Profili:
Tomislav Portada
(autor)
Dean Marković
(autor)
Maria Kolympadi Markovic
(autor)
Davor Šakić
(autor)
Erim Bešić
(autor)
Gabrijel Zubčić
(autor)