Pregled bibliografske jedinice broj: 1265232
Catalytic conversion of CO2 into organic cyclic carbonates
Catalytic conversion of CO2 into organic cyclic carbonates // BOOK OF ABSTRACTS 28th CROATIAN MEETING OF CHEMISTS & CHEMICAL ENGINEERS / Rogošić, Marko (ur.).
Zagreb: Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2023. str. 87-87 (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 1265232 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Catalytic conversion of CO2 into organic cyclic carbonates
Autori
Kolympadi Markovic, Maria ; Matulja, Dario ; Jozanović, Marija ; Sakač, Nikola ; Ambrožić, Gabriela ; Šakić, Davor ; Vrček, Valerije ; Marković, Dean
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
BOOK OF ABSTRACTS 28th CROATIAN MEETING OF CHEMISTS & CHEMICAL ENGINEERS
/ Rogošić, Marko - Zagreb : Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2023, 87-87
Skup
28th CROATIAN MEETING OF CHEMISTS & CHEMICAL ENGINEERS
Mjesto i datum
Rovinj, Hrvatska, 28.03.2023. - 31.03.2023
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
CO2, carbonates, catalyzed reaction, palladium
Sažetak
Carbon dioxide (CO2) gas is considered as an abundant and renewable C1 synthon for the preparation of highly valued chemicals. [1] Catalytic CO2 capture by propargylic substrates – alcohols or amines – affords α-alkylidene cyclic carbonates or carbamates, respectively. [2] Combination of CO2 capture with C–C cross-coupling reactions may give direct access to complex products that otherwise require multistep syntheses. [3] Such transformations are particularly desirable because they follow the principles of green chemistry for atom and step economy. We are accordingly presenting, herein, Pd-catalyzed carboxylative intermolecular or intramolecular C–C cross-coupling reactions on various propargylic alcohol substrates (see Fig. 1). Our experiments are supported by calculations based on density functional theory (DFT) method, which show that these reactions are exergonic because of product stabilization through the formation of additional C–C bonds, thus overcoming the thermodynamic and kinetic inertness of CO2 even under atmospheric pressure. Currently, our efforts are focused on the elucidation of the reaction mechanism.
Izvorni jezik
Engleski
POVEZANOST RADA
Profili:
Nikola Sakač
(autor)
Maria Kolympadi Markovic
(autor)
Valerije Vrček
(autor)
Dean Marković
(autor)
Davor Šakić
(autor)
Gabriela Ambrožić
(autor)
Dario Matulja
(autor)
Marija Jozanović
(autor)