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Cyclopalladation of 4, 4’-disubstituted azobenzenes by palladium(II) acetate (CROSBI ID 649955)

Prilog sa skupa u zborniku | sažetak izlaganja sa skupa | međunarodna recenzija

Barišić, Dajana ; Budimir, Ana ; Juribašić Kulcsar, Marina ; Plavec, Janez ; Ćurić, Manda Cyclopalladation of 4, 4’-disubstituted azobenzenes by palladium(II) acetate // Adriatic NMR Conference : Book of Abstracts / Namjesnik, Danijel ; Pičuljan, Katarina ; Bregović, Nikola et al. (ur.). Zagreb: Prirodoslovno-matematički fakultet Sveučilišta u Zagrebu, 2017. str. 36-36

Podaci o odgovornosti

Barišić, Dajana ; Budimir, Ana ; Juribašić Kulcsar, Marina ; Plavec, Janez ; Ćurić, Manda

engleski

Cyclopalladation of 4, 4’-disubstituted azobenzenes by palladium(II) acetate

Transition-metal mediated activation of a carbon−hydrogen bond is a common method for synthesis of cyclometallated compounds. Cyclopalladated compounds have been vastly investigated due to their unique chemical and physical properties that, when fully explored, enable them for application ranging from catalysts and active units in sensors to cancer treatment agents. Our group focuses on cyclopalladated azobenzenes that show promising photophysical properties in solution and in solid state. Here we report an NMR spectroscopic study of cyclopalladation of 4, 4′-disubstituted azobenzenes L1-L3 (Scheme 1) by palladium(II) acetate in DMF-d7. 1H monitoring of the reaction enabled an insight into the reaction progress and allowed identification of mono- and dicyclopalladated acetate products (major isomers are shown in Scheme 1).

NMR, palladation, azobenzene, acetate

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Podaci o prilogu

36-36.

2017.

objavljeno

Podaci o matičnoj publikaciji

Adriatic NMR Conference : Book of Abstracts

Namjesnik, Danijel ; Pičuljan, Katarina ; Bregović, Nikola ; Novak, Predrag

Zagreb: Prirodoslovno-matematički fakultet Sveučilišta u Zagrebu

978-953-6076-41-3

Podaci o skupu

Adriatic NMR Conference

poster

16.06.2017-18.06.2017

Mali Ston, Hrvatska

Povezanost rada

Kemija