Pregled bibliografske jedinice broj: 825213
Aromatic dinitroso compounds as supramolecular building blocks
Aromatic dinitroso compounds as supramolecular building blocks // Math/Chem/Comp : Book of Abstracts / Vančik, Hrvoj ; Cioslowski, Jerzy (ur.).
Dubrovnik, Hrvatska, 2016. str. 9-9 (poster, nije recenziran, sažetak, znanstveni)
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Naslov
Aromatic dinitroso compounds as supramolecular
building blocks
Autori
Bibulić, Petar ; Špadina, Mario ; Biljan, Ivana ; Rončević, Igor ; Vančik, Hrvoj
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
Math/Chem/Comp : Book of Abstracts
/ Vančik, Hrvoj ; Cioslowski, Jerzy - , 2016, 9-9
Skup
28th MC2 Conference (Math/Chem/Comp)
Mjesto i datum
Dubrovnik, Hrvatska, 20.06.2016. - 25.06.2016
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
dinitroso ; polymerization ; monomers ; dimers ; supramolecular ; photochemistry ; cryogenic ; switches
Sažetak
Aromatic C-nitroso compounds can exist in three different forms, as monomers, Z- or E- dimers (azodioxides). Nitroso compounds also exhibit photochromic and thermochromic behavior in solid state. Azodioxides dissociate under UV irradiation at low temperatures and again dimerize at elevated temperatures. Aromatic nitroso compounds with two or more nitroso groups could be used as supramolecular building blocks. Wuest et al. utilized tetranitroso bocks for construction of covalent organic networks (COFs) by polymerization. Supramolecular structures with azodioxides groups could be disassembled or reassembled by applying external stimuli such as UV radiation or heat. Our goal was to prepare aromatic dinitroso compounds with various spacers between two aromatic rings and to investigate their polymerization properties in solid state. Most of the examined dinitroso compounds form oligomers in the solid state which are mainly in E- configuration. Diphenyl-ether derivative doesn’t form dimers because of the quinoid resonance structure, while diphenylmethane derivative forms Z- oligomers. In the case of diphenylmethane derivative, Z- conformers are stabilized by favorable aromatic ring π-π stacking. Monomers are generated upon UV irradiation at cryogenic temperatures. Monomers dimerize by heating the samples to ~150 K. Methane, ethane, biphenyl and benzophenone derivatives form Eoligomers upon redimerization. In the case of diphenylmethane, E- dimers isomerize to thermodynamically more stable Z- conformation upon further heating.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb
Profili:
Petar Bibulić
(autor)
Hrvoj Vančik
(autor)
Mario Špadina
(autor)
Igor Rončević
(autor)
Ivana Biljan
(autor)