Pregled bibliografske jedinice broj: 1131012
N-(4-halogeno)benzyl-(3-halogeno)pyridinium cations as asymmetric ditopic halogen bond donors
N-(4-halogeno)benzyl-(3-halogeno)pyridinium cations as asymmetric ditopic halogen bond donors // International School of Crystallography, 55th Course: Molecular Crystal Engineering
Erice, Italija, 2021. str. n/a-n/a (poster, podatak o recenziji nije dostupan, sažetak, znanstveni)
CROSBI ID: 1131012 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
N-(4-halogeno)benzyl-(3-halogeno)pyridinium
cations as asymmetric ditopic halogen bond donors
Autori
Fotović, Luka ; Stilinović, Vladimir
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
International School of Crystallography, 55th Course: Molecular Crystal Engineering
/ - , 2021, N/a-n/a
Skup
55th International School of Crystallography Course: Molecular Crystal Engineering
Mjesto i datum
Erice, Italija, 31.05.2021. - 04.06.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Podatak o recenziji nije dostupan
Ključne riječi
halogen bond donor ; halogenopyridinium cation
Sažetak
Halogen bond is a valuable widely used tool for constructing supramolecular assemblies in the solid state. To date, neutral molecules have been highlighted as the most common halogen bond donors. Besides numerous studies on neutral halogen bond donors, a few studies dealing with cationic halogen bond donors such as halogenopyridinium cations have been published. In our previous work we have shown that halogen bonds in protonated iodopyridinium halogenides can even compete with hydrogen bond in binding halogenide anions. In this study, we have been interested in asymmetric cationic ditopic halogen bond donor where one halogen bond donor atom is placed on positively charged pyridine ring while other one on “neutral” benzyl ring (the positive charge is mostly located on the pyridine nitrogen ring). We successfully prepared a series of four N-(4- halogeno)benzyl-(3- halogeno)pyridinium bromides. In order to study the halogen bonding potential of this cations with a wider range of (anionic) halogen bond acceptors the chloride and iodide salts were prepared by ion exchange. Single crystal X-ray diffraction experiments revealed that in these systems halogen bonds with the halogen atoms on pyridinium rings with halogenide anions are generally relatively shorter (as compared to the corresponding van der Waals radii) than the halogen bonds with the halogen atoms on the “neutral” part of cations (benzyl ring).
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
HRZZ-IP-2019-04-1868 - Nove građevne jedinke u supramolekulskom dizajnu složenih višekomponentnih molekulskih kristala temeljenih na halogenskim vezama (HaloBond) (Cinčić, Dominik, HRZZ - 2019-04) ( CroRIS)
Ustanove:
Prirodoslovno-matematički fakultet, Zagreb