Pregled bibliografske jedinice broj: 1165871
N-(4-halogenobenzyl)-(3-halogeno)pyridinium cations as halogen bond donors
N-(4-halogenobenzyl)-(3-halogeno)pyridinium cations as halogen bond donors // 27th Croatian Meeting of Chemists and Chemical Engineers and 5th Symposium Vladimir Prelog : Book of Abstracts / Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna (ur.).
Zagreb: Hrvatsko kemijsko društvo, 2021. str. 186-186 (poster, domaća recenzija, sažetak, znanstveni)
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Naslov
N-(4-halogenobenzyl)-(3-halogeno)pyridinium cations
as halogen bond donors
Autori
Fotović, Luka ; Bedeković, Nikola ; Stilinović, Vladimir
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
27th Croatian Meeting of Chemists and Chemical Engineers and 5th Symposium Vladimir Prelog : Book of Abstracts
/ Marković, Dean ; Meštrović, Ernest ; Namjesnik, Danijel ; Tomašić, Vesna - Zagreb : Hrvatsko kemijsko društvo, 2021, 186-186
Skup
27. hrvatski skup kemičara i kemijskih inženjera (27HSKIKI)
Mjesto i datum
Veli Lošinj, Hrvatska, 05.10.2021. - 08.10.2021
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
pyridinium cations ; halogen bond ; halogenide anions
Sažetak
Halogen bond is a valuable widely used tool for constructing supramolecular assemblies in the solid state.[1] Besides numerous studies on neutral halogen bond donors, [2] a few studies dealing with cationic halogen bond donors such as halogenopyridinium cations have been published. [3, 4] In our previous work we have shown that halogen bonds in protonated iodopyridinium halogenides can even compete with hydrogen bond in binding halogenide anions.[5] In this study, we have been interested in asymmetric ditopic monocationic 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 six N-(4- halogenobenzyl)-(3- halogeno)pyridinium bromides. To study the halogen bonding potential of these 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 the 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