Pregled bibliografske jedinice broj: 309680
Novel adamantane-dipyrromethanes and their anion binding properties
Novel adamantane-dipyrromethanes and their anion binding properties // 15th European Symposium on Organic Chemistry ; ESOC 15
Dublin, 2007. (poster, međunarodna recenzija, sažetak, znanstveni)
CROSBI ID: 309680 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Novel adamantane-dipyrromethanes and their anion binding properties
Autori
Renić, Marija ; Basarić, Nikola ; Mlinarić-Majerski, Kata
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
15th European Symposium on Organic Chemistry ; ESOC 15
/ - Dublin, 2007
Skup
15th European Symposium on Organic Chemistry
Mjesto i datum
Dublin, Irska, 08.07.2007. - 13.07.2007
Vrsta sudjelovanja
Poster
Vrsta recenzije
Međunarodna recenzija
Ključne riječi
Adamantane-dipyrromethanes; aninon binding; 1H-NMR titrations
Sažetak
In the scope of our research on the synthesis of the macrocyclic compounds capable of selective recognitions of different guest molecules (1), we turned our attention to preparation of anion sensors. Anions play key roles in wide range of chemical and biological processes and it is of great importance to design suitable molecular receptors that can recognize and bind anions. A significant number of molecules wich are used as anion sensors are composed of pyrroles which can serve sa binding subunit due to presence of acidic NH proton to which anion can be attached by the hydrogen bonds. Since it was shown that the presence of two NH protons is enough to accomplish binding of an anion with sufficient binding constants (2), we choose to investigate the applicability of dipyrromethanes as anion binding agents. Herein we report the synthesis of four new adamantane-dipyrromethane derivatives (AdD) 1-4, as well as investigation of their anion binding properties. It was anticipated that incorporation of the bulky adamantane would hinder rotational mobility of the pyrrole moietes in the AdD resulting in the increase of the stability of the complexes with anion, as compared to the dipyrromethane bearing aromatic phenyl subdtituent in the meso position (5-phenyldipyrromethane). Moreover, adamantane derivatives are characterized by lipophilicity which may provide the potentional applicability of the AdD molecules as anion extracting agents. In this study we also present the result s of the binding with 5 anions: F-, Cl-, Br-, HSO4- and H2PO4-. Stability constants for the complexes with F- anion are much larger then for the other anions.
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
098-0982933-2911 - Kavezasti spojevi: ugradbene jedinice u molekularnim sustavima (Majerski, Kata, MZOS ) ( CroRIS)
Ustanove:
Institut "Ruđer Bošković", Zagreb