Pregled bibliografske jedinice broj: 998969
Nitrokloranilat – novi heterosubstituirani 2, 5-dihidroksikinonski ligand s velikim potencijalom za dizajn koordinacijskih polimera
Nitrokloranilat – novi heterosubstituirani 2, 5-dihidroksikinonski ligand s velikim potencijalom za dizajn koordinacijskih polimera // SIMPOZIJ STUDENATA DOKTORSKIH STUDIJA PMF-a, Knjiga sažetaka / Primožič, Ines (ur.).
Zagreb, 2019. str. 36-37 (poster, nije recenziran, sažetak, znanstveni)
CROSBI ID: 998969 Za ispravke kontaktirajte CROSBI podršku putem web obrasca
Naslov
Nitrokloranilat – novi heterosubstituirani 2, 5-dihidroksikinonski ligand s velikim potencijalom za dizajn koordinacijskih polimera
(NITROCHLORANILATE – A NOVEL HETEROSUBSTITUTED 2, 5-DIHYDROXYQUINOID LIGAND WITH A GREAT POTENTIAL FOR DESIGN OF COORDINATION POLYMERS)
Autori
Milašinović, Valentina ; Molčanov, Krešimir
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
SIMPOZIJ STUDENATA DOKTORSKIH STUDIJA PMF-a, Knjiga sažetaka
/ Primožič, Ines - Zagreb, 2019, 36-37
ISBN
978-953-6076-49-9
Skup
3. Simpozij studenata doktorskih studija PMF-a = 3rd Faculty of Science PhD Student Symposium
Mjesto i datum
Zagreb, Hrvatska, 22.02.2019
Vrsta sudjelovanja
Poster
Vrsta recenzije
Nije recenziran
Ključne riječi
nitrokloranilat ; Heterosubstituirani ligand ; koordinacijski polimer
(nitrochloranilate ; heterosubstituted ligand ; coordination polymer)
Sažetak
2, 5-dihydroxyquinones (anilic acids) are a class of versatile organic ligands interesting for design of novel coordination polymers and metal-organic frameworks. They are able to coordinate metals in terminal bidentate and bridging (bis)bidentate modes, and are thus able to form coordination polymers of various topologies [1]. The most commonly used ones are unsubstituted 2, 5-dihydroxyquinone [2] and its dichloro-analogue, chloranilic acid (3, 6-dichloro-2, 5-dihydroxyquinone) [3]. Substituents on positions 3 and 6 of the quinoid ring influence electronic structure of the ring through inductive effect, thus enhancing properties such as acidity, electronegativity (the rings may act as electron acceptors), optical properties (colour and possible luminescence) and capability to coordinate metals. The ligands are also able to mediate magnetic exchange interactions [1]. So far, all studied anilic acids were symmetrically substituted (i.e. substituents at positions 3 and 6 are identical), and pioneering work with the first asymmetrically substituted analogue, chlorocyananilic acid (3-chloro-6-cyano-2, 5-dihydroxyquinone) revealed interesting luminescent properties [4], promising for design of optoelectronic materials. Here we present a novel asymmetrically substituted ligand, nitrochloranilic acid (3-nitro-6-chloro-2, 5-dihydroxyquinone, NCA) and first of its transition metal complexes. In a mononuclear complex (Hpy)2[Mn(NCA)2(H2O)2] it behaves as a terminal bidentate ligand, while in 1D coordination polymers [Mn2(NCA)(H2O)5·3H2O]n, {;[Co(NCA)(phen)]·EtOH};n and [Cu(NCA)(H2O)2]n·H2O it acts as a bridging (bis)bidentate ligand. In the binuclear [Cu(NCA)(bpy)]2 it bridges two monomeric units [Cu(NCA)(bpy)] by bonding to Cu atom through its nitro group.
Izvorni jezik
Engleski
POVEZANOST RADA
Projekti:
HRZZ-IP-2014-09-4079 - Novi metal-organsi sustavi s oksalatnim i kinoidnim ligandima s podešenim svojstvima pogodnim za primjenu (NMOSBOQLWTPSFP) (Molčanov, Krešimir, HRZZ - 2014-09) ( CroRIS)