Pregled bibliografske jedinice broj: 1021253
Benzimidazole-1, 2, 3-triazole derivatives and bis-(1, 2, 3-triazolyl-benzimidazolyl)benzenes: synthesis and chemosensing properties
Benzimidazole-1, 2, 3-triazole derivatives and bis-(1, 2, 3-triazolyl-benzimidazolyl)benzenes: synthesis and chemosensing properties // 26. Hrvatski skup kemičara i kemijskih inženjera, Knjiga sažetaka, Šibenik, Hrvatska, 9-12.04.2019. / Galić, Nives ; Rogošić, Marko (ur.).
Zagreb: Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2019. str. 146-146 (poster, domaća recenzija, sažetak, znanstveni)
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Naslov
Benzimidazole-1, 2, 3-triazole derivatives and bis-(1, 2, 3-triazolyl-benzimidazolyl)benzenes: synthesis and chemosensing properties
Autori
Bobanović, Kristina ; Steinberg, Ivana ; Krištafor, Svjetlana
Vrsta, podvrsta i kategorija rada
Sažeci sa skupova, sažetak, znanstveni
Izvornik
26. Hrvatski skup kemičara i kemijskih inženjera, Knjiga sažetaka, Šibenik, Hrvatska, 9-12.04.2019.
/ Galić, Nives ; Rogošić, Marko - Zagreb : Hrvatsko društvo kemijskih inženjera i tehnologa (HDKI), 2019, 146-146
ISBN
9789536894673
Skup
26. hrvatski skup kemičara i kemijskih inženjera (26HSKIKI) ; 4. simpozij Vladimir Prelog
Mjesto i datum
Šibenik, Hrvatska, 09.04.2019. - 12.04.2019
Vrsta sudjelovanja
Poster
Vrsta recenzije
Domaća recenzija
Ključne riječi
benzimidazole ; 1, 2, 3-triazole ; synthesis, chemosensor
Sažetak
Nitrogen-containing heterocycles are widely investigated structures in the field of biology, medicine and chemical sensors. Benzimidazole and its derivatives are one of the most important building blocks in the design of novel biologically active molecules due to their structural similarity with naturally occuring nucleotides. In addition, combination of π-bridging and electron accepting properties of benzimidazole unit together with its metal-ion chelating ability and pH sensitivity, validated benzimidazole derivatives as promising candidates in fluorescent cellular imaging and metal ion sensing. Introduction of different electron donating and/or electron withdrawing substituents in the benzimidazole core can significantlly affect the optical characteristics of the resulting molecule [1]. Click-derived triazoles play important roles in sensing mechanisms because of their π-conjugated character and coordinating ability. 1, 2, 3-triazole ring can act as a covalent linkage between benzimidazole and corresponding functional group or can directly participate in binding of the target analyte [2]. In this work we present the synthesis of novel benzimidazole-1, 2, 3-triazole conjugates and 1, 3- and 1, 4-bis(1, 2, 3-triazolyl-benzimidazolyl)benzenes as novel donor-π-acceptor systems using click-chemistry approach. The influence of aryl-substituted 1, 2, 3-triazole unit at position 2 of benzimidazole is studied. All compounds are examined as potential chemosensor molecules for pH and/or different metal cations using UV-vis absorption and fluorescence spectroscopy. Detailed spectroscopic titrations in solutions are performed and fluorescence intensity changes are discussed as continuation of our ongoing research [3]. This work was funded by the Croatian Science Foundation (project HRZZ-3386, iNFiNiTE–SENS).
Izvorni jezik
Engleski
Znanstvena područja
Kemija
POVEZANOST RADA
Projekti:
HRZZ-IP-2014-09-3386 - Dizajn i sinteza novih dušikovih heterocikličkih fluorofora i fluorescentnih nanomaterijala kao kemijskih senzora za pH i metalne ione (iNFiNiTE–SENS) (Vianello, Robert, HRZZ - 2014-09) ( CroRIS)
Ustanove:
Fakultet kemijskog inženjerstva i tehnologije, Zagreb