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Complexation of Oxonium and Ammonium Ions by Lower-rim Calix[4]arene Amino Acid Derivatives


Požar, Josip; Horvat, Gordan; Čalogović, Marina; Galić, Nives; Frkanec, Leo; Tomišić, Vladislav
Complexation of Oxonium and Ammonium Ions by Lower-rim Calix[4]arene Amino Acid Derivatives // Croatica chemica acta, 85 (2012), 4; 541-552 doi:10.5562/cca2172 (međunarodna recenzija, članak, znanstveni)


Naslov
Complexation of Oxonium and Ammonium Ions by Lower-rim Calix[4]arene Amino Acid Derivatives

Autori
Požar, Josip ; Horvat, Gordan ; Čalogović, Marina ; Galić, Nives ; Frkanec, Leo ; Tomišić, Vladislav

Izvornik
Croatica chemica acta (0011-1643) 85 (2012), 4; 541-552

Vrsta, podvrsta i kategorija rada
Radovi u časopisima, članak, znanstveni

Ključne riječi
Calixarenes ; oxonium cation ; ammonium cation ; complexation ; solvation ; microcalorimetry ; UV spectrometry ; molecular dynamics

Sažetak
Complexation of oxonium and ammonium cations with two calix4arene amino acid derivatives, namely 5, 11, 17, 23-tetra-tert-butyl-26, 28, 25, 27-tetrakis-(O-methyl-D-α-phenylglycylcarbonylmethoxy)-calix[4]arene (1) and 5, 11, 17, 23-tetra-tert-butyl-26, 28, 25, 27-(O-methyl-L-leucylcarbonylmethoxy)calix[4]¬arene (2), in acetonitrile and methanol was studied by means of spectrophotometric and calorimetric titrations at 25 °C. The classical molecular dynamics simulations of the macrocycles and the corresponding complexes with NH4+ and H3O+ were carried out in order to investigate their possible structures in solution. The examined calix[4]arene derivatives were shown to be rather efficient binders for H3O+ cation and moderately efficient for NH4+ in acetonitrile, whereas the complexation of these cations in methanol could not be observed. The structures of the complexes obtained by means of molecular dynamics simulations suggested the involvement of ether and carbonyl oxygen atoms in the complexation of both NH4+ and H3O+. An inclusion of an acetonitrile molecule into the hydrophobic cavity of the free and complexed ligands was observed as well. The difference in binding affinities of 1 and 2 towards NH4+ and H3O+ ions could be explained by taking into account cation solvation, difference in their size and in the strength of hydrogen bonding between cations and the ligand binding sites.

Izvorni jezik
Engleski

Znanstvena područja
Kemija



POVEZANOST RADA


Projekt / tema
098-0982904-2912 - Samo-udruživanje u gelovima i sinteza funkcionalnih hibridnih materijala (Leo Frkanec, )
119-1191342-2960 - Elektroliti i koordinacijske reakcije u otopini (Vladislav Tomišić, )

Ustanove
Institut "Ruđer Bošković", Zagreb,
Prirodoslovno-matematički fakultet, Zagreb

Časopis indeksira:


  • Current Contents Connect (CCC)
  • Web of Science Core Collection (WoSCC)
    • Science Citation Index Expanded (SCI-EXP)
    • SCI-EXP, SSCI i/ili A&HCI
  • Scopus


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