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CATEGORY (Please choose one topic) TopicsCHOOSE XS01Polymer Dynamics.S02Soft Matter Dynamics and Phase Transitions in Amorphous, Partially Ordered and Ordered Systems (Liquid and Plastic Crystals, Ferro-electrics, Ceramics, Pharmaceuticals, etc.).S03Glassy Dynamics and its Scaling under Different Variables (Pressure, Temperature, Electric Fields, etc.).S04Confinement Effects.S05Non-Linear Effects.S06Advancements in Terahertz Spectroscopy.S07Industrial Applications.S08Dielectric Spectroscopy Spatially Resolved at Micro- and Nanoscale.S09Water and Hydrogen Bonded Systems, Application of BDS to Life Science.S10Charge Transport, Relaxation and Interfacial EffectsX High proton conductivity of the homo- and heterometallic oxalate-based compounds of different dimensionality Marijana Juri1, Ana Lozani1, Sanja Renka1, Sanja Burazer and Kreaimir Mol anov1 1 Ruer Boakovi Institute, Bijeni ka cesta 54, 10000 Zagreb, Croatia Recently, proton conductivity of the metal-organic frameworks (MOFs) has been considered as a new functionality, mainly due to their crystallinity, high porosity, designability and tunability in structure and properties, and potential application in solid-state electrolytes. The simplest method to introduce proton carriers is to include a counterion such as hydronium (H3O+), ammonium [NH4+, (CH3)2NH2+,...] or an anion (SO42"), resulting in charged compounds. The counterions form the hydrogen-bonding arrays with the guest water or other constituents of compound, creating proton-conducting pathways.1,2 A very important role in the design and synthesis of multifunctional materials belongs to the oxalate moiety, C2O42", due to its various possibilities of coordination to metal centers and its ability to mediate electronic effects between paramagnetic metal ions. The proton conductive materials must have good water and chemical durability under the influence of humidity and temperature, and in general, oxalate-based systems have regular structures and stable frameworks. In addition, the oxygen atoms of the oxalate group can construct complex hydrogen-bonded networks, which are more than suitable for proton conduction. Although high proton conductivity is often found in two-dimensional (2D) and three-dimensional (3D) oxalate-based compounds, the low-dimensional structures can have excellent proton conductivity properties via the hydrogen-bonding chain because a low void space can be advantageous for proton hopping.2,3 We explored the proton conduction behaviour of three oxalate-based compounds of different nuclearity and dimensionality, prepared and characterized in our group: homometallic discrete mononuclear (NH4)2[Fe(H2O)Cl3(C2O4)]H2O (1) and one-dimensional (1D) {[NH(CH3)(C2H5)2][FeCl2(C2O4)]H2O}n (2), and 2D heterometallic {[NH(CH3)2 (C2H5)]8[Mn4Cl4Cr4(C2O4)12]}n (3). The proton conductivity of 1, 2 and 3 at 298 K increases with increasing relative humidity (RH), achieving values of 2.17 10"3 (&! cm)"1 at 74% RH, 2.70 10"4 (&! cm)"1 at 93% RH and 1.6 10 3 (&! cm) 1 at 90% RH, respectively. 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References (1) X.-X. Xie, Y.-C. Yang, B.-H. Dou, Z.-F. Li, G. Li, Coord. Chem. Rev. 2020, 404, 213100. (2) D-W.;  HYPERLINK "https://pubs.rsc.org/en/results?searchtext=Author%3ADae-Woon%20Lim" Lim, H.  HYPERLINK "https://pubs.rsc.org/en/results?searchtext=Author%3AHiroshi%20Kitagawa" Kitagaw, Chem. Soc. Rev. 2021, 50, 6349-6368. (3) S. Burazer, K. Mol ano, AeeeeeeeeeffffffffdgfgtgvgzgԼԼԏvbvIvbvI1jhMhrCJPJUaJmH nH sH tH 'hrhrCJaJmHnHsH tH u0jhrhrCJUaJmHnHsH tH u(hMhHCJPJaJmH nH sH tH .hMhr5CJPJ\aJmH nH sH tH .hMhr6CJPJ]aJmH nH sH tH (hMhrCJPJaJmH nH sH tH +hMhH5CJPJaJmH nH sH tH zgggggggggggghllll(l,l>lBlRlVlllpltllllllllllл|||z||||||||l^lhMhr5CJPJaJhMhr6CJPJaJUhMhCJPJaJhMhHCJPJaJhMhrCJPJaJ.hMhr6CJPJ\aJmH nH sH tH (hMhrCJPJaJmH nH sH tH +hMhr5CJPJaJmH nH sH tH 1hMhr6CJPJ\]aJmH nH sH tH ". `anti, T. Klase, E. Wenger, D. Paji, Z. Jagli i, J. Popovi, M. Juri, Materials 2021, 14, 5543. 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