@article{63721,
  abstract     = {{<jats:p>Defect engineering offers an effective route to tailor the local coordination environment, gas transport and excited-state processes in metal-organic frameworks (MOFs). We establish a quantitative structure-property relationship linking defect-modulated porosity...</jats:p>}},
  author       = {{Zhao, Zhenyu and Tiemann, Michael}},
  issn         = {{2050-7526}},
  journal      = {{Journal of Materials Chemistry C}},
  pages        = {{4743--4752}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Defect Structure-Performance Correlation in Eu³⁺@UiO-66: Design of Coordination Sites for Rapid Optical O₂ Sensing}}},
  doi          = {{10.1039/d5tc04319k}},
  volume       = {{14}},
  year         = {{2026}},
}

@article{62819,
  abstract     = {{Novel oxalate-bridged heterotrinuclear complexes [A][Mn2Cr(bpy)2(H2O)2Cl2(C2O4)3] (A = (CH3)2(C2H5)NH+ (1) and (CH3)(C2H5)2NH+ (2); bpy = 2,2′-bipyridine) were synthesized using an aqueous solution of [A]3[Cr(C2O4)3] as a building block in reaction with Mn2+ ions and with the addition of the N-donor ligand bipyridine. The isostructural heterometallic complex salts were characterized by single-crystal and powder X-ray diffraction, infrared and impedance spectroscopy, thermal analysis and magnetization measurements. The trinuclear anion [{Mn(bpy)(H2O)Cl(μ-C2O4)}2Cr(C2O4)]− consists of two [Mn(bpy)(H2O)Cl]+ units bridged by the [Cr(C2O4)3]3− anion, which acts as a bidentate ligand towards each of the manganese atoms. The anions are hydrogen bonded to each other via coordinated chloride anions, water molecules and oxygen oxalate atoms, resulting in two-dimensional (2D) hydrogen bonding layers. Compounds exhibit water-assisted proton conductivity behaviour, which was investigated at different temperatures and relative humidities (RH). At 25 °C, an increase in RH from 60% to 93% resulted in an obvious proton conducting switch from 9.1 × 10−11 to 5.6 × 10−5 S cm−1 for 1 and from 7.4 × 10−10 to 1.8 × 10−6 S cm−1 for 2, corresponding to high on/off ratios of about 106 for 1 and 104 for 2. In situ powder X-ray diffraction (PXRD) analysis showed that unit cell parameters of compounds 1 and 2 slightly increase when exposed to humid conditions. This confirmed that incorporation of water molecules into structures with pores and voids causes the proton conductivity switching phenomenon. Magnetic susceptibility measurements indicate a ferromagnetic interaction between Cr3+ and Mn2+ ions bridged by the bis(bidentate) oxalate group. The prepared compounds 1 and 2 were explored as single-source precursors for the formation of spinel oxide by their thermal treatment. With increasing temperature, the spinel composition changed according to the formula Mn1+xCr2–xO4 (0 ≤ x ≤ 1), where x = 0.7 at 500 °C and x = 1 at 900 °C when tet[MnII]oct[MnIIICrIII]O4 is formed. The (micro)structure, morphology, and optical properties of spinel Mn2CrO4 were characterized by PXRD, scanning electron microscopy and UV-Vis diffuse reflectance spectroscopy. The photocatalytic activity of this oxide in degradation of the methylene blue dye under Vis irradiation without and with the support of hydrogen peroxide was further investigated.}},
  author       = {{Lozančić, Ana and Burazer, Sanja and Wagner, Tobias and Molčanov, Krešimir and Pajić, Damir and Androš Dubraja, Lidija and Tiemann, Michael and Jurić, Marijana}},
  issn         = {{2050-7526}},
  journal      = {{Journal of Materials Chemistry C}},
  number       = {{41}},
  pages        = {{21179--21195}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Water-assisted proton conductivity and a magnetic study of heterotrinuclear oxalate-bridged compounds: molecular precursors for the Mn2CrO4 spinel}}},
  doi          = {{10.1039/d5tc02569a}},
  volume       = {{13}},
  year         = {{2025}},
}

@article{49676,
  abstract     = {{<jats:p>Dynamics-induced interchain charge transfer in a polymer aggregate in stack configuration can be understood by single-oligomer polaron energy.</jats:p>}},
  author       = {{Bauch, Fabian and Dong, Chuan-Ding and Schumacher, Stefan}},
  issn         = {{2050-7526}},
  journal      = {{Journal of Materials Chemistry C}},
  keywords     = {{Materials Chemistry, General Chemistry}},
  number       = {{38}},
  pages        = {{12992--12998}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Dynamics-induced charge transfer in semiconducting conjugated polymers}}},
  doi          = {{10.1039/d3tc02263c}},
  volume       = {{11}},
  year         = {{2023}},
}

@article{51093,
  abstract     = {{<jats:p>Dynamics-induced interchain charge transfer in a polymer aggregate in stack configuration can be understood by single-oligomer polaron energy.</jats:p>}},
  author       = {{Bauch, Fabian and Dong, Chuan-Ding and Schumacher, Stefan}},
  issn         = {{2050-7526}},
  journal      = {{Journal of Materials Chemistry C}},
  keywords     = {{Materials Chemistry, General Chemistry}},
  number       = {{38}},
  pages        = {{12992--12998}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Dynamics-induced charge transfer in semiconducting conjugated polymers}}},
  doi          = {{10.1039/d3tc02263c}},
  volume       = {{11}},
  year         = {{2023}},
}

@article{61267,
  abstract     = {{<jats:p>Dynamics-induced interchain charge transfer in a polymer aggregate in stack configuration can be understood by single-oligomer polaron energy.</jats:p>}},
  author       = {{Bauch, Fabian and Dong, Chuan-Ding and Schumacher, Stefan}},
  issn         = {{2050-7526}},
  journal      = {{Journal of Materials Chemistry C}},
  number       = {{38}},
  pages        = {{12992--12998}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Dynamics-induced charge transfer in semiconducting conjugated polymers}}},
  doi          = {{10.1039/d3tc02263c}},
  volume       = {{11}},
  year         = {{2023}},
}

@article{46012,
  abstract     = {{<jats:p>Nickel–iron oxide electrocatalysts prepared <jats:italic>via</jats:italic> a rapid electrodeposition are promising candidates for non-enzymatic glucose sensors.</jats:p>}},
  author       = {{Ni, Ming and Tan, Minyuan and Pan, Ying and Zhu, Chuhong and Du, Haiwei}},
  issn         = {{2050-7526}},
  journal      = {{Journal of Materials Chemistry C}},
  keywords     = {{Materials Chemistry, General Chemistry}},
  number       = {{35}},
  pages        = {{12883--12891}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Rapid preparation of self-supported nickel–iron oxide as a high-performance glucose sensing platform}}},
  doi          = {{10.1039/d2tc03176k}},
  volume       = {{10}},
  year         = {{2022}},
}

@article{40435,
  abstract     = {{<p>Coulomb binding energy is reduced when a few-molecule integer charge transfer complex (ICTC) is formed.</p>}},
  author       = {{Dong, Chuan-Ding and Schumacher, Stefan}},
  issn         = {{2050-7526}},
  journal      = {{Journal of Materials Chemistry C}},
  keywords     = {{Materials Chemistry, General Chemistry}},
  number       = {{34}},
  pages        = {{11929--11935}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Molecular doping in few-molecule polymer-dopant complexes shows reduced Coulomb binding}}},
  doi          = {{10.1039/d0tc02185g}},
  volume       = {{8}},
  year         = {{2020}},
}

@article{22577,
  abstract     = {{<p>A new Ti-precursor for low-temperature PE-ALD of titanium dioxide thin films as gas barrier layers on polymer substrates.</p>}},
  author       = {{Gebhard, M. and Mitschker, F. and Wiesing, M. and Giner, I. and Torun, B. and de los Arcos de Pedro, Maria Teresa and Awakowicz, P. and Grundmeier, G. and Devi, A.}},
  issn         = {{2050-7526}},
  journal      = {{Journal of Materials Chemistry C}},
  pages        = {{1057--1065}},
  title        = {{{An efficient PE-ALD process for TiO2 thin films employing a new Ti-precursor}}},
  doi          = {{10.1039/c5tc03385c}},
  year         = {{2016}},
}

@article{39669,
  abstract     = {{<p>Polymer-stabilized blue phase liquid crystal in-plane switching cell.</p>}},
  author       = {{Nordendorf, Gaby and Schmidtke, Jürgen and Wilkes, David and Kitzerow, Heinz-Siegfried}},
  issn         = {{2050-7526}},
  journal      = {{Journal of Materials Chemistry C}},
  keywords     = {{Materials Chemistry, General Chemistry}},
  number       = {{3}},
  pages        = {{518--521}},
  publisher    = {{Royal Society of Chemistry (RSC)}},
  title        = {{{Temperature-insensitive electro-optic response of polymer-stabilized blue phases}}},
  doi          = {{10.1039/c6tc04679g}},
  volume       = {{5}},
  year         = {{2016}},
}

@article{64039,
  abstract     = {{The preparation of hierarchical and sophisticated particle architectures for mimicking structural colors known from nature still remains a challenge. In this study, the preparation of novel opal and double-inverse opal films based on thermally treated metallopolymer core particles with a silica shell is described. Thermal treatment leads to the formation of magnetic nanorattle-type particles. The main challenge of artificial particles is to ensure sufficient dispersibility after several synthetic steps. Especially silica particles providing surface hydroxyl groups tend to sinter at high temperatures leading to agglomeration. We present the introduction of trimethyl ethoxy silane (TMES) as an excellent functionalization reagent as the key reaction step. The necessity and success of functionalization are investigated by transmission electron microscopy (TEM) and zeta potential measurements. Importantly, solid state NMR techniques are employed to gain deeper insights into the chemical structure of the surface-attached reagent. Finally, by this convenient functionalization the preparation of elastomeric opal films and double-inverse opal films is proven successful revealing excellent optical film properties. Moreover, magnetic properties of these novel films are investigated by using magnetic force microscopy (MFM). The herein established route is expected to pave the way for the preparation of a variety of advanced and stimuli-responsive optical materials.}},
  author       = {{Scheid, D. and Stock, D. and Winter, T. and Gutmann, Torsten and Dietz, C. and Gallei, M.}},
  issn         = {{2050-7526}},
  journal      = {{Journal of Materials Chemistry C}},
  keywords     = {{Materials Science, silica, Physics, nmr, colloidal photonic crystals, light, polymerization, solids, structural color, thermo}},
  number       = {{11}},
  pages        = {{2187–2196}},
  title        = {{{The pivotal step of nanoparticle functionalization for the preparation of functional and magnetic hybrid opal films}}},
  doi          = {{10.1039/c5tc04388c}},
  volume       = {{4}},
  year         = {{2016}},
}

@article{22596,
  author       = {{Xu, Ke and Chaudhuri, Ayan Roy and Parala, Harish and Schwendt, Dominik and de los Arcos de Pedro, Maria Teresa and Osten, H. Jörg and Devi, Anjana}},
  issn         = {{2050-7526}},
  journal      = {{Journal of Materials Chemistry C}},
  title        = {{{Atomic layer deposition of Er2O3 thin films from Er tris-guanidinate and water: process optimization, film analysis and electrical properties}}},
  doi          = {{10.1039/c3tc30401a}},
  year         = {{2013}},
}