Scopus İndeksli Yayınlar Koleksiyonu / Scopus Indexed Publications Collection
Permanent URI for this collectionhttps://hdl.handle.net/11147/7148
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Article Citation - WoS: 31Citation - Scopus: 36Integration of Triboluminescent Eud4tea Crystals To Transparent Polymers: Impact Sensor Application(American Chemical Society, 2017) İncel, Anıl; Eanes, Mehtap; McMillen, Colin D.; Demir, Mustafa MuammerLanthanide-based organometallic materials are well-known candidate triboluminescent (TL) materials that can show bright emission when a mechanical force is applied. These materials are usually in the form of crystalline powders, and it is often useful to integrate these samples into a polymer matrix in order to achieve processability, enabling coating from a solution/molten state or fabrication as a complex-shaped matrix. In this work, micrometer-sized europium tetrakis (dibenzoylmethide) triethylammonium (EuD4TEA) crystals were synthesized and integrated with various transparent polymers (PMMA, PS, PVDF, and PU) using two approaches: (i) blending and (ii) surface impregnation. In the former method, the crystalline particles were molecularly dissolved; therefore, a TL response cannot be achieved. More than 10 wt % TL crystals in the composite is needed to obtain TL signals. However, TL signal was achieved at 2.5 wt % when a composite was prepared by the latter approach. TL intensity shows exponential decay with consecutive mechanical action. The TL emission of PU-based surface impregnated composite expires with long-lived emission, and maximum TL response with respect to applied force was measured between 2.45 and 42.0 N.Article Citation - WoS: 7Citation - Scopus: 7Hydrothermal Synthesis of New Rare Earth Silicate Fluorides: a Novel Class of Polar Materials(Academic Press Inc., 2012) McMillen, Colin D.; Eanes, Mehtap; Stritzinger, Jared T.; Kolis, Joseph K.Polar crystals provide an interesting avenue for materials research both in the structures they form and the properties they possess. This work describes the hydrothermal synthesis and structural characterization of three novel silicate fluorides. Compound (1), LiY 3(SiO 4) 2F 2 crystallizes in space group C2/c, with a=17.651(4) Å, b=4.8868(10) Å, c=11.625(2) Å and β=131.13(3)°. BaY 2(Si 2O 7)F 2 (2) crystallizes in space group P-1, with a=5.1576(10) Å, b=6.8389(14) Å, c=11.786(2) Å, α=93.02(3)°, β=102.05(3)° and γ=111.55(3) °. Finally, the structure of Ba 2Y 3(SiO 4) 2F 5 (3) was determined in the polar orthorhombic space group Pba2, having unit cell parameters a=8.8864(18) Å, b=12.764(3) Å and c=5.0843(10) Å. The structures are compared based on their building blocks and long range polarities. Aligned silicate tetrahedra segregated into a single layer in (3) impart the observed polarity.Article Citation - WoS: 3Citation - Scopus: 5Hydrothermal Synthesis and Characterization of a New Layered Compound Li2vgeo5(Elsevier Ltd., 2004) Eanes, Mehtap; Kolis, Joseph W.The new compound Li2VGeO5 with a layered structure has been synthesized at 580°C via the hydrothermal method. The compound crystallizes in the space group P4/n of the tetragonal system with two formula units in a cell of dimensions a=6.5187(9)Å, c=4.5092(9)Å (T=298K), V=191.61(5)Å3. The structure is composed of layers made of repeating [(VO5)(GeO4)]1- units. Li+ ions reside between the layers. The magnetic susceptibility data show an antiferromagnetic coupling below 5K with C=0.47emuKmol-1, and θ=-13K with μeff=1.89μB for each Li 2VGeO5 unit.Article Citation - WoS: 4Citation - Scopus: 4Hydrothermal Synthesis and Characterization of a Novel Supramolecular Hybrid Based on Keggin and Cu(i) Complex(Elsevier, 2013) Eanes, Mehtap; Önen, BanuA novel inorganic-organic hybrid molecule, [Cu(4,4′bipyH)3(4,4bipy)][HPW12O40]2.12H2O (1), has been hydrothermally synthesized and characterized by IR spectra, TG and single crystal X-ray diffraction analyses. Structural analysis reveals that the novel compound 1 composed of two Kegging polyoxoanion connected with Cu complex fragment forming a big molecule that extends in 3D via hydrogen bonding.
