Chemistry / Kimya
Permanent URI for this collectionhttps://hdl.handle.net/11147/4072
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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: 4Citation - Scopus: 5Crystal Structure of Distrontium Manganese (iii) Tetraoxophosphate Heptaoxodiphosphate, Sr2mn[po4] [p2o 7](Walter de Gruyter GmbH, 2007) Doğan, Leyla; Eanes, MehtapMnO11P3Sr2, monoclinic, P121/c1 (no. 14), a = 6.641(1) Å, b = 6.834(1) Å, c = 19.554(4) Å, β = 99.22(3)°, V = 876.0 Å3, Z = 4, Rgt(F) = 0.051, wRref(F2) = 0.090, T = 298 K.Article Citation - WoS: 6Citation - Scopus: 6Crystal Structure of Lead(ii) Trioxovanadate(v) Chloride, Pb[vo 3]cl(Walter de Gruyter GmbH, 2007) Şahin, Aytaç; Eanes, MehtapClO3PbV, orthorhombic, Pnma (no. 62), a = 10.022(2) Å, b = 5.288(1) Å, c = 7.171(1) Å, V= 380.0 Å3, Z = 4, Rgt(F) = 0.035, wRref(F2) = 0.105, T= 153 K.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: 11Citation - Scopus: 12Hydrothermal Synthesis, Characterization and Magnetic Properties of Navge2o6 and Livge2o6(Elsevier Ltd., 2004) Eanes, Mehtap; Kolis, Joseph W.Supercritical fluids are shown to be an excellent reaction media for the synthesis of novel solid state phases at intermediate temperatures. LiVGe 2O6 and NaVGe2O6 have the common pyroxene structure composed of VO6 linear chains. NaVGe 2O6 crystallizes in the monoclinic space group C2/c with four formula units having cell dimensions a = 9.960(4)Å, b = 8.853(10)Å, c = 5.4861(10)Å, β = 106.403(3)°. The structure was refined until R = 0.0290 and Rw = 0.0370. For LiVGe 2O6 in space group P21/c: a = 9.8508(7)Å, b = 8.754(3)Å, c = 5.3948(13)Å, β = 108(3)°, R = 0.0240 and Rw = 0.0250. The compounds contain edge-shared VO6 octahedral chains and corner-shared GeO4 tetrahedral chains. The presence of these VO6 chains results in spin-Peierls distortion. Structural and physical characterization of the compounds are reported.Article Citation - WoS: 2Citation - Scopus: 2Redetermination of the Crystal Structure of Sodium Trisamarium Digermanate Dihydroxide, Nasm3(geo4)2(oh)2(Walter de Gruyter GmbH, 2002) Eanes, MehtapGe2H2NaO10Sm3, monoclinic, C12/c1 (No. 15), a = 18.323(3)Å, b = 5.2369(8) Å, c = 12.108(2) Å, β= 131.230(2)°, V = 873.8 Å3, Z = 4, R gt(F) = 0.037, wRref(F2) = 0.010, T= 153 K.Article Citation - WoS: 5Citation - Scopus: 5Hydrothermal Synthesis and Characterization of One Dimensional Chain Structures of Monolacunary Keggin Polyoxoanions Substituted With Copper(Elsevier Ltd., 2015) Eanes, Mehtap; Önen, Banu; McMillen, Colin D.Two novel polymeric polyoxometallates constructed from transition metal substituted heteropolytungstates, [(4,4’bpyH2)2(4,4’bpyH)][PCuW11O39]·H2O (1), and [(4,4’bpyH2)(pyH)3][PCuW11O39]·2H2O (2), (4,4’bpy = 4,4’bipyridine, py = pyridine) have been synthesized under hydrothermal conditions and characterized by IR, TGA, single crystal X-ray diffraction and magnetic measurements. The product formation showed a high sensitivity toward experimental factors including pH and stirring. Compounds 1 crystallizes in the monoclinic space group P2(1)/n with a = 13.503(3) Å, b = 26.726(5) Å, c = 15.168(3) Å, = 99.61(3)° and Z=4. The second compound also crystallizes in space group P2(1)/n, but with a = 13.519(3) Å, b = 20.431(4) Å, c =18.655(4) Å, = 96.52(3)° and Z=4. Compound 1 exhibits a zigzag chain structure, while compound 2 exhibits a straight chain structure. Compound 2 is the first example of a polyoxometallate containing 1D chains of transitionmetal- substituted heteropolytungstate designed with two significantly different organic units as the countercations. The Cu2+ ions in 1 exhibit paramagnetic behavior.Article Citation - WoS: 11Citation - Scopus: 11Effect of Alkali Metal Hydroxides on the Morphological Development and Optical Properties of Ceria Nanocubes Under Hydrothermal Conditions(American Scientific Publishers, 2011) Kepenekçi, Özlem; Eanes, Mehtap; Demir, Mustafa MustafaNanocrystalline cerium(IV) oxide (CeO2, ceriaceria) particles were produced via the hydrothermal treatment of cerium nitrate hexahydrate with various alkali metal hydroxides (MOH: M = Li, Na, K). Experimental conditions such as [MOH], reaction temperature, and reaction time were studied. Particle morphology as well as size of crystallites was precisely controlled by choice of experimental conditions. While rod-shaped particles were obtained at 120 C, well-defined nanocubes were formed at higher temperatures regardless of the choice of MOH. Examination of particle growth kinetics, in the final stages of crystallization, showed that particle growth rate is controlled by two different mechanisms. Grain boundary diffusion controls the particle growth in the presence of NaOH with an activation energy of 113.8 kj/mol and surface diffusion for LiOH ad KOH with the activation energy of 43.0–150.9 kj/mol, respectively. In addition, the particles exhibit strong violet and blue emissions at 400 nm and 370 nm. The former emission originates from excitation of a wide band gap of CeO2. The latter one is attributed to the trivalency of the cerium ion and appears to be sensitive to all the experimental conditions studied. Both extending reaction time and increasing temperature reduce the intensity of the 370 nm emission and increase the intensity of the 400 nm emission.Article A Two-Dimensional Organic–inorganic Hybrid Compound, Poly[(ethylenediamine)tri-Μ(International Union of Crystallography, 2008) Gün, Özgül; Emirdağ Eanes, Mehtap; Vanderveer, Don; Eanes, MehtapA new organic–inorganic two-dimensional hybrid compound, [CuMoO4(C2H8N2)], has been hydrothermally synthesized at 443 K. The unit cell contains layers composed of CuN2O4 octahedra and MoO4 tetrahedra. Corner-sharing MoO4 and CuN2O4 polyhedra form CuMoO4 bimetallic sites that are joined together through O atoms, forming an edge-sharing Cu2Mo2O4 chain along the c axis. The one-dimensional chains are further linked through bridging O atoms that join the Cu and Mo atoms into respective chains along the b axis, thus establishing layers in the bc plane. The ethylenediamine ligand is coordinated to the Cu atom through its two N atoms and is oriented perpendicularly to the two-dimensional –Cu—O— Mo– layers. The average distance between adjacent layers, as calculated by consideration of the closest and furthest distances between two layers, is 8.7 Å. The oxidation statesof the Mo and Cu atoms of VI and II, respectively, were confirmed by bond-valence sum calculations.