WoS İndeksli Yayınlar Koleksiyonu
Permanent URI for this collectionhttps://hdl.handle.net/20.500.12573/394
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Article Citation - WoS: 12Citation - Scopus: 11Trans-Cis Isomerization Assisted Synthesis of Solution-Processable Yellow Fluorescent Maleic Anhydrides for White-Light Generation(Elsevier Science SA, 2015-12) Ozdemir, Mehmet; Genc, Sinan; Ozdemir, Resul; Altintas, Yemliha; Citir, Murat; Sen, Unal; Usta, HakanHeterocyclic maleic anhydride derivatives have been extensively studied in natural products chemistry over the past few decades. However, their incorporation into optoelectronic devices has lagged behind that of other pi-conjugated systems, and they have never been studied in white light emitting diodes (WLEDs). The development of emissive pi-conjugated materials for (WLEDs) has been an emerging scientific and technological research area to replace phosphors used in LED-based solid-state lighting. Here, we demonstrate the design, synthesis and characterization of two new highly emissive alkyl-substituted bis(thienyl)maleic anhydrides (C6-Th2MA and C12-Th2MA) with favorable photophysical properties. The new core is synthesized via a novel trans-to-cis isomerization-assisted one-pot reaction, which is demonstrated for the first time in the literature for the synthesis of a bis(heteroaryl)maleic anhydride. Due to its favorable absorption and fluorescence properties in the blue and yellow region of the visible spectrum, respectively, C12-Th2MA is studied as a potential wavelength-upconverting material. A WLED fabricated by drop-casting a polymeric solution of C12-Th2MA on a blue LED (InGaN, 455 nm) yields promising CIE coordinates and color-rendering index (CRI) values of (0.24, 0.20) and 65.0, respectively. Considering the simplicity of the current molecular structure and facile synthesis, alkyl-substituted bis(thienyl)maleic anhydrides stand as ideal phosphor alternatives. Therefore, the current findings may open new perspectives for the development of maleic anhydride-based small molecules for low-cost, energy-efficient, and solution-processed lighting technologies. (C) 2015 Elsevier B.V. All rights reserved.Article Citation - WoS: 25Citation - Scopus: 27Selective Removal of Cationic Micro-Pollutants Using Disulfide-Linked Network Structures(Royal Soc Chemistry, 2017) Atas, Mehmet Sahin; Dursun, Sami; Akyildiz, Hasan; Citir, Murat; Yavuz, Cafer T.; Yavuz, Mustafa SelmanMicropollutants are found in all water sources, even after thorough treatments that include membrane filtration. New ones emerge as complex molecules are continuously produced and discarded after used. Treatment methods and sorbent designs are mainly based on non-specific interactions and, therefore, have been elusive. Here, we developed swellable covalent organic polymers (COP) with great affinity towards micropollutants, such as textile industry dyes. Surprisingly, only cationic dyes in aqueous solution were selectively and completely removed. Studies of the COPs surfaces led to a gating capture, where negatively charged layer attracts cationic dyes and moves them inside the swollen gel through diffusive and hydrophobic interaction of the hydrocarbon fragments. Despite its larger molecular size, crystal violet has been taken the most, 13.4 mg g(-1), surpassing all competing sorbents. The maximum adsorption capacity increased from 12.4 to 14.6 mg and from 8.9 to 11.4 mg when the temperature of dye solution was increased from 20 to 70 degrees C. The results indicated that disulfide-linked COPs are attractive candidates for selectively eliminating cationic dyes from industrial wastewater due to exceptional swelling behaviour, low-cost and easy synthesis.Article Citation - WoS: 104Citation - Scopus: 109Proton Conducting Poly(Vinyl Alcohol) (PVA)/Poly (2-Acrylamido Sulfonic Acid) (PAMPS)/Zeolitic Imidazolate Framework (ZIF) Ternary Composite Membrane(Elsevier, 2016-02) Erkartal, Mustafa; Usta, Hakan; Citir, Murat; Sen, UnalThe design, synthesis and characterization of novel proton exchange membranes (PEMs) are of significant scientific and technological importance for the realization of fuel cells, actuators, and sensors. Here, we demonstrate a novel ternary composite membrane consisting of poly(vinyl alcohol) (PVA), poly (2-acrylamido-2-methylpropane sulfonic acid) (PAMPS), zeolitic imidazolate framework-8 (ZIF-8), which is prepared by physical blending and casting methods. To enhance the water management of the membranes, in situ chemical cross-linking is carried out by glutaraldehyde (GA). During the characterization of the new membranes, FT-IR is used for intermolecular and inter-polymer interactions between different components of the membrane, SEM is used to identify morphology, XRD is used to prove the presence of ZIF-8 nanoparticles, and finally TGA is used for thermal stability. The proton conductivity of the membranes is found to increase with temperature and also with the increasing content of PAMPS. The highest proton conductivity under fully hydrated state at 80 degrees C is measured as 0.134 S cm(-1) for PVA: PAMPS: ZIF-8 (55:40:5) composition. In this study, it is clearly shown that ZIF-8 nanoparticles contribute to the proton conductivity by forming hydrogen bonds with the polymer network in the membrane. The water uptake (WU) and ion exchange capacity (IEC) values are 3.28 (gig) and 1.52 meq g(-1), respectively for the same membrane. To the best our knowledge, this study shows one of the first example of a MOFcontaining membrane with truly high proton conductivities, and both values of proton conductivity and electrochemical properties are comparable to those of well-studied membrane, Nation. (C) 2015 Elsevier B.V. All rights reserved.Article Citation - WoS: 6Citation - Scopus: 7Measuring Temperature Change at the Nanometer Scale on Gold Nanoparticles by Using Thermoresponsive PEGMA Polymers(Wiley-VCH Verlag GmbH, 2017-06-13) Yavuz, Mustafa S.; Citir, Murat; Cavusoglu, Halit; Demirel, GokhanPlasmonic heating of gold nanoparticles (AuNPs) under laser illumination is a highly desirable technique, especially for cancer therapy. However, significant drawbacks still remain including uncontrolled heat release from AuNPs, random exposure duration, and selection of the proper laser power without damaging normal healthy cells. Herein, we demonstrate a simple and versatile method to measure temperature variation on the surface of Au nanoparticles under laser irradiation based on a thermoresponsive polymer, poly(ethylene glycol) methylether methacrylate (PEGMA). In this context, a series of PEGMA polymers were synthesized to have different lower critical solution temperature (LCST) values (28-90 degrees C) and conjugated to the surface of spherical AuNPs by a gold-thiolate linkage. According to our strategy, the AuNPs first photothermally absorb light energy and convert it to heat owing to their tailored photothermal characteristics. The generated heat from the AuNPs subsequently dissipates into the surrounding thermoresponsive PEGMA polymer. When the temperature generated on the Au surface upon laser irradiation for a certain exposure time reaches the LCST value of the surrounding PEGMA polymer, the polymer chain collapses. Therefore, the hydrodynamic diameter of the PEGMA-coated AuNPs changes, which can be easily monitored by using dynamic light scattering (DLS). We systematically measured the temperature (28-90 degrees C) generated on the AuNP surfaces by using different laser power densities with varying durations. We believe that the resulting strategy will be very valuable for oncologists to easily predict the minimum laser power and duration needed to destroy the cancer cells through the photothermal effect of Au nanostructures.Article Citation - WoS: 18Citation - Scopus: 19Infrared Multiple Photon Dissociation Spectroscopy of Protonated Histidine and 4-Phenylmidazole(Elsevier, 2012-12) Citir, Murat; Hinton, Christopher S.; Oomens, Jos; Steill, Jeffrey D.; Armentrout, P. B.The gas-phase structures of protonated histidine (His) and the side-chain model, protonated 4-phenyl imidazole (PhIm), are examined by infrared multiple photon dissociation (IRMPD) action spectroscopy utilizing light generated by the free electron laser FELIX. To identify the structures present in the experimental studies, the measured IRMPD spectra are compared to spectra calculated at a B3LYP/6-311+G(d,p) level of theory. Relative energies of various conformers are provided by single point energy calculations carried out at the B3LYP, B3P86, and MP2(full) levels using the 6-311+G(2d,2p) basis set. On the basis of these experiments and calculations, the IRMPD action spectrum for H+(His) is characterized by a mixture of [N-pi,N-alpha] and [N-pi,CO] conformers, with the former dominating. These conformers have the protonated nitrogen atom of imidazole adjacent to the side-chain (N-pi) hydrogen bonding to the backbone amino nitrogen (N-alpha) and to the backbone carbonyl oxygen, respectively. Comparison of the present results to recent IRMPD studies of protonated histamine, the radical His(center dot+) cation, H+(HisArg), H-2(2+)(HisArg), and M+(His), where M+ = Li+, Na+, K+, Rb+, and Cs+, allows evaluation of the vibrational motions associated with the observed bands. (c) 2012 Elsevier B.V. All rights reserved.Article Citation - WoS: 1Citation - Scopus: 1Highly Efficient Chlorinated Solvent Uptake by Novel Covalent Organic Networks via Thiol-Ene Chemistry(Springer, 2021-07-03) Yavuz, Mustafa Selman; Citir, MuratIn this study, we synthesized an aliphatic-aromatic regular network as a novel covalent organic networks called TEPN-1 (Thiol-ene Polymer Network) and TEPN-2 via thiol-ene chemistry. TEPN-1 and TEPN-2 were analyzed by FTIR, C-13-NMR, Brunauer-Emmett-Teller, thermogravimetric analysis and elemental analysis. Solvent uptake capacity of TEPN-1 and TEPN-2 was employed against 26 solvents which are frequently used in chemical industry. It is found that TEPN-1 has the highest swelling adsorption ratio with chloroform and DCM (13.7 and 11.5 g.g(-1), respectively), while TEPN-2 has 9.2 and 7.5 g.g(-1), respectively. Both TEPN-1 and TEPN-2 have very minimal water uptake (0.165 and 0.189 g.g(-1), respectively). TEPN-1 and TEPN-2 are efficient adsorbents for most of organic solvents including water-miscible organic solvents such as THF, dioxane and pyridine.Article Citation - WoS: 21Citation - Scopus: 21Enhancement of Anhydrous Proton Conductivity of Poly(Vinylphosphonic Acid)-Poly(2,5 Membranes Via in Situ Polymerization(Wiley-VCH Verlag GmbH, 2014-10-16) Sen, Unal; Usta, Hakan; Acar, Oktay; Citir, Murat; Canlier, Ali; Bozkurt, Ayhan; Ata, AliPolymer electrolyte membranes (PEMs) are synthesized via in situ polymerization of vinylphosphonic acid (VPA) within a poly(2,5-benzimidazole) (ABPBI) matrix. The characterization of the membranes is carried out by using Fourier transform infrared (FTIR) spectroscopy for the interpolymer interactions, thermogravimetric analysis (TGA) and differential scanning calorimetry (DSC) for the thermal properties, and scanning electron microscopy (SEM) for the morphological properties. The physicochemical characterizations suggest the complexation between ABPBI and PVPA and the formation of homogeneous polymer blends. Proton conductivities in the anhydrous state (150 degrees C) measured by using impedance spectroscopy are considerable, at up to 0.001 and 0.002 S cm(-1) for (1: 1) and (1: 2) molar ratios, respectively. These conductivities indicate signifi cant improvements (> 1000x) over the physically blended samples. The results shown here demonstrate the great potential of in situ preparation for the realization of new PEM materials in future high-temperature and non-humidified polymer electrolyte membrane fuel cell (PEMFC) applications.Conference Object Citation - WoS: 15Citation - Scopus: 16Development of Highly Transparent Pd-Coated Ag Nanowire Electrode for Display and Catalysis Applications(Elsevier Science Bv, 2015-09) Canlier, Ali; Ucak, Umit Volkan; Usta, Hakan; Cho, Changsoon; Lee, Jung-Yong; Sen, Unal; Citir, MuratAg nanowire transparent electrode has excellent transmittance (90%) and sheet resistance (20 Omega/sq), yet there are slight drawbacks such as optical haze and chemical instability against aerial oxidation. Chemical stability of Ag nanowires needs to be improved in order for it to be suitable for electrode applications. In our recent article, we demonstrated that coating Ag nanowires with a thin layer of Au through galvanic exchange reactions enhances the chemical stability of Ag nanowire films highly and also helps to obtain lower haze. In this study, coating of a thin Pd layer has been applied successfully onto the surface of Ag nanowires. A mild Pd complex oxidant [Pd(en)(2)](NO3)(2) was prepared in order to oxidize Ag atoms partially on the surface via galvanic displacement. The mild galvanic exchange allowed for a thin layer (1-2 nm) of Pd coating on the Ag nanowires with minimal truncation of the nanowire, where the average length and the diameter were 12.5 mu m and 59 nm, respectively. The Pd-coated Ag nanowires were suspended in methanol and then electrostatically sprayed on flexible polycarbonate substrates. It has been revealed that average total transmittance remain around 95% within visible spectrum region (400-800 nm) whereas sheet resistance rises up to 175 Omega/sq. To the best of our knowledge, for the first time in the literature, Pd coating was employed on Ag nanowires in order to design transparent electrodes for high transparency and strong chemical resistivity against nanowire oxidation. The current Pd-coated Ag nanowires may render an excellent catalyst system for fuel cell applications, as well as in organic synthesis with relatively low costs since our approach enables the fabrication of these nanowires with a very thin layer of Pd. We believe that mesh form of Pd-coated Ag nanowires will coin a new catalyst concept to the related areas since their sheet conductivity is high enough, and also little amount of Pd displays a large surface area as thin layers. (C) 2015 Elsevier B.V. All rights reserved.Article Citation - WoS: 55Citation - Scopus: 57Bond Energies of ThO+ and ThC+: A Guided Ion Beam and Quantum Chemical Investigation of the Reactions of Thorium Cation With O2 and CO(AIP Publishing, 2016-05-13) Cox, Richard M.; Citir, Murat; Armentrout, P. B.; Battey, Samuel R.; Peterson, Kirk A.Kinetic energy dependent reactions of Th+ with O-2 and CO are studied using a guided ion beam tandem mass spectrometer. The formation of ThO+ in the reaction of Th+ with O-2 is observed to be exothermic and barrierless with a reaction efficiency at low energies of k/k(LGS) = 1.21 +/- 0.24 similar to the efficiency observed in ion cyclotron resonance experiments. Formation of ThO+ and ThC+ in the reaction of Th+ with CO is endothermic in both cases. The kinetic energy dependent cross sections for formation of these product ions were evaluated to determine 0 K bond dissociation energies (BDEs) of D-0(Th+-O) = 8.57 +/- 0.14 eV and D-0(Th+-C) = 4.82 +/- 0.29 eV. The present value of D-0(Th+-O) is within experimental uncertainty of previously reported experimental values, whereas this is the first report of D-0(Th+-C). Both BDEs are observed to be larger than those of their transition metal congeners, TiL+, ZrL+, and HfL+ (L = O and C), believed to be a result of lanthanide contraction. Additionally, the reactions were explored by quantum chemical calculations, including a full Feller-Peterson-Dixon composite approach with correlation contributions up to coupled-cluster singles and doubles with iterative triples and quadruples (CCSDTQ) for ThC, ThC+, ThO, and ThO+, as well as more approximate CCSD with perturbative (triples) [CCSD(T)] calculations where a semi-empirical model was used to estimate spin-orbit energy contributions. Finally, the ThO+ BDE is compared to other actinide (An) oxide cation BDEs and a simple model utilizing An(+) promotion energies to the reactive state is used to estimate AnO(+) and AnC(+) BDEs. For AnO(+), this model yields predictions that are typically within experimental uncertainty and performs better than density functional theory calculations presented previously. Published by AIP Publishing.