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Publication Metadata only A coarse graining approach in molecular simulations: fuzzy potentials(Istanbul Technical University, 2003) Department of Chemistry; Department of Chemistry; Yurtsever, İsmail Ersin; Eşsiz, Şebnem; Faculty Member; Undergraduated Student; Department of Chemistry; College of Sciences; College of Sciences; 7129; 191615A new representation for interaction potential functions is presented. Unlike the orthodox approaches, the potential function is not a fixed function in terms of internuclear coordinates but a probabilistic one which contains information over a wide range of angular degrees of freedom. It is shown that such approaches can provide practical solutions for bulk systems of high density.Publication Metadata only A two-dimensional Monte Carlo polymerization of 5-membered rings(Scientific Technical Research Council Turkey, 1997) Esentürk, O.; Pamuk, H. A.; Department of Chemistry; Yurtsever, İsmail Ersin; Faculty Member; Department of Chemistry; College of Sciences; 7129A modification of the kinetic growth model in two dimensions for the polymerization of 5-membered rings is presented. The preliminary results reveal the validity of the modified model.Publication Open Access CO2 absorption into primary and secondary amine aqueous solutions with and without copper ions in a bubble column(TÜBİTAK, 2022) Güler, Cansu; Uzunlar, Erdal; Department of Chemical and Biological Engineering; Erkey, Can; Yousefzadeh, Hamed; Faculty Member; Researcher; Department of Chemical and Biological Engineering; College of Engineering; 29633; N/AChemical absorption of CO2 into aqueous amine solutions using a nonstirred bubble column was experimentally investigated. The performance of CO2 absorption of four different primary and secondary amines including monoethanolamine (MEA), piperazine (PZ), 2-piperidineethanol (2PE), and homopiperazine (HPZ) were compared. The effects of initial concentration of amine, the inlet mole fraction of CO2, and solution temperature on the rate of CO2 absorption and CO2 loading (mol CO2/mol amine) were studied in the range of 0.02–1 M, 0.10–0.15, and 25–40 °C, respectively. The effect of the presence of copper ions in the amine solution on CO2 loading was also studied. By comparison of the breakthrough curves of the amines at different operational conditions, it was revealed that the shortest and longest time for the appearance of the breakthrough point was observed for MEA and HPZ solutions, respectively. CO2 loading of MEA, 2PE, PZ, and HPZ aqueous solutions at 25 °C, 0.2 M of initial concentration of amine, and 0.15 of inlet mole fraction of CO2 were 1.06, 1.14, 1.13, and 1.18 mol CO2/mol amine, respectively. By decreasing the inlet mole fraction of CO2 from 0.15 to 0.10, CO2 loading slightly decreased. As the initial concentration of amine and temperature decreased, CO2 loading increased. Also, the presence of copper ions in the absorbent solution resulted in a decrease in the CO2 loading of MEA and HPZ aqueous solutions. In case of PZ and 2PE amines, adding copper ions led to precipitation even at low copper ion concentrations.Publication Metadata only Competitive hydrogen bonding in aspirin-aspirin and aspirin-leucine interactions(Scientific Technical Research Council Turkey-Tubitak, 2012) Department of Chemistry; Department of Chemical and Biological Engineering; Department of Chemistry; Yurtsever, Zeynep; Erman, Burak; Yurtsever, İsmail Ersin; Undergraduate Student; Faculty Member; Faculty Member; Department of Chemical and Biological Engineering; Department of Chemistry; College of Sciences; College of Engineering; College of Sciences; N/A; 179997; 7129Aspirin-aspirin and aspirin-leucine interactions are studied by the density functional theory (DFT) and high level ab initio calculations with second order Moller-Plesset perturbation theory (MP2). The rotational isomers of aspirin are identified by their relative stability both in gaseous phase and in water using the polarizable continuum method (PCM). Local minima of aspirin monomers in water are found to be all highly populated compared to the gas phase behavior. Homodimers of aspirin form hydrogen bonds with bond energies of 10 kcal/mol. Weak hydrogen bonds utilizing phenyl and methyl groups are also found. The interaction between aspirin and leucine is stronger with relatively short bond lengths compared to homodimeric aspirin interactions. The potential energy surface has several minima with comparable stability. This study shows the significance of diverse bonding schemes, which are important for understanding complete interaction mechanisms of aspirin.Publication Open Access Dimerization of pyrrole(TÜBİTAK, 1998) Yurtsever, Mine; Department of Chemistry; Yurtsever, İsmail Ersin; Faculty Member; Department of Chemistry; College of Sciences; 7129Accurate ab-inito quantum mechanical calculations of pyrrole dimers are reported. The thermodynamical stabilities of dimers with alpha - alpha, alpha -beta, and beta - beta type linkages are compared in order to predict the possibilities of branching in polypyrroles. Calculations employing large basis sets and including electron correlation effects predict the alpha - alpha dimers as the most stable form. However, an alpha - beta type bonding requires only 1.5-2.0 kcal/mol, and the energy necessary to introduce a beta - beta type bond is 3.6-4.0 kcal/mol. These values show that a high degree of branching is possible even at room temperatures.Publication Metadata only Dissociation dynamics of small carbon clusters(Scientific Technical Research Council Turkey, 1997) Elmacı, Nuran; Department of Chemistry; Yurtsever, İsmail Ersin; Faculty Member; Department of Chemistry; College of Sciences; 7129The dissociation dynamics of small carbon clusters is studied by classical trajectory analysis. A large number of initial conditions are chosen to analyze the effects of the energy, angular momentum and the initial geometry of the cluster. The dissociation times, decay rate constants, kinetic energy of the dissociating atoms and the geometrical structure of the remaining part of the clusters are computed from microcanonical sampling of the phase space. Distributions of these properties as well as the possibilities of various fragmentation channels are presented.Publication Metadata only Enhanced ionic conductivity and mechanical strength in nanocomposite electrolytes with nonlinear polymer architectures(TÜBİTAK, 2023) N/A; Department of Chemical and Biological Engineering; N/A; Bakar, Recep; Şenses, Erkan; Darvishi, Saeid; PhD Student; Faculty Member; PhD Student; Department of Chemical and Biological Engineering; Koç University Boron and Advanced Materials Application and Research Center (KUBAM) / Koç Üniversitesi Bor ve İleri Malzemeler Uygulama ve Araştırma Merkezi (KUBAM); Koç University Surface Science and Technology Center (KUYTAM) / Koç Üniversitesi Yüzey Teknolojileri Araştırmaları Merkezi (KUYTAM); Graduate School of Sciences and Engineering; College of Engineering; Graduate School of Sciences and Engineering; N/A; 280298; N/ASolvent-free polymer-based electrolytes (SPEs) have gained significant attention to realize safer and flexible lithium-ion batteries. Among all polymers used for preparing SPEs electrolytes, poly(ethylene oxide), a biocompatible and biodegradable polymer, has been the most prevalent one mainly because of its high ionic conductivity in the molten state, the capability for the dissolution of a wide range of different lithium salts as well as its potential for the environmental health and safety. However, linear PEO is highly semicrystalline at room temperature and thus exhibits weak mechanical performance. Addition of nanoparticles enhances the mechanical strength and effectively decreases the crystallization of linear PEO, yet enhancement in mechanical performance often results in decreased ionic conductivity when compared to the neat linear PEO-based electrolytes; new strategies for decoupling ionic conductivity from mechanical reinforcement are urgently needed. Herein, we used lithium bis(trifluoromethane-sulfonyl)-imide (LiTFSI) salts dissolved in various nonlinear PEO architectures, including stars (4-arms and 8-arms) and hyperbranched matrices, and SiO2 nanoparticles (approximately equal to 50 nm diameter) as fillers. Compared to the linear PEO chains, the room temperature crystallinity was eliminated in the branched PEO architectures. The electrolytes with good dispersion of the nanoparticles in the nonlinear PEOs significantly enhanced ionic conductivity, specifically by approximately equal to 40% for 8-arm star, approximately equal to 28% for 4-arms star, and approximately equal to %16 for hyperbranched matrices, with respect to the composite electrolyte with the linear matrix. Additionally, the rheological results of the SPEs with branched architectures show more than three orders of magnitude enhancement in the low-frequency moduli compared to the neat linear PEO/Li systems. The obtained results demonstrate that the solvent-free composite electrolytes made of branched PEO architectures can be quite promising especially for irregularly shaped and environmentally benign battery applications suitable for medical implants, wearable devices, and stretchable electronics, which require biodegradability and biocompatibility. © TÜBİTAK.Publication Metadata only Exploration of novel 6,8,9-trisubstituted purine analogues: synthesis, in vitro biological evaluation, and their effect on human cancer cells(Tubitak Scientific & Technological Research Council Turkey, 2024) Polat, Muhammed Fatih; Atalay, Rengul; Tuncbilek, Meral; N/A; Şahin, İrem Durmaz; Koç University Research Center for Translational Medicine (KUTTAM); School of MedicineCancer, a leading global cause of mortality, demands continuous advancements in therapeutic strategies. This study focuses on the design and synthesis of a novel series of purine derivatives, specifically 6 -(substituted phenyl piperazine)-8-(4-phenoxyphenyl)9-cyclopentyl purine derivatives (5-11). The motivation behind this endeavor lies in addressing acquired resistance mechanisms in cancer cells, a significant hurdle in current treatment modalities. The synthesis, starting from 4,6-dichloro-5-nitropyrimidine, involves a multi -step process, resulting in seven new purine derivatives. Biological evaluation against human liver, colon, and breast cancer cells (Huh7, HCT116, and MCF7, respectively) was performed using the SRB assay. Among the synthesized analogs, compounds 5 and 6, exhibited notable cytotoxic activity, surpassing clinically used positive controls 5-Fluorouracil and Fludarabine in terms of efficacy. This research underscores the potential of purine derivatives with a phenyl group at the C-8 position as a scaffold for developing compounds with improved anticancer properties. The findings offer insights for future exploration and development of novel agents in cancer pharmaceutical research.Publication Open Access Genetic algorithm-driven surface-enhanced Raman spectroscopy substrate optimization(Multidisciplinary Digital Publishing Institute (MDPI), 2021) Yanık, Cenk; Department of Electrical and Electronics Engineering; N/A; Onbaşlı, Mehmet Cengiz; Bilgin, Buse; Torun, Hülya; Faculty Member; Department of Electrical and Electronics Engineering; Koç University Research Center for Translational Medicine (KUTTAM) / Koç Üniversitesi Translasyonel Tıp Araştırma Merkezi (KUTTAM); College of Engineering; Graduate School of Sciences and Engineering; 258783; N/A; N/ASurface-enhanced Raman spectroscopy (SERS) is a highly sensitive and molecule-specific detection technique that uses surface plasmon resonances to enhance Raman scattering from analytes. In SERS system design, the substrates must have minimal or no background at the incident laser wavelength and large Raman signal enhancement via plasmonic confinement and grating modes over large areas (i.e., squared millimeters). These requirements impose many competing design constraints that make exhaustive parametric computational optimization of SERS substrates pro-hibitively time consuming. Here, we demonstrate a genetic-algorithm (GA)-based optimization method for SERS substrates to achieve strong electric field localization over wide areas for recon-figurable and programmable photonic SERS sensors. We analyzed the GA parameters and tuned them for SERS substrate optimization in detail. We experimentally validated the model results by fabricating the predicted nanostructures using electron beam lithography. The experimental Raman spectrum signal enhancements of the optimized SERS substrates validated the model predictions and enabled the generation of a detailed Raman profile of methylene blue fluorescence dye. The GA and its optimization shown here could pave the way for photonic chips and components with arbitrary design constraints, wavelength bands, and performance targets.Publication Metadata only In silico design of novel and highly selective lysine-specific histone demethylase inhibitors(Scientific Technical Research Council Turkey-Tubitak, 2011) Akdogan, Ebru Demet; Yelekci, Kemal; Department of Chemical and Biological Engineering; Erman, Burak; Faculty Member; Department of Chemical and Biological Engineering; College of Engineering; 179997Histone lysine-specific demethylase (LSD1) is involved in a wide range of epigenetic processes and plays important roles in gene silencing, DNA transcription, DNA replication, DNA repair, and heterochromatin formation. Its active site shows a resemblance to those of 2 homologous enzymes, monamine oxidase A and B (MAO-A and MAO-B.) In the present work, starting from suitable scaffolds and generating thousands of structures from them, 10 potential inhibitors were obtained with structural and physicochemical properties selectively suitable for inhibiting LSD1. iLib Diverse software was used to generate the diverse structures and 3 docking tools, CDOCKER, GOLD, and AutoDock, were used to find the most probable potential inhibitor based on its binding affinity. The dispositions of the candidate molecules within the organism were checked by ADMET_PSA_2D (polar surface area) versus ADMET_AlogP98 (the logarithm of the partition coefficient between n-octanol and water), and their suitability is discussed. The LSD1 inhibition activities of the candidates were compared with the properties of trans-2-phenylcyclopropylamine (tranylcypromine) and 2-(4-methoxy-phenyl) cyclopropylamine, which are the 2 known inhibitors of LSD1.