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Relevant bibliographies by topics / Polyl

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Academic literature on the topic 'Polyl'

Author: Grafiati

Published: 4 June 2021

Last updated: 13 February 2022

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Journal articles on the topic "Polyl"

1

Ginsburg, Isaac, Ruth Borinski, Milu Sadovnic, Yael Eilam, and Kim Rainsford. "Polyl-histidine." Inflammation 11, no. 3 (September 1987): 253–77. http://dx.doi.org/10.1007/bf00915832.

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Oprisanu, Alexandra, Ioana Georgiana Lazar, Maria Daniela Pop, Eleonora Mihaela Ungureanu, Raluca Isopescu, and Liviu Birzan. "Polyazulenes Based Materials for Heavy Metal Ions Detection." Revista de Chimie 68, no. 10 (November 15, 2017): 2215–18. http://dx.doi.org/10.37358/rc.17.10.5858.

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Azulene is a special monomer used to functionalize electrodes due to its high polarizability, because it makes possible spontaneous electron drift from the five-membered ring to the seven-membered ring. Our study concerns the electrochemical characterization by cyclic voltammetry, differential pulse-voltammetry and rotating disk electrode voltammetry of a new azulene monomer, 4-(5-isopropyl-3,8-dimethylazulen-1-yl)-2,6-bis((E)-2-(thiophen-2-yl)vinyl) pyridine (L). It has been used to obtain complexing modified electrodes by electrochemical polymerization. PolyL films modified electrodes have been characterized by cyclic voltammetry in ferrocene probe solution. The complexing properties of polyL based functional materials have been investigated towards heavy metals (Pb, Cd Hg, Cu) by preconcentration � anodic stripping technique.

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Lazar, Ioana Georgiana, Elena Diacu, George Octavian Buica, Eleonora Mihaela Ungureanu, Georgiana Luiza Arnold, and Liviu Birzan. "The Heavy Metals Sensing Based on 2,6-Bis(-2-(Thiophen-3-yl)Vinyl)-4-(4,6,8-Trimethylazulen-1-yl)Pyrylium Modified Electrodes." Revista de Chimie 68, no. 11 (December 15, 2017): 2509–13. http://dx.doi.org/10.37358/rc.17.11.5917.

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This paper focuses on electrochemical characterization of new azulene compound 2,6-bis((E)-2-(thiophen-3-yl)vinyl)-4-(4,6,8-trimethylazulen-1-yl)pyrylium (L) by cyclic voltammetry (CV), differential pulse voltammetry (DPV), rotating disk electrode voltammetry (RDE) on glassy carbon disk working electrodes. The character of redox processes was established by CV and RDE using increasing scan rates at different scan domains. PolyL modified electrodes have been prepared by scanning or controlled potential electrolysis (CPE). The complexing properties of L and polyL have been investigated towards detection of heavy metal ions by anodic stripping technique. The voltammetric curves present well defined peaks for Pb2+, Cd2+, Cu2+ and Hg2+, which can be used as analytical signals for their determination. The performances of the modified electrodes obtained at different potentials and charges have been evaluated. The best results have been obtained for Pb2+ and Cd2+ with the achievement of detection limits of 10-7 M.

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Pop, Maria Daniela, Oana Brincoveanu, Mihaela Cristea, George Octavian Buica, Marius Enachescu, and Eleonora Mihaela Ungureanu. "AFM and SEM Characterization of Chemically Modified Electrodes Based on 5-[(azulen-1-yl) methylene]-2-thioxothiazolidin-4-one." Revista de Chimie 68, no. 12 (January 15, 2018): 2799–803. http://dx.doi.org/10.37358/rc.17.12.5981.

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Preparation and microscopy characterization of polymer modified glassy carbon electrodes based on (5-[(azulen-1-yl) methylene]-2-thioxothiazolidin-4-one (L) were reported. Atomic Force Microscopy was used to investigate the morphological and mechanical properties of the deposited polyL films onto glassy carbon. The topography images of the analyzed samples exhibited the presence of some columnar shape features onto the layer surfaces. The surface roughness of the layers deposited at constant charge calculated from topography images, increased with the more positive applied potential for controlled potential electrolysis. At different charges, the roughness parameter showed the same behavior for the layers obtained applying a constant potential without having a noticeable influence on the adhesion properties on the substrate. Analysis using scanning electron microscopy shows a relatively uniform surface arrangement of the polymer and the presence of some clusters which are disturbing the planarity. PolyL chemically modified electrodes have been used for heavy metal ions detection with best results for lead.

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Li, Qing, Yiling Zhang, Jingbing Li, Hao Wang, Hui Lu, Honghao Fan, and Gang Zheng. "Stimulatory effects of poly-para-dioxanone, poly L-lactic acid, polycaprolactone, and poly(lactic-co-glycolic acid)/PLLA in rats." Materials Express 9, no. 8 (November 1, 2019): 962–69. http://dx.doi.org/10.1166/mex.2019.1582.

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Numerous fillers are increasingly used for augmenting volume loss and ameliorating facial wrinkles. Collagen stimulants are the most recent next-generation dermal fillers capable of inducing neocollagenesis. To investigate biophysical characteristics, the safety and efficacy of the newly developed combination, poly(L-lactide) or polyl-lactic acid (PLLA) and poly(lactide-co-glycolide) (PLGA), were compared with those of poly-para-dioxanone (PPDO), poly-l-lactic acid (PLLA), and polycaprolactone (PCL) fillers. PPDO, PLLA, PCL, or PLGA/PLLA was injected into the dorsal skin of 8-week-old rats. Tissue samples were obtained 0, 2, and 4 weeks post treatment for Sirius Red-staining, polarized light microscopy, enzyme-linked immunosorbent assay (ELISA), real-time reverse transcription PCR (qRT-PCR), and western blotting. The MagBeads Total RNA Extraction Kit was used to isolate total cell RNA. The PLGA/PLLA filler demonstrated similar neocollagenesis and inflammatory response as other collagen stimulants, and showed better biodegradability than PPDO, PLLA and PCL fillers. Our data suggest that the newly developed collagen-stimulating PLGA/PLLA filler may be a safe and effective option for correcting volume loss and rejuvenating photoaging skin.

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Bello, Jake, Edward N. Granados, Steven Lewinski, Helene R. Bello, and Thomas Trueheart. "Methylated Polyl(L-lysine): Conformational Effects and Interactions with Polynucleotides." Journal of Biomolecular Structure and Dynamics 2, no. 5 (February 1985): 899–913. http://dx.doi.org/10.1080/07391102.1985.10507608.

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Tonegawa, Toru, Toshiyuki Ikoma, Guo Ping Chen, and M. Tanaka. "Control of Protein Initial Burst from Zinc-Hydroxyapatite / Poly(L-Lactide) System." Key Engineering Materials 330-332 (February 2007): 857–60. http://dx.doi.org/10.4028/www.scientific.net/kem.330-332.857.

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Control of protein release without the initial burst from zinc containing hydroxyapatite porous microparticles (Zn-HAp) was investigated with a novel formulation method. The formulation method was a coat of polyL(L-lactide; PLA) on the microparticle with nano-thickness, which obviously suppressed the initial burst of protein release compared with the microparticles without the formulation, the coat of PLA. The HAp/PLA microparticle with 1-20μm of the size distribution was available for the drug delivery carrier of proteins without the degradation.

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Khajeheian, Mohammad B., and Ari Rosling. "Preparation and characterization of linear and star-shaped polyL-lactide blends." Journal of Applied Polymer Science 133, no. 2 (April 11, 2015): n/a. http://dx.doi.org/10.1002/app.42231.

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Bugean, Ioana-Georgiana, Adinuta Paun, Elena Diacu, Mihaela Cristea, Liviu Birzan, and Eleonora-Mihaela Ungureanu. "Chemically Modified Electrodes Based on 4-(azulen-1-yl)-2,6-bis ((e)-2-(thiophen-2-yl)vinyl) Pyrylium Perchlorate." Revista de Chimie 71, no. 9 (September 5, 2020): 113–24. http://dx.doi.org/10.37358/rc.20.9.8322.

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The electrochemical behavior of 4-(azulen-1-yl)-2,6-bis((E)-2-(thiophen-2-yl)vinyl) pyrylium perchlorate (L) was studied by cyclic voltammetry, differential pulse voltammetry, and rotating disk electrode voltammetry. The electrochemical polymerization of L was studied. Modified electrodes covered by polyL films were obtained by successive scanning or by controlled potential electrolysis (CPE) at different charges and potentials. The new electrodes obtained by CPE were applied for sensing the following heavy metals ions: Cu(II), Pb(II), Cd(II), Hg(II). The best results have been registered for Pb(II) ion with a detection limit of 10-8 M.

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Nakamura, Kosuke, Takahiro Ohtsuki, Haruyo Mori, Hiroo Hoshino, Ariful Hoque, Atsushi Oue, Fumie Kano, et al. "Novel anti-HIV-1 activity produced by conjugating unsulfated dextran with polyl-lysine." Antiviral Research 94, no. 1 (April 2012): 89–97. http://dx.doi.org/10.1016/j.antiviral.2012.02.011.

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Dissertations / Theses on the topic "Polyl"

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Duigou, Stéphane. "Caractérisation génétique et fonctionnelle de PolY1 et PolY2 chez B. Subtilis." Paris 6, 2004. http://www.theses.fr/2004PA066451.

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Neumaier, Sebastian, and Axel Polleres. "Geo-Semantic Labelling of Open Data. SEMANTiCS 2018-14th International Conference on Semantic Systems." Elsevier, 2018. http://epub.wu.ac.at/6452/1/neum%2Dpoll%2D2018SEMANTiCS.pdf.

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In the past years Open Data has become a trend among governments to increase transparency and public engagement by opening up national, regional, and local datasets. However, while many of these datasets come in semi-structured file formats, they use di ff erent schemata and lack geo-references or semantically meaningful links and descriptions of the corresponding geo-entities. We aim to address this by detecting and establishing links to geo-entities in the datasets found in Open Data catalogs and their respective metadata descriptions and link them to a knowledge graph of geo-entities. This knowledge graph does not yet readily exist, though, or at least, not a single one: so, we integrate and interlink several datasets to construct our (extensible) base geo-entities knowledge graph: (i) the openly available geospatial data repository GeoNames, (ii) the map service OpenStreetMap, (iii) country-specific sets of postal codes, and (iv) the European Union's classification system NUTS. As a second step, this base knowledge graph is used to add semantic labels to the open datasets, i.e., we heuristically disambiguate the geo-entities in CSV columns using the context of the labels and the hierarchical graph structure of our base knowledge graph. Finally, in order to interact with and retrieve the content, we index the datasets and provide a demo user interface. Currently we indexed resources from four Open Data portals, and allow search queries for geo-entities as well as full-text matches at http://data.wu.ac.at/odgraph/ .

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Bloomer, Melissa. "Polly." Digital Commons at Loyola Marymount University and Loyola Law School, 2019. https://digitalcommons.lmu.edu/etd/787.

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Le, Van-Ly. "Polly two - a public key cryptosystem based on Polly cracker." [S.l. : s.n.], 2003. http://deposit.ddb.de/cgi-bin/dokserv?idn=967582806.

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Trafton, Robin C. Connelly Frances S. "Polly Apfelbaum redefined /." Diss., UMK access, 2007.

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Thesis (M.A.)--Dept. of Art and Art History. University of Missouri--Kansas City, 2007.
"A thesis in art history." Typescript. Advisor: Frances Connelly. Vita. Title from "catalog record" of the print edition Description based on contents viewed Dec. 18, 2007. Includes bibliographical references (leaves 89-95). Online version of the print edition.

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Sunde, Jadranka. "Polya-type inequalities /." Title page, contents and introduction only, 1997. http://web4.library.adelaide.edu.au/theses/09PH/09phs9578.pdf.

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Toh, Chee-Seng. "Alcohol dehydrogenase biosensor based on poly(aniline)-poly(vinylsulfonate) modified electrode and : enhancement effect of CA'2'+ions on the electrocatalytic oxidation of NADH at poly(aniline)-poly(vinylsulfonate) and poly(aniline)-poly(styrenesulfonate)." Thesis, University of Southampton, 2002. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.393941.

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Flugel, Michael. "Synthese und Charakterisierung von Poly(epoxynorbornan) und Poly(epoxycyclohexan)." [S.l. : s.n.], 1999. http://archiv.ub.uni-marburg.de/diss/z1999/0199.

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Jacobs, Jaco. "Poly(N-vinylpyrrolidone) - Poly(γ-benzyl-L-glutamate) conjugates." Stellenbosch : Stellenbosch University, 2012. http://hdl.handle.net/10019.1/20369.

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Thesis (MSc)--Stellenbosch University, 2012.
ENGLISH ABSTRACT: The combination of natural and synthetic polymers allow for the synthesis of advanced hybrid copolymers. These hybrid copolymers have applications in biomedical areas, one such area being in drug delivery systems (DDS). In this study, a modular approach was used to prepare amphiphilic block copolymers with the ability to self-assemble into three dimensional structures. Reversible addition-fragmentation chain transfer (RAFT) was the synthetic tool used to mediate the polymerization of N-vinylpyrrolidone. RAFT is a versatile method to prepare polymers with control over molecular weight and dispersity. A xanthate chain transfer agent (CTA) was used to obtain the hydrophilic poly(N-vinylpyrrolidone) (PVP) block. An aldehyde functionality could be introduced due to the lability of the xanthate moiety, the procedure of which was effectively optimized to produce quantitative conversion. A dixanthate CTA was synthesized to produce a PVP chain which after the modification reaction, resulted in a α,ω-telechelic polymer. A polypeptide was synthesized via the ring-opening polymerization of Ncarboxyanhydrides (ROP NCA). The living and controllable ROP of NCAs is a method which results in polypeptides, but without a well-defined amino acid order. Poly(γ- benzyl-L-glutamate) (PBLG) was synthesized with a narrow dispersity (Đ = 1.10 – 1.15) using conditions that promote the retention of a terminal primary amine. A protected cysteine functionality was introduced via the terminal amine PBLG chain-end, using peptide synthesis techniques. This resulted in the conjugation of the aldehyde functional PVP and the cysteine terminal PBLG using a covalent, non-reducible thiazolidine linkage. The deprotection of the cysteine, more specifically the deprotection of the thiol was a non-trivial procedure. The thiol protecting acetamidomethyl (Acm) group could not be cleaved using traditional methods, but instead a modified procedure was developed to effectively remove the Acm group while inhibiting hydrolysis of the benzyl esters. It was determined that the conjugation reaction could effectively proceed in N,Ndimethylformamide (DMF) at a slightly elevated temperature and so continued to prepare the amphiphilic hybrid block copolymers, PVP-b-PBLG. A structurally different PBLG chain, namely PBLG-b-Cys was conjugated to the ω-aldehyde PVP and the conjugation efficiency was compared to our PBLG-Cys block. In the case of PBLG-b- Cys the in situ deprotection and conjugation as well as a two-step deprotection and conjugation reaction with PVP resulted in very low conjugation efficiency. The cysteine end-functional PBLG resulted in near quantitative conjugation with PVP. The critical micelle concentration (CMC) for PVP90-b-PBLG54 was determined to be 6 μg/mL, using fluorescence spectroscopy. Particle sizes were determined with TEM and DLS and found to range from 25 nm to 120 nm depending on the polymer block lengths as well as hydrophobic/hydrophilic block length ratios. Furthermore, when the micelles were subjected to an increased acidic environment, the labile benzyl ester bonds were hydrolyzed. This was observed with TEM where the particle sizes increased 10-fold to form vesicular structures. Hydrolysis was further confirmed with ATR-FTIR and 1H-NMR spectroscopy. Cytotoxicity tests confirmed that the copolymer micelles had good cell compatibility at high concentrations such as 0.9 mg/mL. Investigation into drug loading using a pyrene probe confirmed the viability of using PVP-b-PBLG as a responsive DDS.
AFRIKAANSE OPSOMMING: Die kombinasie van natuurlike en sintetiese polimere maak dit moontlik vir die sintese van gevorderde hibried kopolimere. Hierdie kopolimere het aanwending in biomediese gebiede, een so 'n gebied is in medisinale vervoer sisteme (MVS). 'n Modulêre benadering is in hierdie studie gebruik om amfifiliese blok kopolimere te berei. Omkeerbare addisie-fragmentasie kettingoordrag (OAFO) is gebruik as die sintetiese tegniek vir die polimerisasie van N-vinielpirolidoon (NVP). OAFO is 'n veelsydige metode om polimere te berei met beheer oor molekulêre gewig en dispersiteit (Đ). 'n Xantaat kettingoordrag agent (KOA) is gebruik om die hidrofiliese poli(N-vinielpirolidoon) (PVP) blok te sintetiseer. ‘n Aldehied endgroep was deur die terminale xantaat funksionaliteit berei, ‘n proses wat geoptimiseer is tot kwantitatiewe omsetting. 'n Di-xantaat KOA is gesintetiseer om, na modifikasie, 'n α, ω-telecheliese polimeer te produseer. Die polipeptied was gesintetiseer deur middel van ’n ringopening polimerisasie van Nkarboksianhidriede (ROP NKA). Die lewende en beheerbare ROP van NKAe is 'n metode wat lei tot polipeptiede sonder ’n gedefinieerde aminosuur volgorde. Poli(γ- benzyl-L-glutamaat) met 'n lae dispersiteit (Đ = 1.10 – 1.15), is gesintetiseer deur gebruik te maak van kondisies wat die behoud van 'n terminale primêre amien bevorder. 'n Beskermde sistien-funksionaliteit is ingebou via die terminale amien met behulp van peptiedsintese tegnieke. Die tiol beskerming van die asetamidometiel (Asm) groep kon nie gekleef word deur gebruik te maak van tradisionele metodes nie, maar ‘n nuwe proses is ontwikkel om die Asm groep te kleef sowel as om die hidrolise van die bensiel esters te inhibeer. Die koppelings reaksie het effektief verloop in DMF by 'n effens verhoogde temperatuur en sodoende is die amfifiliese hibried blok-kopolimere, PVP-b-PBLG berei. Twee verskillende PBLG kettings is gekoppel aan die ω-aldehied PVP en die koppeling doeltreffendheid is vergelyk. Daar is bevind dat net die sistien end-funksionele PBLG tot kwantitatiewe konjugasie kon lei. Die kritiese misel konsentrasie is bepaal vir PVP90-b-PBLG54 as 6 μg/mL met behulp van fluoressensie spektroskopie. Die deeltjie-groottes is bepaal met TEM en DLS en wissel van 25 nm tot 120 nm, afhangende van die polimeer bloklengtes sowel as hidrofobiese / hidrofiliese blok lengte verhoudings. Die miselle is blootgestel aan 'n verhoogde suur omgewing, wat tot die hidrolise van die bensiel ester groepe gelei het. TEM het getoon dat die deeltjie-groottes met 10-voud vergroot het tot vesikulêre strukture. Hidrolise is verder bevestig met ATR-FTIR en 1H-KMR spektroskopie. Sitotoksiese toetse het bevestig dat die miselle geen of min toksisiteit toon teenoor eukariotiese selle nie, selfs teen 'n hoë konsentrasies soos 0.9 mg/ml. Die medisinale behoud vermoë is met behulp van pireen bevestig en dus ook die potensiaal van PVP-b-PBLG as ‘n moontlike MVS.

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Hobson, Rachel Jane. "The structure of poly(vinyl chloride) and poly(acrylonitrile)." Thesis, University of Cambridge, 1993. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.307019.

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Books on the topic "Polyl"

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Bryant, Amy. Polly. New York: HarperCollins, 2007.

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Polly. London: Harper, 2012.

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Polly. Boston, Mass: G.K. Hall, 1987.

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Polly. London: Arrow, 2002.

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Borntrager, Mary Christner. Polly. Waterville, ME: Thorndike Press, 2002.

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Neels, Betty. Polly. Bath: Lythway, 1987.

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Borntrager, Mary Christner. Polly. Scottdale, Pa: Herald Press, 1994.

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Killman, Murray. Polly. [S.l: s.n.], 2000.

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Linde, Freda. Polly Pink. Pretoria: Daan Retief Publishers, 1991.

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Little, Jean. Pretty Polly. New York: Crown Publishers, 1992.

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Book chapters on the topic "Polyl"

1

Steiner, G., and C. Zimmerer. "Poly(adenylic acid) potassium salt (PolyA)." In Polymer Solids and Polymer Melts – Definitions and Physical Properties I, 446–53. Berlin, Heidelberg: Springer Berlin Heidelberg, 2013. http://dx.doi.org/10.1007/978-3-642-32072-9_39.

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Bährle-Rapp, Marina. "poly..., Poly..." In Springer Lexikon Kosmetik und Körperpflege, 435. Berlin, Heidelberg: Springer Berlin Heidelberg, 2007. http://dx.doi.org/10.1007/978-3-540-71095-0_8082.

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Groot, Wim, Jan van Krieken, Olav Sliekersl, and Sicco de Vos. "Production and Purification of Lactic Acid and Lactide." In Poly(Lactic Acid), 1–18. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470649848.ch1.

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Dorgan, John R. "Rheology of Poly(Lactic Acid)." In Poly(Lactic Acid), 125–39. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470649848.ch10.

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Perego, Gabriele, and Gian Domenico Cella. "Mechanical Properties." In Poly(Lactic Acid), 141–53. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470649848.ch11.

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Almenar, Eva, and Rafael Auras. "Permeation, Sorption, and Diffusion in Poly(Lactic Acid)." In Poly(Lactic Acid), 155–79. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470649848.ch12.

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Soto-Valdez, Herlinda. "Migration." In Poly(Lactic Acid), 181–88. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470649848.ch13.

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Lim, Loong-Tak, Kevin Cink, and Tim Vanyo. "Processing of Poly(Lactic Acid)." In Poly(Lactic Acid), 189–215. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470649848.ch14.

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Yu, Long, Eustathios Petinakis, Katherine Dean, and Hongshen Liu. "Poly(Lactic Acid)/Starch Blends." In Poly(Lactic Acid), 217–26. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470649848.ch15.

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Detyothin, Sukeewan, Ajay Kathuria, Waree Jaruwattanayon, Susan E. M. Selke, and Rafael Auras. "Poly(Lactic Acid) Blends." In Poly(Lactic Acid), 227–71. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470649848.ch16.

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Conference papers on the topic "Polyl"

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Kratz, Sven, Don Kimber, Weiqing Su, Gwen Gordon, and Don Severns. "Polly." In the 16th international conference. New York, New York, USA: ACM Press, 2014. http://dx.doi.org/10.1145/2628363.2628430.

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Cunei, Antonio, and Jan Vitek. "PolyD." In the 20th annual ACM SIGPLAN conference. New York, New York, USA: ACM Press, 2005. http://dx.doi.org/10.1145/1094811.1094849.

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Maskey, Ashish, Fransciso Almeida, Carol F. Farver, and Faud Hajjar. "Endobronchial Fibroepithelial Polyp." In American Thoracic Society 2012 International Conference, May 18-23, 2012 • San Francisco, California. American Thoracic Society, 2012. http://dx.doi.org/10.1164/ajrccm-conference.2012.185.1_meetingabstracts.a4566.

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Li, Lingliang, Fujun Zhang, Changrong Guan, Zuliang Zhuo, Bangzhi Cao, and Yitao Liu. "Photoluminescence and photovoltaic performance of poly3-octylthiophene and poly3-alkylthiophene." In 5th International Symposium on Advanced Optical Manufacturing and Testing Technologies, edited by Ya-Dong Jiang, Bernard Kippelen, and Junsheng Yu. SPIE, 2010. http://dx.doi.org/10.1117/12.865727.

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Omiya, Tan, Doudou Fall, and Youki Kadobayashi. "IoT-Poly." In Koli Calling '19: 19th Koli Calling International Conference on Computing Education Research. New York, NY, USA: ACM, 2019. http://dx.doi.org/10.1145/3364510.3364519.

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Dao, Thuy, Todd Roggenbauer, and Jim Colclasure. "STI fill effect on poly-poly comb IL." In 2014 IEEE International Conference on IC Design & Technology (ICICDT). IEEE, 2014. http://dx.doi.org/10.1109/icicdt.2014.6838581.

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Hwang, J. S., G. S. Lee, K. J. Kong, D. J. Ahn, S. W. Hwang, and D. Ahn. "Electrical Conduction Through Poly(dG) Single-stranded, Poly(dC) Single-stranded, and Poly(dG)-poly(dC) Double-stranded DNA Molecules." In 2002 International Conference on Solid State Devices and Materials. The Japan Society of Applied Physics, 2002. http://dx.doi.org/10.7567/ssdm.2002.f-1-6.

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Araneda, E., L. Gargallo, A. Leiva, N. Hadjichristidis, I. Mondragon, D. Radic, A. D’Amore, Domenico Acierno, and Luigi Grassia. "Blends of PEO in Poly(ethylene oxide)∕Poly(2-vinyl pyridine)-b-poly(ethylene oxide)." In V INTERNATIONAL CONFERENCE ON TIMES OF POLYMERS (TOP) AND COMPOSITES. AIP, 2010. http://dx.doi.org/10.1063/1.3455606.

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9

Mohamad, A. S., J. C. Jeynes, and M. P. Hughes. "Dielectrophoresis of poly AT and poly GC DNA Nanomanipulation." In 2012 IEEE 12th International Conference on Nanotechnology (IEEE-NANO). IEEE, 2012. http://dx.doi.org/10.1109/nano.2012.6321928.

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Quattrocchi, C., D. A. dos Santos, J. M. Toussaint, and J. L. Bredas. "Electronic structure of poly(p-phenylene) - poly(acetylene) copolymers." In International Conference on Science and Technology of Synthetic Metals. IEEE, 1994. http://dx.doi.org/10.1109/stsm.1994.834846.

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Reports on the topic "Polyl"

1

Matyjaszewski, Krzysztof, and Jeffrey S. Hrkach. Epoxides as Activators for Grafting of Poly(Tetrahydrofuran) from Poly(Methylphenylsilylene). Fort Belvoir, VA: Defense Technical Information Center, May 1992. http://dx.doi.org/10.21236/ada251086.

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2

Moore, J. A., and Ji-Heung Kim. Blends of Poly(enaminonitriles). Fort Belvoir, VA: Defense Technical Information Center, June 1989. http://dx.doi.org/10.21236/ada208441.

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3

Bruno, Thomas J., Tara J. Fortin, Marcia L. Huber, Arno Laesecke, Eric W. Lemmon, Elisabeth Mansfield, Mark O. McLinden, et al. Thermophysical properties of polyol ester lubricants. Gaithersburg, MD: National Institute of Standards and Technology, August 2019. http://dx.doi.org/10.6028/nist.ir.8263.

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4

Emanuel, Stacy, Sean M. Marsh, Kara Marsh, Jason Fors, Matt Boehmer, and Andrea Zucker. Youth Poll Report and Crosstabulations. Fort Belvoir, VA: Defense Technical Information Center, November 2004. http://dx.doi.org/10.21236/ada431127.

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5

Marsh, Sean M., Kara Marsh, Jason Fors, Stacy Emanuel, and Matt Boehmer. Influencer Poll Report and Crosstabulations. Fort Belvoir, VA: Defense Technical Information Center, November 2004. http://dx.doi.org/10.21236/ada431156.

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Tzamaloukas, Asimakis, and J. J. Garcia-Luna-Aceves. Poll-before-Data Multiple Access. Fort Belvoir, VA: Defense Technical Information Center, January 1999. http://dx.doi.org/10.21236/ada461597.

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Pyda, M., A. Boller, B. Wunderlich, J. Grebowicz, and H. Chuah. Heat capacity of poly(trimethylene terephthalate). Office of Scientific and Technical Information (OSTI), December 1997. http://dx.doi.org/10.2172/554761.

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Haddad, Timothy S., Andre Lee, and Shawn H. Phillips. Poly(Dimethysiloxanes) Modified with Inorganic Polyhedra. Fort Belvoir, VA: Defense Technical Information Center, January 2001. http://dx.doi.org/10.21236/ada410326.

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9

Lin, Terri C. Poly(amido amine) Dendrimers in Supercapacitors. Office of Scientific and Technical Information (OSTI), August 2013. http://dx.doi.org/10.2172/1091321.

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10

Stern, S. A. Mechanisms of gas permeation through polymer membranes: Summary technical report, January 1986--December 1989. [Poly(alkyl methacrylates), poly-(1-trimethylsylil-1-propyne), and poly(vinyl acetate)]. Office of Scientific and Technical Information (OSTI), January 1989. http://dx.doi.org/10.2172/6182255.

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