Relevant bibliographies by topics / Monolayer structure

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  1. Journal articles
  2. Dissertations / Theses
  3. Books
  4. Book chapters
  5. Conference papers
  6. Reports

Academic literature on the topic 'Monolayer structure'

Author: Grafiati
Published: 4 June 2021
Last updated: 4 February 2022

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Journal articles on the topic "Monolayer structure"

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Kajiyama, Tisato. "Novel Concepts of the Aggregation Structure of Organic Monolayers on the Surface of Water." MRS Bulletin 20, no. 6 (June 1995): 32–38. http://dx.doi.org/10.1557/s0883769400036952.

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Langmuir-Blodgett (LB) films have been applied to molecular electronics, nonlinear optics, and biosensors. Their useful properties can be accessed by using a defect-free monolayer—the precursor of LB films. In order to prepare a defect-free or defect-diminished monolayer, it is necessary to estimate the molecular arrangements and structural defects in the monolayer. The actual structure of monolayers on the surface of water have been proposed on the basis of recent morphological and structural studies. Molecular-aggregation processes or monolayer-formation processes do not always match the general concept concluded from surface pressure-area (π-A) isotherms. Therefore, a universal understanding has not been reached. Here we present a novel and systematic classification for the aggregation structure of monolayers on the water surface and also demonstrate how to prepare defect-diminished monolayers.
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Kazak, Alexandr, Margarita Marchenkova, Antonina Smirnova, Tatiana Dubinina, Alexey Seregin, Alexandr Rogachev, and Nadezhda Usol'tseva. "Thin-film materials based on phthalocyanine derivatives: structure and physico-chemical properties." ITM Web of Conferences 30 (2019): 08006. http://dx.doi.org/10.1051/itmconf/20193008006.

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In order to establish the effect of the molecular structure of mix-substituted phthalocyanine derivatives on its supramolecular organization in thin-films, the floating layers of three A3B-type phthalocyanine derivatives were obtained. Their supramolecular organization was determined and it was found that the studied compounds form homogeneous stable floating layers on the water surface. Structure parameters of floating layers depend both on the length of aliphatic substituents (R = CnH2n+1) and the metal complexing agent. Ligands I and II form stable monolayer structures, which the layer packing periods increase with the elongation of aliphatic substituents: the lattice parameter (d) is 1.93 and 2.3 nm for ligands I (n = 6) and II (n = 8), correspondingly. During further compression of the formed monolayers, ligands I and II form stable bilayers, in which the arrangement of molecules remains similar to the structure of the previous monolayers. These bilayers contain minor inclusions of 3D aggregates. Metal complex III forms only stable monolayer (d = 2.06 nm), upon further compression of which 3D- aggregates included in the monolayer are formed.
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Martínez, Hector, Enrique Chacón, Pedro Tarazona, and Fernando Bresme. "The intrinsic interfacial structure of ionic surfactant monolayers at water–oil and water–vapour interfaces." Proceedings of the Royal Society A: Mathematical, Physical and Engineering Sciences 467, no. 2131 (February 16, 2011): 1939–58. http://dx.doi.org/10.1098/rspa.2010.0516.

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Using computer simulations, we investigate the interfacial structure of sodium dodecyl sulphate (SDS) monolayers adsorbed at the water surface and water–oil interfaces. Using an algorithm that removes the averaging effect of the capillary waves, we obtain a detailed view of the solvation structure of water around the monolayer. We investigate surface concentrations between 45 and 33 Å 2 per surfactant, which are near experimental conditions corresponding to the critical micellar concentration and the formation of Newton black films. The surfactants induce a layering structure in water, which disappears at approximately 1 nm from the monolayer plane. The water molecules exhibit a preferred orientation with the dipoles pointing towards the monolayer. The orientational order decays slowly, but it does not influence the hydrogen bond structure of water, which is significantly disrupted in the interfacial region only. These structural changes are qualitatively the same in SDS–water and oil–SDS–water interfaces. In the latter case, we find a small degree of penetration of oil in the monolayer (between 0.2 and 0.25 molecules per SDS). This small penetration has a measurable effect on the monolayer, which increases its thickness by approximately 10 per cent. The bending modulus of the SDS monolayers is of the order of the thermal energy, k B T .
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Herr, Brian R., and Chad A. Mirkin. "Self-Assembled Monolayers of Ferrocenylazobenzenes: Monolayer Structure vs Response." Journal of the American Chemical Society 116, no. 3 (February 1994): 1157–58. http://dx.doi.org/10.1021/ja00082a058.

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Zhang, Bo, Tomas Mikysek, Veronika Cicmancova, Stanislav Slang, Roman Svoboda, Petr Kutalek, and Tomas Wagner. "2D GeSe2 amorphous monolayer." Pure and Applied Chemistry 91, no. 11 (November 26, 2019): 1787–96. http://dx.doi.org/10.1515/pac-2019-0501.

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Abstract In this paper, GeSe2 thin film and glass ingot were prepared in a layered structure. Subsequently, the 2D amorphous monolayers were achieved from layered thin film and layered glass ingot. The thicknesses of monolayers from thin film range from 1.5 nm to 5 nm. And the thickness of monolayer from glass ingot is 7 μm. The fast cooling of material results in the formation of self-assembled monolayers. In the case of thin film, layers are connected with “bridge”. After doping of Ag, the precipitation of nano particles exfoliates the adjacent monolayers which can be further dispersed by etching of Ag particles. In the case of glass ingot, the composition changes at 1 % between adjacent monolayers, according to EDX (energy-dispersive X-ray spectroscopy) spectra. And the glass 2D monolayer can be mechanically peeled off from the glass ingot.
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Dabkowska, A. P., D. J. Barlow, A. V. Hughes, R. A. Campbell, P. J. Quinn, and M. J. Lawrence. "The effect of neutral helper lipids on the structure of cationic lipid monolayers." Journal of The Royal Society Interface 9, no. 68 (August 10, 2011): 548–61. http://dx.doi.org/10.1098/rsif.2011.0356.

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Successful drug delivery via lipid-based systems has often been aided by the incorporation of ‘helper lipids’. While these neutral lipids enhance the effectiveness of cationic lipid-based delivery formulations, many questions remain about the nature of their beneficial effects. The structure of monolayers of the cationic lipid dimethyldioctadecylammonium bromide (DODAB) alone, and mixed with a neutral helper lipid, either diolelyphosphatidylethanolamine or cholesterol at a 1 : 1 molar ratio was investigated at the air–water interface using a combination of surface pressure–area isotherms, Brewster angle microscopy (BAM) and specular neutron reflectivity in combination with contrast variation. BAM studies showed that while pure DODAB and DODAB with cholesterol monolayers showed fairly homogeneous surfaces, except in the regions of phase transition, monolayers of DODAB with diolelyphosphatidylethanolamine were, in contrast, inhomogeneous exhibiting irregular bean-shaped domains throughout. Neutron reflectivity data showed that while the thickness of the DODAB monolayer increased from 17 to 24 Å as it was compressed from a surface pressure of 5–40 mN m −1 , the thickness of the helper lipid-containing monolayers, over the same range of surface pressures, was relatively invariant at between 25 and 27 Å. In addition, the monolayers containing diolelyphosphatidylethanolamine were found to be more heavily hydrated than the monolayers of cationic lipid, alone or in combination with cholesterol, with hydration levels of 18 molecules of water per molecule of lipid being recorded for the diolelyphosphatidylethanolamine-containing monolayers at a surface pressure of 30 mN m −1 compared with only six and eight molecules of water per molecule of lipid for the pure DODAB monolayer and the cholesterol-containing DODAB monolayer, respectively.
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Somorjai, G. A., and U. Starke. "Monolayer surface structure analysis." Pure and Applied Chemistry 64, no. 4 (January 1, 1992): 509–27. http://dx.doi.org/10.1351/pac199264040509.

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Голубев, О. Л. "Некоторые особенности конденсации атомов кремния на поверхности монокристалла вольфрама." Журнал технической физики 90, no. 3 (2020): 465. http://dx.doi.org/10.21883/jtf.2020.03.48933.283-19.

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Using the methods of the field emission microscopy, the condensation of Si on the W surface at various temperatures T of the substrate and numbers n of monoatomic layers of the deposited condensate is studied. At low temperatures T ~ 600 K, a low-temperature Si-monolayer with the structure of pure W is formed on the surface, whereas another structure of a high-temperature monolayer, namely surface siliside is formed at T > 1000 K. The low-temperature monolayer and surface siliside are differ in their orienting effect when constructing the Si layers. In the case of condensation on a low-temperature monolayer, crystallites of Si are formed starting already from the third monolayer at n > 3, whereas the Si crystallites grow during the condensation on surface siliside starting from n > 300 monolayers. The energy activation of the volume diffusion Qdif of the Si-atoms into W and desorption Qdes from W surface are determined.
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Zhou, Yuan, Xiao Fang Bi, Jia Xiang Shang, and Hui Bin Xu. "Study of Electronic Structure In Ni3Fe/Al2O3/Ni3Fe Magnetic Tunnel Junction with Various Ferromagnetic Layer Thicknesses." Materials Science Forum 475-479 (January 2005): 3909–14. http://dx.doi.org/10.4028/www.scientific.net/msf.475-479.3909.

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A series models of Ni3Fe/Al2O3/Ni3Fe magnetic tunnel junction with Al-terminated interfaces have been established for investigating the influence of ferromagnetic layer thickness on the electronic structure, employing first-principle methods based on local spin-density approximation theory. The spin polarization of the interfacial Ni3Fe monolayer shows a maximum value as the thickness of ferromagnetic layer increases. The Al monolayers at the ferromagnetic/insulating interface and the O monolayer in the interior of insulating layer are also studied in terms of the change of spin polarization with the ferromagnetic layer thickness. In addition, we have found that the structure of Ni3Fe monolayer has a great influence on the spin polarization.
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Razinkov, Vladimir I., Grigory B. Melikyan, Richard M. Epand, Raquel F. Epand, and Fredric S. Cohen. "Effects of Spontaneous Bilayer Curvature on Influenza Virus–mediated Fusion Pores." Journal of General Physiology 112, no. 4 (October 1, 1998): 409–22. http://dx.doi.org/10.1085/jgp.112.4.409.

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Cells expressing the hemagglutinin protein of influenza virus were fused to planar bilayer membranes containing the fluorescent lipid probes octadecylrhodamine (R18) or indocarbocyanine (DiI) to investigate whether spontaneous curvature of each monolayer of a target membrane affects the growth of fusion pores. R18 and DiI lowered the transition temperatures for formation of an inverted hexagonal phase, indicating that these probes facilitate the formation of negative curvature structures. The probes are known to translocate from one monolayer of a bilayer membrane to the other in a voltage-dependent manner. The spontaneous curvature of the cis monolayer (facing the cells) or the trans monolayer could therefore be made more negative through control of the polarity of voltage across the planar membrane. Electrical admittance measurements showed that the open times of flickering fusion pores were shorter when probes were in trans monolayers and longer when in cis monolayers compared with times when probe was symmetrically distributed. Open times were the same for probe symmetrically distributed as when probes were not present. Thus, open times were a function of the asymmetry of the spontaneous curvature between the trans and cis monolayers. Enriching the cis monolayer with a negative curvature probe reduced the probability that a small pore would fully enlarge, whereas enriching the trans monolayer promoted enlargement. Lysophosphatidylcholine has positive spontaneous curvature and does not translocate. When lysophosphatidylcholine was placed in trans leaflets of planar membranes, closing of fusion pores was rare. The effects of the negative and positive spontaneous curvature probes do not support the hypothesis that a flickering pore closes from an open state within a hemifusion diaphragm (essentially a “flat” structure). Rather, such effects support the hypothesis that the membrane surrounding the open pore forms a three-dimensional hourglass shape from which the pore flickers shut.
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Dissertations / Theses on the topic "Monolayer structure"

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Wei, Ling 1961. "Structure and reactivity of monolayer and micelle interfaces." Thesis, McGill University, 1992. http://digitool.Library.McGill.CA:80/R/?func=dbin-jump-full&object_id=56973.

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The research in this thesis is focused on the structure and reactivity of monolayer and micelle interfaces.
The kinetic results of ring formations of a series of $ sigma$-($ omega$-bromoalkoxy)phenoxides in a cationic micellar environment (CTAB) revealed that the ring closure rate constants from the 7-membered ring to the 14-membered ring decrease by $ sim$6-fold. This is much smaller than that observed for a homogeneous reaction environment ($ sim$1500-fold). In addition, micellar effective molarities (EM)$ sb{ rm m}$ for these reactions are found to be 7 to 1900 fold greater than in homogeneous solution. This catatysis can be reasoned to originate from an increase in the ground-state free energy of the substrate induced by localization of the phenolate oxygen and alkyl bromide moieties at the polar micelle interface.
Monolayer isotherm studies establish a dependence of isotherm features on the structure of the phospholipid. It is found that the liftoff area increases as the position of the second hydrophilic group is located further from the dominate polar group. The transition pressure reaches its highest value when the substituent is in the 7-position. The condensed area for almost all these substrates gives nearly the same value ($ sim$45 A$ sp2$/molecule). These may be explained by that the molecules lie flatly on the air/water interface at high surface concentration after which the hydrophobic parts in a molecule are forced out of the water surface. The hydrophilic groups remain on the water surphase so as to produce a loop conformation. At high pressure all the molecules are approximately perpendicular to the water surface so as to form a highly dense packing state. The unusually broad first order phase transition in isotherms of some boloform and macrocyclic phospholipids is consistent with these substrates being reorientated at large areas to yield stable bilayers, trilayers, etc.
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York, Ian. "Structure and reactivity of titania-supported bismuth molybdates." Thesis, Brunel University, 2000. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.311658.

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Arnold, Thomas. "The adsorption of alkanes from their liquids and binary mixtures." Thesis, University of Oxford, 2001. http://ethos.bl.uk/OrderDetails.do?uin=uk.bl.ethos.249654.

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Rödner, Sandra. "Interfacial colloidal particle films and their structure formation." Licentiate thesis, KTH, Chemistry, 2002. http://urn.kb.se/resolve?urn=urn:nbn:se:kth:diva-1505.

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Abstract to“Interfacial colloidal particle films andtheir structure formation”; a licentiate thesis, whichwill be presented by Sandra Rödner in Q2, 29 November 2002at 13.00.

Colloidal particles can be made to organise themselves intoordered arrays. These colloidal structures acquire interestingand useful properties, not only from their constituentmaterials but also from the spontaneous emergence of mesoscopicorder that characterises their internal structure. Orderedarrays of colloidal particles, with lattice constants rangingfrom a few nanometers to a few microns, have potentialapplications as optical computing elements and chemicalsensors, and also has an important influence on the mechanicalproperties and optical appearance of paint films and papercoatings.

The control of colloidal structure formation starts with theparticle interactions (attractive or repulsive) and colloidaldynamics, which is the topic of this thesis. To enable adetailed understanding of the different factors that controlthe formation of dense 2D colloidal films, a method forstructural characterisation was developed. The degree of orderin the hexagonal close-packed structure, displayed by thecolloidal films, was characterised by the size of ordereddomains and by the distribution of pore sizes. The size ofordered domains was obtained from the pair distributionfunction, and the distribution of pores from a Delaunaytriangulation procedure. These methods are based on theparticle positions in the film, which were determined by lightmicroscopy and processed digital images.

The two methods were used to study the effect of particleinteractions on the structure of colloidal monoparticulatefilms, formed at the air-liquid interface. The size of theordered domains decreased exponentially with increasing bondstrength, while the pore density increased. The transfer andsubsequent drying of the formed film on a solid substrateinduced structural changes; the capillary forces transformedsmall pores into triangular order while some of the largervoids and cracks increased in size.

The structural features of colloidal monolayers, formed bydrying a dilute silica suspension on a substrate, wereinvestigated. Addition of small amounts of salt resulted indrastic changes of the particle film structure. The size of theordered domains decreased exponentially with increasing amountsof added salt (0-2.9% NaCl/Silica ratio), with a simultaneousincrease of the concentration of large defects. This suggeststhat loss of colloidal stability and onset of particle adhesionto the substrate inhibit rearrangement and ordering. Theevaporation rate was controlled by varying the relativehumidity during drying. Colloidal monolayers with the largestordered domains and the lowest concentration of stacking faultswere formed at an intermediate humidity (55% RH).

The rearrangement process during drying of dilute silicasuspensions was followed in detail by studying the changes inthe structural features during growth of colloidal monolayers.Low crystal growth rate promoted the transition of squarelattice domains to a hexagonal close-packed structure. Additionof salt to the electrostatically stabilised dispersionincreased the formation of square structured regions at thecrystal-suspension interface, due to increasing adhesion to thesubstrate. The loss of colloidal stability inhibited therearrangement process, resulting in higher concentrations ofsquare lattice domains at large distances from the crystal edgecompared to systems without added salt.

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Kaur, Sandeep. "Modify the electronic structure of monolayer MoS2 through electron-beam-activated fluorination." Thesis, Uppsala universitet, Institutionen för fysik och astronomi, 2020. http://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-426011.

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Mohammed, Avaise [Verfasser], and Hidenori [Akademischer Betreuer] Takagi. "Structure and electronic properties of epitaxial monolayer WSe2 / Avaise Mohammed ; Betreuer: Hidenori Takagi." Stuttgart : Universitätsbibliothek der Universität Stuttgart, 2019. http://d-nb.info/1215573952/34.

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Castorano, Nicholas Joseph. "The Structure and Dynamics of Diacetylene-Lipid Langmuir Monolayers." Case Western Reserve University School of Graduate Studies / OhioLINK, 2010. http://rave.ohiolink.edu/etdc/view?acc_num=case1279558411.

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Zhang, Minhui. "Investigation of structure and permeability of surfaces modified with self-assembled monolayers." Thesis, This resource online, 1996. http://scholar.lib.vt.edu/theses/available/etd-08222008-063703/.

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Becfraft, Kevin Allan. "In-situ spectroscopic investigations of molecular structure at aqueous/solid and aqueous/monolayer/solid interfaces /." view abstract or download file of text, 2004. http://wwwlib.umi.com/cr/uoregon/fullcit?p3147813.

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Thesis (Ph. D.)--University of Oregon, 2004.
Typescript. Includes vita and abstract. Includes bibliographical references (leaves 163-173). Also available for download via the World Wide Web; free to University of Oregon users.
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Li, Huimin. "Relationship between molecular structure and surface properties of self-assembled monolayers." Diss., Virginia Tech, 2004. http://hdl.handle.net/10919/29056.

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Polyimides are frequently used as insulating layers in the microelectronics industry. These polymers are tough, have high thermal stability, and have favorable dielectric properties; consequently, polyimides are excellent materials for insulating layers in microelectronic devices. In this research, self-assembled monolayers are investigated for use as an adhesion promoter for metal substrates, and for corrosion protectors of the metal surface. Gold substrates modified by adsorption of 3- and 4-aminothiophenol monolayers, 3- and (4-mercaptophenyl) phthalimide (MPP) monolayers, and by reaction of the 3- and 4-aminothiophenol monolayers with the phthalic anhydride were studied using reflection absorption infrared spectroscopy, contact angle measurement, ellipsometry, and electrochemical measurements. Reactions on the monolayers are used to model the attachment of an insulating polyimide to the substrate. The covalent attachment of the anhydride is confirmed, and the efficiency of the reaction of the aminothiolphenol monolayers is investigated. The reactivity of the aminothiolphenol monolayers is found to depend on the position of the amino-group around the phenyl ring. Impedance spectroscopy is used to investigate the ionic insulating properties of these systems. The 4-mercaptophthalimide monolayer is found to have the highest monolayer resistance to ion transport. This result suggests that it forms the most densely packed monolayer. The monolayer resistance of the surfaces prepared by adsorption of the aminothiolphenol isomers followed by reaction with phthalic anhydride is much lower than the corresponding deposited mercaptophthalimide monolayers. These results suggest that the reaction efficiency is low. Impedance spectroscopy and polarization measurements suggests a higher protection efficiency for 3-mercaptophenylphthalimide. These results will be discussed in the context of the ability of the isomeric mercaptophthalimide monolayers to serve as protectors against substrate corrosion.
Ph. D.
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Books on the topic "Monolayer structure"

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Birdi, K. S. Self-assembly monolayer structures of lipids and macromolecules at interfaces. New York: Kluwer Academic, 2002.

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Birdi, K. S. Self-assembly monolayer structures of lipids and macromolecules at interfaces. New York: Kluwer Academic/Plenum Publishers, 1999.

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D, Möbius, and Miller Reinhard, eds. Organized monolayers and assemblies: Structure, processes, and function. Amsterdam: Elsevier, 2001.

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Organized Monolayers and Assemblies: Structure, Processes and Function. Elsevier, 2002. http://dx.doi.org/10.1016/s1383-7303(02)x8001-6.

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Birdi, K. S. Self-Assembly Monolayer Structures of Lipids and Macromolecules at Interfaces. Springer, 2013.

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Self-Assembly Monolayer Structures of Lipids and Macromolecules at Interfaces. Boston: Kluwer Academic Publishers, 2002. http://dx.doi.org/10.1007/b114152.

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Shin, Seokmin. Theoretical studies of the structure and phase transitions of liquid supported monolayers. 1992.

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(Editor), Dietmar Mobius, and Reinhard Miller (Editor), eds. Organized Monolayers and Assemblies: Structure, Processes and Function (Studies in Interface Science). Elsevier Science, 2002.

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Cai, Zhonghou. The structure of the liquid metal-adsorbate interface and phase transitions in Langmuir monolayers. 1991.

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Fleming, Ingrid, Brenda R. Kwak, and Merlijn J. Meens. The endothelial cell. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780198755777.003.0006.

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The endothelium, a monolayer of cells that lines blood vessels, acts as a physical barrier between circulating blood and vascular smooth muscle cells. The purpose of this chapter is to provide a general overview on the structural heterogeneity of the endothelium. Moreover, the most important physiological functions of the vascular endothelium in blood vessels are discussed. More detailed insights into the pathogenesis of specific diseases, including atherosclerosis and hypertension, are provided in other chapters of this book.
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Book chapters on the topic "Monolayer structure"

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Hann, R. A. "Molecular Structure and Monolayer Properties." In Langmuir-Blodgett Films, 17–92. Boston, MA: Springer US, 1990. http://dx.doi.org/10.1007/978-1-4899-3716-2_2.

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Zasadzinski, Joseph A., Coralie Alonso, Junqi Ding, Frank Bringezu, Heidi Warriner, Tim Alig, Siegfried Steltenkamp, and Alan J. Waring. "Relationships Between Surface Viscosity, Monolayer Phase Behavior, and the Stability of Lung Surfactant Monolayers." In Structure and Dynamics of Membranous Interfaces, 341–83. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2014. http://dx.doi.org/10.1002/9780470388495.ch13.

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Sasaki, Kotaro, Miomir B. Vukmirovic, Jia X. Wang, and Radoslav R. Adzic. "Platinum Monolayer Electrocatalysts: Improving Structure and Activity." In Fuel Cell Science, 215–36. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2010. http://dx.doi.org/10.1002/9780470630693.ch6.

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Shlimak, I., A. V. Butenko, E. Zion, V. Richter, Yu Kaganovskii, L. Wolfson, A. Sharoni, et al. "Structure and Electron Transport in Irradiated Monolayer Graphene." In Future Trends in Microelectronics, 217–31. Hoboken, NJ, USA: John Wiley & Sons, Inc., 2016. http://dx.doi.org/10.1002/9781119069225.ch2-9.

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Dluhy, Richard A., and Donald G. Cornell. "Monolayer Structure at Gas—Liquid and Gas—Solid Interfaces." In ACS Symposium Series, 192–207. Washington, DC: American Chemical Society, 1990. http://dx.doi.org/10.1021/bk-1990-0447.ch011.

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Maultzsch, J., S. Reich, A. R. Goñi, and C. Thomsen. "Resonant Raman scattering in an InAs/GaAs monolayer structure." In Springer Proceedings in Physics, 697–98. Berlin, Heidelberg: Springer Berlin Heidelberg, 2001. http://dx.doi.org/10.1007/978-3-642-59484-7_329.

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Blasie, J. Kent. "Structure of Integral Membrane Proteins within Membranes via X-Ray and Neutron Diffraction: From Oriented Multilayers to a Single Monolayer." In Membrane Protein Structure, 268–80. New York, NY: Springer New York, 1994. http://dx.doi.org/10.1007/978-1-4614-7515-6_12.

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Aston, M. S. "The Anamolous Effect of Electrolytes on Surfactant Monolayer Surface Pressure-Area Isotherms." In The Structure, Dynamics and Equilibrium Properties of Colloidal Systems, 551–55. Dordrecht: Springer Netherlands, 1990. http://dx.doi.org/10.1007/978-94-011-3746-1_36.

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Als-Nielsen, J. "Synchrotron X-ray and Cold Neutron Studies of Amphiphilic Monolayer Structures." In Structure and Dynamics of Strongly Interacting Colloids and Supramolecular Aggregates in Solution, 589–616. Dordrecht: Springer Netherlands, 1992. http://dx.doi.org/10.1007/978-94-011-2540-6_30.

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Penfold, J., R. K. Thomas, E. M. Lee, E. A. Simister, J. R. Lu, and A. R. Rennie. "The Determination of the Structure of a Mixed Surfactant Monolayer by Specular Neutron Reflection." In Springer Proceedings in Physics, 19–23. Berlin, Heidelberg: Springer Berlin Heidelberg, 1992. http://dx.doi.org/10.1007/978-3-642-84763-9_3.

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Conference papers on the topic "Monolayer structure"

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Megnafi, Hicham, Noureddine Boukli Hacene, Henri Baudrand, Nathalie Raveu, and Ikram Allam. "A monolayer passive structure analysis by WCIP method." In 2012 6th International Conference on Sciences of Electronic, Technologies of Information and Telecommunications (SETIT). IEEE, 2012. http://dx.doi.org/10.1109/setit.2012.6481916.

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Shan, Shengyu, Cunjun Ruan, and Yufei Wang. "Magnifying Near-field Image Structure Based on Monolayer Graphene." In 2018 43rd International Conference on Infrared, Millimeter, and Terahertz Waves (IRMMW-THz 2018). IEEE, 2018. http://dx.doi.org/10.1109/irmmw-thz.2018.8509922.

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Zubko, I. Yu, and V. I. Kochurov. "Estimation of elastic moduli of graphene monolayer in lattice statics approach at nonzero temperature." In ADVANCED MATERIALS WITH HIERARCHICAL STRUCTURE FOR NEW TECHNOLOGIES AND RELIABLE STRUCTURES. AIP Publishing LLC, 2015. http://dx.doi.org/10.1063/1.4932931.

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Kapoor, Pooja, Munish Sharma, Ashok Kumar, and P. K. Ahluwalia. "Structural, electronic and magnetic properties of Au-based monolayer derivatives in honeycomb structure." In DAE SOLID STATE PHYSICS SYMPOSIUM 2015. Author(s), 2016. http://dx.doi.org/10.1063/1.4947734.

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Xiaomi Zhang, Dedong Han, Yingying Cong, Junchen Dong, Guodong Cui, Shengdong Zhang, Xing Zhang, and Yi Wang. "Strain effect on electronic structure of La-doped monolayer graphene." In 2016 13th IEEE International Conference on Solid-State and Integrated Circuit Technology (ICSICT). IEEE, 2016. http://dx.doi.org/10.1109/icsict.2016.7999055.

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Valsaraj, Amithraj, Jiwon Chang, Leonard F. Register, and Sanjay K. Banerjee. "Effect of HfO2 and Al2O3 on monolayer MoS2 electronic structure." In 2014 72nd Annual Device Research Conference (DRC). IEEE, 2014. http://dx.doi.org/10.1109/drc.2014.6872310.

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Sharma, Vaishali, and Prafulla K. Jha. "Investigating the lattice dynamics and electronic structure of monolayer PdTe2." In DAE SOLID STATE PHYSICS SYMPOSIUM 2019. AIP Publishing, 2020. http://dx.doi.org/10.1063/5.0016688.

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Cho, H. Jeremy, Shalabh C. Maroo, and Evelyn N. Wang. "Characterization of Lipid Membrane Properties for Tunable Electroporation." In ASME 2012 Third International Conference on Micro/Nanoscale Heat and Mass Transfer. American Society of Mechanical Engineers, 2012. http://dx.doi.org/10.1115/mnhmt2012-75321.

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Abstract:
Lipid bilayers form nanopores on the application of an electric field. This process of electroporation can be utilized in different applications ranging from targeted drug delivery in cells to nano-gating membrane for engineering applications. However, the ease of electroporation is dependent on the surface energy of the lipid layers and thus directly related to the packing structure of the lipid molecules. 1,2-dipalmitoyl-sn-glycero-3-phosphocholine (DPPC) lipid monolayers were deposited on a mica substrate using the Langmuir-Blodgett (LB) technique at different packing densities and analyzed using atomic force microscopy (AFM). The wetting behavior of these monolayers was investigated by contact angle measurement and molecular dynamics simulations. It was found that an equilibrium packing density of liquid-condensed (LC) phase DPPC likely exists and that water molecules can penetrate the monolayer displacing the lipid molecules. The surface tension of the monolayer in air and water was obtained along with its breakthrough force.
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Fan, H. B., Cell K. Y. Wong, and Matthew M. F. Yuen. "Hydrophobic self-assembly monolayer structure for reduction of interfacial moisture diffusion." In High Density Packaging (ICEPT-HDP). IEEE, 2009. http://dx.doi.org/10.1109/icept.2009.5270758.

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Kumar, Ashok, Ravindra Pandey, P. K. Ahluwalia, and K. Tankeshwar. "Topological insulator behavior of WS2 monolayer with square-octagon ring structure." In DAE SOLID STATE PHYSICS SYMPOSIUM 2015. Author(s), 2016. http://dx.doi.org/10.1063/1.4948215.

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Reports on the topic "Monolayer structure"

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Dutta, P., and J. B. Ketterson. Structure and shear response of lipid monolayers. Office of Scientific and Technical Information (OSTI), February 1992. http://dx.doi.org/10.2172/5523952.

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Dutta, P., and J. B. Ketterson. Structure and shear response of lipid monolayers. Office of Scientific and Technical Information (OSTI), February 1990. http://dx.doi.org/10.2172/5189708.

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Edwards, Grant Alvin. Structure and Function Evolution of Thiolate Monolayers on Gold. Office of Scientific and Technical Information (OSTI), January 2006. http://dx.doi.org/10.2172/888936.

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Edwards, Grant Alvin. Structure and function evolution of thiolate monolayers on gold. Office of Scientific and Technical Information (OSTI), January 2006. http://dx.doi.org/10.2172/882309.

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Downer, Nancy W., Jianguo Li, Leslie W. DeLuca, Elizabeth M. Penniman, and H. G. Smith. Surface-Bound Alkyl Monolayers: Electrochemical and Structural Characterization. Fort Belvoir, VA: Defense Technical Information Center, June 1991. http://dx.doi.org/10.21236/ada237604.

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Dutta, P., and J. Ketterson. Studies of the structure and properties of organic monolayers, multilayers and superlattices. Office of Scientific and Technical Information (OSTI), January 1990. http://dx.doi.org/10.2172/6998604.

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Dutta, P., and J. B. Ketterson. Structure and shear response of lipid monolayers. Progress report, August 1, 1990--July 31, 1991. Office of Scientific and Technical Information (OSTI), February 1992. http://dx.doi.org/10.2172/10137966.

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Duran, R. S. Structure and Physical Properties of Monolayers and Multilayers of Liquid Crystals Showing Bulk Ferroelectric Properties. Fort Belvoir, VA: Defense Technical Information Center, March 1997. http://dx.doi.org/10.21236/ada323138.

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Dutta, P., and J. B. Ketterson. Structure and shear response of lipid monolayers. Progress report, July 1, 1989--June 31, 1990. Office of Scientific and Technical Information (OSTI), February 1990. http://dx.doi.org/10.2172/10148411.

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Tang, Xiaoyan, Thomas Schneider, and Daniel A. Buttry. A Vibrational Spectroscopic Study of the Structure of Electroactive Self-Assembled Monolayers of Viologen Derivatives. Fort Belvoir, VA: Defense Technical Information Center, May 1993. http://dx.doi.org/10.21236/ada265705.

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You might also be interested in the extended bibliographies on the topic 'Monolayer structure' for particular source types:
Journal articles Dissertations / Theses
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