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Artykuły w czasopismach na temat „Self-assembled monolayer”

Autor: Grafiati

Data publikacji: 4 czerwca 2021

Data aktualizacji: 25 lipca 2025

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1

Baker, MV, and J. Landau. "Self Assembled Alkanethiolate Monolayers as Thin Insulating Films." Australian Journal of Chemistry 48, no. 6 (1995): 1201. http://dx.doi.org/10.1071/ch9951201.

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Simple devices that contain alkanethiolate monolayers sandwiched between conducting films were prepared by fixing a gold film to the surface of an alkanethiolate monolayer (on a gold substrate) with silver paint. These devices, and similar devices that did not contain alkanethiolate monolayers, were tested as resistors in d.c . circuits. The devices that contained octadecanethiolate monolayers had resistances of approximately 1012 Ω, 10 orders of magnitude higher than the resistance of devices that contained no monolayers. Sulfur- terminated alkanethiolate monolayers were prepared by treatment

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2

Schön, J. H., H. Meng, and Z. Bao. "Self-Assembled Monolayer Transistors." Advanced Materials 14, no. 4 (2002): 323–26. http://dx.doi.org/10.1002/1521-4095(20020219)14:4<323::aid-adma323>3.0.co;2-5.

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3

Losic, Dusan, Ken Short, Joe G. Shapter, and Justin J. Gooding. "Atomic Force Microscopy Imaging of Glucose Oxidase using Chemically Modified Tips." Australian Journal of Chemistry 56, no. 10 (2003): 1039. http://dx.doi.org/10.1071/ch03122.

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Atomic force microscopy (AFM) tips have been chemically modified using a variety of approaches mostly based on self-assembled monolayers (SAMs). Tips with both a hydrophobic and hydrophilic nature have been prepared and used to image glucose oxidase covalently attached to a self-assembled monolayer.

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4

Tao, Feng. "Nanoscale surface chemistry in self- and directed-assembly of organic molecules on solid surfaces and synthesis of nanostructured organic architectures." Pure and Applied Chemistry 80, no. 1 (2008): 45–57. http://dx.doi.org/10.1351/pac200880010045.

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This article briefly reviews the interplay of weak noncovalent interactions involved in the formation of self-assembled monolayers of organic molecules and the strong chemical binding in directed-assembly of organic molecules on solid surfaces. For a self-assembled monolayer, each molecule involves at least three categories of weak interactions, including molecule-substrate interactions, molecule-molecule interactions in a lamella, and molecule-molecule interactions between two adjacent lamellae. Basically, molecule-substrate interactions play a major role in determining molecular configuratio

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5

Dickie, Adam J., Ashok K. Kakkar, and Michael A. Whitehead. "Molecular modelling of self-assembled alkynyl monolayer structures Unnatural symmetry units, surface bonding, and topochemical polymerization1." Canadian Journal of Chemistry 81, no. 11 (2003): 1228–40. http://dx.doi.org/10.1139/v03-110.

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Geometric modelling techniques are used to map the potential energies of packing for self-assembled alkyl- and phenyl-backboned monolayers across a range of intermolecular separations. Natural packing distances of 4.24.4 Å produce less stable, more isotropic monolayers because of repulsive interchain contacts. Optimizations at unnatural surface densities found thin films of lower energy and higher symmetry existed at increased chainchain separations. Head-group bonding is therefore identified as a force for controlling monolayer order. Analysis of the natural monolayer structures on a silico

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6

Chandrashekhar, Channapura Halappa. "Photoswitchable Polysiloxane Self-Assembled Monolayer." International Journal for Research in Applied Science and Engineering Technology 7, no. 7 (2019): 350–56. http://dx.doi.org/10.22214/ijraset.2019.7053.

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7

Korolkov, Vladimir V., Stephanie Allen, Clive J. Roberts, and Saul J. B. Tendler. "Subsecond Self-Assembled Monolayer Formation." Journal of Physical Chemistry C 114, no. 45 (2010): 19373–77. http://dx.doi.org/10.1021/jp106289p.

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8

Mellott, James M., and Daniel K. Schwartz. "Supercritical Self-Assembled Monolayer Growth." Journal of the American Chemical Society 126, no. 30 (2004): 9369–73. http://dx.doi.org/10.1021/ja0489588.

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9

Kudernac, Tibor, Natalia Shabelina, Wael Mamdouh, Sigurd Höger, and Steven De Feyter. "STM visualisation of counterions and the effect of charges on self-assembled monolayers of macrocycles." Beilstein Journal of Nanotechnology 2 (October 11, 2011): 674–80. http://dx.doi.org/10.3762/bjnano.2.72.

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Despite their importance in self-assembly processes, the influence of charged counterions on the geometry of self-assembled organic monolayers and their direct localisation within the monolayers has been given little attention. Recently, various examples of self-assembled monolayers composed of charged molecules on surfaces have been reported, but no effort has been made to prove the presence of counterions within the monolayer. Here we show that visualisation and exact localisation of counterions within self-assembled monolayers can be achieved with scanning tunnelling microscopy (STM). The p

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10

Jadhav, Sushilkumar. "Self-assembled monolayers (SAMs) of carboxylic acids: an overview." Open Chemistry 9, no. 3 (2011): 369–78. http://dx.doi.org/10.2478/s11532-011-0024-8.

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AbstractThe field of self-assembled monolayers (SAMs) of organic compounds on different substrates is of importance because it provides a suitable and efficient method of surface modification. The formation of robust, stable monolayers from carboxylic acids on two and three dimensional surfaces of different substrates have been reported. Carboxylic acids are promising class of organic compounds for monolayer formations where traditional alkanethiols or alkoxysilanes show limitations.

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11

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 (1994): 1157–58. http://dx.doi.org/10.1021/ja00082a058.

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12

Goutev, Nikolay, and Masayuki Futamata. "Attenuated Total Reflection Surface-Enhanced Infrared Absorption Spectroscopy of Carboxyl Terminated Self-Assembled Monolayers on Gold." Applied Spectroscopy 57, no. 5 (2003): 506–13. http://dx.doi.org/10.1366/000370203321666506.

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A new recipe for surface-enhanced infrared absorption (SEIRA) active island Au films with improved adhesion in aqueous solution, low resistivity, and enhancement of the infrared (IR) absorption of about 300 was developed. The Au films prepared were utilized in studies of the ionization of self-assembled monolayers of 11-mercaptoundecanoic acid in Na2SO4 aqueous solutions by attenuated total reflection surface-enhanced infrared absorption (ATR-SEIRA) spectroscopy. It was found that the carboxyl end groups of the self-assembled monolayer turn into carboxylate anions on going from anodic to catho

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13

Santiago, Jecksan R., E. Barry Troughton, Richard A. Dennis, and Phillip E. Russell. "Atomic Force Microscopy Studies of Microstructure and Properties of Self Assembled Monolayers." Microscopy and Microanalysis 4, S2 (1998): 308–9. http://dx.doi.org/10.1017/s1431927600021668.

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Ex-situ and in-situ studies were performed for self-assembled monolayers (SAMs) formation on mica. The behavior of two surfactants [octadecylphosphonic acid (OPA) and dodecylphosphonic acid (DPA)] in two different solutions [ethanol or tetrahydrofuran (THF)] were studied at different concentrations. A cross section analysis of the monolayer images at partial coverage showed thickness of 1.8 nm, 0.7 nm, and 1.0 nm for OPA, DPA and mixed OPA/DPA, respectively. These values are similar to the ones presented by Xiao and those expected for a monolayer of mixed surfactants as proposed by Whitesides.

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14

Seelenbinder, John A., Chris W. Brown, and Daniel W. Urish. "Self-Assembled Monolayers of Thiophenol on Gold as a Novel Substrate for Surface-Enhanced Infrared Absorption." Applied Spectroscopy 54, no. 3 (2000): 366–70. http://dx.doi.org/10.1366/0003702001949645.

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A unique method of obtaining surface-enhanced infrared absorption (SEIRA) spectra for chemicals that will not chemically attach to a metal surface has been investigated. Surface enhancements are greatest for molecules that bind to metals. In order to achieve greater enhancement for those analytes that do not bind to SEIRA metals, we have investigated self-assembled monolayers as a means of linking analytes to a gold substrate. Monolayers of thiophenol were formed onto sputter-coated gold–silicon substrates. Analytes were deposited onto the thiophenol-coated gold–silicon wafers, and external re

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15

Reese, R. Scott, and Marye Anne Fox. "Spectral and cyclic voltammetric characterization of self-assembled monolayers on gold of pyrene end-labeled oligonucleotide duplexes." Canadian Journal of Chemistry 77, no. 5-6 (1999): 1077–84. http://dx.doi.org/10.1139/v99-098.

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Self-assembled monolayers of sulfur-terminated oligonucleotide duplexes were formed on flat gold surfaces, either by exposure of a self-assembled monolayer bearing one oligonucleotide strand to the complementary strand or by preformation of a oligonucleotide duplex that was then deposited on a fresh gold surface. Virtually identical spectral behavior was observed whether the duplex was produced before deposition or by in situ complementary association. With a duplex bearing an appropriate pyrene end-label, the resulting thin film was photoresponsive. Surface emission measurements show no evide

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16

Carson, George A., and Steve Granick. "Self-assembly of octadecyltrichlorosilane monolayers on mica." Journal of Materials Research 5, no. 8 (1990): 1745–51. http://dx.doi.org/10.1557/jmr.1990.1745.

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A method is described to deposit a securely attached, self-assembled monolayer of octadecyltrichlorosilane (OTS) on the surface of freshly cleaved muscovite mica. Comparison of the infrared methylene spectra with those of closely packed Langmuir-Blodgett films implies that the surface coverage of the OTS films was a fraction 0.8–0.9 that of films formed by Langmuir-Blodgett (LB) methods. However, LB monolayers are less securely attached to the substrate. The contact angle of water on these self-assembled monolayers remained over 100° for over 24 h and it suffered no noticeable degradation afte

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17

Brothers, Michael C., David Moore, Michael St. Lawrence, et al. "Impact of Self-Assembled Monolayer Design and Electrochemical Factors on Impedance-Based Biosensing." Sensors 20, no. 8 (2020): 2246. http://dx.doi.org/10.3390/s20082246.

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Real-time sensing of proteins, especially in wearable devices, remains a substantial challenge due to the need to convert a binding event into a measurable signal that is compatible with the chosen analytical instrumentation. Impedance spectroscopy enables real-time detection via either measuring electrostatic interactions or electron transfer reactions while simultaneously being amenable to miniaturization for integration into wearable form-factors. To create a more robust methodology for optimizing impedance-based sensors, additional fundamental studies exploring components influencing the d

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18

Chang, Chia-Chi, Toyoko Imae, Liang-Yih Chen, and Masaki Ujihara. "Efficient surface enhanced Raman scattering on confeito-like gold nanoparticle-adsorbed self-assembled monolayers." Physical Chemistry Chemical Physics 17, no. 48 (2015): 32328–34. http://dx.doi.org/10.1039/c5cp05490g.

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Confeito-like gold nanoparticles adsorbed on the self-assembled monolayer hierarchy of dendrimer/polystyrene spheres can strongly enhance Raman scattering, being superior to those on the self-assembled monolayer of 3-aminopropyltriethoxysilane.

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19

Wakamatsu, Satoshi, Jun-ichi Nakada, Shintaro Fujii, Uichi Akiba, and Masamichi Fujihira. "Self-assembled nanostructure of Au nanoparticles on a self-assembled monolayer." Ultramicroscopy 105, no. 1-4 (2005): 26–31. http://dx.doi.org/10.1016/j.ultramic.2005.06.014.

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20

Aslam, M., N. K. Chaki, Jadab Sharma, and K. Vijayamohanan. "Device applications of self-assembled monolayers and monolayer-protected nanoclusters." Current Applied Physics 3, no. 2-3 (2003): 115–27. http://dx.doi.org/10.1016/s1567-1739(02)00180-3.

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21

Koo, Ja-Ryong, Sang-Woo Pyo, Jun-Ho Kim, Hyun-Koo Lee, and Young Kwan Kim. "Self Assembled Monolayer for Molecular Electronics." Japanese Journal of Applied Physics 44, no. 1B (2005): 566–69. http://dx.doi.org/10.1143/jjap.44.566.

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22

Bounichou, Matthieu, Olivier Alévêque, Tony Breton, et al. "Self-assembled monolayer-assisted mass spectrometry." Journal of Materials Chemistry 19, no. 43 (2009): 8032. http://dx.doi.org/10.1039/b904175n.

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23

Mu, Xiaoyan, Aiting Gao, Dehui Wang, and Peng Yang. "Self-Assembled Monolayer-Assisted Negative Lithography." Langmuir 31, no. 9 (2015): 2922–30. http://dx.doi.org/10.1021/la504516e.

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24

Stolarczyk, Elżbieta, Katarzyna Sidoryk, Marcin Cybulski, Marek Kubiszewski, and Krzysztof Stolarczyk. "Design of Therapeutic Self-Assembled Monolayers of Thiolated Abiraterone." Nanomaterials 8, no. 12 (2018): 1018. http://dx.doi.org/10.3390/nano8121018.

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The aim of our work was to synthetize of a new analogue of abiraterone—thiolated abiraterone (HS-AB) and design a gold surface monolayer, bearing in mind recent advances in tuning monolayer structures and using them as efficient drug delivery systems. Therapeutic self-assembled monolayers (TSAMs) were prepared by chemically attaching HS-AB to gold surfaces. Their properties were studied by voltammetry and atomic force microscopy (AFM). A gold electrode with immobilized thioglycolic acid (HS-GA) was used for comparison. The surface concentration of HS-AB on the gold surface was 0.572 nmol/cm2,

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25

Yan, Yan, Ye Zhou, Long-Biao Huang, et al. "Enhanced self-assembled monolayer treatment on polymeric gate dielectrics with ultraviolet/ozone assistance in organic thin film transistors." RSC Advances 5, no. 79 (2015): 64471–77. http://dx.doi.org/10.1039/c5ra13246k.

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Chemical vapor deposition (CVD) is utilized to form self-assembled monolayers on polymeric insulators. Ultraviolet/ozone (UVO) treatment is used to enhance the alignment of HMDS monolayer on polymeric insulator surface and a time dependent effect is observed for UVO.

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26

Breton, Gary W. "1-[2,6-Dimethyl-4-(pent-4-yn-1-yloxy)phenyl]-4-phenyl-1,2,4-triazolidine-3,5-dione." Molbank 2023, no. 1 (2023): M1578. http://dx.doi.org/10.3390/m1578.

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Urazolyl radicals are a class of persistent nitrogen-centered radicals. In a previous work, we successfully formed self-assembled monolayers of substituted urazolyl radicals on gold surfaces. To extend the scope of these investigations, we sought to form a self-assembled monolayer using a urazolyl radical species that we knew existed predominantly in the dimerized N-N form instead of existing predominantly as free N-centered radical species, as had previously been investigated. We successfully synthesized the precursor urazole compound needed to generate the desired urazolyl radical, and compl

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27

Taglietti, Angelo, Giacomo Dacarro, Daniele Barbieri, et al. "High Bactericidal Self-Assembled Nano-Monolayer of Silver Sulfadiazine on Hydroxylated Material Surfaces." Materials 12, no. 17 (2019): 2761. http://dx.doi.org/10.3390/ma12172761.

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Anti-infective surfaces are a modern strategy to address the issue of infection related to the clinical use of materials for implants and medical devices. Nanocoatings, with their high surface/mass ratio, lend themselves to being mono-layered on the material surfaces to release antibacterial molecules and prevent bacterial adhesion. Here, a “layer-by-layer” (LbL) approach to achieve a self-assembled monolayer (SAM) with high microbicidal effect on hydroxylated surfaces is presented, exploiting the reaction between a monolayer of thiolic functions on glass/quartz surfaces and a newly synthesize

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28

Jee, Seung-Hyun, Soo-Ho Kim, Jae-Hwan Ko, and Young-Soo Yoon. "Work Function Increase of ITO Modified by Self Assembled Monolayer for Organic Electrical Devices." Journal of the Korean Institute of Electrical and Electronic Material Engineers 19, no. 6 (2006): 563–67. http://dx.doi.org/10.4313/jkem.2006.19.6.563.

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Wang, Zhen, Yan-Li Shi, and Hu-Lin Li. "Investigation of two-component mixed self-assembled monolayers on gold." Canadian Journal of Chemistry 79, no. 3 (2001): 328–36. http://dx.doi.org/10.1139/v01-022.

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Two-component mixed self-assembled monolayers (SAMs) composed of 2-mercapto-5-methyl-1,3,4-oxadiazole (MMO) and 1-dodecanethiol (C12SH) in various molar percentages were prepared on gold surfaces by self-assembly. X-ray photoelectron spectroscopy (XPS) and wettability results gave evidence that the coverage of MMO was controlled by the composition of MMO in the assembling solution. The monolayer coverage and apparent rate constant of the redox active probes in solution of different molar ratios of mixed SAMs could be calculated using impedance measurements. The cyclic voltammetry reveals that

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30

KRATOCHVÍLOVÁ, IRENA, ADRIANA ZAMBOVA, JEREMIAH MBINDYO, BAHARAK RAZAVI, and JOSEF HOLAKOVSKÝ. "CURRENT-VOLTAGE CHARACTERIZATION OF ALKANETHIOL SELF-ASSEMBLED MONOLAYERS IN METAL NANOWIRES." Modern Physics Letters B 16, no. 05n06 (2002): 161–69. http://dx.doi.org/10.1142/s0217984902003609.

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An electric-field assisted assembly has been used to place rod-shaped, metal-organic, molecule-metal nanowires onto lithographically defined metal pads allowing the electrical characterization of metal-molecule self-assembled monolayer-metal containing nanowires. Our results show that the parameters of metal-molecule metal junctions are close to previously published data, so we have constructed systems containing insulating monolayers with reasonable properties.

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31

KONGKANAND, Anusorn, and Susumu KUWABATA. "Preparation of Pt Monolayer Islands Using Self-assembled Monolayer Technique." Electrochemistry 72, no. 6 (2004): 412–14. http://dx.doi.org/10.5796/electrochemistry.72.412.

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32

Hinckley, Adam P., and Anthony J. Muscat. "Wet Chemical Cleaning of Organosilane Monolayers." Solid State Phenomena 314 (February 2021): 54–59. http://dx.doi.org/10.4028/www.scientific.net/ssp.314.54.

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Thin organic self-assembled monolayer films are used to promote adhesion and seal the pores of metal oxides as well as direct the deposition of layers on patterned surfaces. Defects occur as the self-assembled monolayer forms, and the number and type of defects depend on surface preparation, deposition solvent, temperature, time and other parameters. Particles commonly deposit during organosilane self-assembly on metal oxide surfaces. The particles are defects because they are prone to react in subsequent processing, which may not be desirable if the organosilane serves as a pore sealant or pa

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33

Jennane, Jamila, Tanya Boutros, and Richard Giasson. "Photolithography of self-assembled monolayers: optimization of protecting groups by an electroanalytical method." Canadian Journal of Chemistry 74, no. 12 (1996): 2509–17. http://dx.doi.org/10.1139/v96-281.

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Patterned surfaces presenting a high density of chemically reactive functional groups can be prepared through photolithography of self-assembled monolayers (SAM). In this paper, we report the synthesis and the evaluation of three reagents that can be used in SAM-photolithographic applications. These reagents are made up of a triethoxysilylpropylamine moiety in which the amine is temporarily blocked by photolabile protecting groups: NVOC (o-nitroveratryloxycarbonyl), ONB (o-nitrobenzyl), or DDZ (α,α-dimethyl-3,5-dimethoxybenzyloxycarbonyl). The presence of the triethoxysilyl group allows self-a

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34

Wang, Yue Hui. "Large-Area Self-Assembled Monolayer of Silica Microspheres by Convective Assembly." Key Engineering Materials 609-610 (April 2014): 479–82. http://dx.doi.org/10.4028/www.scientific.net/kem.609-610.479.

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We reported here a convective assembly process for the formation of large-area self-assembled monolayers of silica microspheres on silicon and glass substrates. Uniformly coated monolayers of silica spheres were achieved on silicon wafers with and without coated SiN2 of 3 inch of diameter and large glass substrate of 6 × 6 in2 in size. The coating of large-area uniform monolayers of silica microspheres was characterized with scanning electron microscopy and optical microscopy. The mechanism of the convective assembly has been explained by the convective flux that is generated by capillary imme

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35

Zhang, Bo, Tomas Mikysek, Veronika Cicmancova, et al. "2D GeSe2 amorphous monolayer." Pure and Applied Chemistry 91, no. 11 (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 et

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36

Kumar, Sowmya M., Parvathi K. Balakrishnan, Chethan Hedge, and Shilpa Dandekeri. "Self-Assembled Monolayer- A Nano Surface Modification." Journal of Evolution of Medical and Dental Sciences 9, no. 20 (2020): 1608–12. http://dx.doi.org/10.14260/jemds/2020/351.

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Miller, Johanna L. "A new kind of self-assembled monolayer." Physics Today 67, no. 6 (2014): 20–21. http://dx.doi.org/10.1063/pt.3.2406.

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Zhou, C., M. R. Deshpande, M. A. Reed, L. Jones, and J. M. Tour. "Nanoscale metal/self-assembled monolayer/metal heterostructures." Applied Physics Letters 71, no. 5 (1997): 611–13. http://dx.doi.org/10.1063/1.120195.

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Rozenfeld, O., Y. Koltypin, H. Bamnolker, S. Margel, and A. Gedanken. "Self-Assembled Monolayer Coatings on Amorphous Iron." Langmuir 10, no. 11 (1994): 3919–21. http://dx.doi.org/10.1021/la00023a001.

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Schön, Jan Hendrik, Hong Meng, and Zhenan Bao. "Self-assembled monolayer organic field-effect transistors." Nature 413, no. 6857 (2001): 713–16. http://dx.doi.org/10.1038/35099520.

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Le Liepvre, Sylvain, Ping Du, David Kreher, et al. "Fluorescent Self-Assembled Molecular Monolayer on Graphene." ACS Photonics 3, no. 12 (2016): 2291–96. http://dx.doi.org/10.1021/acsphotonics.6b00793.

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Chinwangso, Pawilai, Andrew C. Jamison, and T. Randall Lee. "Multidentate Adsorbates for Self-Assembled Monolayer Films." Accounts of Chemical Research 44, no. 7 (2011): 511–19. http://dx.doi.org/10.1021/ar200020s.

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Shin, Chong Kyu, Hoosung Lee, Changsoo Jung, Doseok Kim, and Bum Ku Rhee. "Self-Assembled Polythiophene Monolayer on Gold Surface." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 349, no. 1 (2000): 167–70. http://dx.doi.org/10.1080/10587250008024891.

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Nakamura, Fumio, Keita Mitsui, Tomohide Murase, et al. "Immobilization of DNA on Self-Assembled Monolayer." Molecular Crystals and Liquid Crystals Science and Technology. Section A. Molecular Crystals and Liquid Crystals 349, no. 1 (2000): 219–22. http://dx.doi.org/10.1080/10587250008024904.

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Woodward, J. T., and D. K. Schwartz. "In SituObservation of Self-Assembled Monolayer Growth." Journal of the American Chemical Society 118, no. 33 (1996): 7861–62. http://dx.doi.org/10.1021/ja961524v.

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Lin, Yu-Pu, Oualid Ourdjini, Luca Giovanelli, et al. "Self-Assembled Melamine Monolayer on Cu(111)." Journal of Physical Chemistry C 117, no. 19 (2013): 9895–902. http://dx.doi.org/10.1021/jp401496s.

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Nováková, Zuzana, Renáta Oriňáková, Andrea Straková Fedorková, and Andrej Oriňák. "Electrochemical study of self-assembled monolayer adsorption." Journal of Solid State Electrochemistry 18, no. 8 (2014): 2289–95. http://dx.doi.org/10.1007/s10008-014-2455-6.

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Ion, Ana, Vassilia Partali, Hans-Richard Sliwka, and Florinel Gabriel Banica. "Electrochemistry of a carotenoid self-assembled monolayer." Electrochemistry Communications 4, no. 9 (2002): 674–78. http://dx.doi.org/10.1016/s1388-2481(02)00430-7.

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Park, Jun Hyung, Buyng Su Park, Gu Huh, et al. "Specific Immobilization of Streptavidin on Mixed Self-Assembled Monolayers as Mixing Ratio." Solid State Phenomena 121-123 (March 2007): 495–98. http://dx.doi.org/10.4028/www.scientific.net/ssp.121-123.495.

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We report on the distribution of mixed self-assembled monolayers (SAMs) composed of biotinylated and diluent alkylthiolates for streptavidin immobilization. Two thiol derivatives, 11-mercapto-1-undecanol (MUOH) and 11-mercaptoundecanoic-(8-biotinylamido-3,6-dioxaoctyl) amide (MBDA), were employed for mixed SAM. These thiols formed self-assembled monolayer without local domain, and streptavidins were immobilized onto biotinylated gold surface without nonspecific binding. In order to find the optimized condition of immobilization of streptavidin, we controlled the mixing ratio of two kind thiols

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Škugor Rončević, Ivana, Nives Vladislavić, Marijo Buzuk, and Maša Buljac. "Electrodeposition of hydroxyapatite coating on Mg alloy modified with organic acid self-assembled monolayers." Journal of Chemical Research 44, no. 3-4 (2019): 212–20. http://dx.doi.org/10.1177/1747519819895980.

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Calcium phosphate coatings are used in orthopedics due to their excellent bioactivity, which improves the bonding between the metal implant and the bone. The use of self-assembling monolayers of long-chain organic acids can induce calcium phosphate growth. In this article, the self-assembling monolayers of stearic acid and octadecylphosphonic acid formed on the Mg alloy surface were additionally modified with electrodeposited hydroxyapatite coating to increase the bioactivity and biocompatibility of the Mg alloy in a physiological solution. Hydroxyapatite coating was prepared by a two-step rea

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