Relevant bibliographies by topics / Trichlorosilanes

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  1. Journal articles
  2. Dissertations / Theses
  3. Book chapters
  4. Conference papers

Academic literature on the topic 'Trichlorosilanes'

Author: Grafiati
Published: 4 June 2021
Last updated: 16 February 2022

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Journal articles on the topic "Trichlorosilanes"

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Ackerhans, Carsten, Bodo Räke, Ralph Krätzner, Peter Müller, Herbert W. Roesky, and Isabel Usón. "Ammonolysis of Trichlorosilanes." European Journal of Inorganic Chemistry 2000, no. 5 (2000): 827–30. http://dx.doi.org/10.1002/(sici)1099-0682(200005)2000:5<827::aid-ejic827>3.0.co;2-j.

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Sasaki, Manabu, and Krzysztof Matyjaszewski. "Synthesis of branched copolysilanes from trichlorosilanes." Journal of Polymer Science Part A: Polymer Chemistry 33, no. 5 (1995): 771–78. http://dx.doi.org/10.1002/pola.1995.080330503.

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Hshieh, Fu-Yu, David B. Hirsch, and James H. Williams. "Short communication: Autoignition temperature of trichlorosilanes." Fire and Materials 26, no. 6 (2002): 289–90. http://dx.doi.org/10.1002/fam.804.

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Oyola-Reynoso, Stephanie, Jiahao Chen, Boyce S. Chang, Jean-Francis Bloch, and Martin M. Thuo. "Surface polymerization of perfluorosilane treatments on paper mitigates HF production upon incineration." RSC Advances 6, no. 85 (2016): 82233–37. http://dx.doi.org/10.1039/c6ra20582h.

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Burning perfluoro trichlorosilanes (R<sup>F</sup>) treated paper leads to depolymerization of the crosslinked polysilane, distilling off liquid R<sup>F</sup> and emitting CO<sub>2</sub> and H<sub>2</sub>O as the only gaseous products.
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SOGA, Mamoru, Kazufumi Ogawa, Shinji OZAKI, Yasushi MASUDA, and Kunio GOTO. "Hydrophobic Treatment of Glass Plates with Perfluoroalkyl Trichlorosilanes." Hyomen Kagaku 14, no. 10 (1993): 630–35. http://dx.doi.org/10.1380/jsssj.14.630.

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St. John, Pamela M., and H. G. Craighead. "Microcontact printing and pattern transfer using trichlorosilanes on oxide substrates." Applied Physics Letters 68, no. 7 (1996): 1022–24. http://dx.doi.org/10.1063/1.116216.

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Booth, Brandon D., Nathaniel J. Martin, Edward A. Buehler, Clare McCabe, and G. Kane Jennings. "Tribological characterization of gradient monolayer films from trichlorosilanes on silicon." Colloids and Surfaces A: Physicochemical and Engineering Aspects 412 (October 2012): 57–63. http://dx.doi.org/10.1016/j.colsurfa.2012.07.015.

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Fairbank, R. W. Peter, and Mary J. Wirth. "Role of surface-adsorbed water in the horizontal polymerization of trichlorosilanes." Journal of Chromatography A 830, no. 2 (1999): 285–91. http://dx.doi.org/10.1016/s0021-9673(98)00908-x.

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Wang, Jiandong, Xuan Xiang, Xiang Yao, Wen-Jing Xiao, Jian Lin, and Wei-Shi Li. "Efficient perovskite solar cells using trichlorosilanes as perovskite/PCBM interface modifiers." Organic Electronics 39 (December 2016): 1–9. http://dx.doi.org/10.1016/j.orgel.2016.09.018.

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Okamoto, Hidenori, and Shozo Kato. "A Facile Reduction of Certain Schiff Bases with Di- and Trichlorosilanes." Bulletin of the Chemical Society of Japan 64, no. 11 (1991): 3466–67. http://dx.doi.org/10.1246/bcsj.64.3466.

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Dissertations / Theses on the topic "Trichlorosilanes"

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Kysilka, Ondřej. "Functionalised trichlorosilanes in the asymmetric allylation." Thesis, University of Glasgow, 2013. http://theses.gla.ac.uk/4377/.

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We present a synthetic route to the homoallylic alcohols, using the well-established asymmetric organocatalysed allylation of aldehydes. These alcohols were transformed in one step into the substituted tetrahydrofurans in the presence of achiral Lewis acids, forming three chiral centres for the price of two. A synthetic route towards chiral substituted tetrahydropyrans and unsaturated 1,5 diol-building blocks has also been developed.
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Adamkiewicz, Malgorzata. "Self-assembled monolayers on silicon : deposition and surface chemistry." Thesis, University of St Andrews, 2013. http://hdl.handle.net/10023/3938.

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Fabrication of surfaces with versatile functional groups is an important research area. Hence, it is essential to control and tune the surface properties in a reliable manner. Vinyl-terminated self-assembled monolayers (SAMs) offer significant flexibility for further chemical modification and can serve as a versatile starting point for tailoring of surface properties. Here a synthetic route for the preparation of vinyl-terminated trichlorosilane self-assembling molecules: 9-decenyltrichlorosilane (CH₂=CH-(CH₂)₈-SiCl₃), 10-undecenyltrichlorosilane (CH₂=CH-(CH₂)₉-SiCl₃), and 14-pentadecenyltrich
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Vrankova, Kvetoslava. "Scope of enantioselective reduction of imines with trichlorosilane." Thesis, University of Glasgow, 2009. http://theses.gla.ac.uk/1390/.

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Herein, we report the results of research continuing previous successI in the field of enantioselective organocatalytic reduction of imines with trichlorosilane. Syntheses of various precursors (ketones) and substrates (imines) for the reduction reaction and their reduction following the protocol (Scheme A1) are described in this thesis. 1. Aromatic heterocycles containing nitrogen – good yields of the reduced product (68-85 %), the enantioselectivity depended on steric bulk in proximity to the nitrogen, steric bulk improved the enantioselectivity (up to 78 % ee), probably due to thwarting the
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MacDougall, Kenneth N. "Organocatalysts for the asymmetric reduction of aromatic ketimines with trichlorosilane." Thesis, University of Glasgow, 2008. http://theses.gla.ac.uk/123/.

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Asymmetric reduction of N-aryl ketimines 189a j, 212, and 213 with trichlorosilane can be catalyzed by new N-methyl L-amino acid-derived Lewis-basic organocatalysts, such as bisamide 197c (10 mol%), in toluene at room temperature with high enantioselectivity (≤92% ee). The structure-reactivity investigation shows that the product configuration is controlled by the nature of the side chain of the catalyst scaffold (e.g., i Pr vs Me, as in 197c and 208c), so that catalysts of the same absolute configuration may induce the formation of the opposite enantiomers of the product. Arene-arene interact
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Fetzer, Molly M. "Comparative risk assessment of a cylinder handling system and a bulk liquid distribution system for Trichlorosilane." Online version, 1998. http://www.uwstout.edu/lib/thesis/1998/1998fetzerm.pdf.

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Liu, Ke-Hung, and 劉柯宏. "Extinguishing efficiency of liquid nitrogen against trichlorosilane fires." Thesis, 2015. http://ndltd.ncl.edu.tw/handle/70550598999117915661.

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碩士<br>國立雲林科技大學<br>環境與安全衛生工程系<br>103<br>Trichlorosilane ( SiHCl3,TCS ) and other silanes were toxic, water-reactive and corrosive. They were used in the semi-conductor, solar, petrochemical industries functioned as the major process materials for the ultrapure silicon. As they were released and ignited, several byproducts were harmful to health and environment, such as silica oxides, chlorine and hydrogen gases etc. They also reacted with water to produce hydrochloride acid, which dispersed easily to threat public and to create the difficulties for response and rescue actions. In recent year
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Kao, Chi-yueh. "Doping polythiophene derivatives with tridecafluoro-1,1,2,2-tetrahydrooctyl trichlorosilane vapor." 2007. http://hdl.rutgers.edu/1782.2/rucore10001600001.ETD.16406.

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Siou-RongLi and 黎秀蓉. "Emissions of acid aerosols and gases associated with the releasing and burning of trichlorosilane under various humidity conditions." Thesis, 2010. http://ndltd.ncl.edu.tw/handle/39286925755072679265.

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碩士<br>國立成功大學<br>環境醫學研究所<br>98<br>This study investigated the emission characteristics of acid aerosols (HCl-p), acid gases (HCl-g) and chlorine (Cl2) during the releasing and burning of trichlorosilane (TCS). An exposure chamber was established and its uniformity and stability were tested under various test conditions prior to conducting experimental campaigns. Five relative humidity conditions (RH= 44.0 %, 57.3 %, 65.5 %, 79.8 % and 89.8 %) were selected and the air exchange rate (ACH) was specified at 6. Each test condition was repeated three times and HCl-p, HCl-g and Cl2 were collected dur
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Book chapters on the topic "Trichlorosilanes"

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Martin, Donald R., John F. Suttle, Harold Simmons Booth, and Frederic B. Dutton. "2-Chloroethyl Chlorosulfonate and (2-Chloroethoxy)Trichlorosilane." In Inorganic Syntheses. John Wiley & Sons, Inc., 2007. http://dx.doi.org/10.1002/9780470132357.ch30.

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Hirota, E., K. Kuchitsu, T. Steimle, J. Vogt, and N. Vogt. "126 C2H4Cl6Si2 1,1'-(1,2-Ethanediyl)bis[1,1,1-trichlorosilane]." In Molecules Containing No Carbon Atoms and Molecules Containing One or Two Carbon Atoms. Springer Berlin Heidelberg, 2014. http://dx.doi.org/10.1007/978-3-540-70614-4_327.

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Kočcovský, Pavel, and Sigitas Stončcius. "Reduction of Imines with Trichlorosilane Catalyzed by Chiral Lewis Bases." In Chiral Amine Synthesis. Wiley-VCH Verlag GmbH & Co. KGaA, 2010. http://dx.doi.org/10.1002/9783527629541.ch4.

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Leone, Stefano, Marco Mauceri, Giuseppe Pistone, et al. "SiC-4H Epitaxial Layer Growth Using Trichlorosilane (TCS) as Silicon Precursor." In Silicon Carbide and Related Materials 2005. Trans Tech Publications Ltd., 2006. http://dx.doi.org/10.4028/0-87849-425-1.179.

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Porter, M. J. "Oxidation of Trichlorosilanes." In Alcohols. Georg Thieme Verlag KG, 2008. http://dx.doi.org/10.1055/sos-sd-036-00017.

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Sarkar, T. K. "From Allyl Halides by Copper(I)-Catalyzed Silylation with Trichlorosilane." In Compounds of Groups 15 (As, Sb, Bi) and Silicon Compounds. Georg Thieme Verlag KG, 2002. http://dx.doi.org/10.1055/sos-sd-004-00935.

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Wicha, J. "Deoxygenation of Aromatic Acids, Aldehydes, and Ketones Using the Trichlorosilane–Tripropylamine Couple." In Alkanes. Georg Thieme Verlag KG, 2009. http://dx.doi.org/10.1055/sos-sd-048-00037.

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Ehrich, H., T. Lobreyer, K. Hesse, and H. Lieske. "Some phenomenological and mechanistic aspects of the use of copper as catalyst in trichlorosilane synthesis." In Studies in Surface Science and Catalysis. Elsevier, 2000. http://dx.doi.org/10.1016/s0167-2991(00)80806-x.

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Conference papers on the topic "Trichlorosilanes"

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Martin, Cristina, and Aarash Y. N. Sofla. "A Method for Bonding PDMS Without Using Plasma." In ASME 2010 International Mechanical Engineering Congress and Exposition. ASMEDC, 2010. http://dx.doi.org/10.1115/imece2010-38790.

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The vapor-assisted treatment constitutes a simple and inexpensive method to increase the adhesion strength of polydimethylsiloxane and glass without using plasma. In this method, the targeted PDMS-glass sample is exposed to a vapor in an enclosed container for a certain time. Different chemicals were tested as possible vapor sources. No increase in the adhesion strength of PDMS-glass samples was observed when silanes without chloro functional groups were used. On the other hand, all alkyl trichlorosilanes tested in this study led to permanent bondings. In addition, an increase in the strength
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Guangxia, Zhang, Zhang Qiaoyun, and Chen Zemin. "Methyl Trichlorosilane Preparation of Methyl Aluminum Silicate." In 2012 Third International Conference on Digital Manufacturing and Automation (ICDMA). IEEE, 2012. http://dx.doi.org/10.1109/icdma.2012.124.

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del Coso, G., J. C. Zamorano, C. del Canizo, J. F. Lelievre, J. Hofstetter, and A. Luque. "Solar Grade Silicon production through trichlorosilane decomposition." In 2009 Spanish Conference on Electron Devices (CDE). IEEE, 2009. http://dx.doi.org/10.1109/sced.2009.4800507.

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Park, Won-Ju. "P068 Health effects after exposure to accidental release of silicon tetrachloride and trichlorosilane." In Occupational Health: Think Globally, Act Locally, EPICOH 2016, September 4–7, 2016, Barcelona, Spain. BMJ Publishing Group Ltd, 2016. http://dx.doi.org/10.1136/oemed-2016-103951.390.

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Chen, Jian-Zhang. "Thermally Actuated Droplet Motion on Chemically Homogeneous, Striated, and Defected Surfaces." In 2008 Second International Conference on Integration and Commercialization of Micro and Nanosystems. ASMEDC, 2008. http://dx.doi.org/10.1115/micronano2008-70096.

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Experiments have demonstrated thermocapillary actuation on uniformly grafted partial-wettable surfaces. Droplet mobilization only occurs above a threshold thermal gradient or threshold droplet radius [1]. We characterized the motion instead in terms of a threshold depinning force, which successfully describes all the liquids tested. Above the depinning transition, the droplet speed, which is controlled by thermocapillary, capillary and viscous forces, increases monotonically with this reduced force parameterization. These results agree well to numerical predictions of a generalized Ford and Na
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Zang, Xinxiang, Yang Yuan, Haisheng Chen, Liang Zhang, Shaofeng Wang, and Kejin Huang. "Performance of reactive distillation columns with multiple reactive sections for the disproportionation of trichlorosilane to silane." In 2017 6th International Symposium on Advanced Control of Industrial Processes (AdCONIP). IEEE, 2017. http://dx.doi.org/10.1109/adconip.2017.7983791.

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Doms, Marco, and Jo¨rg Mu¨ller. "Design, Fabrication and Characterization of a Fully Integrated Micro Vapor-Jet Vacuum Pump." In ASME 2006 2nd Joint U.S.-European Fluids Engineering Summer Meeting Collocated With the 14th International Conference on Nuclear Engineering. ASMEDC, 2006. http://dx.doi.org/10.1115/fedsm2006-98137.

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A MEMS vapor-jet pump for vacuum generation in miniaturized analytical systems, e.g. micro mass-spectrometers [1, 2], is presented. A high velocity gas- or vapor-jet is used for vacuum generation. Starting from atmospheric pressure, a high throughput of more than 23 ml/min and an absolute pressure of 495 mbar were obtained with this new type of micropump. An approach for the full integration of all components of the pump is presented, validated by experimental results. The pump is fabricated from silicon and glass substrates using standard MEMS fabrication techniques including DRIE, trichloros
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Heo, J. C., K. S. Kim, and K. W. Kim. "Tribological Characteristics of Materials for MEMS/NEMS by Using Chemically Modified AFM Tip." In ASME/STLE 2007 International Joint Tribology Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/ijtc2007-44226.

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Friction and adhesion tests were conducted in order to investigate the tribological characteristics of materials for MEMS/NEMS using AFM. AFM Si tips were chemically modified with self-assembled monolayer (SAM) derived from trichlorosilane like OTS and FOTS, and various materials such as Si, Al, Au, Cu, Ti, PMMA and PDMS were prepared for the tests. The friction and adhesion forces between AFM Si tip modified with SAM and MEMS/NEMS materials were measured and compared to those forces when AFM tip was uncoated. According to the results, however, the effect of SAM on the reduction of friction an
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Yamada, Toru, Chungpyo Hong, Otto J. Gregory, and Mohammad Faghri. "Fluid Flow Characteristics in Microchannels With Rib-Patterned Surface." In ASME/JSME 2011 8th Thermal Engineering Joint Conference. ASMEDC, 2011. http://dx.doi.org/10.1115/ajtec2011-44631.

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The effects of rib-patterned surfaces and surface wettability on liquid flow in microchannels were experimentally investigated in this study. Microchannels were fabricated on single-crystal silicon wafers by photolithographic and wet-etching techniques. Rib structures were patterned in the silicon microchannel, and the surface was chemically treated by trichlorosilane to create the hydrophobic condition. Experiments with water as the working fluid were performed with these microchannels over a wide range of Reynolds number between 110 and 1914. The results for the rib-patterned microchannels s
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Kim, K. S., J. H. Kang, and K. W. Kim. "Effect of Process Conditions on Adhesion Between Stamp and Polymer Film Used in Thermal Nanoimprint Lithography." In ASME/STLE 2007 International Joint Tribology Conference. ASMEDC, 2007. http://dx.doi.org/10.1115/ijtc2007-44291.

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In this study, the adhesion characteristics between stamp and thermoplastic polymer film were studied in order to investigate the effect of process conditions on the adhesion between two materials. Imprint pressure, separation speed and coating of anti-sticking layer (ASL) were considered as the process conditions. A piece of fused silica without patterns on its surface was used as a stamp and the thermoplastic polymer film was made on Si substrate by the spin-coating of commercial polymer solution such as mr-I PMMA and mr-I 7020. The ASL was derived from (1H, 1H, 2H, 2H - perfluorooctyl) tric
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