3 edition of Organosilanes found in the catalog.
|Statement||editors, Elias B. Wyman and Mathis C. Skief.|
|Contributions||Wyman, Elias B., Skief, Mathis C.|
|LC Classifications||QD305.S54 O735 2009|
|The Physical Object|
|LC Control Number||2009054173|
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Organosilanes book in Radical Chemistry 1st Edition by Chryssostomos Chatgilialoglu (Author) › Visit Amazon's Chryssostomos Chatgilialoglu Page.
Find all the books, read about the author, and more. See search results for this author. Are you an author. Learn about Author Central Cited by: Organosilanes: Properties, Performance and Applications (Materials Science and Technologies) UK ed.
Edition by Elias B. Wyman (Editor), Mathis C. Skief (Editor) ISBN ISBN Why is ISBN important. ISBN. This bar-code number lets you verify that you're getting exactly the right version or edition of a book. Price: $ Organosilanes in Radical Chemistry.
Author(s): Chryssostomos Chatgilialoglu; The aim of this book is to offer for the first time a description of silyl radicals within an interdisciplinary context, connecting structural characteristics and chemical properties to their application in different areas of chemistry.
and cofounder of the. Discusses the use of organosilanes as anchoring layers for biomolecules on different materials. This book also examines the biofunctionalization of organosilanes and their applications. This book gives an excellent overview to readers wish to work in this field of chemistry, giving some interesting examples and applications of organosilanes.
"Organosilanes in Radical Chemistry" can be strongly recommended to all researchers working in the field of radical chemistry and look for a harmless alternative to tributyl tin hydride. () Organosilanes. In: Bhushan B. (eds) Encyclopedia of Nanotechnology.
Springer, Papers Reference Manager Search within book. Type for suggestions. Table of contents Previous. Page Navigate to page number. of Next. About this reference work. Organosilanes are examples of molecules used to form SAMs on a wide variety of hydroxylated surfaces.
APTES is one of the most widely used organosilanes for surface modification as it is an economical and efficient method. Organosilane polymers (polysilanes) are not typical NLO polymers because they do not have delocalized π-electrons in the polymer main chain. However, the σ-electrons forming the silicon-silicon single bonds do exhibit some degree of delocalization along the backbone and this σ-conjugation is the source of a rich variety of photophysical properties including the NLO behavior.
Organosilanes have varied uses in organic chemistry from the most frequently employed protecting groups to intermediates in organic synthesis. The Acros Organics portfolio of organosilanes is continuously expanding to meet your chemistry needs. In this brochure you will find an overview of four of the most important applications of organosilanes.
How Does a silane Modify a surface. Most of the widely used organosilanes have one organic substituent and three hydrolyzable substituents. In the vast majority of surface treatment applications, the alkoxy groups of the trialkoxysilanes are hydrolyzed to form silanol-containing species.
Reaction of these silanes involves four steps. Hydrolysis of organosilanes is a first-order reaction. The hydrolysis rate of the Si-H bond depends on the type and number of organic residues.
Thus, the hydrolysis rate of trialkylsilanes is significantly slower than that of triarylsilanes. This can be explained by a stronger increase in electron density on the silicon atom by the alkyl groups. Ionic and Organometallic-Catalyzed Organosilane Reductions is an essential reference book for all synthetic organic chemists working in academic and industrial by: Organosilicon Chemistry provides information pertinent to the fundamental aspects and application of organosilicon chemistry.
This book discusses the exact manner and extent of d-orbital involvement in organosilicon compounds in ground, electronic, and transition excited states.
About this book Ionic and Organometallic-Catalyzed Organosilane Reductions provides an up-to-date, comprehensive review of reductions with organosilanes. "This is an impressive piece of work." (JACS, ). Organosilanes in Radical Chemistry By Chryssostomos Chatgilialoglu.
Wiley: Chichester, UK. £90, Euros. ISBN: XAuthor: David C. Harrowven. Organosilicon Chemistry: 2 provides information pertinent to the fundamental aspects of organosilicon chemistry.
This book discusses the organosilicon substituents in anionic rearrangements as well as examines the production of tetrakis allene from a large number. Silicon in Organic Synthesis provides an introduction to the organic chemistry of silicon. This book places particular emphasis on the concept of silicon as a “ferryman,” mediating the transformation of one wholly organic molecule into another.
The book begins by reviewing the discovery and development of organosilicon compounds. () Organosilanes. In: Bhushan B. (eds) Encyclopedia of Nanotechnology. Springer, Papers Reference Manager Search within book.
Type for suggestions. Table of contents Previous. Page Navigate to page number. of Next. About this reference work. An Inefficient Hydrogen-atom transfer.
Radical reactions with triethylsilane (10) as the hydrogen-atom transfer are similar to those in which phenyl-substituted silanes fill this role in that repeated addition of substantial amounts initiator is neces low reactivity of 10 as a hydrogen-atom transfer for carbon-centered radicals can be partially compensated for by using.
Organosilicon compounds are organometallic compounds containing carbon–silicon bonds. Organosilicon chemistry is the corresponding science of their preparation and properties. Most organosilicon compounds are similar to the ordinary organic compounds, being colourless, flammable, hydrophobic, and stable to air.
Organosilanes for Cross-coupling. ChemFiles, 7. Dimethylsilanols. Over the past several years, Pd-catalyzed cross-coupling of silicon compounds has rapidly gained acceptance as a suitable alternative to more commonly known methods such as: Stille (Sn), Kumada (Mg), Suzuki (B), and Negishi (Zn) cross-couplings.
1 Organosilicon. A comprehensive, up-to-date reference to synthetic applications of organosilicon chemistry Organic, organometallic, and polymer chemistry as well as materials science all utilize silicon in various forms, yet there is little cross-fertilization of ideas and applications among the by: This book comprises 12 chapters, and begins with a general discussion of the chemistry and molecular structure of the silicones.
The following chapters then discuss preparation of silanes with nonfunctional organic substituents; monomeric organosilicon compounds RnSiX4-n; and organosilanes with organofunctional Edition: 1. Silane is an inorganic compound with chemical formula, Si H 4, making it a group 14 is a colourless, pyrophoric, toxic gas with a sharp, repulsive smell, somewhat similar to that of acetic acid.
Silane is of practical interest as a precursor to elemental silicon. "Silanes" refers to many compounds with four substituents on silicon, including an organosilicon al formula: H₄Si.
Silicon-centered radicals play an important role in organic synthesis, polymer chemistry and material sciences. This book offers a description of silyl radicals within an interdisciplinary context, connecting structural characteristics and chemical properties to their application in different areas of chemistry.
In recent years silicon-centered radicals have played an important role in organic synthesis, polymer chemistry and material sciences. The aim of this book is to offer for the first time a description of silyl radicals within an interdisciplinary context, connecting structural characteristics and chemical properties to their application in different areas of chemistry.
Deals with biosensors and microarrays that take advantage of the specific biological recognition between a surface-immobilised 'probe' and a biological 'target' in solution. This book gives a brief definition of biosensors and their requirements. It discusses the use of organosilanes as anchoring layers for biomolecules on different materials.
Low mechanical stability of superhydrophobic surfaces is the bottle neck we are facing for their practical applications. Here we report facile fabrication of durable superhydrophobic textiles by dip coating in a nanocomposite solution of fluoro-free organosilanes.
The kind of organosilane, molar ratio of orgCited by: Organosilanes have long been considered an environmentally superior alternative to their corresponding tin analogues.
We have been especially interested in Pd-mediated reductions employing polymethylhydrosiloxane (PMHS). PMHS is an easily handled, inexpensive, non.
Get this from a library. Organosilanes in radical chemistry. [Chryssostomos Chatgilialoglu] -- In recent years silicon-centered radicals have played an important role in organic synthesis, polymer chemistry and material sciences.
The aim of this book is to offer for the first time a. Organosilicon Chemistry Michael A. Brook (McMaster University, Hamilton, Canada) ISBN: s Cloth s Nov.
s pp. s Price $ Comprehensive and focused, this book provides a broad overview of silicon chemistry—with an emphasis on both the preparation and reactivity of silicon compounds—helping scientists utilize. Electronic books: Additional Physical Format: Print version: Use of organosilanes in biosensors.
New York: Nova Science Publishers, © (DLC) (OCoLC) Material Type: Document, Internet resource: Document Type: Internet Resource, Computer File: All Authors / Contributors: V Dugas. Silicone Surface Science offers a survey of the major topics concerning the properties and behavior of silicone surfaces.
It covers all main aspects of the subject, including: polydimethylsiloxane, spread monolayers, self-assembled monolayers, hydrophobicity and super-hydrophobicity, coupling agents, surfactants, fluorosilicones, surface treatments and surface analysis. Organosilanes have also been used as molecular resists in electron beam lithography 5 and scanning probe lithography.
27 Patterning can also be achieved through microcontact or nanocontact printing. 44, 47, References. Ulman A., Chem. Rev. 96, (). /cr ; Hahn C Cited by: the roadway since budgets often do not allow for the use of extra equipment and manpower on gravel roads. The recommended shape of each part of the cross section will be discussed in.
The third edition of this well-known textbook discusses some modern methods used in organic synthesis, and aims to show the value and scope of these methods and how they are used in the synthesis of complex molecules.
The general plan of the book follows that of the second edition, but the opportunity has been taken to bring the book up to date and to take account of advances in knowledge and 5/5(1).
Check out the new look and enjoy easier access to your favorite features. We herein report supported Pd nanoparticles on N,O-doped hierarchical porous carbon as a single operation catalyst-enabled additive-modulated reaction pathway for alkynes addition with organosilanes between hydrosilyation and semihydrogenation.
In the case Cited by: 8. ThriftBooks sells millions of used books at the lowest everyday prices. We personally assess every book's quality and offer rare, out-of-print treasures.
We deliver the joy of reading in % recyclable packaging with free standard shipping on US orders over $ Organosilanes in Radical Chemistry Chryssostomos Chatgilialoglu Hardcover, Pages First Edition, December ISBN: X Wiley.
A brief outline or organosilicon chemistry, including the synthesis of organosilanes, chemical bonding in silicon compounds, silicone polymers, and catenated by: Temperature (K) - - A: B: C D: E: F: An increasingly serious and widespread problem is the introduction of plastics into the water cycle.
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