Radical Reactions of Fullerenes and their Derivatives (Developments in Fullerene Science) by B.L. Tumanskii

Cover of: Radical Reactions of Fullerenes and their Derivatives (Developments in Fullerene Science) | B.L. Tumanskii

Published by Springer .

Written in English

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Subjects:

  • Biochemistry,
  • Inorganic Chemistry,
  • Science,
  • Science/Mathematics,
  • Science / Chemistry / Inorganic,
  • Science / Chemistry / Physical & Theoretical,
  • Fullerenes,
  • Chemistry - Inorganic

Book details

The Physical Object
FormatHardcover
Number of Pages212
ID Numbers
Open LibraryOL8369804M
ISBN 101402001762
ISBN 109781402001765

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Radical Reactions of Fullerenes and their Derivatives (Developments in Fullerene Science Book 2) - Kindle edition by Tumanskii, B.L., Kalina, O. Download it once and read it on your Kindle device, PC, phones or tablets.

Use features like bookmarks, note taking and highlighting while reading Radical Reactions of Fullerenes and their Derivatives (Developments in Fullerene Science Book 2).Manufacturer: Springer. Radical Reactions of Fullerenes and their Derivatives (Developments in Fullerene Science) st Edition by B.L.

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Cited by: The discovery of fullerenes, species belonging to the electronodeficient polyalkenes with weakly conjugated double bonds, has opened novel opportunities for the radical chemistry. Pioneering study in this field was performed by P.

Krusic, E. Wasserman, P. Keizer, J. Morton, and K. Radical Reactions of Fullerenes and their Derivatives. Authors (view affiliations) reactions of fullerenes in bulk amounts opens the door to large-scale preparation of new organic and organoelement derivatives of including biologically active ones.

Radical reactions of fullerenes find wide application in the synthesis of fullere- containing. Get this from a library. Radical reactions of fullerenes and their derivatives.

[Boris Tumanskiĭ; Oleg Kalina] -- "The discovery of fullerenes has opened novel opportunities for the radical chemistry. The fullerenyl radical adducts formed via addition of atoms or free radicals to fullerenes have no analogs in.

Cite this chapter as: () Ion Radical Reactions of Fullerenes. In: Radical Reactions of Fullerenes and their Derivatives. Developments in Fullerene Science, vol 2. Radical Reactions of Fullerenes: From Synthetic Organic Chemistry to Materials Science and Biology Manolis D.

Tzirakis * and Michael Orfanopoulos * Department of Chemistry, University of Crete, Voutes, Heraklion, Greece. Fullerenes: Chemistry and Reactions. Author(s): Prof. Andreas Hirsch the book is logically arranged such that information is easy to retrieve, and the style lends itself to effortless reading and to learning more about the chemical properties of this family of molecules.

activities have been focussed on the development of. Fullerenes have the ability to assume different forms and to encage compounds. The unique physical, chemical, electrical, and optical properties of fullerenes and their derivatives have led to their incorporation into new or improved devices and materials, and.

Fullerene chemistry is a field of organic chemistry devoted to the chemical properties of fullerenes. Research in this field is driven by the need to functionalize fullerenes and tune their properties. For example, fullerene is notoriously insoluble and adding a suitable group can enhance solubility.

By adding a polymerizable group, a fullerene polymer can be obtained. Functionalized. Fullerenes From Synthesis To Optoelectronic Properties English Paperback Book The Chemical - $ The Chemical Physics Of Fullerenes 10 And 5 Years Later The Far-reaching Impa.

Request PDF | Fullerenes: Chemistry and Reactions | In this handbook, the leading experts in the field presents important and fundamental aspects of the organic and organometallic chemistry of.

Fullerenes and their derivatives were found to have a neuroprotective effect in the central nervous system [32]. In addition, because of the good biocompatibility and selective release mechanism of fullerenes as well as their ability to penetrate the intact skin, the applications of fullerenes as drug or gene carriers has attracted much attention.

Fullerenes were initially found to be inert, but their unique cage structure and solubility in organic solvents opened up their susceptibility to functionalization via addition and redox reactions. In: Radical Reactions of Fullerenes and their Derivatives.

Taylor, Lecture Notes on Fullerene Chemistry: A Handbook for Chemists, Imperial College Press, London, 4. In this handbook, the leading experts in the field presents important and fundamental aspects of the organic and organometallic chemistry of fullerenes.

Naturally they also cover the applications in material and medicinal science for these fascinating molecules. Completely self-contained, the book is logically arranged such that information is easy to retrieve, and the style lends itself to.

The book begins with introductory chapters that provide the necessary background in experimental and theoretical techniques.

This is followed by experimental results and theoretical calculations covering the wide range of available gas-phase fullerene collision experiments. Radical Reactions of Fullerenes and their Derivatives.

Boris. A fullerene is an allotrope of carbon whose molecule consists of carbon atoms connected by single and double bonds so as to form a closed or partially closed mesh, with fused rings of five to seven atoms.

The molecule may be a hollow sphere, ellipsoid, tube, or many other shapes and sizes. Graphene (isolated atomic layers of graphite), which is a flat mesh of regular hexagonal rings, can be.

Fullerene Collision Reactions provides a comprehensive overview of the state-of-the-art of fullerene collision studies.

The book begins with introductory chapters that provide the necessary background in experimental and theoretical techniques. Free radical reactions which took place upon warming the glasses to temperatures at which the electron adducts become mobile were studied.

For carboxylic acids (C/sub n/H/sub 2n+1/CO/sub 2/D, n = 2,3) the deuterated anion radicals (RCH/sub 2/C(OD)/sub 2/) give results which suggest abstraction of a hydrogen from the parent acid to produce.

this book, which contains the complete important literature, the reader will find all aspects of fullerene chemistry as well as the properties of fullerene derivatives.

After a short description of the discovery of the fullerenes all methods of the production and isolation of the parent fullerenes and endohedrals are.

Fullerenes, especially C60, exhibit great potential applications in biology field, due to their excellent antibacterial, antiviral, antitumor and other properties.

Many water-soluble fullerene derivatives have been designed, synthesized and used as photo-dynamic therapy agents, antiviral agents, bioimaging agents, drug carriers and so by: 3. The mechanism of the reaction of azafullerene radical C59N• with diphenylmethane and 9-methyl-9H-fluorene has been investigated.

The primary and secondary kinetic isotope effects provide strong evidence for a stepwise mechanism in which the hydrogen-atom abstraction is the rate-determining by: 4. The photo, electrochemical and physical properties of C 60 and other fullerene derivatives finds applications in medical fields.

The ability of fullerenes to fit inside the hydrophobic cavity of HIV proteases makes them potential inhibitor for substrates to catalytic active site of enzyme.

It possesses radical scavenging and antioxidant by: 6. The description of the chemistry of the fullerenes the reduction (Chapter 2), nucleophilic additions (Chapter 3), cycloadditions (Chapter 4), hydrogenation (Chapter 3, radical additions (Chapter 6), transition metal complex formation am also indebted to my co-workers for their assistance in preparing figures and illustrations.

C(60), vitamin E, and three C(60) derivatives (polar 1 and water-soluble C(3)/D(3)C(60)s) were examined for their antioxidant effects on prevention of lipid peroxidation induced by superoxide and hydroxyl by: The fullerenes, particularly the highly symmetrical C 60 sphere, have a beauty and elegance that excites the imagination of scientists and nonscientists alike, as they bridge aesthetic gaps between the sciences, architecture, mathematics, engineering, and the visual to their discovery, only two well-defined allotropes of carbon were known—diamond (composed of a three-dimensional.

Since the first discovery of the well-known class of spherical molecules [], fullerenes have attracted worldwide attention due to their unique structure and paved the way in many research areas [2,3,4,5].The research interest in studying such unique molecules is due to their fascinating physical and chemical properties such as the capability of forming endohedral and exohedral derivatives Author: Hamad M.

Al-Matar, Mohammad H. BinSabt, Mona A. Shalaby. Fullerenes and their derivatives have been proposed as free radical scavengers, and a number of investigations have studied fullerene derivatives as potential free radical antioxidant therapeutics, neuroprotectants, anti-inflammatories and others [5,10].

Fullerenes (both pristine and derivatized fullerenes) have a tendency toward aggregation Cited by: Buckminsterfullerene is a type of fullerene with the formula C It has a cage-like fused-ring structure (truncated icosahedron) that resembles a soccer ball, made of twenty hexagons and twelve pentagons, with a carbon atom which has one π bond and two σ bonds at each corner of the shape to create a Chemical formula: C₆₀.

Indices of the fullerenes reactivity Denis Sh. estimation of the stability of fullerene derivatives which can be successfully used in medicine, nanotechnologies, taken into account in kinetic analysis of competitive reactions of radical addition to C Fullerene is able to fit inside the hydrophobic cavity of HIV proteases, inhibiting the access of substrates to the catalytic site of the enzyme.

It can be used as radical scavenger; in fact some water-soluble derivatives are able to reduce ROS by: The halogen derivatives of fullerene are of particular interest on account of their application as synthons for preparing novel derivatives on their basis.3 The bromination and chlorination will add maximum of 24 halogens, whereas fluorination will readily add 48 fluorines.3 The important distinction of halogenation reactions from other radical.

31 Manganese(III) Acetate, CAN, and Fe(III) Salts in Oxidative Radical Chemistry Jonathan W. Burton. 32 Halogen and Chalcogen Transfer Chemistry Chaozhong Li. 33 Xanthates and Related Derivatives as Radical Precursors Samir Z.

Zard. 34 Epoxides in Titanocene-Mediated and -Catalyzed Radical Reactions Andreas Gansäuer and André. Fullerenes can be of a different type C60, C70, etc., depending on the content of carbon atoms.

The most stable and best studied - is the C60, containing 60 carbon atoms. Fullerene is the only molecular form of carbon, in contrast to the diamond and graphite, which are only crystalline forms with a certain spatial arrangement of carbon atoms in. Fullerenes act as ‘radical sponges’ scavenging around 20 free radicals per molecule of fullerene.

This action is due to the electron deficient alkene nature of fullerenes which take up the electrons and scavenge the radicals. The efficiency of these entities goes up to around times the leading antioxidants. Oxidation causes cell death.

Guan-Wu Wang,* Ting-Hu Zhang, Er-Hong Hao, Li-Juan Jiao, Yasujiro Murata, and Koichi Komatsu, “Solvent-Free Reactions of Fullerenes with N-Alkylglycines with and without Aldehydes under High-Speed Vibration Milling”, Tetrahedron59, 4.

Fullerenes synonyms, Fullerenes pronunciation, Fullerenes translation, English dictionary definition of Fullerenes. An allotrope of carbon composed of any of various cagelike molecules that consist only of an even number of carbon atoms, are often spherical in shape.

The separation and functionalization of fullerenes is a recent and exciting area of research. The separation methods outlined are intended to increase the availability of endohedral metallofullerenes by decreasing their cost of production.

Functionalized fullerene species were achieved through Bingel and Prato reactions to provide materials. Novel mechanism of antioxidant activity of buckminsterfullerene C60 based on protons absorbing and mild uncoupling of mitochondrial respiration and phosphorylation was postulated.

In the present study we confirm this hypothesis using computer modeling based on Density Functional Theory. Fullerene's geroprotective activity is sufficiently higher than those of the most powerful Cited by:. Due to their attractive physical, chemical, and biological properties and the availability of various methods for surface modification, fullerenes and their derivatives have been studied for their numerous biomedical applications, not only in tumor diagnosis and therapy, but also as an anti-HIV agent [77, 78], antimicrobial photosensitizer [Download Radical Reactions of Fullerenes and their Derivatives!

or any other file from Books category. HTTP download also available at fast speeds.activity is an intrinsec property of fullerenes, the mechanism of radical scavenging and neuroprotection are still unclear.

The aim of this work is to study the mechanism and kinetics of the gas phase reaction between fullerene C60 and hydroxyl radicals, using quantum File Size: 1MB.

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