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Advances in chemistry research. Volume 16 /

Detalles Bibliográficos
Clasificación:Libro Electrónico
Otros Autores: Taylor, James C.
Formato: Electrónico eBook
Idioma:Inglés
Publicado: New York : Nova Science Publishers, Inc., 2012.
Temas:
Acceso en línea:Texto completo

MARC

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245 0 0 |a Advances in chemistry research.  |n Volume 16 /  |c James C. Taylor, editor. 
260 |a New York :  |b Nova Science Publishers, Inc.,  |c 2012. 
300 |a 1 online resource (x, 236 pages) :  |b illustrations (some color) 
336 |a text  |b txt  |2 rdacontent 
337 |a computer  |b c  |2 rdamedia 
338 |a online resource  |b cr  |2 rdacarrier 
504 |a Includes bibliographical references and index. 
588 0 |a Online resource; title from pdf information screen (Ebsco, viewed April 2, 2013). 
505 0 |a ADVANCES IN CHEMISTRY RESEARCH VOLUME 16 ; ADVANCES IN CHEMISTRY RESEARCH VOLUME 16 ; CONTENTS; PREFACE ; QUANTUM CHEMISTRY OF NITRIC ACID: ELECTRONIC STRUCTURE AND REACTIVITY OF ITS DECOMPOSITION PRODUCTS; ABSTRACT ; INTRODUCTION; 1.1. Structural and Thermodynamic Parameters of Known Isomers of HNO3 ; 1.2. Structural and Thermodynamic Parameters of New Isomers of HNO3 ; 2. THE MOLECULAR STRUCTURE OF N2O5 IN THE GAS AND SOLID PHASES ; 3. THE ELECTRONIC STRUCTURE OF THE HIGH-ENERGY STATES OF NITROGEN DIOXIDE NO2. 
505 8 |a 4.1. Photochemical Water Decomposition in the Presence of Nitrogen Dioxide in Troposphere 4.2. Hydrolysis of NO2* ; 5.1. Structural and Thermodynamic Parameters of an NO3 Molecule in Different Electronic States ; 5.2. The Reactivity of High-Energy Nitrogen Trioxide NO3 (2A1) in the Oxidation of N2 and N2O ; 6.1. The Molecular Structures of Dinitrogen Tetraoxide N2O4 Isomers and Quantum-Chemical Evidence for a New Isomer -- Nitrosonium Nitrate NO+NO3- ; 6.2. The NO2 Dimerization, Isomerization and Hydrolysis of N2O4 in the Acid-Formation Process. 
505 8 |a 7.1. Molecular Mechanism of the NO Oxidation by Oxygen in the Gas Phase 7.2. Experimental Data for the Trimolecular Reaction of O2 with Two NO Molecules ; 7.3. Quantum-Chemical Data for the Trimolecular Reaction of O2 with Two NO Molecules; CONCLUSION ; REFERENCES ; FURAN RESINS: SYNTHESIS, CHARACTERIZATION AND APPLICATIONS; ABSTRACT ; 1. INTRODUCTION ; 2. FURAN DERIVATIVES AS SOLVENTS ; 2.1. Furfural ; 2.2. Furan ; 2.3. Furfuryl Alcohol ; 2.4. Hydroxymethyl Furfural ; 2.5. Dimethylfuran ; 3. FURAN DERIVATIVES AS INHIBITORS; 3.1. Inhibition of Free Radical Polymerization. 
505 8 |a 3.2. Corrosion Inhibitors3.3. Biological Inhibition ; 4. DIELS-ALDER REACTIONS APPLIED TO FURAN DERIVATIVES ; 4.1. Conditions and Versatility ; 4.2. Furan Rings as Functional Group Modifiers: Synthetic Applications; 4.2.1. Natural Products; 4.2.2. Polymers ; 4.2.3. Strategies for Structure Modification ; 4.3. Exploitation of the Thermal Reversibility; 4.3.1. Recyclable Materials ; 4.3.2. Self-Healing Materials; 4.3.3. Biomedical Applications: Hydrogels and Drug Delivery ; 5. CHEMICAL AND THERMAL RESISTANT MATERIALS BASED ON FURAN DERIVATIVES ; 6. HIGH CARBON YIELDS: CARBONACEOUS MATERIALS. 
505 8 |a 7. REPLACEMENT OF CLASSICAL MATERIALS 8. HIGHLY REGULAR STRUCTURES: GRAFTING AND POLYMER MODIFICATION ; 9. HIGHLY CONJUGATED STRUCTURES ; 10. NANOTECHNOLOGICAL APPLICATIONS OF FURAN BASED STRUCTURES ; REFERENCES ; A NEW RELATIONSHIP BETWEEN BOND DISTANCES AND BOND STRETCHING WAVENUMBERS OF NO IN COMPLEXES, CLUSTERS, AND ADSORBED ON SINGLE CRYSTAL METAL SURFACES: A VIBRATIONAL SPECTRODIFFRACTOMETRIC ANALYSIS ; ABSTRACT ; LIGAND ABBREVIATIONS ; ABBREVIATIONS ; 1. INTRODUCTION ; 2. RESULTS AND DISCUSSION ; 2.1. The Data ; 2.2. Structure and Bonding. 
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