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1. |
Record Nr. |
UNINA9910144325103321 |
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Titolo |
The Formation of bonds to halogens . Part 1 [[electronic resource] /] / founding editor, J.J. Zuckerman; editor, A.P. Hagen |
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Pubbl/distr/stampa |
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ISBN |
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1-282-30815-7 |
9786612308154 |
0-470-14517-X |
0-470-14538-2 |
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Descrizione fisica |
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1 online resource (745 p.) |
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Collana |
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Inorganic reactions and methods ; ; 3 |
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Altri autori (Persone) |
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HagenA. P |
ZuckermanJ. J <1936-1987.> (Jerold J.) |
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Disciplina |
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Soggetti |
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Halogenation |
Chemical bonds |
Chemical kinetics - Effect of temperature on |
Electronic books. |
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Lingua di pubblicazione |
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Formato |
Materiale a stampa |
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Livello bibliografico |
Monografia |
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Note generali |
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Description based upon print version of record. |
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Nota di bibliografia |
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Includes bibliographical references and indexes. |
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Nota di contenuto |
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Inorganic Reactions and Methods; Contents; How to Use this Book; Preface to the Series; Editorial Consultants to the Series; Contributors to Volume 3; Formation of Bonds to Halogens (Part 1); Introduction; Formation of Halogen-Halogen Bonds; Introduction; Preparation of the Elemental Halogens; by Anodic Oxidation; of Fluoride Ion.; of Chloride Ion.; of Bromide Ion.; of Iodide Ion.; by Chemical Oxidation; of FIuoride.; of ChIoride.; of Bromide.; of Iodide.; by Reduction.; by Dissociation of Halides.; Diastatine Synthesis.; Preparation of Cationic Polyhalogens (Homonuclear and Heteronuclear) |
by Halide-Anion Transfer in Acid-Base Reactions.by Oxidation of Elemental Halogens or Interhalogens.; Preparation of Neutral Interhalogens; from the Elements.; by Fluorination of CI2, Br2, and I2.; by Chlorination of Br2 and I2.; by Bromination of I2.; from the Oxidation of Anionic Halides.; from the Oxidation of Organoiodides; by F2 or CI2.; by Oxidizing Fluorinating Agents (Excluding F2).; |
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Preparation of Neutral and Cationic lnterhalogen Compounds Containing Astatine; Preparation of Aryliodo Fluorides from Aryliodo Oxides; from Aryliodoso and Aryliodo Compounds and HF. |
from Aryliodo Compounds and SF4.by Electrochemical Fluorination of Aryliodo Compounds.; from Aryliodo Compounds and XeF2.; from Aryliodo Compounds and F2.; Preparation of Anionic Polyhalides (Homonuclear and Heteronuclear); from Elemental Halogens with Halide Anion.; from lnterhalogen Compounds with Halide Anion.; Preparation of Anionic Polyhalides Containing Astatine.; Preparation of HaIogen OxyfIuorides; from Halogen Oxides with F2.; from Halogen Oxides with Fluorinating Agents Other than F2.; from Halogen Oxyfluorides with Fluorinating Agents. |
by Disproportionation of Halogen Oxyfluorides.from Positive Halogen Compounds with Fluorinating Agents.; from Halogen Oxyacids and Their Salts with Fluorinating Agents.; by Elimination.; Formation of Bonds between Halogens and Group-VB (0, S, Se, Te, Po) Elements; Introduction; from the Elements; from Halogenation by Elemental Halogens; to Give the Oxygen-Halogen Bond.; to Give the Sulfur-Halogen Bond.; to Give the Se-Halogen Bond.; to Give the Te-Halogen Bond.; to Give the Po-Halogen Bond.; from Halogenation by Hydrogen Halides.; from Halogenation by Oxidizing Halides |
to give the Oxygen-Halogen Bond.to Give the Sulfur-Halogen Bond.; to Give the Se-Halogen Bond.; to Give the Te-Halogen Bond.; from Halogenation by Organic Halides.; from Oxidation of Elementai halogens by Ozone.; from Cleavage of the Group VIB-Hydrogen Bond (Excluding Polonium); by Halogens.; by Oxidizing Halides.; from Cleavage of the Group VIB-Carbon bond; by Halogens.; by Oxidizing Halides or Electrochemical Fluorination.; from Cleavage of the Group VIB-Group IVB Element Bond; by Halogens.; by Oxidizing Halides.; from Cleavage of the Group VIB-Oxygen Bond; by Halogens. |
to Give the Sulfur-Halogen Bond. |
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Sommario/riassunto |
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For the first time the discipline of modern inorganic chemistry has been systematized according to a plan constructed by a council of editorial advisors and consultants, among them three Nobel laureates (E.O. Fischer, H. Taube and G. Wilkinson). Rather than producing a collection of unrelated review articles, the series creates a framework which reflects the creative potential of this scientific discipline. Thus, it stimulates future development by identifiying areas which are fruitful for further research. The work is indexed in a unique way by a structured system which maximizes its usefulne |
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