Systematic nomenclature of organic, organometallic and coordination chemistry : chemical-abstracts guidelines with IUPAC recommendations and many trivial names / Ursula Bünzli-Trepp.

Format:

Book

Author/Creator:

Bünzli-Trepp, Ursula, 1943- author.

Contributor:

Rosengarten Family Fund.

Language:

English

German

Subjects (All):

Chemistry, Organic--Nomenclature.

Chemistry, Organic.

Organometallic chemistry--Nomenclature--Handbooks, manuals, etc.

Organometallic chemistry.

Coordination compounds--Handbooks, manuals, etc.

Coordination compounds.

Names.

Genre:

Handbooks and manuals.

Physical Description:

ix, 685 pages : illustrations (some color) ; 30 cm

Edition:

Second English Edition.

Place of Publication:

Berlin : Logos Verlag Berlin, [2021]

Language Note:

English text.

Contents:

Machine generated contents note: 1. Directions for Use of the Book

2. Fundamentals

2.1. Nomenclature terms and definitions used in the Book

2.2. Conventions for enclosing marks and vowels in names

2.2.1. Enclosing marks

2.2.2. Vowels

3. Guide to Name Construction and Name Interpretation

3.1. General procedure and choice of the senior compound class (choice of the principal group)

3.2. Nomenclature types

3.2.1. Substitutive nomenclature

3.2.2. Conjunctive nomenclature

3.2.3. Multiplicative nomenclature: compounds with identical structural units

3.2.4. Additive nomenclature

3.2.5. Subtractive nomenclature

3.2.6. Functional-class nomenclature

3.3. Determination of the molecular-skeleton parent

3.4. Numbering of the molecular-skeleton parent and of other structure components

3.5. Alphabetical order of prefixes or parent-substituent names

4. Molecular-Skeleton Parents

4.1. Preliminary notes

4.2. Hydrocarbon chains

4.3. Heterochains

4.3.1. Preliminary notes

4.3.2. Heterochains with irregularly placed heteroatoms: replacement nomenclature (`a' nomenclature)

4.3.3. Heterochains with regularly placed heteroatoms: homogeneous and heterogeneous heterochains

4.4. Carbomonocycles

4.5. Heteromonocycles

4.5.1. Preliminary notes

4.5.2. Heteromonocycles with compulsory trivial names

4.5.3. Heteromonocycles with ten or fewer ring members: extended Hantzsch-Widman nomenclature

4.5.4. Heteromonocycles with more than ten ring members: replacement nomenclature (`a' nomenclature)

4.5.5. Silicon-containing heteromonocycles

4.6. Fused polycycles (carbo- and heterocycles)

4.6.1. Preliminary notes

4.6.2. Fused polycycles with compulsory semitrivial or trivial names

4.6.3. Fused polycycles consisting of a parent component and attached components: fusion names: fusion names

4.6.4. Fused polycycles with replacement names (`a' names)

4.7. Von Baeyer bridged polycycles (carbo- and heterocycles)

4.8. Bridged fused polycycles (carbo- and heterocycles)

4.9. Spiropolycycles (carbo-and heterocycles)

4.9.1. Preliminary notes

4.9.2. Spiropolycycles with carbomonocycle or heteromonocycle components

4.9.3. Spiropolycycles with at least one fused-polycyde component or one von Baeyer bridged-polycycle component

4.10. Ring assemblies of identical ring components (carbo- and heterocycles)

5. Substituent Prefixes

5.1. Preliminary notes

5.2. Prefixes of mononuclear substituents

5.3. Prefixes of hydrocarbon-chain substituents

5.4. Prefixes of heterochain substituents

5.5. Prefixes of carbocycle substituents

5.6. Prefixes of heterocycle substituents

5.7. Prefixes of ring-assembly substituents

5.8. Prefixes of composite substituents: choice of the parent substituent

5.9. Prefixes of carbonyl-containing substituents and analogs

6. Compound Classes

6.1. Preliminary notes

6.2. Radicals

6.2.1. Preliminary notes

6.2.2. Radical center at a molecular-skeletal parent

6.2.3. Radical center at a characteristic group

6.2.4. Polyradicals

6.3. Cations

6.3.1. Preliminary notes

6.3.2. Cation center by the formal addition of electrophiles E+

6.3.3. Cation center by the formal removal of hydride ions H-

6.3.4. Cation center resulting from skeletal bonding of a heteroatom

6.3.5. Cation center in spiropolycydes

6.3.6. Cation substituents (prefixes)

6.3.7. Polycations

6.4. Anions

6.4.1. Preliminary notes

6.4.2. Anion center by the formal removal of protons H+

6.4.3. Anion center by the formal addition of hydride ions H-

6.4.4. Anion substituents (prefixes)

6.4.5. Polyanions

6.5. Zwitterions

6.6. Radical ions

6.7. Carboxylic, carbothioic, carboselenoic, carbotelluroic, carbohydrazonic, carboximidic, and corresponding carboperoxoic acids and salts

6.7.1. Preliminary notes

6.7.2. Carboxylic acids

6.7.3. Carbothioic, carboselenoic, carbotelluroic, carbohydrazonic, and carboximidic acids

6.7.4. Carboperoxoic acids (peroxy acids) and their chalcogeno, hydrazono, and imido replacement analogs

6.7.5. Salts of carboxylic acids and of their chalcogeno, hydrazono, imido, and peroxy replacement analogs

6.8. Sulfonic, sulfinic, and sulfenic acids, selenonic, seleninic, and selenenic acids, telluronic, tellurinic, and tellurenic acids, their chalcogeno, hydrazono, imido, and peroxy replacement analogs, and corresponding salts

6.9. C-Oxoacids: carbonic and formic acid and their replacement analogs and corresponding salts

6.10. S-, Se-, Te-, and N-Oxoacids

6.11. P-and As-Oxoacids

6.12. Sb-, Bi-, Si-, and B-Oxoacids

6.13. Anhydrides

6.14. Esters and lactones

6.15. Acidhalides

6.16. Amides, lactams, cyclic imides, and amidines

6.17. Hydrazides

6.18. Nitriles

6.19. Aldehydes and their oxime and hydrazone derivatives

6.20. Ketones and their oxime and hydrazone derivatives

6.21. Alcohols and phenols

6.22. Hydroperoxides

6.23. Amines

6.24. Imines

6.25. Nitrogen compounds

6.26. Phosphorus and arsenic compounds

6.27. Antimony and bismuth compounds

6.28. Boron compounds

6.29. Silicon, germanium, tin, and lead compounds

6.30. Oxygen compounds

6.31. Sulfur, selenium, and tellurium compounds

6.32. Carbon compounds

6.33. Halogen compounds

6.34. Organometallic and coordination compounds

Appendixes

A.1. Specialist nomenclatures

A.1.1. Preliminary notes

A.1.2. Alkaloids

A.1.3. Amino acids and peptides

A.1.4. Carbohydrates

A.1.5. Cyditols

A.1.6. Nucleosides, nucleotides, and nucleic acids

A.1.7. Steroids

A.1.8. Terpenes, carotenoids, and retinoids

A.1.9. Vitamins

A.1.10. Porphyrins and bile pigments

A.1.11. Polymers

A.1.12. References for specific compound classes, Internet addresses, and nomenclature software

A.2. Multiplying affixes

A.3. Modifying syllables

A.4. Heteroatom syllables and element names

A.5. Indicated H atom `H' (indicated hydrogen) and tautomers

A.6. Configuration descriptors in names

A.6.1. Definitions

A.6.2. The CIP system for the specification of the configuration of a stereogenic center, axis or plane, or double bond

A.6.3. Stereodescriptors for the denotation of the absolute and relative configuration in names

A.6.4. Configuration of organometallic and coordination compounds

A.7. Lambda (X) convention

A.8. Isotopically modified compounds

A.8.1. Preliminary notes

A.8.2. Isotopically modified compounds: IUPAC Recommendations

A.8.3. Isotopically modified compounds: CA Guidelines

A.9. List of substituent prefixes.

Notes:

Translation of "Handbuch für die systematische Nomenklatur der organischen Chemie, metallorganischen Chemie und Koordinationschemie".

Includes bibliographical references and index.

Local Notes:

Acquired for the Penn Libraries with assistance from the Rosengarten Family Fund.

ISBN:

9783832553746

3832553746

OCLC:

1285492754

Publisher Number:

99990839972