Phane Nomenclature

Part II: Modification of the Degree of Hydrogenation and Substitution Derivatives of Phane Parent Hydrides

(IUPAC Recommendations 2002)

Prepared for publication by H. A. Favre¹ and W. H. Powell²

¹ 2031, rue Leclaire, Montréal, QUÉ, H1V 3A1, Canada

² 1436 Havencrest Ct., Columbus, OH 43220-3841, USA

https://iupac.qmul.ac.uk/phane2/

Members of Working Party (1998-2002):
H. A. Favre (Convener), D. Hellwinkel, W. H. Powell, H. A. Smith, Jr, S. S.-C. Tsay.

World Wide Web version Prepared by G. P. Moss

School of Physical and Chemical Sciences, Queen Mary University of London,
Mile End Road, London, E1 4NS, UK
g.p.moss@qmul.ac.uk

These Rules are as close as possible to the published version [see Pure Appl. Chem., 2002, 74, 809-834. Copyright IUPAC; reproduced with the permission of IUPAC]. If you need to cite these rules please quote this reference as their source.

A PDF of this document is available.

In setting up the World Wide Web version some errors have been detected. The changes have been marked by which is a link to details of the change and where it applies. For problems in converting the text into a World Wide Web version see the IUPAC nomenclature home page.

Any comments, corrections or suggestions for a future edition should be e-mailed to g.p.moss@qmul.ac.uk

Abstract: Cyclophane and linear phane systems are considered as parent hydrides. Their derivatives are named in conformity with the principles, rules and conventions prescribed for naming organic compounds. The following nomenclatural features are described: indicated and added hydrogen, order of seniority for numbering, substituents expressed as suffixes, substituents cited as prefixes, phane parent hydrides modified by addition or subtraction of hydrogen atoms, and polyfunctional derivatives.

Contents

Introduction
PhII-1. Numbering
- PhII-1.1. Starting point and direction of numbering.
- PhII-1.2. 'Hydro-' and 'dehydro-' prefixes.
- PhII-1.3. Lowest locants.
- PhII-1.4. Termination of acyclic phane parent hydrides.
PhII-2. Specification of indicated hydrogen
PhII-3. Substituent groups derived from phane parent hydrides
- PhII-3.1. General method.
- PhII-3.2. The 'added hydrogen' method
PhII-4. Substitutive nomenclature for phane parent hydrides
- PhII-4.1. Phane parent hydrides with characteristic group suffixes.
- PhII-4.2. Radicals and ions derived from phane parent hydrides.
- PhII-4.3. Substituents of phane parent hydrides cited as prefixes
PhII-5. Phane parent hydrides modified by the addition or subtraction of hydrogen atoms
- PhII-5.1. 'Hydro-' prefixes.
- PhII-5.2. 'Dehydro-' prefixes
- PhII-5.3. Ene and yne endings
  - PhII-5.3.1. Double and triple bonds.
  - PhII-5.3.2. Double bonds in amplificants and in simplified phane skeletons.
  - PhII-5.3.3. Triple bonds
  - PhII-5.3.4. Double and triple bonds in a phane structure.
- PhII-5.4. Double bonds between mancude amplificants and alternating atoms or chains.
- PhII-5.5. Double bonds between hydrogenated mancude amplificants and atoms or chains.
PhII-6. Polysubstituted derivatives of phane parent hydrides
- PhII-6.1. Principal characteristic groups.
- PhII-6.2. Name component order for polysubstituted phane derivatives.
- PhII-6.3. Order for assignment of lowest locants for phane derivatives.
References

Continued with Introduction
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