Nomenclature numerical prefixes

Nomenclature based on a parent term with an appended suffix accounts for most natural product names. However, as related compounds are identified, or even when a suffix has to denote multiple functional groups, a variety of modifying terms can be employed. For example, the common prefix nor- denotes the removal of a skeletal atom from the parent structure the loss of two or more skeletal atoms is indicated by combining an appropriate numerical prefix with nor- , e.g., dinor- , trinor- (Giles 1999). Table 1.2 lists additional examples of commonly encountered modifying terms. 

Binary npe nomenclature. In this system, the composition of a substance is specified by ihe juxtaposition of dement group names, modified or unmodified, together with appropriate numerical prefixes, if considered necessary. 

In compositional nomenclature, ligands are given in alphabetical order before central atoms. Central atoms are listed in alphabetical order as well. Bridging ligands to the extent known are indicated by the p notation (see Section 3.2.3.4). The numbers of ligands and central atoms are indicated by the appropriate numerical prefixes (see Section 3.3.2). Anions, cations, oxidation states and ionic charges are indicated in the same manner as in mononuclear compounds (see Section 3.3.3). For examples see Table 14. 

Owing to the numerous possibilities in which a 1,4-diene can be assembled, especially when heteroatoms are included, a nomenclature issue arises that needs to be addressed from the outset. According to the Hantzsch-Widman nomenclature system in combination with the lUPAC rules, hetera-di-ir-meth-ane reactions are those transformations in which a particular heteroatom replaces the caiixin atom of the 1,4-diene moiety the position is specified by means of a numerical prefix. We will use this suggested nomenclature for the di-Tr-methane photorearrangement as indicated for the substrates shown in Scheme 1. 

The Stock Oxidation-Number System. Stock sought to correct many nomenclature difficulties by introducing Roman numerals in parentheses to indicate the state(s) of oxidation, eg, titanium(II) chloride for TiCl2, iron(II) oxide for FeO, titanium(III) chloride for TiCl, iron(III) oxide for Fe203, titanium(IV) chloride for TiCl, and iron(II,III) oxide for Fe O. In this system, only the termination -ate is used for anions, followed by Roman numerals in parentheses. Examples are potassium manganate(IV) for K2Mn02, potassium tetrachloroplatinate(II) for K PtCl, and sodium hexacyanoferrate(III) for Na3Fe(CN)3. Thus a set of prefixes and terminations becomes uimecessary. 

When a system does not have a retained name or a name that can be composed systematically as above, and when ortho- and ortho-peri- x% on are possible, it is named using fusion nomenclature, i.e. by combining the names of the two or more systems that are fused. One system is adjudged to be the senior according to criteria described elsewhere and is taken as a parent hydride, and the other is denoted in the name by a non-detachable prefix. The junction of the two systems is indicated in a specific manner. Instead of numerical locants, italic letters a , 6 , c , etc. are used to identify bonds in the parent hydride. The final letter o and normal locants are characteristic of the prefix. The examples below illustrate the fusion operation and the resulting fusion name. 

Metallocene derivatives may be named by either standard organic suffix (functional)7 or prefix nomenclature. Substituents are given the lowest numerical locants in the usual manner on the equivalent cyclopentadienyl rings of the ocene entity. The first ring is numbered 1 to 5 and the second ring is numbered V to 5. In metallocenes composed of multiple ocene groupings the cyclopentadienyl rings are further numbered 1" to 5", V" to 5", etc. The radical names -ocenyl, -ocenediyl, -ocenetriyl, etc. are used. For examples see Table 25. 

Nomenclature follows IUPAC recommendations (79PAC2251). The basic macrocyclic system I is named porphyrin, which implies that the pyrrolic nitrogen atoms are placed in positions-21 and -23, regardless of the structure of the actual tautomer. Hydro prefixes are then considered in ascending numerical order. I attempt here to maintain the arrangements of the formulas of hydroporphyrins resulting from these rules. 

In Chap. 6 we placed Roman numerals at the ends of names of metals to distinguish the charges on monatomic cations. It is really the oxidation number that is in parentheses. This nomenclature system is called the Stock system. For monatomic ions, the oxidation number is equal to the charge. For other cations, again the oxidation number is used in the name. For example, Hg2 + is named mercury(I) ion. Its charge is 24- the oxidation number of each atom is 4-1. Oxidation numbers are also used for other cations, such as dioxovanadium(V) ion, V02". The prefix 0x0- stands for oxygen. Oxidation numbers can be used with nonmetal-nonmetal compounds, as in sulfur(VI) oxide for SO3, but the older system using prefixes (Table 6-2) is still used more often. 

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