Anions nomenclature

Boraanthracene — see Dibenzo[6,e]borin 9-Boraanthracene anions nomenclature, 1, 631 Borabenzene anions nomenclature, 1, 631... 

Ammonophosphorous acids, nomenclature of, 2 265 Anatase, formation of, by 7-ti-tanium(IV) oxide, 6 82 Aniline, compound with thorium acetylacetonate, 2 215 5-Anilino-l,2,3,4-thiatriazole, 6 45 Anions, nomenclature of, 2 258 Antimony(III) cesium chloride, 2SbCl3-3CsCl, precipitation in extraction of cesium from pollu-cite, 4 6... 

Electron acceptor Radical anion nomenclature Solvated electron nomenclature... 

Table 6.3 Prefixes and Suffixes in Acid and Anion Nomenclature (Acids and Anions of Chlorine Given as Examples)...

Nitric, sulfuric, and phosphoric acids have important variations with different numbers of oxygen atoms. The acid and anion nomenclature system in Table 6.3... 

The following example gives you the opportunity to practice what you have learned about acid and anion nomenclature. If you have memorized what is necessary and know how to apply the rules, you will be able to write the required names and formulas with reference to nothing other than a periodic table. If you have really mastered the system, you will be able to extend it to the last substance in each column. 

See Secs. 3.1.2.2 and 3.1.2.8 for naming monatomic and certain polyatomic anions. When an organic group occurs in an inorganic compound, organic nomenclature (q.v.) is followed to name the organic part. 

Protonated Anions. Ions such as HSOy are recommended to be named hydrogensulfate with the two words written as one following the usual practice for polyatomic anions. However, in the Nomenclature of Organic Chemistry, 1979 edition, hydrogen is used as a separate word this practice is followed in this Handbook. 

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. 

Eor the many details of constmcting or interpreting stmctures and systematic names, the Hterature on nomenclature and indexing (6) can be consulted. Systematic nomenclature is illustrated by the Chemicaly hstracts name of the sodium iron(III) EHPG chelate sodium [[N,N -l,2-ethanediylbis[2-(2-hydroxyphenyl)glyciQatol]](4-)-N,N, 0,0, 0, 0 ]ferrate(l-) [16455-61-1], The ferrate anion (12) [20250-28-6] and the potassium salt [22569-56-8] are also Hsted ia Chemical Abstracts (7). 

Anions derived from cyclic imides may, of course, be named by the foregoing principles, but it is often desirable to name them so as to emphasize their functional character. To do so, the -imide name is changed to -imidide . Such anions are obviously mesomeric, but for nomenclature purposes they are considered to be derived from the more stable tautomer, the imide form, as shown in (201). 

Another type of anion, confined for practical purposes to boron compounds, has no unshared electrons at the anionic site, and must be thought of as being formed by addition of hydride to a boron atom (or other atom with an incomplete valence shell). Such structures were not anticipated at the time general heterocyclic nomenclature was developed, and they are only recently being fitted into systematic nomenclature (lUPAC Provisional Recommendation 83.2). Proposals for a suffix to indicate such structures are under consideration (1982). 

Meanwhile, the A convention combined with replacement nomenclature may be used to indicate the changed bonding number of the anionic site, and the suffix -ide appended, as shown in (202) and (203). Proposals for an anionic replacement prefix, analogous to the cationic -onia prefixes, are under consideration. 

Specific polymers discussed in this chapter and the type of column used for their characterization are summarized in Table 20.1. The polymers are categorized as nonionic, anionic, or cationic. The nomenclature (acronyms) used for the different polymer types are also listed in Table 20.1. 

Protonation of the anion [SN2] by acetic acid in diethyl ether produces the thermally unstable sulfur diimide S(NH)2. Like all sulfur diimides, the parent compound S(NH)2 can exist as three isomers (Scheme 5.5). Ab initio molecular orbital calculations indicate that the (cis,cis) configuration is somewhat more stable than the (cis,trans) isomer, while the (trans,trans) isomer is expected to possess considerably higher energy. The alternative syn,anti or E,Z nomenclatures may also be used to describe these isomers. The structures of organic derivatives S(NR)2 (R = alkyl, aryl) are discussed in Section 10.4.2. 

In the 1,3-dipolar cycloaddition reactions of especially allyl anion type 1,3-dipoles with alkenes the formation of diastereomers has to be considered. In reactions of nitrones with a terminal alkene the nitrone can approach the alkene in an endo or an exo fashion giving rise to two different diastereomers. The nomenclature endo and exo is well known from the Diels-Alder reaction [3]. The endo isomer arises from the reaction in which the nitrogen atom of the dipole points in the same direction as the substituent of the alkene as outlined in Scheme 6.7. However, compared with the Diels-Alder reaction in which the endo transition state is stabilized by secondary 7t-orbital interactions, the actual interaction of the N-nitrone p -orbital with a vicinal p -orbital on the alkene, and thus the stabilization, is small [25]. The endojexo selectivity in the 1,3-dipolar cycloaddition reaction is therefore primarily controlled by the structure of the substrates or by a catalyst. 

Ligand A molecule or anion bonded to the central metal in a complex ion, 409 characterization, 411-412 nomenclature, 648-649 Light, 159q absorption, 421 particle nature of, 135-136 wave nature of, 133-135 Limiting reactant The least abundant... 

These will be represented by (Res.A )B , where Res. is the basic polymer of the resin, A is the anion attached to the polymeric framework, B+ is the active or mobile cation thus a sulphonated polystyrene resin in the hydrogen form would be written as (Res.SO J)H. A similar nomenclature will be employed for anion exchange resins, e.g. (Res. NMeJ )CI . 

The radical and the anion, R-N2 and R-N2, derived (formally) from a diazonium ion by addition of one and two electrons respectively, are named as diazenyl ( radical at the end is not necessary ) and diazenide (IUPAC, 1993). The radical derived formally from a diazoalkane by addition of a hydrogen atom (R=N-NH) is named diazanyl . In order to be consistent with the nomenclature of diazonium ions, the name of the parent compound should precede the words mentioned, e. g., benzenediazenyl for C6H5 - NJ (the term phenyldiazenyl radical is, however, used by Chemical Abstracts). 

Chromium, (ri6-benzene)tricarbonyl-stereochemistry nomenclature, 1,131 Chromium complexes, 3,699-948 acetylacetone complex formation, 2,386 exchange reactions, 2,380 amidines, 2,276 bridging ligands, 2,198 chelating ligands, 2,203 anionic oxo halides, 3,944 applications, 6,1014 azo dyes, 6,41 biological effects, 3,947 carbamic acid, 2,450 paddlewheel structure, 2, 451 carboxylic acids, 2,438 trinuclear, 2, 441 carcinogenicity, 3, 947 corroles, 2, 874 crystal structures, 3, 702 cyanides, 3, 703 1,4-diaza-1,3-butadiene, 2,209 1,3-diketones... 

Macropolycyclic ligands, 2,942 classification, 2,917 metal complexes binding sites, 2, 922 cavity size, 2,924 chirality, 2, 924 conformation, 2,923 dimensionality, 2, 924 electronic effects, 2, 922 shaping groups, 2,923 structural effects, 2,922 molecular cation complexes, 2,947 molecular neutral complexes, 2,952 multidentate, 2,915-953 nomenclature, 2,920 Macro tetrolide actins metal complexes, 2,973 Macrotricycles anionic complexes, 2,951 cylindrical... 

The abbreviations for the investigation methods are also taken from the nomenclature of Sillen and Martel 1 (76) aiex = anion exchange cal = calorimetry ciex = cation exchange dis = distribution between two phases est = estimate red = e.m.f. with redox electrode sp = spectrophotometry. Our selected data, rather limited in number, arise from the present status of the IAEA assessment of inorganic complexes of the actinides (12). 

A remarkable variety of compounds in the Ca-(B,C,N) system has opened a window for research in related fields. With the elements boron, carbon and nitrogen, substance classes such as borocarbides, boronitrides, and carbonitrides can be considered to contain anionic derivatives of binary compounds B4C, BN, and C3N4. Until now, most compounds in these substance classes have been considered to contain alkali, alkaline-earth, or lanthanide elements. Lanthanide borocarbides are known from the work of Bauer [1]. Lanthanide boronitrides represent a younger family of compounds, also assigned as nitridoborates [2] following the nomenclature of oxoborates. 

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