Rules and Naming Conventions for Coordination Complexes: Anions, Ligands, and Metal Ions, Study notes of Latin

The rules for naming coordination complexes, focusing on the order of writing names, Greek prefixes, and common names for ligands. It also explains how to indicate the oxidation number of the metal atom and the naming conventions for negatively charged complexes. Jørgensen's Chain Theory is discussed as a theory that explains the linking of ammonia molecules in metal compounds.

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RULES FOR NAMING COORDINATION COMPLEXES
The name of the positive ion is written before the name
of the negative ion.
The name of the ligand is written before the name of the
metal to which it is coordinated.
Ligands are listed in the following order: negative ions,
neutral molecules, and positive ions. Ligands with the
same charge are listed in alphabetical order.
The Greek prefixes mono-, di-, tri-, tetra-, penta-, hexa-,
and so on are used to indicate the number of ligands
when these ligands are relatively simple. The Greek
prefixes bis-, tris-, andtetrakis- are used with more
complicated ligands.
The names of negative ligands always end in o, as
in fluoro (F-), chloro (Cl-), bromo (Br-), iodo (I-), oxo (O2-
), hydroxo (OH-), and cyano (CN-).
A handful of neutral ligands are given common names,
such as aquo (H2O), ammine (NH3), andcarbonyl (CO).
The oxidation number of the metal atom is indicated by
a Roman numeral in parentheses after the name of the
metal atom.
The names of complexes with a net negative charge end
in -ate. Co(SCN)42-, for example, is the
tetrathiocyanatocobaltate(II) ion. When the symbol for
the metal is derived from its Latin name,-ate is added to
the Latin name of the metal. Thus, negatively charged
iron complexes are ferrates and negatively charged
copper complexes are cuprates.
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RULES FOR NAMING COORDINATION COMPLEXES

The name of the positive ion is written before the name of the negative ion.The name of the ligand is written before the name of the metal to which it is coordinated.Ligands are listed in the following order: negative ions, neutral molecules, and positive ions. Ligands with the same charge are listed in alphabetical order.The Greek prefixes mono - , di - , tri - , tetra - , penta - , hexa - , and so on are used to indicate the number of ligands when these ligands are relatively simple. The Greek prefixes bis - , tris - , and tetrakis - are used with more complicated ligands.The names of negative ligands always end in o , as in fluoro (F-), chloro (Cl-), bromo (Br-), iodo (I-), oxo (O^2 - ), hydroxo (OH-), and cyano (CN-).A handful of neutral ligands are given common names, such as aquo (H 2 O), ammine (NH 3 ), and carbonyl (CO).The oxidation number of the metal atom is indicated by a Roman numeral in parentheses after the name of the metal atom.The names of complexes with a net negative charge end in - ate****. Co(SCN) 42 - , for example, is the tetrathiocyanatocobaltate(II) ion. When the symbol for the metal is derived from its Latin name, - ate is added to the Latin name of the metal. Thus, negatively charged iron complexes are ferrates and negatively charged copper complexes are cuprates.

List of common ion names

Monatomic anions:

Cl−^ chloride S2−^ sulfide P3−^ phosphide Polyatomic ions: NH 4 +^ ammonium H 3 O+^ hydronium NO 3 −^ nitrate NO 2 −^ nitrite ClO−^ hypochlorite ClO 2 −^ chlorite ClO 3 −^ chlorate ClO 4 −^ perchlorate SO 3 2−^ sulfite SO 4 2−^ sulfate HSO 3 −^ hydrogen sulfite (or bisulfite) HCO 3 −^ hydrogen carbonate (or bicarbonate) CO 3 2−^ carbonate PO 4 3−^ phosphate HPO 4 2−^ hydrogen phosphate H 2 PO 4 −^ dihydrogen phosphate CrO 4 2−^ chromate Cr 2 O 7 2−^ dichromate BO 3 3−^ borate AsO 4 3−^ arsenate C 2 O 4 2−^ oxalate CN−^ cyanide SCN−^ thiocyanate MnO 4 −^ permanganate

For negatively charged complex ions

A negatively charged complex ion is called an anionic complex. An anion is a negatively charged ion.

In this case the name of the metal is modified to show that it has ended up in a negative ion. This is shown by the ending -ate.

With many metals, the basic name of the metal is changed as well - sometimes drastically!

Common examples include:

metal changed to

cobalt cobaltate

aluminium aluminate

chromium chromate

vanadium vanadate

copper cuprate

iron ferrate

J"rgensen's Chain Theory J~rgensen's chain theory links ammonia molecules in metal compounds similar to the linking of carbon units in hydrocarbons. Like carbon, each metal center is thought to have a fixed valence (valency being defined as the number of bonds formed by the atom of interest), with each metal stabilizing different chain lengths. stabilizing an ammine chain length of two while trivalent cobalt in structure V favors an amrnine chain length of four, Water linkages in metal hydrates (V) were treated similarly. Further, Jergensen astutely noticed that anions such as chloride (CI-) and nitrite (NOz- ) found in the complex show two distinct reactivities. Chain theory suggests that these anions occupy two different positions, proximal to (or bound directly to) and distal to (far from) the metal ion. Anions far from the metal can be readily removed during a chemical reaction, for example, CI-removal with AgNO:J, equation (2.1), whereas those bound directly to the metal do not react. AgN0 3 (aq) + Cl-(aq) ----+ AgCI(s) + N03(.q)

TABLE 1 Taessert's Cobalt Amine Complexes

Formula Original Name Color Compound CoC13' 6NH CoC13' 5NH CoCI3' 4NH CoCI3' 4NH

Yellow Purple Green Violet

complex Praseocomplex Violeto complex

[Co(NH3)61Ch [Co(NH3lsCllClz [Co(NH3) 4ClzlCI [Co(NH3) 4ClzlCI

Co (^) NH 3 NH 3 NH 3 NH 3 Cl

NH 3 Cl

NH 3 Cl

structure (1)

Co (^) NH 3 NH 3 NH 3 NH 3 Cl

NH 3 Cl

Cl

structure (2)