2.1: Introduction
- Page ID
- 189925
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\(\newcommand{\avec}{\mathbf a}\) \(\newcommand{\bvec}{\mathbf b}\) \(\newcommand{\cvec}{\mathbf c}\) \(\newcommand{\dvec}{\mathbf d}\) \(\newcommand{\dtil}{\widetilde{\mathbf d}}\) \(\newcommand{\evec}{\mathbf e}\) \(\newcommand{\fvec}{\mathbf f}\) \(\newcommand{\nvec}{\mathbf n}\) \(\newcommand{\pvec}{\mathbf p}\) \(\newcommand{\qvec}{\mathbf q}\) \(\newcommand{\svec}{\mathbf s}\) \(\newcommand{\tvec}{\mathbf t}\) \(\newcommand{\uvec}{\mathbf u}\) \(\newcommand{\vvec}{\mathbf v}\) \(\newcommand{\wvec}{\mathbf w}\) \(\newcommand{\xvec}{\mathbf x}\) \(\newcommand{\yvec}{\mathbf y}\) \(\newcommand{\zvec}{\mathbf z}\) \(\newcommand{\rvec}{\mathbf r}\) \(\newcommand{\mvec}{\mathbf m}\) \(\newcommand{\zerovec}{\mathbf 0}\) \(\newcommand{\onevec}{\mathbf 1}\) \(\newcommand{\real}{\mathbb R}\) \(\newcommand{\twovec}[2]{\left[\begin{array}{r}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\ctwovec}[2]{\left[\begin{array}{c}#1 \\ #2 \end{array}\right]}\) \(\newcommand{\threevec}[3]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\cthreevec}[3]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \end{array}\right]}\) \(\newcommand{\fourvec}[4]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\cfourvec}[4]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \end{array}\right]}\) \(\newcommand{\fivevec}[5]{\left[\begin{array}{r}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\cfivevec}[5]{\left[\begin{array}{c}#1 \\ #2 \\ #3 \\ #4 \\ #5 \\ \end{array}\right]}\) \(\newcommand{\mattwo}[4]{\left[\begin{array}{rr}#1 \amp #2 \\ #3 \amp #4 \\ \end{array}\right]}\) \(\newcommand{\laspan}[1]{\text{Span}\{#1\}}\) \(\newcommand{\bcal}{\cal B}\) \(\newcommand{\ccal}{\cal C}\) \(\newcommand{\scal}{\cal S}\) \(\newcommand{\wcal}{\cal W}\) \(\newcommand{\ecal}{\cal E}\) \(\newcommand{\coords}[2]{\left\{#1\right\}_{#2}}\) \(\newcommand{\gray}[1]{\color{gray}{#1}}\) \(\newcommand{\lgray}[1]{\color{lightgray}{#1}}\) \(\newcommand{\rank}{\operatorname{rank}}\) \(\newcommand{\row}{\text{Row}}\) \(\newcommand{\col}{\text{Col}}\) \(\renewcommand{\row}{\text{Row}}\) \(\newcommand{\nul}{\text{Nul}}\) \(\newcommand{\var}{\text{Var}}\) \(\newcommand{\corr}{\text{corr}}\) \(\newcommand{\len}[1]{\left|#1\right|}\) \(\newcommand{\bbar}{\overline{\bvec}}\) \(\newcommand{\bhat}{\widehat{\bvec}}\) \(\newcommand{\bperp}{\bvec^\perp}\) \(\newcommand{\xhat}{\widehat{\xvec}}\) \(\newcommand{\vhat}{\widehat{\vvec}}\) \(\newcommand{\uhat}{\widehat{\uvec}}\) \(\newcommand{\what}{\widehat{\wvec}}\) \(\newcommand{\Sighat}{\widehat{\Sigma}}\) \(\newcommand{\lt}{<}\) \(\newcommand{\gt}{>}\) \(\newcommand{\amp}{&}\) \(\definecolor{fillinmathshade}{gray}{0.9}\)A general introduction to coordination compounds is given in the context of Lewis acids and bases on another page.
Much of reactivity can be understood in Lewis acidity terms. Perhaps the simplest examples of reactions are the formation of Lewis acid-base complexes. In a Lewis acid-base complex, a Lewis base has simply shared a pair of electrons with a Lewis acid, forming a new bond.

Frequently, metal atoms or ions act as Lewis acids. They can often accept electrons from a number of different Lewis bases at once, forming "complexes" or "complex ions" ("complex" meaning they are formed from individual parts that connect together). These Lewis bases (also called "ligands") are said to be "coordinated" to the metal, meaning they are stuck to the metal via the electron pair that they share with it.

A number of examples of ligands (compounds with lone pairs that can bind to metals) are shown in the following table.
Table \(\PageIndex{1}\): Some Common Ligands.

"Coordination complexes" play important roles in biology as well as economically important processes. Probably the most familiar coordination complex in biology is hemoglobin. It can coordinate with an additional dioxygen molecule and carry the oxygen through the bloodstream, delivering oxygen to tissues much more efficiently.

A very common coordination complex in industrial use is Wilkinson's catalyst, (PPh3)3RhCl. Wilkinson's catalyst is used to make a number of transformations more efficient; most notably, it is used in hydrogenation reactions. Chemical transformations of this sort are commonly used in making pharmaceuticals and other high-demand materials.

Because coordination compounds can sometimes be anions or cations, there is a convention used to tell the reader which part of the formula is connected together, and which part is the counterion(s). The part listed in square brackets consists of ligands bonding to a central metal; the part outside the brackets is the counterion(s). For example, [(H2O)6Co]Cl2 consists of a Co2+ ion bound to six waters. Two separate chloride anions are found nearby.

Draw structures for the following coordination compounds.
- K2[PtCl6]
- K3[Fe(CN)6]
- [(NH3)4CoCl2]Cl (two isomers)
- [(NH3)3CoCl3] (two isomers)
- [(NH3)2Ag]PF6 (it's Ag+; that's a single PF6- counterion)
- Na[HgCl3]
- Cd(NH3)4Cl2 (two isomers)
- Li2[CoCl4]
- K[Rh(CO)2I2]
- [Fe(OH2)6])NO3)2
- [Cu(NH3)4](SO4)2
- Na2[Ni(CN)4]
- [Fe(OH2)6])NO3)2 (repeat of j.)
- K3[Fe(SCN)6]
- K2[Zn(OH)4]
- Pt(NH3)2Cl2 (two isomers)
- [Ru(NH3)5Cl]Cl2
- Li[Sn(OH)3]
- K4[Mn(CN)6]
- Ni(CO)4
- [Co(NH3)5NO2](NO2)2 (two isomers based on how the ligand connects to the metal)
- [Co(NH3)5SCN]Cl2 (two isomers possible)
- [VO]SO4 (challenge: why might you draw the V-O bond differently than the other metal-ligand bonds so far?)
- [VO2]PF6
- Na2[HgS2]
- K[MnO4]
- Answer
-
Identify the geometries of each of the complexes in Exercise \(\PageIndex{1}\)