Transition Metals•Mercury (Hg) is the only transition metal that is

not a solid.•The transition metals all have valence electrons in a d subshell.•Like other metals, transition metals form cations not anions.•We shall see that many transitions cations form beautifully coloured compounds.

•Co-ordination complexes are compounds in which several ligands are co-ordinated to a transition metal cation. A ligand is any substance (neutral or anion) which can act as a Lewis base, donating electrons to the transition metal cation (which acts as a Lewis acid). If the complex has a charge, it is a complex ion.

•[Cu(OH2)6]2+ is Cu2+ with six water (“aqua ligands”)

•[Zn(CN)4]2- is Zn2+ with four cyanide (“cyano ligands”)

The ligands around the metal do not all have to be the same!

Ligands and Coordiantion Complexes

Cu

H2O

H2O OH2

OH2

OH2

OH2

2+

ZnNC

NC CN

CN

2-

Ligands and Coordiantion Complexes

This is a cartoon! Heme (the porphyrin in hemoglogin) has chains branching off the porphyrin ring.

•A very important co-ordination complex is found in hemoglobin:

•Classifying Ligands•Ligands co-ordinated to a transition metal through one atom are called monodentate ligands. •Ligands co-ordinated to a transition metal through two atoms are called bidentate (“two-toothed”) ligands. •Polydentate ligands can also be called chelating ligands, or chelates (“claws”). We saw one such ligand in the Chemistry 1000 “Hardness of Water” lab. EDTA was able to “grip” a cation by co-ordinating to it with six different atoms! (For clarity, individual carbon atoms are not shown.)

Ligands and Coordiantion Complexes

Fe

O

O

O

ON

N

O

O

O

O

1-

FeOO

O

O

O

O

C

C

C

C

O

O

O

O

O

O

C

C

3-

FeOH2

H2O

H2O

OH2

OH2

OH2

3+

monodentate ligand bidentate ligand polydentate ligand

•The number of atoms attached to the transition metal is referred to as the co-ordination number. It doesn’t matter whether these atoms come from the same molecule/ion or from several different ones. Go back and assign a co-ordination number to each complex ion on the previous three pages.•Co-ordination complexes can be charged or neutral. To make a neutral precipitate, charged co-ordination complexes (complex ions) need one or more counterions to balance the charge. This gives a complex salt.

•In the CHEM 2000 lab, you will make the bright green complex salt, K3[Fe(C2O4)3].3H2O containing Fe3+. Break this formula into a complex ion, counterion and water of hydration, clearly indicating each ion’s charge. Identify the ligands and their charge.

Ligands and Coordiantion Complexes

FeOO

O

O

O

O

C

C

C

C

O

O

O

O

O

O

C

C

3-

3 x K+ counter ions + +3 x H2O water of hydration. Water is not coordinated to the metal

Ligands and Coordiantion Complexes

•Some co-ordination complexes and complex salts contain extra water molecules which were trapped during crystallization. These complexes are also hydrates. Water of hydration can be removed by heating a complex salt in a dry oven.

•If 5.00 grams of K3[Fe(C2O4)3].3H2O is heated until all of the water has evaporated, what mass of solid will remain?

MW of K3[Fe(C2O4)3].3H2O = 491.24274 g/molMW of K3[Fe(C2O4)3] = 437.1969 g/mol

Calculate the number of moles of K3[Fe(C2O4)3].3H2O (which is also the moles of K3[Fe(C2O4)3]). Multiply the number of moles by the mass of K3[Fe(C2O4)3] to get the mass of K3[Fe(C2O4)3] remaining.

•A co-ordination complex must contain a transition metal cation and several ligands. It may also have counterion(s) (to balance charge) and/or extra water molecules. When naming a co-ordination complex or complex salt, look for these components.

•The first step in naming a complex salt is to identify the complex ion. To name the complex ion:

•List the ligands using prefixes to indicate the number of each type of ligand. Use alphabetical order if there are multiple ligands.

•For ligands with simple names (e.g. chloro, hydroxo), use di, tri, tetra, penta, hexa, etc. •For ligands with complicated names (e.g. oxalato), use bis, tris, and tetrakis.

•Name the transition metal. If the complex ion is an anion, use the metal’s Latin name and change the suffix to ‘ate’•List the metal’s oxidation state using Roman numerals.

•Once you have named the complex ion, name the complex salt like any other ionic compound: cation then anion then hydration.

e.g. K3[Fe(C2O4)3].3H2O

Naming Complex Salts

potassium trisoxalatoferrate(III) trihydrate(cation) (complex anion) (hydration)

Naming Complex Salts (Ligand Names)

Anions Formula Name

fluoride :F- fluoro

chloride :Cl- chloro

bromide :Br- bromo

iodide :I- iodo

cyanide :CN- cyano

oxide :O2- oxo

hydroxide :OH- hydroxo

carbonate carbonato

oxalate oxalato

Neutral Molecules Formula Name

carbon monoxide :CO carbonyl

water :OH2 aqua

ammonia :NH3 ammine

ethylenediamine (“en”) NH2CH2CH2NH2 ethylenediamine

OO

:OCCO:[ ] 2-O

:OCO:[ ] 2-

When cobalt is in a complex anion, it is cobaltate. Similarly, zinc is zincate and chromium is chromate. The elements below have names that are not directly derived from the english name for the element.

Naming Complex Salts (Latin Names)

Element Symbol Latin Name Name in Anionic Complex

copper Cu cuprum cuprate

gold Au aurum aurate

iron Fe ferrum ferrate

silver Ag argentum argentate

•Name the following complex salts. Note that complex ions are typically written inside square brackets.

•[Ni(OH2)6] CO3

•[Cu(NH3)4] SO4 · H2O

•[CoCl3(NH3)3]

•[Co(NH3)6] [Cr(CN)6]

Naming Complex Salts

Hexaaquanickel(II) carbonate

Tetraaminecopper(II) sulfate monohydrate

Triamminetrichlorocobalt(III)

Hexaamminecobalt(III) hexacyanochromate(III)

•Note that there is a difference between water as a ligand and “water of crystallization”. The bright blue crystals commonly referred to as CuSO4·5H2O are really [Cu(OH2)4]SO4·H2O. Give the name corresponding to each of these two formulas.

•CuSO4·5H2O =

•[Cu(OH2)4]SO4·H2O =

•The only way to determine this information is by experiment, but you should recognize that, in many hydrated salts, at least some of the water molecules serve as ligands.

Naming Complex Salts

Copper(II) sulfate pentahydrate

Tetraaquacopper(II) sulfate monohydrate

•We have seen that main group metals are somewhat limited in what oxidation states they can adopt. Many transition metals, on the other hand, can take on a wide variety of different oxidation states. This distribution is not entirely random, as show in the graph below (common oxidation states in dark red):

•Note that the elements in the middle can exist in a wider variety of oxidation states than those on either end of the d-block.

Why are Transition Metals Special?

Why are Transition Metals Special?

•Compared to s and p electrons, d electrons can be added or removed relatively easily.

•The electron configuration of neutral vanadium is:

•The first two electrons removed will be those in the 4s orbital. After that, electrons are removed from the 3d orbitals giving three stable oxidation states:

•vanadium(III)

•vanadium(IV)

•vanadium(V)

[Ar]4s23d3

[Ar]3d2

[Ar]3d1

[Ar]

Electronic Structure and Colour

One of the more fun consequences of these partially filled d subshells is that the co-ordination complexes of transition metals are often brightly coloured. The flasks below contain aqueous solutions of several nitrate salts. Note that, since all nitrates are water-soluble, these solutions contain aqua complexes of the transition metal cation.

Fe3+ Cu2+Ni2+Co2+Zn2+

•Why is the Zn2+ complex the only colourless one?•Consider the electron configurations of the five cations:

•Fe3+

Co2+

•Ni2+

•Cu2+

•Zn2+

Electronic Structure and Colour

[Ar]4s23d6 [Ar]3d5

[Ar]4s23d7 [Ar]3d7

[Ar]4s23d8 [Ar]3d8

[Ar]4s13d10 [Ar]3d9

[Ar]4s23d10 [Ar]3d10

Electronic Structure and Colour•Where does the variety in colour come from?

•Many co-ordination complexes have octahedral geometry. This means that two of the d orbitals on the transition metal point directly at ligands while the other three do not:

•A simple electrostatic model, called the crystal field theory, assumes that there will be a certain degree of electron-electron repulsion between the electron pair a ligand donates and any electrons already in the metal d orbitals. This repulsion is felt most strongly by electrons in d orbitals pointing at the ligands.

•Thus, the dz2 and dx2-y2 orbitals are pushed to higher energy than the dxy, dxz and dyz orbitals. This separation in energy is referred to as crystal field splitting (Δo where ‘o’ is for ‘octahedral’).

Electronic Structure and Colour

In co-ordination complexes with crystal field splitting, there are two ways to distribute d electrons. Which one is favoured depends on the size of Δo.

•The high spin distribution maximizes the alignment of spin of the d electrons. It is favoured when Δo is small (when the metal is bonded to weak field ligands). Why?

•The low spin distribution puts electrons in the lowest energy orbitals first. It is favoured when Δo is large (when the metal is bonded to strong field ligands). Why?

Electronic Structure and Colour

CN- > en > NH3 > EDTA4- > H2O > ox2- > OH- > F- > Cl- > Br- > I-

strong field weak field

•How does this make for coloured solutions?•Recall that photons are emitted when electrons drop from a higher energy orbital to a lower energy orbital. (see Atomic Line Spectra) Similarly, the electrons get to the higher energy orbital by absorbing photons of light.•Electrons in the lower energy d orbitals can absorb photons and be excited into the higher energy d orbitals. Since Δo corresponds to the energy of light in the visible region (and there is more than one way to absorb a photon), some wavelengths of visible light are absorbed. The wavelengths that are not absorbed give the colour of solution.•+To absorb coloured light, the transition metal needs to have electrons in at least one of the low-energy d orbitals and an empty space in at least one of the high-energy d orbitals. Which of these two requirements does Zn2+ lack (making it colourless)?

Electronic Structure and Colour

Electronic Structure and Colour

•Note that different ligands provide different amounts of crystal field splitting. Fe(OH2)6

3+ and Fe(C2O4)33- are both complexes of

Fe3+ but Fe(OH2)63+ is extremely pale purple (frequently

appearing colourless) while Fe(C2O4)33- is green.

•What colour of light is each compound most likely absorbing?

•Which of these two ligands is splitting the d orbitals of Fe3+ more? (i.e. which complex has a larger Δo)

Electronic Structure and Colour

YG

C

M

BR

•Even a very small change in the structure of a complex ion can change its colour drastically.

•Draw two different Lewis structures for [CoCl2(NH3)4]+.

•One of these compounds is purple while one is green! The purple one is referred to as cis-[CoCl2(NH3)4]+ while the green one is trans-[CoCl2(NH3)4]+

•These compounds are referred to as isomers. They have the same molecular formula butone cannot be superimposed on the other, no matter how they are rotated.

Isomers

Co

H3N

H3N Cl

Cl

NH3

NH3

+

CoCl

H3N Cl

NH3

NH3

NH3

+

purple green

Draw two isomers of diamminedichloroplatinum(II), a square planar complex.

Draw two isomers of [CoCl3(NH3)3], an octahedral complex.

Isomers

The cis isomer is an anti-cancer drug while the trans isomer is toxic!

PtH3N

H3N Cl

ClPt

Cl

H3N Cl

NH3

Co

H3N

H3N Cl

Cl

NH3

Cl

Co

H3N

Cl Cl

Cl

NH3

NH3

facial (fac)meridional (mer)