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Chem. 1B – Chem. 1B –

Chem. 1B – - PowerPoint Presentation

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Chem. 1B – - PPT Presentation

1117 Lecture Announcements I Lab Last Quiz MondayTues on Exp 10 14 and Chapter 24 No Lab next Wednesday Experiment 10 report due Exam 3 Two weeks and three lectures from today On electrochemistry and Chapter 24 ID: 551438

metals complex chapter transition complex metals transition chapter coordination orbitals electrons complexes octahedral axis bonding cont energy states light

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Slide1

Chem. 1B – 11/17 LectureSlide2

Announcements I

Lab

Last Quiz Monday/Tues on

Exp

10, 14 and Chapter 24

No Lab next Wednesday

Experiment 10 report due

Exam 3

Two weeks (and three lectures) from today

On electrochemistry and Chapter 24

Last year’s exam did not cover last parts of Ch. 24Slide3

Announcements II

Mastering

Ch

. 24 assignment due

11/26

Today’s Lecture

Transition Elements (Ch. 24)

Bonding in Coordination Complexes - TheorySlide4

Chapter 24 Transition Metals

Optical Isomer Demonstration

Show with models of MX

2

YZ and MWXYZSlide5

Chapter 24 Transition Metals

Coordination Complex – Bonding Theory – cont.

To understand how electrons in the d shells influence bonding, we must understand the shapes of d orbitals

Two different classes of d orbitals occurs

Off axes orbitals

x

y

z

x

y

z

d

xy

– lies in xy plane

x

y

z

d

xz

d

yz

Slide6

Chapter 24 Transition Metals

Coordination Complex – Bonding Theory – cont.

Two different classes of d orbitals occurs

On axes orbitals

x

y

z

x

y

z

d

x^2 – y^2

d

z^2

Slide7

Chapter 24 Transition Metals

Coordination Complex – Bonding Theory – cont.

In octahedral binding, because the ligands bring the electrons, lower energy results when the binding axes orbitals (d

z2

and d

x2-y2

) are UNFILLED

Or alternatively, the ligands cause a split in energy levels of d shell orbitals

E

Free atom

Metal in octahedral complex

On axis

Off axis

DSlide8

Chapter 24 Transition Metals

Coordination Complex – Bonding Theory – cont.

How does d orbital splitting affect coordination complexes?

Electrons go to low energy states first

Example: [Cr(CN)

6

]

3-

has 4 – 1 = 3 d shell electrons – they should occupy the three off-axes orbitals

On axis

Off axisSlide9

Chapter 24 Transition Metals

Coordination Complex – Bonding Theory – cont.

When we add more than 3 electrons (e.g. 4 electrons), there are two possibilities:

fill bottom orbitals first

or go to top orbitals

Filling depends on

D

gap (larger leads to “low spin” states – first shown, while smaller leads to “high spin” states – second shown)Slide10

Chapter 24 Transition Metals

Coordination Complex – Bonding Theory – Role of Ligands

Particular metals, such as Fe, can form complexes with different properties (e.g. colors or magnetic properties) depending on ligands

Ligands affect size of

D

gap

“Strong” ligands result in large

D

gap, while “weak” ligand results in smaller

D

gap (with the idea that more tightly held electrons will overlap more with d shell electrons)Slide11

Chapter 24 Transition Metals

Coordination Complex – Bonding Theory – Role of

Ligands

and Metal

Ligand Strength (see text for full range)

Metal Ion Strength (greater charge, Fe

3+

vs. Fe

2+

, increases

D

)

strongest

CN

-

weakest

NH

3

Cl

-

I

-

H

2

O

Weak Field Ligands – tend to give high spin statesSlide12

Chapter 24 Transition Metals

Coordination Complex – Magnetic and Light Absorbing Properties

Magnetic Properties:

Compounds or atoms with unpaired electrons are magnetic (since half filled shells will have electrons with the same spin)

Example: Fe [Kr]4s

2

3d

6

will have 4 unpaired electrons and is magnetic

Other metals, e.g. Zn (d

10

), are not magnetic

E

4s

3dSlide13

Chapter 24 Transition Metals

Coordination Complex – Magnetic Properties – cont.

Octahedral Complexes will have d electrons split into to energy states by ligand field

Large

D

gap complexes give rise to “low spin” states that are less magnetic vs. “high spin” states

Examples: [Fe(CN)

6

]

4-

vs. [Fe(Br)

6

]4-

large

D

small

DSlide14

Chapter 24 Transition Metals

Coordination Complex – Light Absorbing Properties

Gap between on- and off-axes d orbitals can also lead to transitions between two states

Example: [Cr(CN)

6

]

3-

Absorption of light causes electronic transition from low energy to high energy state:Slide15

Chapter 24 Transition Metals

Coordination Complex – Light Absorbing Properties – cont.

Many coordination complexes absorb visible light (

l

green light

~ 525 nm or E = hc/

l

= 3.8 x 10

-19

J)

The larger the

D

gap, the greater the E, and the smaller the l value energy

Visible colors go ROYGBIV (red, orange, yellow, green, blue, indigo, violet – from longer to shorter wavelength)Slide16

Chapter 24 Transition Metals

Coordination Complex – Light Absorbing Properties – cont.

Example: [Co(H

2

O)

6

]

2+

(used for the

Drierite

color demonstration)

Color is pink/purple (but pink is red + white = seen color because complex absorbs other colors)

Using color wheel (text) expected absorbance is in green (measured in Chem 31 as 510 nm)

Color wheel used because we see reflected lightED = ?If we switched to NH3 as a ligand (stronger), what shift would be expected?Slide17

Chapter 24 Transition Metals

Coordination Complex – Other Geometries

Besides octahedral geometries, tetrahedral and square planar geometries have different overlaps with d orbitals resulting in different d orbital splitting

In tetrahedral complexes, the complex can be positioned (see Fig. 24.17) where ligand bonds interact with “off-axis” d orbitals (d

xy

, d

xz

, and d

yz

) making these orbitals higher in energy and on-axis d orbitals lower in energy (however with small

D

values and high spin states)

Metal in tetrahedral complex

On axis

Off axis

DSlide18

Chapter 24 Transition Metals

Coordination Complex – Other Geometries

In square planar geometry, overlap is most with d

x^2 – y^2

(but is more complex as shown below)

Square planar geometry is common for d

8

ions in which d

x2 – y2

orbitals are unoccupied (low spin)

Metal in square planar complex

d

x2 – y2

d

xy

on axis and off axis in xy plane

d

Z2

d

xz

d

yzSlide19

Chapter 24 Transition Metals

Questions

Which two d orbitals do octahedral complexes overlap with the most?

Which d orbital is there the greatest overlap in square planar complexes?

Give the number of unpaired electrons for the following metals in octahedral complexes for low spin states/high spin states

a) Fe

3+

- octahedral b) Co

2+

– octahedral

c) Cu

2+

- tetrahedral d) Mn

3+ - octahedralSlide20

Chapter 24 Transition Metals

Questions – cont.

Ti

3+

is purple while Ti

4+

is uncolored. Explain.

For which of the following metals in octahedral complexes does the ligand NOT play a role in the number of unpaired electrons?

a) Mn

2+

b) Fe

3+

c) Co

2+ d) Ni

2+6. [Fe(en)3]3+ undergoes a ligand replacement reaction and forms [FeX6]3-. The new complex absorbs at shorter wavelengths. What do we know about the strength of X as a ligand?