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Module proposal
UNIVERSITY OF WARWICK
Proposal Form for New or Revised Modules (MA1- version 3)
For consideration by the Undergraduate Studies Committee/Sub-Faculty or Graduate
Studies Committee only.
NB:
1.
1.
If it is unclear whether or not a change to an existing module should be
proposed on this form, the Chair or Secretary of the Undergraduate
Studies Committee/Sub-Faculty or Graduate Studies Committee should
be consulted.
2.
In order to reduce printing costs please delete the text provided as
guidance in the body of the form before submission to the Faculty
Secretariat. However, all sections must be completed to the satisfaction of
the Faculty Undergraduate/Graduate Studies Committee.
Title of Module:
CH267 Transition Metal Chemistry: structure, reactivity and organometallic chemistry.
2.
New or Revised Module:
New module?
[X]
Revised module?
[]
Level: D (Doctorate)
M (Masters)
H (Honours)
I (Intermediate)
C (Certificate)
[ ]
[ ]
[X]
[ ]
[ ]
If this new module replaces an existing approved module specify the code and
title of the module to be discontinued and date on which change will occur:
Replaces CH245 and CH262, October 2009
If this is a proposal for a revised module, specify which sections have been
amended, and give an outline rationale for the changes:
3.
Date of Introduction of new module or revised version of existing module:
October 2009
4.
Department Responsible for Teaching:
Chemistry
If the module is taught by more than one department please indicate this (for
matrix purposes):
Department
Department
%
%
Name of Module Leader:
JP Rourke
1
Module proposal
If the module leader is not a member of Warwick staff and has not previously
been appointed as a module leader/tutor, please include a C.V with this form.
5.
Availability/Location of module within courses:
List the degree courses on which this module is available, indicating the year of
study, whether the module is core or an option and the credit weighting in each
case. Include any part-time or 2+2 degrees on which this module is available.
Degree
Code
F100
F101
F102
F105
F106
F107
F108
F121
F122
F125
F126
F127
F128
F1N1
F1N2
BF91
B9F1
FC11
F1C1
Title
Chemistry BSc
Chemistry BSc with Intercalated year
General Chemistry BSc
Chemistry MChem
Chemistry MChem with Professional Experience
Chemistry MChem with Intercalated Year
Chemistry MChem with Industrial Training
Chemistry with Medicinal Chemistry BSc
Chemistry with Medicinal Chemistry BSc with
Intercalated Year
Chemistry with Medicinal Chemistry MChem
Chemistry with Medicinal Chemistry MChem with
Professional Experience
Chemistry with Medicinal Chemistry MChem with
Intercalated Year
Chemistry with Medicinal Chemistry MChem with
Industrial Training
Chemistry with Management BSc
Chemistry with Management BSc with Intercalated
Year
Biomedical Chemistry BSc
Biomedical Chemistry BSc with Intercalated Year
Chemical Biology MChem
Chemical Biology MChem with Intercalated Year
Visiting Students
Year of
study
2
2
2
2
2
2
2
2
2
Core Optional Option list CATS*
core?
A,B or C
Core
15
Core
15
Core
15
Core
15
Core
15
Core
15
Core
15
Core
15
Core
15
2
2
Core
Core
15
15
2
Core
15
2
Core
15
2
2
Core
Core
15
15
2
2
2
2
Core
Core
Core
Core
15
15
15
15
15
*Credit should be in one of the following tariffs:
6, 12, 18, 24, 48 credits; or
7.5, 15, 30, 45, 60 credits; or
(for postgraduate courses only) 10, 20, 30, 40, 50,60 credits
6.
Consultation with other Departments:
It is important that any departments affected by the introduction of this
module are consulted before the module is considered by the relevant
Faculty committee.
Which other departments will be affected by the introduction/revision of this
module (i.e. other departments offering the module as an option in their degree
courses, including joint degree courses involving the department proposing the
module)? Please give details of any consultations undertaken and indicate
whether the other departments have approved the proposal.
2
Module proposal
N/A
7.
Context:
Describe the relationship to any other modules with which the new module has a
close connection and any prerequisite relationships.
This module follows on from the transition metal component of Year 1 CH160. The one-electron
(orbital) picture is extended to the many-electron (Russell-Saunders) regime for d states in cubic
symmetry. Qualitative electric-dipole selection rules for first-row metal complexes. Totally new
material on organometallic chemistry is discussed leading to an appreciation of the bonding
modes of most ligand types and a brief introduction to their reactivity.
Pre-requisite
CH160
Post-requisites
CH266
CH3A2
CH3A3
8.
Module Aims:
These should identify the module’s broad educational purposes. Indicate how the
module will contribute to the achievement of the aims of the degree courses on
which it is available.


9.
To develop a formal understanding of bonding in transition metal complexes, as a
platform for understanding the reactivity of such complexes
To develop a systematic knowledge of organometallic chemistry, and thereby explore
some of the conceptual links between organic and inorganic
Learning Outcomes:
Successful completion of the module leads to the learning outcomes. The
learning outcomes identify the knowledge, skills and attributes developed by the
module. Learning Outcomes should be presented in the following format using the
table below:
By the end of the module students should be able to...
Learning Outcomes should include reference to subject knowledge and
understanding, key skills, cognitive skills and subject-specific practical and
professional skills and be clearly relevant to fulfilling the educational aims.
Learning Outcomes should be measurable by the assessment methods for the
module. Indicate how the module will contribute to the achievement of degree
course learning objectives.
(a)
Subject knowledge and understanding
The knowledge and understanding that a student will be expected to have
upon completion, such as : ‘a theoretical knowledge of the principles and
methods of archaeology’ or ‘a knowledge of the major types of chemical
reaction and the main characteristics associated with them.’
(b)
Key Skills
Communication (written, verbal, graphical...)
Numeracy
Use of information technology (e.g. WP, www, databases, spreadsheets,
specialist packages)
Ability to learn
Others (e.g. teamwork)
(c)
Cognitive Skills
3
Module proposal
For example: ability in critical analysis; the ability to formulate and test
concepts and hypotheses.
(d)
Subject-Specific/Professional Skills
For example: laboratory skills; scientific support writing; research skills
and methods.
4
Module proposal
LEARNING OUTCOMES
(By the end of the module the student should
be able to....)
Which teaching and learning methods enable
students to achieve this learning outcome?
Which assessment methods will measure the
achievement of this learning outcome?
Use group theory to assign a point group to a
Lectures, tutorial problems and directed reading.
Unseen exam
Feedback from tutor
Lectures, tutorial problems and directed reading.
Unseen exam
Feedback from tutor
Lectures, tutorial problems and directed reading.
Unseen exam
Feedback from tutor
Lectures, tutorial problems and directed reading.
Unseen exam
Feedback from tutor
molecule and understand the key features of the
associated character table.
Understand why d-d repulsion leads to multiple
transitions in electronic spectroscopy.
Understand the thermodynamics of complex
formation and how it leads to an appreciation of
the kinetics of ligand substitution (as exemplified
by associative, interchange and dissociative
processes).
Understand the difference between inner and
outer sphere redox reaction, and how to tell them
apart. Use the Marcus cross-relation to
approximate reaction rates.
5
Module proposal
Understand and describe the factors affecting
Lectures, tutorial problems and directed reading.
Unseen exam
Feedback from tutor
Lectures, tutorial problems and directed reading.
Unseen exam
Feedback from tutor
Lectures, tutorial problems and directed reading.
Unseen exam
Feedback from tutor
Lectures, tutorial problems and directed reading.
Unseen exam
Feedback from tutor
reactivity of s and p block alkyls and aryls.
Explain successes and limitations of synthetic
methods.
Describe the MO basis for understanding the 18e
rule
Explain why classical complexes and squareplanar organometallics do not follow the 18e rule
Count electrons in organometallic complexes
Use an MO bonding description to describe the
bonding of common ligands to transition metals.
Appreciate synthetic methods to make simple
complexes.
Understand basic reactivity of TM organometallic
complexes, exemplified by ligand substitution,
oxidative addition, reductive elimination and
migratory insertion reactions.
6
Module proposal
10.
Syllabus:
Give an outline of the syllabus for the module.
The module will be divided into a number of different components, as outlined below.
Group theory
Recognition of symmetry elements. Identification of point groups. Elementary uses of
character tables such as assigning appropriate symmetry labels to molecular orbitals.
d-d spectroscopy of cubic metal complexes
d-d interelectron repulsion. Microstates and many-electron term symbols for d2. Term
symbols for remaining d configurations. Term splittings in cubic symmetry. Qualitative
electric-dipole selection rules. Selected examples.
Compound formation: thermodynamic considerations
Stepwise and overall formation constants; extension of concepts developed in CH160
Substitution reations
Classification scheme, A, D, I. Activation parameters and reaction profiles. Solvent
exchange rates and relationships to d configurations/spin states/LFSE. Ligand substitution at
octahedral complexes – Eigen-Wilkins mechanism and its associated rate law. Ligand
substitution at square planar centres. Rate laws. Trans effects and trans influence.
Stereospecific synthesis.
Redox reactions
Outer sphere processes and simple Marcus theory. Inner sphere reaction. Diagnostic tests
for inner versus outer sphere.
Main group organometallics
Systematic review. Reactivity (source of R- etc). Oxidative addition as applied to Grignard
synthesis.
d-Block organometallics – the 18 electron rule
MO diags for octahedral complexes: sigma and pi bonding. Electron counting, co-ordination
compounds vs organometallics. Exceptions to the 18 electron rule, including
16 electron square planar complexes.
Bonding of ligands to metal centres.
Carbon monoxide: sigma donation, pi backbonding, effect on IR spectra
Phosphines: bonding and steric effects
Hydrides and dihydrogen: bonding, backbonding and transformation to dihydride. Recognition
that is oxidative addition.
Organic molecules as ligands, exemplified through systems such as: 1 bonding with alkyls;
2 with alkenes; 3 with allyls; 4 with cyclobutadiene; 5 with cyclopentadienyl; 6 with
benzene
Carbenes: Fischer, Schrock and NHC
Alkanes, agostic hydrogens and noble gases.
Reactions of organometallics
Ligand substitution exemplified by carbonyl replacement, the differences between 16e and
18e complexes (associative vs dissociative substitution). Masked dissociative pathways.
Oxidative Addition and Reductive Elimination.
1,1-Migratory insertion reactions, as exemplified by migration onto carbonyl ligands.
1,2-Insertions and β-hydride elimination. Brief discussion.
11.
Illustrative Bibliography:
List the core texts only. The illustrative bibliography should provide an
indication of the focus and level of the reading required by this module, rather
than the full range (this should not be more than half a page):
Inorganic Chemistry 4ed by Shriver and Atkins (OUP)
7
Module proposal
12.
Teaching:
Give the number of each type of teaching event per week and the length of
each session in hours.
30hrs in total
Lectures
problem classes
Tutorials
Laboratory sessions
Total contact hours
Module duration (weeks, if applicable)
Self Study/Revision
13.
Assessment Methods:
Type of assessment
Examinations
14.
0
4hrs in total
0
34hrs (total)
10 weeks
116 hrs
Length
3 hrs
% weighting
100%
Resources:
Are any resources required for this module which are not already available
from the Department’s own baseline resources (e.g. staff costs,
accommodation, equipment, minor works, library costs, audio visual and
computing facilities, vacation study requirements)? Is the module likely to
require high usage of centrally timetabled teaching rooms or specific slots
(e.g. for a module on a part time postgraduate course)?
Any additional requirements should be discussed with the appropriate Officer
(see list below) before submitting the proposal.
List any additional requirements and indicate the outcome of any discussions.
Signature of Module Leader:
Date
Signature of Chair of Department:
Date
8
Exams Office
Assessment Details (information required by the Exams Office)
This form should be completed only for modules to be assessed by an exam organised by the Exams Office
The form does not have to be submitted for approval but should be sent to Andrea Humber in the Exams
Office. If this information is not provided the module cannot be set up on the Student Record System
and students will therefore be unable to register for the module and exam. If you have any queries about
this form please contact Andrea Humber in the Examination Office (ext 74160)
Module Title
Department
Module Leader
Name of Examiner
Transition metal chemistry: reactions in solution and organometallic
chemistry
Chemistry
Dr Jon Rourke
Indicate all available methods of assessment in the table below
% Examined
% Assessed by other methods
100
Length of examination paper
3hrs
Examination Details
Will this module be examined together with any other module (sectioned paper)? If so please give
details.
No
Is the module to be examined by 1 paper
[ X]
or 2 papers
[ ]
When will the exam take place (e.g. Jan, April, Summer)? Summer . . . . . . . . . . . . . . . . . . .
Is reading time required?
Yes [ ]
No [ ]
Give any special exam timetable arrangements
Stationery Requirements
No. of Answer Books
Graph Paper
Calculator
List any other special stationery requirements (e.g. Data books, tables etc):
Type of Paper
Seen:
Yes [ ] No [ ]
Open Book : Yes [ ] No [ ]
Restricted:
Yes [ ] No [ ]
Where restricted please provide list of texts permitted here:
8