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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