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<CourseUnit xmlns="http://www.manchester.ac.uk/CUICourseUnitDetails" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xsi:schemaLocation="http://www.manchester.ac.uk/CUICourseUnitDetails.xsd">
  <UnitCode Applicant="Y" Label="Unit code" Student="Y">
    <Code>CHEM60112</Code>
  </UnitCode>
  <UnitTitle Applicant="Y" Label="Unit title" Student="Y">
    <Title>Advanced Chemistry Topics</Title>
  </UnitTitle>
  <MaxUnits Applicant="Y" Label="Credit rating" Student="Y">
    <Units>15</Units>
  </MaxUnits>
  <TeachingPeriods Applicant="Y" Label="Teaching period(s)" Student="Y">
    <Period>Semester 2</Period>
  </TeachingPeriods>
  <AcademicCareer Applicant="Y" Label="Academic career" Student="Y">
    <Value>Postgraduate Taught</Value>
  </AcademicCareer>
  <UnitLevel Applicant="Y" Label="Unit level" Student="Y">
    <Level>Level 6</Level>
  </UnitLevel>
  <StaffList Applicant="Y" Label="Teaching staff" RoleLabel="Course Unit Role" Student="Y">
    <StaffMember>
      <Name>Andrew Regan</Name>
      <Role>Unit coordinator</Role>
    </StaffMember>
  </StaffList>
  <OfferedBy Applicant="Y" Label="Offered by" Student="Y">
    <OrganisationList>
      <Organisation>
        <OrgName>Department of Chemistry</OrgName>
      </Organisation>
    </OrganisationList>
    <GroupList>
      <Group>
        <GroupName></GroupName>
      </Group>
    </GroupList>
    <FheqLevels>
      <FheqLevel>
        <LevelNumber>1</LevelNumber>
        <LevelName>FHEQ level (Framework for Higher Education Qualifications) ' Masters/Integrated Masters P4 ' </LevelName>
      </FheqLevel>
    </FheqLevels>
    <Ects>
      <MaxUnits>European Credit Transfer &amp; Accumulation System Rating :   7.5</MaxUnits>
    </Ects>
  </OfferedBy>
  <MarketingOverview Applicant="Y" Label="Marketing Course unit overview" Student="">
    <Content>&lt;p&gt;The over-arching aim of the personalised learning unit is to prepare students for a professional career in Chemistry by expanding core chemistry knowledge into advanced topics, to provide a wider and deeper understanding of particular areas of chemistry.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;The key aims of each of the topics are:&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Contemporary f-Element Chemistry (D. Mills)&lt;/strong&gt; – This topic introduces students to the use of molecular design to achieve landmark advances in non-aqueous f-element synthetic chemistry.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Catalytic Asymmetric Synthesis (A. Trowbridge)&lt;/strong&gt; – This topic introduces students to the catalytic processes that are routinely used for the stereoselective synthesis of target molecules. &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;New topic to be confirmed &amp;nbsp;(J. Abbenseth)&lt;/strong&gt; – &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main Group Reagents in Synthesis (A.C. Regan) &lt;/strong&gt;– This topic introduces students to the use of silicon-, sulfur- selenium- and phosphorus-containing reagents in organic synthesis.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Metal-Organic Frameworks (Y. Ma)&lt;/strong&gt; - This topic introduces students to porous metal-organic framework materials.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Chemical Concepts from Quantum Mechanics (P. Popelier)&lt;/strong&gt; – This topic introduces students to Quantum Chemical Topology, the most comprehensive and coherent way of extracting chemical insight from modern wavefunctions.The course will also introduce research-level topics in this area.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;</Content>
  </MarketingOverview>
  <UnitOverview Applicant="" Label="Course unit overview" Student="Y">
    <Content>&lt;p&gt;The over-arching aim of the personalised learning unit is to prepare students for a professional career in Chemistry by expanding core chemistry knowledge into advanced topics, to provide a wider and deeper understanding of particular areas of chemistry.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;The key aims of each of the topics are:&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Contemporary f-Element Chemistry (D. Mills) &lt;/strong&gt;– This topic introduces students to the use of molecular design to achieve landmark advances in non-aqueous f-element synthetic chemistry.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Catalytic Asymmetric Synthesis (A. Trowbridge) &lt;/strong&gt;– This topic introduces students to the catalytic processes that are routinely used for the stereoselective synthesis of target molecules. &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;New topic to be confirmed &amp;nbsp;(J. Abbenseth) &lt;/strong&gt;– &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main Group Reagents in Synthesis (A.C. Regan)&lt;/strong&gt; – This topic introduces students to the use of silicon-, sulfur- selenium- and phosphorus-containing reagents in organic synthesis.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Metal-Organic Frameworks (Y. Ma)&lt;/strong&gt; - This topic introduces students to porous metal-organic framework materials.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Chemical Concepts from Quantum Mechanics (P. Popelier) &lt;/strong&gt;– This topic introduces students to Quantum Chemical Topology, the most comprehensive and coherent way of extracting chemical insight from modern wavefunctions.The course will also introduce research-level topics in this area.&amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;</Content>
  </UnitOverview>
  <Aims Applicant="Y" Label="Aims" Student="Y">
    <Content>&lt;p&gt;The over-arching aim of this module is to prepare students for a professional career in Chemistry by expanding core chemistry knowledge into advanced topics to provide a wider and deeper understanding of particular areas of chemistry.&lt;/p&gt;</Content>
  </Aims>
  <LearningOutcomes Applicant="Y" Label="Learning outcomes" Student="Y">
    <Content>&lt;p&gt;&lt;span style="background-color:rgb(255,255,255);color:rgb(0,0,0);"&gt;&lt;i&gt;&lt;span class="TextRun SCXW9933502 BCX8 NormalTextRun" style="-webkit-tap-highlight-color:transparent;-webkit-text-stroke-width:0px;-webkit-user-drag:none;font-family:&amp;quot;Microsoft Sans Serif&amp;quot;, &amp;quot;Microsoft Sans Serif_EmbeddedFont&amp;quot;, &amp;quot;Microsoft Sans Serif_MSFontService&amp;quot;, sans-serif;font-size:11pt;font-variant-caps:normal;font-variant-ligatures:none !important;font-weight:400;letter-spacing:normal;line-height:17.2667px;margin:0px;orphans:2;padding:0px;text-align:left;text-decoration-color:initial;text-decoration-style:initial;text-decoration-thickness:initial;text-indent:0px;text-transform:none;user-select:text;white-space:pre-wrap;widows:2;word-spacing:0px;" data-contrast="none" xml:lang="EN-GB" lang="EN-GB"&gt;On successful completion of the course students should be able to:&amp;nbsp;&lt;/span&gt;&lt;/i&gt;&lt;span class="EOP SCXW9933502 BCX8" style="-webkit-tap-highlight-color:transparent;-webkit-text-stroke-width:0px;-webkit-user-drag:none;font-family:&amp;quot;Microsoft Sans Serif&amp;quot;, &amp;quot;Microsoft Sans Serif_EmbeddedFont&amp;quot;, &amp;quot;Microsoft Sans Serif_MSFontService&amp;quot;, sans-serif;font-size:11pt;font-style:normal;font-variant-caps:normal;font-variant-ligatures:normal;font-weight:400;letter-spacing:normal;line-height:17.2667px;margin:0px;orphans:2;padding:0px;text-align:left;text-decoration-color:initial;text-decoration-style:initial;text-decoration-thickness:initial;text-indent:0px;text-transform:none;user-select:text;white-space:pre-wrap;widows:2;word-spacing:0px;" data-ccp-props="{}"&gt;&amp;nbsp;&lt;/span&gt;&lt;/span&gt;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Contemporary f-Element Chemistry (D. Mills)&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;ILO1 – Apply knowledge of f-element coordination/organometallic chemistry to create synthetic routes to complexes with designer geometries, coordination numbers and bonding regimes. &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO2 – Interpret a range of experimental data to rationalise physicochemical properties and to propose f-element complex formulations and formal oxidation states at metal and ligand sites. &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO3 – Apply knowledge of metal coordination spheres and redox chemistry to generate synthetic routes to f-element complexes with low and high formal metal oxidation states. &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO4 – Predict and explain the outcomes of small molecule activation reactions of f-element complexes by consideration of experimental data, ligand effects, covalency and redox chemistry. &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO5 – Classify f-element complexes containing redox non-innocent ligands and appraise data to interpret or to hypothesise aspects of structure, bonding and reactivity. &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO6 – Compare and contrast lanthanide- and actinide-ligand multiple bonding regimes in order to rationalise relative complex stabilities and their reactivity profiles.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Catalytic Asymmetric Synthesis (A. Trowbridge) &amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;ILO1 – Interpret reactions commonly used in catalytic asymmetric synthesis.&lt;/p&gt;&lt;p&gt;ILO2 - Predict the outcomes of unseen catalytic asymmetric reactions based on theoretical models.&lt;/p&gt;&lt;p&gt;ILO3 – Develop strategies for the synthesis of unseen molecules using catalytic, asymmetric transformations.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;New topic to be confirmed (J. Abbenseth)&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO1 - &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO2 – &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO3 – &amp;nbsp;&lt;/p&gt;&lt;p&gt;ILO4 – &amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main Group Reagents in Synthesis (A.C. Regan) &amp;nbsp;&lt;/strong&gt;&lt;/p&gt;&lt;p&gt;ILO1 – describe the effects of heteroatoms on the reactivity of organic molecules containing them.&lt;/p&gt;&lt;p&gt;ILO2 – explain how the presence of a heteroatom modifies the reactivity of an organic compound containing it.&lt;/p&gt;&lt;p&gt;ILO3 – deduce the structure of appropriate heteroatom-containing reagents required to achieve given transformations.&lt;/p&gt;&lt;p&gt;ILO4 – deduce the structure of products formed from organic reactions involving given heteroatom-containing reagents.&lt;/p&gt;&lt;p&gt;ILO5 – write curly-arrow mechanisms for reactions i</Content>
  </LearningOutcomes>
  <Knowledge Applicant="Y" Label="Knowledge and understanding" Student="Y">
    <Content></Content>
  </Knowledge>
  <IntellectualSkills Applicant="Y" Label="Intellectual skills" Student="Y">
    <Content></Content>
  </IntellectualSkills>
  <PracticalSkills Applicant="Y" Label="Practical skills" Student="Y">
    <Content></Content>
  </PracticalSkills>
  <TransferableSkills Applicant="Y" Label="Transferable skills and personal qualities" Student="Y">
    <Content>&lt;div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;Problem solving, analytical skills, time management.&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;</Content>
  </TransferableSkills>
  <EmployabilitySkillsList Applicant="Y" Label="Employability skills" Student="Y">
    <Skill>
      <SkillId></SkillId>
      <SkillDescription></SkillDescription>
    </Skill>
  </EmployabilitySkillsList>
  <Syllabus Applicant="Y" Label="Syllabus" Student="Y">
    <Content>&lt;p&gt;Students choose 4 of these:&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Contemporary f-Element Chemistry&lt;/strong&gt; (D. Mills)&amp;nbsp;&lt;br/&gt;General coordination chemistry and oxidation states&lt;br/&gt;Achieving the highest oxidation states&lt;br/&gt;Achieving the lowest oxidation states&lt;br/&gt;Redox non-innocent ligands and arenes&lt;br/&gt;Small molecule activation reactions&lt;br/&gt;Metal-ligand multiple bonding&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Metal organic Frameworks, MOFs&lt;/strong&gt; (Y. Ma)&lt;br/&gt;Synthesis of MOFs&lt;br/&gt;Characterisation of MOFs&amp;nbsp;&lt;br/&gt;Applications of MOFs&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Inorganic Computational Chemistry&lt;/strong&gt; (H. Morgan)&amp;nbsp;&lt;br/&gt;&lt;strong&gt;Catalytic Asymmetric Synthesis&lt;/strong&gt; (A. Trowbridge)&amp;nbsp;&lt;br/&gt;Principles of asymmetric synthesis;&lt;br/&gt;Asymmetric hydrogenation of alkenes and ketones;&lt;br/&gt;Asymmetric &amp;nbsp;epoxidation: i. allylic alcohols, ii. unfunctionalised alkenes, iii. synthetic applications of epoxides;&lt;br/&gt;Asymmetric C-C bond forming reactions: i. Aldol reactions, ii. Michael reactions, iii. Asymmetric cycloaddition reactions.&amp;nbsp;&lt;br/&gt;Biological perspectives.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Main Group Reagents in Synthesis &lt;/strong&gt;(A.C. Regan)&amp;nbsp;&lt;br/&gt;Properties of bonds to silicon; effects of silicon on charges.&lt;br/&gt;Silicon-oxygen bonds: protecting groups, trapping reagents, silyl enol ethers.&lt;br/&gt;Formation and reactions of vinyl silanes&lt;br/&gt;Formation and reactions of allyl silanes&lt;br/&gt;Formation and reactions of anions stabilised by silicon.&lt;br/&gt;Formation and reactions of carbanions stabilised by sulphur: dithianes, sulfoxides and sulfones.&lt;br/&gt;Formation and reactions of sulfur ylids.&lt;br/&gt;Reactions of allyl sulfoxides: [2,3]-sigmatropic rearrangements.&lt;br/&gt;Reactions of electrophilic sulfur and selenium reagents.&lt;br/&gt;The Pummerer rearrangement.&lt;br/&gt;Hydroboration reactions.&lt;br/&gt;Reactions of allyl boranes and boronates.&lt;/p&gt;&lt;p&gt;&lt;strong&gt;Quantum Chemistry&lt;/strong&gt; (P. Popelier, J. Skelton)&lt;br/&gt;Generalisation of the quantum harmonic oscillator (QHO) model of vibrations to polyatomic systems and its extension to phonons in periodic solids&lt;br/&gt;Key concepts in the lattice dynamics of solids: the phonon Brillouin zone, wave vectors, the phonon dispersion and density of states, and acoustic and optic modes&lt;br/&gt;Relationship between the phonon spectrum and thermodynamic functions, and the use of statistical thermodynamics to predict material properties&lt;br/&gt;Relationship between imaginary harmonic modes, the potential-energy surface (PES), and “soft-mode” phase transitions&lt;br/&gt;Predicting the infrared activity of vibrations&lt;br/&gt;&amp;nbsp;&lt;/p&gt;</Content>
  </Syllabus>
  <TeachingMethods Applicant="Y" Label="Teaching and learning methods" Student="Y">
    <Content></Content>
  </TeachingMethods>
  <AssessmentMethods Applicant="Y" Label="Assessment methods" Student="Y">
    <IntroText> </IntroText>
    <Method>
      <MethodId>1</MethodId>
      <MethodName>Written exam</MethodName>
      <MethodWeight>100%</MethodWeight>
    </Method>
  </AssessmentMethods>
  <FeedbackMethods Applicant="Y" Label="Feedback methods" Student="Y">
    <Content>&lt;div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;p&gt;Lecturing staff will provide office hours during the course&lt;/p&gt;&lt;p&gt;After the exam marking has been completed, students are provided with feedback&amp;nbsp;&lt;/p&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;&lt;/div&gt;&lt;p&gt;&amp;nbsp;&lt;/p&gt;</Content>
  </FeedbackMethods>
  <RequirementsList Applicant="Y" Label="Pre/co-requisites" Student="Y">
    <Requirement>
      <UnitCode></UnitCode>
      <UnitTitle></UnitTitle>
      <RequirementType></RequirementType>
      <Description></Description>
    </Requirement>
    <AdditionalRequirement></AdditionalRequirement>
  </RequirementsList>
  <AcademicPrograms Applicant="Y" Label="Academic programmes" Student="Y">
    <AcademicProgram>
      <Program>MSc Chemistry</Program>
      <Plan>MSc Chemistry</Plan>
      <Level>PGDT Taught Component</Level>
      <Requirement>Mandatory</Requirement>
    </AcademicProgram>
  </AcademicPrograms>
  <FreeChoice Applicant="Y" Label="Available as a free choice unit?" Student="Y">
    <Content>N</Content>
  </FreeChoice>
  <Accreditation Applicant="Y" Label="Accreditation" Student="Y">
    <Content></Content>
  </Accreditation>
  <RecommendedReading Applicant="Y" Label="Recommended reading" Student="Y">
    <Content>&lt;p&gt;Specific reading material will be provided separately for each topic.&amp;nbsp;&lt;/p&gt;</Content>
  </RecommendedReading>
  <StudyHours Applicant="Y" Label="Study hours" Student="Y">
    <IntroText> </IntroText>
    <ScheduledHours Applicant="Y" Label="Scheduled activity hours" Student="Y">
      <ActivityHours>
        <ActivityType>Assessment written exam</ActivityType>
        <Hours>3</Hours>
      </ActivityHours>
      <ActivityHours>
        <ActivityType>Lectures</ActivityType>
        <Hours>28</Hours>
      </ActivityHours>
      <ActivityHours>
        <ActivityType>Practical classes &amp; workshops</ActivityType>
        <Hours>12</Hours>
      </ActivityHours>
    </ScheduledHours>
    <PlacementHours Applicant="Y" Label="Placement hours" Student="Y">
      <ActivityHours>
        <ActivityType></ActivityType>
        <Hours>0</Hours>
      </ActivityHours>
    </PlacementHours>
    <TotalHours Applicant="Y" Label="Independent study hours" Student="Y">
      <Hours>0</Hours>
    </TotalHours>
  </StudyHours>
  <Notes Applicant="Y" Label="Additional notes" Student="Y">
    <Content></Content>
  </Notes>
</CourseUnit>
