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Option one Mechanisms Displaying 44 mechanisms: Molecular materials and polymers- Dyes- Chemoluminescence Molecular materials and polymers- Dyes- Phenolphthalien as a pH indicator Molecular materials and polymers- Dyes- Photoinduced electron transfer Molecular materials and polymers- Dyes- Photoinduced electron transfer- Ion detector (anthracene derivative) Molecular materials and polymers- Dyes- Photoinduced electron transfer- pH indicator (anthracene derivative) Molecular materials and polymers- Dyes- Reactive binding to fibre Molecular materials and polymers- Dyes- Synthesis of Azo dyes Molecular materials and polymers- Dyes- Synthesis of cyanines Molecular materials and polymers- Organic conductors- Polyacetylene- Durham synthesis Molecular materials and polymers- Organic conductors- Polyacetylene- Ziegler-Natta synthesis Molecular materials and polymers- Organic conductors- Polyparaphenylene- preparation from Diels-Alder route Molecular materials and polymers- Organic conductors- Polyparaphenylene- preparation from oxidation of benzene Molecular materials and polymers- Organic conductors- Polyparaphenylene- preparation of PPP planar ladder Molecular materials and polymers- Organic conductors- Polyparaphenylene- preparation via modified ICI route Molecular materials and polymers- Polymers- Chain growth polymerisation- Anionic ring opening Molecular materials and polymers- Polymers- Living polymerisation- Anionic Molecular materials and polymers- Polymers- Living polymerisation- Atom transfer radical polymerisation (ATRP) Molecular materials and polymers- Polymers- Living polymerisation- Radical Molecular materials and polymers- Polymers- Living polymerisation- Ring opening metathesis (ROMP) Molecular materials and polymers- Polymers- Step growth polymerisation- PET Organometallics option- Arene chromium tricarbonyl complexes- Aryl anion as nucleophile Organometallics option- Arene chromium tricarbonyl complexes- Aryl anion from removal of TMS group Organometallics option- Arene chromium tricarbonyl complexes- Benzylic anion as nucleophile Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic addition Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic addition- formation of benzaldehyde Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic addition- indol Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic addition- with methoxy substituent Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic addition- with methoxy substituent- intramolecular Organometallics option- Arene chromium tricarbonyl complexes- Nucleophilic aromatic substitution Organometallics option- Arene chromium tricarbonyl complexes- Preparation Organometallics option- Arene chromium tricarbonyl complexes- Reduction of attached carbonyl- stereoselectivity Organometallics option- Arene chromium tricarbonyl complexes- SN1 via carbonium ion Organometallics option- Arene chromium tricarbonyl complexes- Stereochemistry of nucleophilic substitution of alpha leaving group Organometallics option- Iron chemistry- η2 alkene complexes- Conversion of epoxides to alkenes Organometallics option- Iron chemistry- η2 alkene complexes- Synthesis Organometallics option- Iron chemistry- η2 alkene complexes- Synthesis of β-Lactams Organometallics option- Iron chemistry- η2 alkene complexes- Synthesis of four membered amide rings Organometallics option- Iron chemistry- η4 alkene complexes- Decomplexation Organometallics option- Iron chemistry- η4 alkene complexes- Synthesis Organometallics option- Iron chemistry- η5 alkene complexes- Nucleophilic attack Organometallics option- Iron chemistry- η5 alkene complexes- Synthesis Organometallics option- Iron chemistry- Fp- Reduction of Fp2 to Fp- Organometallics option- Iron chemistry- Fp- Decomplexation to Fp alkyls to form carbonyl compounds Organometallics option- Iron chemistry- Fp- Synthesis of Fp2