Publication | Open Access
Click Chemistry: Versatility and Control in the Hands of Materials Scientists
693
Citations
116
References
2007
Year
Materials ScienceSynthetic Organic ConceptsOrganic Material ChemistryEngineeringMacromolecular EngineeringReaction EngineeringNatural SciencesOrganic-inorganic Hybrid MaterialDiversity-oriented SynthesisMaterials ScientistsOrganic ChemistryReactivity (Chemistry)Click ChemistryChemistryHybrid MaterialsPolymer ChemistryPolymers
Abstract The increasing need for materials with tightly controlled structures will continue to fuel the induction of synthetic organic concepts into materials science. One powerful example is the embracement of “click chemistry” by the materials science community. Because of their high selectivity, near‐perfect reliability, high yields, and exceptional tolerance towards a wide range of functional groups and reaction conditions click reactions have recently attracted increased attention, specifically for use in polymer synthesis as well as for the modification of surfaces and nanometer‐ and mesoscale structures. As outlined in this Review article, click chemistry, such as the Cu I ‐catalyzed Huisgen 1,3‐dipolar cycloaddition and the Diels–Alder reaction, presents a synthetic concept that lends itself superbly to the controlled preparation of multifunctional materials.
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