The mechanical bond: a work of art.
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Summary
It is argued that the many aspects of beauty in MIMs are relevant, not only to the pleasure chemists derive from their research, but also to the progress of the research itself.
- Type
- review
- Published
- 2012-01-01
- Cited by
- 49
- References
- 233
- OpenAlex
- https://openalex.org/W65794241
- Semantic Scholar
- https://api.semanticscholar.org/CorpusID:38046440
Keywords
Ingenuity, Beauty, Creativity, Pleasure, Art
References
- C60: Buckminsterfullerene
- Hybrid organic–inorganic rotaxanes and molecular shuttles
- Structural classification and general principles for the design of spherical molecular hosts.
- Supramolecular Chemistry: Concepts And Perspectives
- Catenanes, Rotaxanes, and Knots
- The art of chemistry : myths, medicines, and materials
- The origins of creativity
- Molecular Devices and Machines: Concepts and Perspectives for the Nanoworld
- Elegant Solutions: Ten Beautiful Experiments in Chemistry
- The thyme polyethers: An approach to the synthesis of a molecular knotted ring
- Spontaneous assembly of ten components into two interlocked, identical coordination cages
- Knots and Links
- Design and synthesis of an exceptionally stable and highly porous metal-organic framework
- The enzymatic basis of processivity in λ exonuclease
- A photochemically driven molecular-level abacus
- Multiring Catenanes with a Macrobicyclic Core
- Noninvasive remote-controlled release of drug molecules in vitro using magnetic actuation of mechanized nanoparticles.
- Self-Assembled M24L48 Polyhedra and Their Sharp Structural Switch upon Subtle Ligand Variation
- Fabrication and Transport Properties of Single-Molecule-Thick Electrochemical Junctions
- Une nouvelle famille de molecules : les metallo-catenanes
Cited by
- Three-dimensional aromatic networks.
- Mechanically Interlocked Linkers for Dynamic Metal-Organic Frameworks
- Beauty in Chemistry: Artistry in the Creation of New Molecules
- A dynamic [1]catenane with pH-responsiveness formed via threading-followed-by-complexation.
- Organic Switches for Surfaces and Devices
- Design and efficient synthesis of a pillar[5]arene-based [1]rotaxane.
- Active-template synthesis of “click” [2]rotaxane ligands: self-assembly of mechanically interlocked metallo-supramolecular dimers, macrocycles and oligomers
- Formation of [3]catenanes from 10 precursors via multicomponent coordination-driven self-assembly of metallarectangles.
- Solvent-driven selective π-cation templating in dynamic assembly of interlocked molecules
- A neutral naphthalene diimide [2]rotaxane.
- Metal-binding studies of linear rigid-axle [2]pseudorotaxanes with in situ generated anionic metal halide complexes
- Modular synthesis of bipyridinium oligomers and corresponding donor-acceptor oligorotaxanes with crown ethers.
- Hybrid inorganic-organic polyrotaxane, pseudorotaxane, and sandwich.
- Photoresponsive Host-Guest Functional Systems.
- The chameleonic nature of diazaperopyrenium recognition processes.
- Topological isomerism in a chiral handcuff catenane
- CuAAC "click" active-template synthesis of functionalised [2]rotaxanes using small exo-substituted macrocycles: how small is too small?
- Rapid thermally assisted donor-acceptor catenation.
- A Star of David catenane.
- Synthesis and solution-state dynamics of donor–acceptor oligorotaxane foldamers
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