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Supramolecular Polymers containing Sequence-Specific Hydrogen-Bonded End Units
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| | Quick description: |
| A supramolecular chemistry based on modification of existing polymers with functional end groups capable of selective reactions with other molecules to form hydrogen bonds
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| | Posted by: |
| WORLDiscoveries
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| | Published: |
| 25 August 2009
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| | File number: |
| W-AH-010
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| | Patent: |
| PCT
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| | Project Type: |
| Out-Licensing Opportunity
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| | Primary sector: |
| Physical Sciences
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| | Seeking / Offering: |
| Collaboration or Partnership, Non-Exclusive Licensing, Exclusive Licensing
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| | Areas of interest: |
| adhesives, chemical tagging, chemicals, chemistry, hydrogen bonding, hydrogen-bonded, inkjet inks, materials, molecular information coding...
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Supramolecular polymers are large molecules composed of repeating
structural units (monomers) connected by noncovalent bonds rather than
typical covalent chemical bonds. Conventional polymers have excellent
properties as materials, but when they melt they become highly viscous.
Applications are limited by the high temperature, energy and pressure
typically required to provide a melt of sufficiently low viscosity for
processing. Noncovalent bonds, such as hydrogen bonding, make
supramolecular polymers thermodynamically less stable, adaptable, and
more flexible than covalent polymers. Therefore, supramolecular
polymers combine good material properties with low-viscosity melts that
are easy to handle. The focus on weaker and reversible noncovalent
interactions between molecules give rise to interesting and dynamic
properties for supramolecular polymers and open up the prospect of many
new commercial applications.
Western has available a supramolecular chemistry based on modification of existing polymers with functional end groups capable of selective reactions with other molecules to form hydrogen bonds. These subunits added to the ends of polymers are helical when bonded together, resulting in links which are reinforced by intertwining structure in addition to hydrogen bonding. The result is a system of oligomers which self-assemble with complementary partners in a similar - but entirely synthetic - manner analogous to formation of the DNA double helix (i.e. sequence-specifically). The strength and reversibility of the bonding between monomers can be precisely tuned by installing an array of end groups in the monomers thus allowing several bonds to form. The resulting molecules have completely and repeatedly reversible melting properties, responses to shear stress or solvent effects which are tuneable to suit particular applications.
- Ease of synthesis
- Readily compatible with existing polymer systems
- May be incorporated simply and inexpensively into existing covalent polymer frameworks
- Precise viscosity or melt properties for a wide range of polymers
- Tuneable response to temperature, solvent and stress effects
- Reversible noncovalent bonding interactions make the materials easily removable
- Polymer
- Self-assembly
- Supramolecular chemistry
- Hydrogen bonding
- Materials
- Adhesives
- Inkjet inks
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Patrick Therrien University of Western Ontario London, Canada
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