Sustainable glucose-based block copolymers exhibit elastomeric and adhesive behavior
Literature Information
Mohammadreza Nasiri, Theresa M. Reineke
Herein, we present the direct modification of glucose, an abundant and inexpensive sugar molecule, to produce new sustainable and functional polymers. Glucose-6-acrylate-1,2,3,4-tetraacetate (GATA) has been synthesized and shown to provide a useful glassy component for developing an innovative family of elastomeric and adhesive materials. A series of diblock and triblock copolymers of GATA and n-butyl acrylate (n-BA) were created via Reversible Addition–Fragmentation Chain Transfer (RAFT) polymerization. Initially, poly(GATA)-b-poly(n-BA) copolymers were prepared using 4-cyano-4-[(ethylsulfanylthiocarbonyl)sulfanyl] pentanoic acid (CEP) as a chain transfer agent (CTA). These diblock copolymers demonstrated decomposition temperatures of 275 °C or greater and two glass transition temperatures (Tg) around −45 °C and 100 °C corresponding to the PnBA and PGATA domains, respectively, as measured by differential scanning calorimetry (DSC). Triblock copolymers of GATA and n-BA, with moderate dispersities (Đ = 1.15–1.29), were successfully synthesized when S,S-dibenzyl trithiocarbonate (DTC) was employed as the CTA. Poly(GATA)-b-poly(nBA)-b-poly(GATA) copolymers with 14–58 wt% GATA were prepared and demonstrated excellent thermomechanical properties (Td ≥ 279 °C). Two well-separated glass transitions near the values for homopolymers of n-BA and GATA (∼−45 °C and ∼100 °C, respectively) were measured by DSC. The triblock with 14% GATA exhibited peel adhesion of 2.31 N cm−1 (when mixed with 30 wt% tackifier) that is superior to many commercial pressure sensitive adhesives (PSAs). Use of 3,5-bis(2-dodecylthiocarbonothioylthio-1oxopropoxy)benzoic acid (BTCBA) as the CTA provided a more efficient route to copolymerize GATA and n-BA. Using BTCBA, poly(GATA)-b-poly(nBA)-b-poly(GATA) triblock copolymers containing 12–25 wt% GATA, with very narrow molar mass distributions (Đ ≤ 1.08), were prepared. The latter series of triblock copolymers showed excellent thermal stability with Td ≥ 275 °C. Only the Tg for the PnBA block was observed by DSC (∼−45 °C), however, phase-separation was confirmed by small-angle X-ray scattering (SAXS) for all of these triblock copolymers. The mechanical behavior of the polymers was investigated by tensile experiments and the triblock with 25% GATA content demonstrated moderate elastomeric properties, 573 kPa stress at break and 171% elongation. This study introduces a new family of glucose-based ABA-type copolymers and demonstrates functionality of a glucose-based feedstock for developing green polymeric materials.
Recommended Journals

Journal of Chemical Sciences

Critical Reviews in Solid State and Materials Sciences

Heteroatom Chemistry

Journal of the Indian Institute of Science

Chinese Journal of Chemistry

Acta Metallurgica Sinica-English Letters

Main Group Chemistry

Polycyclic Aromatic Compounds

Bioorganic & Medicinal Chemistry Letters

Medicinal Chemistry Research
Related Literature
Nonenzymatic peptide-based catalytic asymmetric phosphorylation of inositol derivatives
Bianca R. Sculimbrene, Adam J. Morgan, Scott J. Miller
DOI: 10.1039/B304015C
Chemical modification of diamond powder using photolysis of perfluoroazooctane
Takako Nakamura, Masatou Ishihara, Tsuguyori Ohana, Yoshinori Koga
DOI: 10.1039/B211807F
Luminescent heterohexanuclear complexes with platinum alkynyl and silver diphosphine as components
Qiao-Hua Wei, Gang-Qiang Yin, Zhen Ma, Lin-Xi Shi
DOI: 10.1039/B305284B
Macro-cellular silica foams: synthesis during the natural creaming process of an oil-in-water emulsion
G. J. T. Tiddy, J. L. Casci
DOI: 10.1039/B303349J
Diastereoselective formation of a dipalladium(i) complex supported by a bridging tetradentate ligand, and oxidative addition of RS–H across a phosphine-bridged PdI–PdI bond
S. Jo Ling Foo, Nathan D. Jones, Brian O. Patrick, Brian R. James
DOI: 10.1039/B300177F
Glyco-helix: parallel lactose-lactose interactions stabilize an α-helical structure of multi-glycosylated peptide
Tomikazu Sasaki
DOI: 10.1039/B212364A
De novo design of non-hydrogen-bonded helical pseudopeptides composed of oxanipecotic acid oligomers
Myung-ryul Lee, Kwang-Yon Kim, Ung-In Cho, Doo Wan Boo, Injae Shin
DOI: 10.1039/B301382K
Stereoselective formation of dinuclear complexes with anomalous CD spectra
Shane G. Telfer, Tomohiro Sato
DOI: 10.1039/B301267K
Decomposition of Pt-intercalated hydrotalcite-like nanocomposites to produce micro/mesoporous catalysts
Masato Machida, Shin Hamada
DOI: 10.1039/B304352E
Homochiral 3D open frameworks assembled from 1- and 2-D coordination polymers
Yong Cui, Helen L. Ngo, Peter S. White, Wenbin Lin
DOI: 10.1039/B211916A
You might also like
What precautions should be taken when handling 2-Methyl-2-propanyl 5-amino-2-thiophenecarboxylate (CAS: 1498311-57-1)?
When handling 2-Methyl-2-propanyl 5-amino-2-thiophenecarboxylate (CAS: 1498311-5...
What are the physical and chemical properties of 5-Bromo-1,2-dichloro-3-fluorobenzene (CAS: 1000572-93-9)?
5-Bromo-1,2-dichloro-3-fluorobenzene (CAS: 1000572-93-9) is a crystalline solid ...
How should (2R)-2-Amino-2-(4-bromophenyl)ethanol (CAS: 354153-64-3) be stored?
(2R)-2-Amino-2-(4-bromophenyl)ethanol (CAS: 354153-64-3) should be stored in a c...
What regulatory guidelines apply to Methyl 4-(aminomethyl)tetrahydro-2H-pyran-4-carboxylate hydrochloride (CAS: 362707-24-2)?
Methyl 4-(aminomethyl)tetrahydro-2H-pyran-4-carboxylate hydrochloride (CAS: 3627...
What are the main uses of 1,4-dimethyl-1H-pyrazole-5-sulfonyl chloride (CAS: 1174834-52-6)?
1,4-Dimethyl-1H-pyrazole-5-sulfonyl chloride is primarily used as an intermediat...
Is Dinaphtho[1,2-b:2',1'-d]furan (CAS: 239-69-0) safe?
Dinaphtho[1,2-b:2',1'-d]furan is generally safe when handled with appropriate pe...
What is the market or research trend for 7-Methyl-7,9-dihydro-1H-purine-2,6,8(3H)-trione (CAS: 612-37-3)?
The market for 7-Methyl-7,9-dihydro-1H-purine-2,6,8(3H)-trione (CAS: 612-37-3) i...
What are the physical and chemical properties of 2-(4-Chlorophenyl)malonaldehyde (CAS: 205676-17-1)?
2-(4-Chlorophenyl)malonaldehyde (CAS: 205676-17-1) is a colorless or light yello...
How is 2-Methylchrysene (CAS: 3351-32-4) typically synthesized?
2-Methylchrysene (CAS: 3351-32-4) is typically synthesized via the reaction of c...
Is N-(6-aminopyrimidin-4-yl)acetamide (CAS: 89533-23-3) safe?
N-(6-aminopyrimidin-4-yl)acetamide (CAS: 89533-23-3) is generally considered saf...
Source Journal
Polymer Chemistry

Polymer Chemistry welcomes submissions in all areas of polymer science that have a strong focus on macromolecular chemistry. Manuscripts may cover a broad range of fields, yet no direct application focus is required.
![1-Oxa-8-azaspiro[4.5]decan-3-ol structure 1-Oxa-8-azaspiro[4.5]decan-3-ol structure](https://static.chemtradehub.com/structs/757/757239-76-2-a0ec.webp)

![4-Chloro-N-{[4-(dimethylamino)phenyl]carbamoyl}benzenesulfonamide structure 4-Chloro-N-{[4-(dimethylamino)phenyl]carbamoyl}benzenesulfonamide structure](https://static.chemtradehub.com/structs/558/5581-42-0-7dcb.webp)
![3-[7-Amino-3-(3-pyridinyl)pyrazolo[1,5-a]pyrimidin-6-yl]phenol structure 3-[7-Amino-3-(3-pyridinyl)pyrazolo[1,5-a]pyrimidin-6-yl]phenol structure](https://static.chemtradehub.com/structs/861/861249-77-6-025b.webp)
