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Cooling rate uncovers epimer-dependent supramolecular organization of carbohydrate amphiphiles.
Castro, Vânia I B; Gao, Yuting; Brito, Alexandra; Chen, Jie; Reis, Rui L; Pashkuleva, Iva; Pires, Ricardo A.
Afiliación
  • Castro VIB; 3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barc
  • Gao Y; ICVS/3B's-PT Government Associate Laboratory, Braga/Guimarães, Portugal.
  • Brito A; 3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barc
  • Chen J; ICVS/3B's-PT Government Associate Laboratory, Braga/Guimarães, Portugal.
  • Reis RL; Department of Chemical Engineering, School of Environmental and Chemical Engineering, Shanghai University, Shangda Road 99, Shanghai 200444, P. R. China.
  • Pashkuleva I; 3B's Research Group, I3Bs - Research Institute on Biomaterials, Biodegradables and Biomimetics, University of Minho, Headquarters of the European Institute of Excellence on Tissue Engineering and Regenerative Medicine, AvePark, Parque de Ciência e Tecnologia, Zona Industrial da Gandra, 4805-017 Barc
  • Pires RA; ICVS/3B's-PT Government Associate Laboratory, Braga/Guimarães, Portugal.
J Mater Chem B ; 12(29): 6996-7000, 2024 Jul 24.
Article en En | MEDLINE | ID: mdl-38949321
ABSTRACT
We show distinct CH-π interactions and assembly pathways for the amphiphile N-(fluorenylmethoxycarbonyl)-galactosamine and its epimer N-(fluorenylmethoxycarbonyl)-glucosamine. These differences result in the formation of supramolecular nanofibrous systems with opposite chirality. Our results showcase the importance of the carbohydrates structural diversity for their specific biointeractions and the opportunity that their ample interactome offers for synthesis of versatile and tunable supramolecular (bio) materials.
Asunto(s)

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tensoactivos Idioma: En Revista: J Mater Chem B Año: 2024 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Tensoactivos Idioma: En Revista: J Mater Chem B Año: 2024 Tipo del documento: Article