Filtern
Dokumenttyp
Sprache
- Englisch (2)
Referierte Publikation
- ja (2)
Schlagworte
- Azobenzene (1)
- Demethoxylation (1)
- Guest uptake/release (1)
- Metal– organic frameworks (1)
- PH-influence (1)
- Pectin (1)
- Photochromism (1)
- Thermal stability (1)
- Visible light (1)
- Water sorption (1)
Organisationseinheit der BAM
- 6 Materialchemie (1)
- 6.3 Strukturanalytik (1)
A two-component core-shell UiO-68 type metal-organic framework (MOF) with a nonfunctionalized interior for efficient guest uptake and storage and a thin light-responsive outer shell was prepared by initial solvothermal MOF synthesis followed by solvent-assisted linker exchange. The bulky shell linker features two tetra-ortho-fluorinated azobenzene moieties to exploit their advantageous photoisomerization properties. The obtained perfect octahedral MOF single crystals can be switched repeatedly and with an unprecedented efficiency between E- and Z-rich states using visible light only. Due to the high photoswitch density per pore of the shell layer, its steric demand and thus molecular uptake (and release) can be conveniently modulated upon green and blue light irradiation. Therefore, the "smart" shell acts as a light-controlled kinetic barrier or "gate" for the diffusion of cargo molecules in and out of the MOF crystals.
Aim of the present study was to investigate the effect of the method of demethoxylation on the particle structure and techno-functional properties of pectins with different degree of methoxylation and distribution of free carboxyl groups. Two groups of model pectins, one with 57% and one with 42% degree of methoxylation have been prepared from one single commercial pectin. Modifications were performed by an acidic and two enzymatic methods using fungal and plant-derived pectin methyl esterases. Thermal stability was investigated by thermal analysis and water uptake was determined by a sorption and a capillary sucking method.
The enzyme-treated pectins were thermally less stable than the acid-treated. The water uptake of enzyme-treated pectins was higher than in acid-treated samples in the sorption method and lower in the capillary sucking tests. The different behaviour is explained by differences in pH during demethoxylation and a co-occurring variation in sodium content. Both parameters affected intermolecular interactions of the pectin macromolecules in solution, which resulted in differences in the particle morphology. The effect of the distribution of free carboxyl groups (statistical or block-wise) on the techno-functional properties was more pronounced in high-methoxylated pectins than in low-methoxylated pectins.