A1 Alkuperäisartikkeli tieteellisessä aikakauslehdessä
Phase-selective low molecular weight organogelators derived from allylated D-mannose (2022)


Mattsson, I., Lahtinen, M., Sitdikov, R., Wank, B., Saloranta-Simell, T., & Leino, R. (2022). Phase-selective low molecular weight organogelators derived from allylated D-mannose. Carbohydrate research, 518, Article 108596. https://doi.org/10.1016/j.carres.2022.108596


JYU-tekijät tai -toimittajat


Julkaisun tiedot

Julkaisun kaikki tekijät tai toimittajatMattsson, Ida; Lahtinen, Manu; Sitdikov, Ruzal; Wank, Bianca; Saloranta-Simell, Tiina; Leino, Reko

Lehti tai sarjaCarbohydrate research

ISSN0008-6215

eISSN1873-426X

Julkaisuvuosi2022

Ilmestymispäivä01.06.2022

Volyymi518

Artikkelinumero108596

KustantajaElsevier BV

JulkaisumaaAlankomaat

Julkaisun kielienglanti

DOIhttps://doi.org/10.1016/j.carres.2022.108596

Linkki tutkimusaineistoonhttps://dx.doi.org/10.5517/ccdc.csd.cc2b4qfn

Julkaisun avoin saatavuusAvoimesti saatavilla

Julkaisukanavan avoin saatavuusOsittain avoin julkaisukanava

Julkaisu on rinnakkaistallennettu (JYX)https://jyx.jyu.fi/handle/123456789/81974

LisätietojaComplete crystallographic data for the structural analysis have been deposited with the Cambridge Crystallographic Data Centre, CCDC no. 2149491 (compound 3) and 2149492 (compound 4),
https://dx.doi.org/10.5517/ccdc.csd.cc2b4qfn and https://dx.doi.org/10.5517/ccdc.csd.cc2b4qgp.


Tiivistelmä

In the last decades, synthesis and design of low molecular weight organogelators has gained increasing attention due to their versatile use in, for example, cosmetics, biomedicine and oil spill remediation. In this work, three potential gelators have been prepared from allylated d-mannose. Both the gelators and the corresponding gels formed were thoroughly characterized by crystallography, FTIR spectroscopy, SEM, rheometry and NMR spectroscopy, in solution and in solid state. The results showed that two of the compounds phase-selectively form gels with hydrocarbon solvents. The most promising gelator compound is alkene terminated, with the unsaturated end functionality not critical for gel formation, tentatively providing the possibility for customizing the gelation properties by further chemical modification. Alternatively, the alkene group could possibly be utilized as a linker for future coupling to carrier materials or surfaces to further increase the mechanical strength of the gel.


YSO-asiasanatgeelitmonosakkaridithiilihydraatitkidetiedeNMR-spektroskopiainfrapunaspektroskopiahyötykäyttö

Vapaat asiasanatD-mannoosi


Liittyvät organisaatiot

JYU-yksiköt:


OKM-raportointiKyllä

Raportointivuosi2022

JUFO-taso1


Viimeisin päivitys 2024-22-04 klo 13:59