Riziwanguli Wufu

Ms. Riziwanguli Wufu

University of Helsinki
orcid

Research Focus & Metrics

Academic Career Length

15Years (2012-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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16 February 2021 in Molecules
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Journal Article
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HLHarri Latva-Mäenpää
Harri Latva-Mäenpää
Riziwanguli WufuRiziwanguli Wufu
Riziwanguli Wufu
DMDaniel Mulat
Daniel Mulat
TSTytti Sarjala
Tytti Sarjala
PSPekka Saranpaa
Pekka Saranpaa
KWKristiina Wähälä
Kristiina Wähälä
Stilbenes or stilbenoids, major polyphenolic compounds of the bark of Norway spruce (Picea abies L. Karst), have potential future applications as drugs, preservatives and other functional ingredients due to their antioxidative, antibacterial and antifungal properties. Stilbenes are photosensitive and UV and fluorescent light induce trans to cis isomerisation via intramolecular cyclization. So far, the characterizations of possible new compounds derived from trans-stilbenes under UV light exposure have been mainly tentative based only on UV or MS spectra without utilizing more detailed structural spectroscopy techniques such as NMR. The objective of this work was to study the stability of biologically interesting and readily available stilbenes such as astringin and isorhapontin and their aglucones piceatannol and isorhapontigenin, which have not been studied previously. The effects of fluorescent and UV light and storage on the stability of trans stilbenes were assessed and the identification and characterisation of new compounds formed during our experiments were carried out by chromatographic (HPLC, GC) and spectroscopic techniques (UV, MS, NMR). The stilbenes undergo a trans to cis isomerisation under extended UV irradiation by intramolecular cyclisation (by the formation of a new C-C bond and the loss of two hydrogens) to phenanthrene structures. The characterised compounds are novel and not described previously.

24 August 2012 in CrystEngComm
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Journal Article
Closed access
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HGHong-Ling Gao
Hong-Ling Gao
YYYong-Ling Yi
Yong-Ling Yi
YHYao-Min Hu
Yao-Min Hu
JQJing Qu
Jing Qu
CHCong-Cong Hu
Cong-Cong Hu
BZBin Zhai
Bin Zhai
Three new 3D lanthanide(III) coordination polymers with the formulas {K[Ln(pdtc)(H2O)]·H2O}n(Ln = Nd(1), Dy(2), Er(3); K4pdtc = potassium pyridine-2,3,5,6-tetracarboxylate) have been synthesized via hydrothermal methods and structurally characterized by X-ray single crystal diffraction analysis, elemental analysis and thermal gravimetric analysis. In complexes 1–3, the pdtc4− ligands adopt new coordination modes and the three complexes have similar 3D network structures which consist of dinuclear building units and novel K–O chains inserted into the structure. Furthermore, complex 2 shows corresponding characteristic luminescence and complex 3 exhibits weak antiferromagnetic properties.