Riziwanguli Wufu
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Research Subjects
Riziwanguli Wufu has a total of 12 co-authors. Here are the top co-authors by number of shared publications:
Bin Zhai
Chemistry & Chemical Engineering, Shangqiu Normal University, Henan 476000, P. R. China
1 shared publicationCong-Cong Hu
Department of Chemistry, Tianjin University, Tianjin 300072, P. R. China
1 shared publication- Daniel Mulat
Department of Chemistry, University of Helsinki, P.O. Box 55, FI-00014 Helsinki, Finland
1 shared publication - Harri Latva-Mäenpää
Department of Chemistry, University of Helsinki, P.O. Box 55, FI-00014 Helsinki, Finland
1 shared publication Hong-Ling Gao
Department of Chemistry, Tianjin University, Tianjin 300072, P. R. China
1 shared publication- Jian-Zhong Cui
Department of Chemistry
1 shared publication
Latest Publications
- Open Access
Stability and Photoisomerization of Stilbenes Isolated from the Bark of Norway Spruce Roots
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.
Open AccessStability and Photoisomerization of Stilbenes Isolated from the Bark of Norway Spruce Roots
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
- Published by Royal Society of Chemistry (RSC) in CrystEngComm
- Vol. 14 (23) , 7965-7971
Syntheses, structures, and properties of 3D lanthanide coordination polymers based on pyridine-2,3,5,6-tetracarboxylate
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.
- 24 August 2012
- Published by Royal Society of Chemistry (RSC) in CrystEngComm
- Vol. 14 (23) , 7965-7971
Syntheses, structures, and properties of 3D lanthanide coordination polymers based on pyridine-2,3,5,6-tetracarboxylate
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.