Daqian Xu
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
Daqian Xu has a total of 30 co-authors. Here are the top co-authors by number of shared publications:
Guohu Zhao
Provincial Key Laboratory of Gansu Higher Education for City Environmental Pollution Control, School of Chemical Engineering, Lanzhou City University, Lanzhou 730070, China
2 shared publications- Wei Sun
State Key Laboratory of Low Carbon Catalysis and Carbon Dioxide Utilization, Lanzhou Institute of Chemical Physics, Chinese Academy of Sciences, Lanzhou 730000, China
2 shared publications Dongmei Ran
College of Chemistry, Chemical Engineering and Materials Science, Soochow University, Suzhou 215123, China
1 shared publicationFangzheng Yao
Provincial Key Laboratory of Gansu Higher Education for City Environmental Pollution Control, School of Chemical Engineering, Lanzhou City University, Lanzhou 730070, China
1 shared publication- Fengli Dai
Institute of Polymer, College of Chemistry and Chemical Engineering, Northwest Normal University, Lanzhou 730070, China
1 shared publication - Fuxiang Jin
School of Chemistry and Chemical Engineering, Lanzhou City University, Lanzhou, China
1 shared publication
Latest Publications
- 11 July 2025
- Published by Springer Nature in Catalysis Letters
- Vol. 155 (8) , 1-12
Phosphorylated Imidazole-Functionalized Chloromethylated Polystyrene-Supported Rhodium Catalyst for Hydroformylation of Dihydrofurans
- 11 July 2025
- Published by Springer Nature in Catalysis Letters
- Vol. 155 (8) , 1-12
Phosphorylated Imidazole-Functionalized Chloromethylated Polystyrene-Supported Rhodium Catalyst for Hydroformylation of Dihydrofurans
- 29 April 2025
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 61 (45) , 8192-8195
Isolable GaN-based analogues of Thiele's and Chichibabin's hydrocarbons
Treatment of two equivalents of Trip2GaCl (Trip = 2,4,6-triisopropylphenyl) with pyrazine and 4,4′-bipyridine affords adducts 1 and 2 in high yields.
- 29 April 2025
- Published by Royal Society of Chemistry (RSC) in Chemical Communications
- Vol. 61 (45) , 8192-8195
Isolable GaN-based analogues of Thiele's and Chichibabin's hydrocarbons
Treatment of two equivalents of Trip2GaCl (Trip = 2,4,6-triisopropylphenyl) with pyrazine and 4,4′-bipyridine affords adducts 1 and 2 in high yields.
- 13 January 2023
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 47 (8) , 3921-3927
Direct use of hydroxyl ions as an oxygen source for oxidation of isoquinolinium salts to isoquinolinones in water solution
Environmentally friendly synthesis of isoquinolinones and quinolinones has been achieved in water solution by oxidation of isoquinolinium and quinolinium salts using oxygen under mild conditions. This reaction is compatible with numerous isoquinolinium and quinolinium salts. The results of the isotope labeling experiment (using 18O2 and H2 18O) suggest that OH− is the oxygen source of the forming products, and oxygen serves as the oxidant. Moreover, this method can be used to synthesize bioactive molecules such as a topoisomerase I inhibitor.
- 13 January 2023
- Published by Royal Society of Chemistry (RSC) in New Journal of Chemistry
- Vol. 47 (8) , 3921-3927
Direct use of hydroxyl ions as an oxygen source for oxidation of isoquinolinium salts to isoquinolinones in water solution
Environmentally friendly synthesis of isoquinolinones and quinolinones has been achieved in water solution by oxidation of isoquinolinium and quinolinium salts using oxygen under mild conditions. This reaction is compatible with numerous isoquinolinium and quinolinium salts. The results of the isotope labeling experiment (using 18O2 and H2 18O) suggest that OH− is the oxygen source of the forming products, and oxygen serves as the oxidant. Moreover, this method can be used to synthesize bioactive molecules such as a topoisomerase I inhibitor.
- Open Access
An Eco-Friendly Polymer Composite Fertilizer for Soil Fixation, Slope Stability, and Erosion Control
In the Loess Plateau region, the poor structure and properties of loess slopes will cause many types of geological disasters such as landslides, mudflow, land collapse, soil erosion, and ground cracking. In this paper, an eco-friendly polymer composite fertilizer (PCF) based on corn straw wastes (CS) and geopolymer synthesized from loess was studied. The characterization by FT-IR of the PCF confirmed that graft copolymer is formed, while morphological analysis by scanning electron microscopy and energy dispersive spectroscopy showed that geopolymer and urea were embedded in the polymer porous network. The effects of PCF contents on the compressive strength of loess were investigated. The PCF was characterized in terms of surface curing test, temperature and freeze-thaw aging property, water and wind erosion resistance, and remediation soil acidity and alkalinity property, which indicates that PCF can improve loess slope fixation and stability by physical and chemical effects. Moreover, the loess slope planting experiment showed that PCF can significantly increase the germination rate of vegetation from 31% to 68% and promote the survival rate of slope vegetation from 45.2% to 67.7% to enhance biological protection for loess slopes. The PCF meets the demands of building and roadbed slope protection and water-soil conservation in arid and semi-arid regions, which opens a new application field for multifunctional polymer composite fertilizers with low cost and environmental remediation.
Open AccessAn Eco-Friendly Polymer Composite Fertilizer for Soil Fixation, Slope Stability, and Erosion Control
In the Loess Plateau region, the poor structure and properties of loess slopes will cause many types of geological disasters such as landslides, mudflow, land collapse, soil erosion, and ground cracking. In this paper, an eco-friendly polymer composite fertilizer (PCF) based on corn straw wastes (CS) and geopolymer synthesized from loess was studied. The characterization by FT-IR of the PCF confirmed that graft copolymer is formed, while morphological analysis by scanning electron microscopy and energy dispersive spectroscopy showed that geopolymer and urea were embedded in the polymer porous network. The effects of PCF contents on the compressive strength of loess were investigated. The PCF was characterized in terms of surface curing test, temperature and freeze-thaw aging property, water and wind erosion resistance, and remediation soil acidity and alkalinity property, which indicates that PCF can improve loess slope fixation and stability by physical and chemical effects. Moreover, the loess slope planting experiment showed that PCF can significantly increase the germination rate of vegetation from 31% to 68% and promote the survival rate of slope vegetation from 45.2% to 67.7% to enhance biological protection for loess slopes. The PCF meets the demands of building and roadbed slope protection and water-soil conservation in arid and semi-arid regions, which opens a new application field for multifunctional polymer composite fertilizers with low cost and environmental remediation.
- 20 May 2020
- Published by Bentham Science Publishers Ltd. in Letters in Organic Chemistry
- Vol. 17 (6) , 438-442
One-Pot, Regioselective Synthesis of Homopropargyl Alcohols using Propargyl Bromide and Carbonyl Compound by the Mg-mediated Reaction under Solvent-free Conditions
The elimination of volatile organic solvents in organic synthesis is the most important goal in “Green” chemistry. We report a simple, efficient and facile method for the addition of progargyl bromide to carbonyl compounds using Mg metal as a mediator under solvent-free conditions which could regioselectively generate homopropargyl alcohols efficiently in good to excellent yields. The procedure has advantages such as short reaction time, operationally simple, excellent product yields, high regioselectivity and organic solvent-free.
- 20 May 2020
- Published by Bentham Science Publishers Ltd. in Letters in Organic Chemistry
- Vol. 17 (6) , 438-442
One-Pot, Regioselective Synthesis of Homopropargyl Alcohols using Propargyl Bromide and Carbonyl Compound by the Mg-mediated Reaction under Solvent-free Conditions
The elimination of volatile organic solvents in organic synthesis is the most important goal in “Green” chemistry. We report a simple, efficient and facile method for the addition of progargyl bromide to carbonyl compounds using Mg metal as a mediator under solvent-free conditions which could regioselectively generate homopropargyl alcohols efficiently in good to excellent yields. The procedure has advantages such as short reaction time, operationally simple, excellent product yields, high regioselectivity and organic solvent-free.
- 30 March 2018
- Published by Wiley in Chemistry – An Asian Journal
- Vol. 13 (17) , 2458-2464
Efficient Aliphatic C−H Bond Oxidation Catalyzed by Manganese Complexes with Hydrogen Peroxide
A tetradentate nitrogen ligand containing a benzimidazole ring and an electron‐rich pyridine ring was developed, the resulting manganese complex exhibited good activity in the C−H oxidation of simple alkanes. In particular, cyclic aliphatic alkanes were transformed into ketones in very good yields (up to 89 %) by using environmentally benign H2O2 as the terminal oxidant. This protocol was also applied successfully in benzylic C−H oxidation, giving the corresponding ketones with very good selectivities. In addition, tertiary C−H bond oxidation of complex molecules by the manganese complex showed potential utility for assembling alcohols with good selectivity in late‐stage chemical synthesis.
- 30 March 2018
- Published by Wiley in Chemistry – An Asian Journal
- Vol. 13 (17) , 2458-2464
Efficient Aliphatic C−H Bond Oxidation Catalyzed by Manganese Complexes with Hydrogen Peroxide
A tetradentate nitrogen ligand containing a benzimidazole ring and an electron‐rich pyridine ring was developed, the resulting manganese complex exhibited good activity in the C−H oxidation of simple alkanes. In particular, cyclic aliphatic alkanes were transformed into ketones in very good yields (up to 89 %) by using environmentally benign H2O2 as the terminal oxidant. This protocol was also applied successfully in benzylic C−H oxidation, giving the corresponding ketones with very good selectivities. In addition, tertiary C−H bond oxidation of complex molecules by the manganese complex showed potential utility for assembling alcohols with good selectivity in late‐stage chemical synthesis.