Guoquan Zhou

ORCID: 0000-0002-3712-2429
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Research Areas
  • Crystallization and Solubility Studies
  • Chemical and Physical Properties in Aqueous Solutions
  • Pharmacological Effects of Natural Compounds
  • Analytical Chemistry and Chromatography
  • X-ray Diffraction in Crystallography
  • Phase Equilibria and Thermodynamics
  • Organic and Molecular Conductors Research
  • Crystallography and molecular interactions
  • Chemical Thermodynamics and Molecular Structure
  • Nanomaterials for catalytic reactions
  • Cyclopropane Reaction Mechanisms
  • Click Chemistry and Applications
  • Intermetallics and Advanced Alloy Properties
  • Crystal structures of chemical compounds
  • Thermodynamic properties of mixtures
  • Synthesis and Catalytic Reactions
  • Membrane Separation Technologies
  • Advancements in Battery Materials
  • Metallurgical and Alloy Processes
  • Photonic and Optical Devices
  • Orbital Angular Momentum in Optics
  • Bauxite Residue and Utilization
  • Catalytic Cross-Coupling Reactions
  • Ammonia Synthesis and Nitrogen Reduction
  • Magnetism in coordination complexes

Ningbo University of Technology
2012-2023

Zhejiang University of Water Resource and Electric Power
2022

North University of China
2022

Prairie View A&M University
2018

Zhejiang University
2001-2015

Zhejiang A & F University
2003

The solubility values of 5-chloro-8-hydroxyquinoline and 5,7-dichloro-8-hydroxyquinoline in six pure solvents at temperatures ranging from 283.15 to 323.15 K was determined by the isothermal saturation method. In investigated temperature range, are larger than those all studied temperatures. They decrease according sequence N-methyl-2-pyrrolidone > N,N-dimethylformamide 1,4-dioxane ethyl acetate toluene acetonitrile. data were correlated using modified Apelblat equation, Buchowski–Ksiazaczak...

10.1021/acs.jced.9b00028 article EN Journal of Chemical & Engineering Data 2019-10-21

Abstract Cu II ‐catalysed diazo transfer and I azide–alkyne 1,3‐dipolar cycloaddition (CuAAC) “click chemistry” were used to synthesis C 7 N aminocyclitol‐derivatised 1,2,3‐triazoles. In the course of this work, ‐N=N‐ moiety was transferred onto aminocyclitols such as validamine, valienamine valiolamine by employing imidazole‐1‐sulfonyl azide reagent with catalysis , Zn Ni in moderate good yields. The obtained azidocyclitols coupled various terminal alkynes under modified Meldal's conditions...

10.1002/ejoc.201301874 article EN European Journal of Organic Chemistry 2014-04-17

Intermetallic compounds are atomically ordered inorganic materials containing two or more transition metals and main-group elements in unique crystal structures. Intermetallics based on group 10 14 have shown enhanced activity, selectivity, durability comparison to simple alloys many catalytic reactions. While high-temperature solid-state methods prepare intermetallic exist, softer synthetic can provide key advantages, such as enabling the preparation of metastable phases smaller particles...

10.1021/acs.organomet.9b00803 article EN Organometallics 2020-03-03

The aim of this work is to study the solubility aniracetam and discuss molecular interaction between solute solvent in dissolution process. This would be important optimize crystallization extraction process aniracetam. equilibrium data seven pure solvents including methanol, ethanol, n-propanol, isopropyl alcohol, acetone, toluene, ethyl acetate, three binary mixtures were measured by using isothermal saturation method from T = 273.15 318.15 K. mixed increased with increasing temperature....

10.1021/acs.jced.8b00023 article EN Journal of Chemical & Engineering Data 2018-07-10

A green and biodegradable carbohydrate-derived alkylamine was designed employed as ligand for Ullmann type C–N coupling catalyzed by copper in water. The of aryl iodide N-nucleophiles were examined moderate to excellent yields obtained. In addition, the in-water strategy expanded successfully reaction indoles with 4-iodoanisole. By measuring solubility, it is speculated that plays role chelating promoting dissolution 4-iodoanisole Remarkably, this methodology environmentally friendly...

10.1055/s-0037-1611695 article EN Synlett 2018-12-17

The present study investigating the experimental equilibrium solubility of 2-chloro-4-amino-6,7-dimethoxyquinazoline (CADQ) dissolved in 12 kinds neat organic solvents, including methanol, ethanol, n-propanol, isopropanol, n-butanol, isobutyl alcohol, ethyl acetate, toluene, N,N-dimethyl formamide (DMF), N-methylpyrrolidone (NMP), 1,4-dioxane, and cyclohexanone, was determined an state by means isothermal saturation method at temperature ranges 273.15–313.15 K under normal atmospheric...

10.1021/acs.jced.0c00506 article EN Journal of Chemical & Engineering Data 2020-11-23

The solubility of 5-methyl-2-pyrazinecarboxylic acid (MPCA) in 12 pure solvents within the temperature range from 273.15 to 313.15 K under 101.3 kPa was determined and correlated by some thermodynamic models including modified Apelblat equation, λh Wilson model. results increased with rising temperature, it decreased following sequence (at a certain temperature): 1,4-dioxane > ethanol n-propanol 1-butanol methanol isopropanol acetone 2-butanone ethyl acetate water acetonitrile toluene....

10.1021/acs.jced.9b00406 article EN Journal of Chemical & Engineering Data 2019-08-21

The solubility profiles of sancycline in methanol, ethanol, n-propanol, isopropanol, 1-butanol, isobutyl alcohol, n-octanol, cyclohexane, n-hexane, acetonitrile, ethyl acetate, and 1,4-dioxane were determined experimentally by using the isothermal dissolution equilibrium method at temperature range from 278.15 to 318.15 K under a pressure 101.2 kPa. As expected, data mole fraction increased with rising temperature. maximum value was obtained (3.364 × 10–3 K), lowest cyclohexane (8.979 10–5...

10.1021/acs.jced.9b00693 article EN Journal of Chemical & Engineering Data 2019-10-21

Zonisamide is moderately soluble in water with a reported solubility of 0.8 mg·mol–1 (6.78 × 10–5 mole fraction). The objective to study the zonisamide methanol, ethanol, n-propanol, isopropanol, 1-butanol, acetonitrile, ethyl acetate, toluene, 2-butanone, cyclohexanone, 1,4-dioxane, and N,N-dimethylformamide (DMF) at temperature range from 273.15 313.15 K, which was measured using isothermal dissolution equilibrium method under pressure 101.2 kPa. largest value found DMF followed by...

10.1021/acs.jced.0c00249 article EN Journal of Chemical & Engineering Data 2020-06-19

The basis of purification and further theoretical studies iohexol is the solubility in different solvents. 12 monosolvents (ethanol, n-propanol, isopropanol, n-butanol, acetone, acetonitrile, ethyl acetate, 1,4-dioxane, cyclohexane, 2-butanone, dimethyl sulfoxide (DMSO), toluene) (ethanol + acetate) solvents system was determined using a static gravimetric method, with following conditions: temperature T = (283.15 to 323.15) K pressure p 101.2 kPa. To sum up, ethanol highest, cyclohexane...

10.1021/acs.jced.8b01101 article EN Journal of Chemical & Engineering Data 2019-03-06

The experimental gramine solubilities in pure organic monosolvents containing methanol, ethanol, n-propanol, isopropanol, n-butanol, acetone, toluene, acetonitrile, ethyl acetate, 1,4-dioxane, n-octanol, and binary solvent mixtures (ethanol + acetate) were determined by means of the isothermal equilibrium method at evaluated temperatures from (273.15 to 313.15) K under a pressure 101.2 kPa. solubility neat solvents rose with rising temperature. data high small selected was as follows:...

10.1021/acs.jced.9b00911 article EN Journal of Chemical & Engineering Data 2020-02-05

The solid–liquid phase equilibrium of ticagrelor in methanol, ethanol, n-propanol, isopropanol, 1-butanol, isobutanol, n-octanol, acetonitrile, ethyl acetate, toluene, 2-butanone, and cyclohexanone at the temperature range from 273.15 to 313.15 K was measured by using isothermal dissolution method under pressure 101.2 kPa. solubility data were analyzed high-performance liquid chromatography, results increased with rising temperature. maximum value obtained 2-butanone (in mole fraction, 7.758...

10.1021/acs.jced.0c00127 article EN Journal of Chemical & Engineering Data 2020-06-29
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