Hai-Tao Wang

ORCID: 0000-0002-3640-159X
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About
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Crystal structures of chemical compounds
  • Non-Invasive Vital Sign Monitoring
  • Oxidative Organic Chemistry Reactions
  • Magnetism in coordination complexes
  • Hemodynamic Monitoring and Therapy
  • Simulation and Modeling Applications
  • Advanced Sensor Technologies Research
  • Flow Measurement and Analysis
  • Catalysis for Biomass Conversion
  • Catalysts for Methane Reforming
  • Metal-Organic Frameworks: Synthesis and Applications
  • Vanadium and Halogenation Chemistry
  • Power Systems and Technologies
  • Radical Photochemical Reactions
  • Multimedia Communication and Technology
  • Fluorine in Organic Chemistry
  • Industrial Technology and Control Systems
  • Synthesis of Organic Compounds
  • Microbial Metabolic Engineering and Bioproduction
  • Advanced Measurement and Metrology Techniques
  • Metal complexes synthesis and properties
  • Innovative Educational Techniques
  • Synthesis and biological activity

Zero to Three
2019-2020

Jinan University
2019-2020

Tianjin University
2004-2015

Northwest A&F University
2012

Abstract Novel amino‐acid‐derived phthalazine reagents have been designed and synthesized for the enantioselective fluorocyclizations of prochiral indoles. The scope reaction is evidenced by 28 examples fluorinated furoindole pyrroloindole heterocycles bearing various functionalities with up to 99% ee. resulting enantioenriched products are found be potent AChE inhibitors. Advantages current new chiral include ease in synthesis analogues readily tunable steric/electronic demands. magnified image

10.1002/adsc.201900814 article EN Advanced Synthesis & Catalysis 2019-10-15

Abstract We apply a chiral anionic phase‐transfer system for the catalytic asymmetric bromoaminocyclization and bromocycloetherification of momo‐functional benzo‐cyclic alkenes. Various brominated tricyclic benzo‐heterocycles were produced with up to 99% yields enantiomeric excess. The resulting enantioenriched hexahydro‐benzoindoles are key building blocks bioactive molecules. magnified image

10.1002/adsc.202000845 article EN Advanced Synthesis & Catalysis 2020-09-23

10.1007/s10877-013-9541-7 article EN Journal of Clinical Monitoring and Computing 2013-12-05

End-tidal carbon dioxide (P(ET)CO₂) monitoring has become an important tool in clinical monitoring, but there are still limitations practice. Low-frequency modulation was used to reliably acquire respiratory information. Then the disturbances of humidity and flow rate were removed by signal decomposition. Finally, real-time concentration CO₂ calculated displayed adjusted calibration function. Targeted experiments confirm that a period 180 ms depth 50% optimal choice. In this case, effects...

10.1364/ao.53.002145 article EN Applied Optics 2014-03-26

The micro force measuring technology is widely used in the area of friction test, liquid surface tension analysis, organism micro-structure measurement and calibration MEMS NEMS, etc. In view realization approach value, a system proposed. A control electrostatic generator adopted to reproduce force. basic working principle an exact designed cylindrical capacitor with characteristics long range, fine linearity faint border effect. linear axletree high precision ensure concentricity movement....

10.1109/icemi.2009.5274813 article EN 2009-08-01

The cation and the anion of title complex, [Cu(CHO2)(C12H8N2)2]BF4 or [Cu(phen)2HCOO]BF4 (phen = 1,10-phenanthroline), both lie on crystallographic twofold rotation axes. CuII ion is in a distorted square-pyramidal geometry, coordinated by four N atoms from two chelating phen ligands one O atom formate ligand. A axis causes H ligand to be disordered.

10.1107/s1600536807002875 article EN Acta Crystallographica Section E Structure Reports Online 2007-01-26

The mol­ecular structure of the title compound, C13H17NO4, has no symmetry plane because one C atom ethyl group lies out defined by other non-H atoms. In crystal structure, mol­ecules stack along a axis. Symmetry-related are linked C—H⋯O hydrogen bond, forming zigzag chains extending in b-axis direction.

10.1107/s1600536805039590 article EN Acta Crystallographica Section E Structure Reports Online 2005-12-07

Mol­ecules of the title compound, C12H26N4S2, have 2/m symmetry. Intra­molecular N—H⋯N and N—H⋯S hydrogen bonds are observed.

10.1107/s1600536805035828 article EN Acta Crystallographica Section E Structure Reports Online 2005-11-05
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