Jinxing Jiang

ORCID: 0000-0003-1817-1054
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About
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Research Areas
  • biodegradable polymer synthesis and properties
  • Carbon dioxide utilization in catalysis
  • Polyoxometalates: Synthesis and Applications
  • Organometallic Complex Synthesis and Catalysis
  • Blood Pressure and Hypertension Studies
  • Copper-based nanomaterials and applications
  • Transition Metal Oxide Nanomaterials
  • Pharmaceutical Practices and Patient Outcomes
  • Advanced battery technologies research
  • Analytical Methods in Pharmaceuticals

Tianshui Normal University
2025

State Key Laboratory of Applied Organic Chemistry
2018-2021

Lanzhou University
2018-2021

Lanzhou City University
2019

China Nonferrous Metal Mining (China)
2019

Fu Wai Hospital
2011

Chinese Academy of Medical Sciences & Peking Union Medical College
2011

Synthesizing different types of sequence-controlled copolyesters can enrich the diversity and modify their properties more precisely, but it is still a challenge to synthesize complicated copolyester using hydroxy acids in living polymerization manner. In this work, highly regioselective stereoselective catalytic system was developed biorenewable biodegradable mandelic acid lactic with isotactic-alternating, heterotactic-alternating, ABAA-type precise sequences. Because regular incorporation...

10.1021/jacs.1c00902 article EN Journal of the American Chemical Society 2021-03-16

A novel two-dimensional (2D) amorphous VOPO4/graphene (A-VOP/G) heterostructure, which features rapid ion diffusion pathways, numerous active sites, high conductivity, and superior stability, serves as a high-voltage cathode for zinc-ion batteries (ZIBs). The A-VOP/G achieves platform (1.50 V) is stable over 2000 cycles at 5 g-1.

10.1039/d5cc00765h article EN Chemical Communications 2025-01-01

Three potassium crown ether complexes supported with bulky amidinate ligands were synthesized for the ring-opening polymerization (ROP) of rac-lactide. The side reaction initiated directly by ligand anion was suppressed well in presence alcohol as our design, and synthesis linear polylactide a molecular weight high 117.7 kg/mol successful together an isoselectivity value Pm = 0.88 at −70 °C. In this system, lactide can be deprotonated to give enolate, which initiate ROP absence alcohol;...

10.1021/acs.inorgchem.7b03184 article EN Inorganic Chemistry 2018-03-01

Ring-opening polymerization (ROP) of rac-O-carboxyanhydride mandelic acid (rac-manOCA) is a promising method to synthesize isotactic biodegradable polyester poly(mandelic acid), which has high glass-transition temperature (Tg) and melting (Tm) due the formation stereocomplex. However, it still big challenge poly(rac-manOCA) so far because easy epimerization manOCA in progress. In this work, highly isoselective ROP rac-manOCA system as first stereoselective example reported using weak Lewis...

10.1021/acs.macromol.9b02302 article EN Macromolecules 2020-01-28

A series of mononuclear salen–sodium anions, as the first examples, were synthesized with tetra-alkyl ammonium a counterpart cation. These complexes are efficient catalysts for isoselective ring-opening polymerization rac-lactide; molecular weights polymers under control and weight distributions narrow when five equivalents BnOH is used an initiator. The best isoselectivity value Pm = 0.82 was achieved at −70 °C. experimental results together density functional theory calculation show that...

10.1021/acs.inorgchem.8b02290 article EN Inorganic Chemistry 2018-12-13

To control the monomer sequence in copolymers of different hydroxyl acids remains a big challenge so far, which is valuable for tuning properties copolyesters. In this work, perfectly alternating sequence-controlled copolymer mandelic acid and glycolic acid, as first example, was synthesized via highly regioselective ring-opening polymerization (ROP) cyclic diester (3-phenyl-1, 4-dioxane 2, 5-diketone, PDD). The high molecular weight poly(mandelate-alt-glycolate) (66.8 kg/mol) achieved too,...

10.1021/acs.macromol.9b01515 article EN Macromolecules 2019-10-01

The stereoselective ring-opening polymerization (ROP) of O-carboxyanhydrides (OCAs) remains a major challenge due to the easy epimerization monomers. In this work, using zinc alkoxide initiator, highly efficient ROP enantiopure 5-methyl-1,3-dioxolane-2,4-dione (LacOCA), 5-benzyl-1,3-dioxolane-2,4-dione (PheOCA), and 5-(4-(benzyloxy)benzyl)-1,3-dioxolane-2,4-dione (Try(Bn)OCA) was achieved without obvious epimerization. Moreover, isoselective rac-LacOCA, rac-PheOCA, rac-Try(Bn)OCA successful...

10.1039/c9cc06108h article EN Chemical Communications 2019-01-01

Monomer sequence controllable syntheses of copolymers, including copolyesters, remain a challenge in polymer science. Although alternating sequence-controlled copolymerization O-carboxyanhydrides (OCAs) can be achieved via using syndioselective initiators, the lactic acid-derived O-carboxyanhydride (LacOCA) with other monomers still suffers from lack highly initiators. In this work, system for ring-opening polymerization (ROP) LacOCA was bulky amine tris(phenolate) hafnium alkoxide initiator...

10.1021/acs.inorgchem.0c01499 article EN Inorganic Chemistry 2020-06-25

The synthesis of highly stereoregular poly(mandelic acid) (PMA) via controllable polymerization is a considerable challenge because the easy racemization monomers during polymerization; consequently, precise stereoblock copolymers PMA have not been reported so far. In this work, was synthesized through living ring-opening O-carboxyanhydrides (OCAs) mandelic acid using active OOO-tridentate bis(phenolate)/zinc catalysts. system, side reaction suppressed very well decreasing basicity ligands...

10.1021/acs.macromol.0c02730 article EN Macromolecules 2021-02-16

To compare the pharmacokinetic (PK) profiles and evaluate PK interaction of hydrochlorothiazide (HCTZ) used alone in combination with benazepril (BENA) or valsartan (VAL) healthy Chinese volunteers.Data from two Phase I clinical trials (Study A Study B) were combined analyzed. was an open, randomized, three-period crossover study. Eligible male volunteers randomly assigned to receive a single dose HCTZ (25 mg), BENA (20 mg) HCTZ/BENA (25/20 mg). B open two-period study VAL/HCTZ (160/12.5...

10.5414/cp201583 article EN International Journal of Clinical Pharmacology and Therapeutics 2011-11-28
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