Weiwei Zuo

ORCID: 0000-0002-9146-7612
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About
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Research Areas
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Asymmetric Hydrogenation and Catalysis
  • Organometallic Complex Synthesis and Catalysis
  • Carbon dioxide utilization in catalysis
  • Synthetic Organic Chemistry Methods
  • N-Heterocyclic Carbenes in Organic and Inorganic Chemistry
  • Metal complexes synthesis and properties
  • biodegradable polymer synthesis and properties
  • Surface Chemistry and Catalysis
  • Axial and Atropisomeric Chirality Synthesis
  • Electrospun Nanofibers in Biomedical Applications
  • Asymmetric Synthesis and Catalysis
  • Chemical Synthesis and Analysis
  • Nanomaterials for catalytic reactions
  • Natural product bioactivities and synthesis
  • Electrohydrodynamics and Fluid Dynamics
  • Nanoplatforms for cancer theranostics
  • Advancements in Battery Materials
  • Oxidative Organic Chemistry Reactions
  • Catalytic Cross-Coupling Reactions
  • Supercapacitor Materials and Fabrication
  • Tannin, Tannase and Anticancer Activities
  • Magnetism in coordination complexes
  • Crystallography and molecular interactions

Donghua University
2015-2025

State Key Laboratory for Modification of Chemical Fibers and Polymer Materials
2022

University of Toronto
2013-2015

Université de Strasbourg
2010-2012

Hebei Medical University
2012

Xingtai People's Hospital
2012

Centre National de la Recherche Scientifique
2010-2012

Laboratoire de Chimie de Coordination
2010-2011

Institut de Chimie de Strasbourg
2010-2011

Beijing National Laboratory for Molecular Sciences
2007-2009

Lighter Hydrogenation Catalysts Enzymes have evolved to use abundant metals such as iron, cobalt, and nickel for redox catalysis. However, synthetic catalysis has generally relied on the rarer, heavier relatives of these elements: ruthenium, rhodium, iridium, palladium, platinum (see Perspective by Bullock ). Friedfeld et al. (p. 1076 ) used high-throughput screening show that right cobalt precursor can be activated asymmetric hydrogenation using traditional ligands developed precious...

10.1126/science.1244466 article EN Science 2013-11-28

Ultrafine fibers produced by electrospinning often exhibit bead-on-string structures, which have generally been considered to be undesirable "by-products" or defects. Theoretical analysis in the literature predicted three types of instabilities for an electrically driven jet: axisymmetric Rayleigh instability, electric field-induced axisymmetric, and whipping instability. The process bead formation revealed that a beaded structure resulted from deformation flow jet. Applied voltage, solution...

10.1002/pen.20304 article EN Polymer Engineering and Science 2005-01-01

A series of iron(II) (7a−11a) and cobalt(II) (7b−11b) 2-(1-methyl-2-benzimidazolyl)-6-(1-(arylimino)ethyl)pyridyl complexes were synthesized, as well bidentate ligated by 2-(2-benzimidazolyl)-6-methylpyridine, 2-(carboethoxyl)-6-(2-benzimidazolyl)pyridine, 2-(1-methyl-2-benzimidazolyl)-6-acetylpyridine. All organic compounds fully characterized NMR IR spectroscopy elemental analysis, while the metal carefully examined analysis. Their molecular structures determined single-crystal X-ray...

10.1021/om0700819 article EN Organometallics 2007-04-04

Nitrogen-rich conjugated microporous polymers (NCMPs) have attracted great attention in recent years owing to their polarity, basicity, and ability coordinate metal ions. Herein, three NCMPs, structurally close polyaniline, were facilely synthesized via chemical oxidative polymerization between multiconnected aniline precursors. The NCMPs with high N content (11.84 wt %), intrinsic ultramicroporosity (<1 nm), moderate surface area (485 m2 g–1) show wide-ranging adsorption functionality,...

10.1021/acsami.7b09553 article EN ACS Applied Materials & Interfaces 2017-10-18

When activated with base, the iron(II) complexes tetradentate amine(imine)diphosphine ligands, (S,S)-trans-[FeCl(CO)(PAr2-NH-N-PAr′2)]BF4 (1: Ar, Ar′ = Ph; 2: Ar Ph, 4-MeC6H4; 3: 3,5-Me2C6H3), are very active for asymmetric transfer hydrogenation (ATH) of ketones in KOtBu/2-propanol. For ATH, better enantioselectivity, but lower catalytic activity, was observed general when using catalyst precursors bulkier dixylylphosphino groups compared to those diphenylphosphino groups. The were much...

10.1021/om500479q article EN publisher-specific-oa Organometallics 2014-06-13

An efficient decolorization strategy for waste polyester textiles and a new purification the glycolysis product were developed combined to enable repeatable use of in textile industry.

10.1039/d3gc00407d article EN Green Chemistry 2023-01-01

The reaction of 1,3-bis(imidazolyl)benzene with excess 1-bromoadamantane at 170 °C for 14 h afforded 1,3-bis(1-adamantylimidazolium)benzene dibromide (1), which was characterized by IR, NMR, and X-ray diffraction. Metathetical anion exchange sodium iodide yielded the N-heterocyclic dicarbene precursor diiodide, (CHimidCHCHimid)I2 (2), in high yield. [Ir(μ-Cl)2(cod)]2 (cod = 1,5-cyclooctadiene) 2 presence 2.2 equiv Cs2CO3 refluxing acetonitrile led to formation unsymmetrical iridium(III)...

10.1021/om200444q article EN Organometallics 2011-07-29

The excellent ketone asymmetric transfer hydrogenation (ATH) systems using the precatalysts (S,S)-trans-[FeCl(CO)(PPh2CH2CH2NHCHPhCHPhNCHCH2PAr2)]BPh4 (Ar = Ph (1), p-tolyl (2)) have a fascinating dependence of activity on base concentration, which is investigated here. reaction complex 1 or 2 with equiv strong potassium tert-butoxide in THF for 2–7 days produces neutral amine(ene-amido) complexes [FeCl(CO)(PPh2CH2CH2NHCHPhCHPhNCHCHPAr2)] (8 and 9). These monodeprotonated been completely...

10.1021/acscatal.5b01979 article EN publisher-specific-oa ACS Catalysis 2015-12-01

Catalytic asymmetric transfer hydrogenation (ATH) reactions of ketones have become an important tool for producing enantiomerically pure alcohols that are widely used in the syntheses bioactive compounds. However, high toxicities and low abundances traditionally employed precious metals serving as catalyst centers impeded widespread application metal-based catalysts synthesis. Development from abundant less toxic 3d is highly desirable but still challenging. We report herein development...

10.1021/acscatal.2c06204 article EN ACS Catalysis 2023-03-14

Iron and cobalt complexes are a new family of catalysts for ethylene oligomerization polymerization. The extensive researches on bis(imino)pyridyl metal have been carried out with the aim synthesizing their derivatives finding suitable reaction parameters optimum activity. Beyond modification works complexes, several alternative models similar coordination sphere developed in our group. This review article describes experiences innovating iron as

10.1016/j.crci.2007.09.002 article EN other-oa Comptes Rendus Chimie 2007-10-25

PET-RAFT polymerization enables precise polymer synthesis, yet conventional systems require an excess chain transfer agent (CTA) over unbound photocatalysts (PCs). Herein, a self-catalyzed strategy employing polymerizable porphyrin MTPPZnH as dual-functional PC effectively embeds high photosensitizer content into glycopolymers for photodynamic therapy (PDT). Three galactose-bearing monomers (acrylate, methacrylate, 4-vinylbenzoate) were polymerized via under optimized light conditions,...

10.1021/acs.biomac.5c00090 article EN Biomacromolecules 2025-03-24

We describe a stepwise synthesis of the hydrido, N-heterocyclic dicarbene iridium(III) pincer complex [Ir(H)I(C(NHC)CC(aNHC))(NCMe)] (3) which features combination normal and abnormal NHC ligands. The reaction bis(imidazolium) diiodide [(CH(imid)CHCH(imid))]I(2) (1) with [Ir(μ-Cl)(cod)](2) afforded first mono-NHC Ir(I) [IrI(cod)(CH(imid)CHC(NHC))]I (2), was then reacted 2 equiv. Cs(2)CO(3) in acetonitrile at 60 °C for 40 h to yield 3. These observations support our previously proposed...

10.1039/c1dt11511a article EN Dalton Transactions 2011-11-07

The unsymmetrical salphen ligand (3,5-tBu-1-OH-C6H2)CH═N-C6H4-N═CH(3-Ph-1-OH-C6H3) (tBu-PhLH2) was designed and synthesized to support aluminum complexes. Its symmetric analogues, (3,5-tBu-1-OH-C6H2)CH═N-C6H4-N═CH(3,5-tBu-1-OH-C6H2) (tBuLH2) (3-Ph-1-OH-C6H3)CH═N-C6H4-N═CH(3-Ph-1-OH-C6H3) (PhLH2), were also explored compared. methane elimination reactions between ligands AlMe3 resulted in formation of tBu-PhLAlMe (1), tBuLAlMe (2), PhLAlMe (3) high yields, which characterized by elemental...

10.1021/acs.organomet.7b00106 article EN Organometallics 2017-04-17

Bis-quaternary ammonium betulin-based dimethacrylate derivatives (Bis-QADM-Bet) were synthesized. Regulating the alkyl chain length of Bis-QADM-Bet endows dental resins with superior antibacterial effects and acceptable physicochemical properties.

10.1039/d3ma00016h article EN cc-by-nc Materials Advances 2023-01-01

Targeted photodynamic therapy (PDT) offers advantages over nontargeted approaches, including improved selectivity, efficacy, and reduced side effects. This study developed star-shaped glycopolymeric photosensitizers using porphyrin-based initiators via ATRP. Incorporating a porphyrin core gave the polymers fluorescence ROS generation, while adding fructose solubility targeting capabilities. The had high light absorption, singlet oxygen production, specificity, low dark toxicity,...

10.1021/acs.biomac.3c01378 article EN Biomacromolecules 2024-02-09
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