Dawei Yang

ORCID: 0000-0002-7646-3891
Publications
Citations
Views
---
Saved
---
About
Contact & Profiles
Research Areas
  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Metalloenzymes and iron-sulfur proteins
  • Crystallography and molecular interactions
  • Electrocatalysts for Energy Conversion
  • Molten salt chemistry and electrochemical processes
  • Organometallic Complex Synthesis and Catalysis
  • Advanced battery technologies research
  • Metal-Catalyzed Oxygenation Mechanisms
  • Asymmetric Hydrogenation and Catalysis
  • Magnetism in coordination complexes
  • Extraction and Separation Processes
  • Carbon dioxide utilization in catalysis
  • Ammonia Synthesis and Nitrogen Reduction
  • Algal biology and biofuel production
  • Nanomaterials for catalytic reactions
  • Metal complexes synthesis and properties
  • Nuclear materials and radiation effects
  • Marine and coastal ecosystems
  • Photosynthetic Processes and Mechanisms
  • Metallurgical Processes and Thermodynamics
  • Advancements in Battery Materials
  • CO2 Reduction Techniques and Catalysts
  • Metal-Organic Frameworks: Synthesis and Applications
  • Thermodynamic and Structural Properties of Metals and Alloys

Dalian University
2016-2025

Dalian University of Technology
2016-2025

Chinese Academy of Sciences
2011-2024

Beijing National Laboratory for Molecular Sciences
2023-2024

Institute of High Energy Physics
2019-2023

Harbin Engineering University
2007-2021

Ningbo Institute of Industrial Technology
2020

North China University of Science and Technology
2019

Beihang University
2018

National Chung Hsing University
2018

Batch Normalization (BN) is capable of accelerating the training deep models by centering and scaling activations within mini-batches. In this work, we propose Decorrelated (DBN), which not just centers scales but whitens them. We explore multiple whitening techniques, find that PCA causes a problem call stochastic axis swapping, detrimental to learning. show ZCA does suffer from problem, permitting successful DBN retains desirable qualities BN further improves BN's optimization efficiency...

10.1109/cvpr.2018.00089 preprint EN 2018-06-01

Interaction of a diiron thiolate-bridged complex, [Cp*Fe(μ-η2:η4-bdt)FeCp*] (1) (Cp* = η5-C5Me5; bdt benzene-1,2-dithiolate) with proton gives an FeIIIFeIII hydride bridged [Cp*Fe(μ-bdt)(μ-H)FeCp*][BF4] (3[BF4]). According to in situ variable temperature 1H NMR studies, the formation 3[BF4] was evidenced occur through stepwise pathway: protonation occurring at iron center produce terminal [Cp*Fe(μ-bdt)(t-H)FeCp*][BF4] (2) and subsequent intramolecular isomerization bridging 3[BF4]. A...

10.1021/acs.inorgchem.5b01508 article EN Inorganic Chemistry 2015-10-19

Batch Normalization (BN) is capable of accelerating the training deep models by centering and scaling activations within mini-batches. In this work, we propose Decorrelated (DBN), which not just centers scales but whitens them. We explore multiple whitening techniques, find that PCA causes a problem call stochastic axis swapping, detrimental to learning. show ZCA does suffer from problem, permitting successful DBN retains desirable qualities BN further improves BN's optimization efficiency...

10.48550/arxiv.1804.08450 preprint EN other-oa arXiv (Cornell University) 2018-01-01

Electrochemical behaviors of lanthanide (i.e. La, Ce, Pr and Nd) chlorides in LiCl-KCl melt were demonstrated via cyclic voltammetry (CV) open circuit potential (OCP) techniques at temperatures from 723 K to 873 K. An electrochemical galvanostatic intermittent titration technique (GITT) was performed obtain the thermodynamic data (Ln) on liquid bismuth electrode. The relationship between activity coefficient temperature determined. Galvanostatic pulse (GP) impedance spectroscopy (EIS) as...

10.1149/1945-7111/abb0f4 article EN Journal of The Electrochemical Society 2020-08-20

Viscosity, at the subcellular level, plays a crucial role as physicochemical factor affecting microenvironment homeostasis. Abnormal changes in mitochondrial viscosity often lead to various diseases organism. Based on twisted intramolecular charge transfer mechanism, four hemicyanine dye fluorescent probes (HT-SA, HT-SA-S, HT-Bzh, and HT-NA) were designed synthesized for response. The single bond between nitrogen-containing heterocycle carbon–carbon double structure of probe served response...

10.1021/acs.jpcb.4c00161 article EN The Journal of Physical Chemistry B 2024-04-12

Thiolate‐bridged diiron complexes have drawn extensive attention due to their wide applications in the biomimetic simulation for structure and function of various metalloenzymes related bioinspired catalysis. Through introduction functional subunit into bridging thiolate ligands, resulting thiolate‐bridged with different geometric electronic structures can exhibit distinct reactivity. Herein, we utilize a half‐sandwich type mononuclear iron complex as reaction precursor construct two novel...

10.1002/ejic.202400643 article EN European Journal of Inorganic Chemistry 2025-01-12

A series of novel monothiolate-bridged dirhodium complexes, [Cp*Rh(μ-SR)(μ-Cl)2RhCp*][BF4] {Cp* = η5-C5Me5, R tertiary butyl (tBu), 1a; ferrocenyl (Fc), 1b; adamantyl (Ad), 1c} were designed and successfully synthesized, which can smoothly facilitate highly regioselective stereoselective hydrosilylation terminal alkynes to afford β(Z) vinylsilanes with good functional group compatibility. Furthermore, the hydride bridged complex [Cp*Rh(μ-StBu)(μ-Cl)(μ-H)RhCp*][BF4] (5) as a potential...

10.1021/acs.orglett.8b02267 article EN Organic Letters 2018-08-28

The novel thioether-dithiolate-bridged diiron complex [Cp*Fe(μ-1κ3SSS′:2κ2SS-tpdt)FeCp*] (1, Cp* = η5-C5Me5; tpdt S(CH2CH2S−)2) has been prepared by the reaction of [Cp*FeCl]2 with Li2(tpdt) in THF. Given thermodynamic instability 1, a one-electron oxidation was performed Fc·PF6 (Fc ferrocene) affording 1[PF6]. Treatment 1[PF6] CO or tBuNC CH2Cl2 gave complexes [Cp*Fe(μ-1κ3SSS′:2κ2SS-tpdt){Cp*Fe(η1-CO)}][PF6] (2[PF6]) and [Cp*Fe(μ-1κ3SSS′:2κ2SS-tpdt){Cp*Fe(η1-tBuNC)}][PF6] (3[PF6]). In...

10.1021/acs.organomet.5b00118 article EN Organometallics 2015-04-23

A series of nitrile-coordinating complexes [Cp*Fe(μ-SEt)RCN]2[PF6]2 (1, R = alkyl, aryl, vinyl, amine) have been obtained by the reaction [Cp*Fe(μ-SEt)MeCN]2[PF6]2 (1a) with various nitriles in acetone. Complexes 1 can realize hydration a nitrile ligand under ambient conditions. [Cp*Fe(μ-SEt)2(μ-η1:η1-NH(O)CR)FeCp*][PF6] (2) were successfully isolated as intermediates during process, 2b and 2e (R CH2═CH Et2N) being characterized spectrometry X-ray crystallography. Treatment 2 HBF4·Et2O...

10.1021/acs.organomet.5b00387 article EN Organometallics 2015-07-13

Abstract By using 3,7‐dithianonane‐1,9‐dithiol (S 4 ) and N , N′ ‐dimethyl‐ ‐bis(2‐mercaptoethyl)ethylenediamine (N 2 S as ligands, two CH 3 CN‐coordinated nickel‐iron heterodimetallic complexes, [NiS Fe(CH CN)Cp*][PF 6 ] ( 1a [NiN 1b (Cp* = η 5 ‐C Me ), were synthesized characterized spectroscopically crystallographically. Reactivities of towards CO, Cl HBF NOPF have also been investigated. A series complexes coordinated with small molecules Fe(L)Cp*][PF n [ 1, L 2a CO 3a ); 2, NO 4a )], [L...

10.1002/ejic.201500304 article EN European Journal of Inorganic Chemistry 2015-05-28

Using an assembly method, dinuclear CoCo and CoFe complexes supported by a bdt ligand, [Cp*Co(μ–η<sup>2</sup>:η<sup>2</sup>-bdt)(μ-I)CoCp*][PF<sub>6</sub>] (<bold>1[PF6]</bold>, Cp* = η<sup>5</sup>-C<sub>5</sub>Me<sub>5</sub>, benzene-1,2-dithiolate), [Cp*Co(μ–η<sup>2</sup>:η<sup>4</sup>-bdt)FeCp′][PF<sub>6</sub>] (<bold>3[PF6]</bold>, Cp′ η<sup>5</sup>-C<sub>5</sub>Me<sub>4</sub>H) were synthesized in high yields.

10.1039/c6dt03275c article EN Dalton Transactions 2016-01-01
Coming Soon ...