Wei Sheng

ORCID: 0000-0002-9044-905X
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About
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Research Areas
  • Photochemistry and Electron Transfer Studies
  • X-ray Diffraction in Crystallography
  • Crystallization and Solubility Studies
  • Photochromic and Fluorescence Chemistry
  • Organic Light-Emitting Diodes Research
  • Click Chemistry and Applications
  • Nanoplatforms for cancer theranostics
  • Advanced Fluorescence Microscopy Techniques
  • Radical Photochemical Reactions
  • Luminescence and Fluorescent Materials
  • solar cell performance optimization
  • Perovskite Materials and Applications
  • Fluorine in Organic Chemistry
  • Porphyrin and Phthalocyanine Chemistry
  • RNA Interference and Gene Delivery
  • Lanthanide and Transition Metal Complexes
  • Copper Interconnects and Reliability
  • Oxidative Organic Chemistry Reactions
  • Photosynthetic Processes and Mechanisms
  • Integrated Circuits and Semiconductor Failure Analysis
  • Photodynamic Therapy Research Studies
  • Inorganic Fluorides and Related Compounds
  • Chemical Reactions and Mechanisms
  • Quantum optics and atomic interactions
  • Molecular spectroscopy and chirality

Michigan State University
2016-2024

Roche (United States)
2023

Cayman Chemical (United States)
2020

Chinese Academy of Medical Sciences & Peking Union Medical College
2016

Shanghai Huali Microelectronics (China)
2015

University of Science and Technology
2015

Korea University of Science and Technology
2015

Jiangsu University
2011-2013

Academia Sinica
1991

The incredible potential for fluorescent proteins to revolutionize biology has inspired the development of a variety design strategies address an equally broad range photophysical characteristics, depending on applications. Of these, that simultaneously exhibit high quantum yield, red-shifted emission, and wide separation between excitation emission wavelengths (Large Stokes Shift, LSS) are rare. pursuit LSS systems led formation complex, obtained from marriage rationally engineered protein...

10.1021/jacs.1c05039 article EN Journal of the American Chemical Society 2021-09-13

Abstract Transparent luminescent solar concentrators (TLSCs) selectively harvest ultraviolet and near‐infrared photons. Due to the absence of electrodes, busbars, collection grids over harvesting area, device structure enables these devices achieve highest levels transparency aesthetics. Recently, CO i 8DFIC has been developed as a nonfullerene acceptor in organic photovoltaics with unprecedented performance. In this work, acceptors are introduced into TLSCs luminophores. The impact...

10.1002/adom.201901536 article EN publisher-specific-oa Advanced Optical Materials 2020-02-24

Abstract Visibly transparent luminescent solar concentrators (TLSC) can optimize both power production and visible transparency by selectively harvesting the invisible portion of spectrum. Since primary applications TLSCs include building envelopes, greenhouses, automobiles, signage, mobile electronics, maintaining aesthetics functionalities is as important achieving high conversion efficiencies (PCEs) in practical deployment. In this work, massive‐downshifting phosphorescent nanoclusters...

10.1002/aenm.202003581 article EN Advanced Energy Materials 2021-02-04

Visibly transparent luminescent solar concentrators (TLSC) have the potential to turn existing infrastructures into net-zero-energy buildings. However, reabsorption loss currently limits device performance and scalability. This is typically defined by Stokes shift between absorption emission spectra of luminophores. In this work, shifts (SS) near-infrared selective-harvesting cyanines are altered substitution central methine carbon with dialkylamines. We demonstrate varying SS values over 80...

10.1038/s41598-018-34442-3 article EN cc-by Scientific Reports 2018-10-30

Abstract Molecular reactivity can change dramatically with the absorption of a photon due to difference electronic configurations between excited and ground states. Here we report on discovery modular system (Schiff base formed from an aldehyde amine) that upon photoexcitation yields more basic imine capable intermolecular proton transfer protic solvents. Ultrafast dynamics state conjugated Schiff reveals pathway for transfer, culminating in 14‐unit increase p K give * >20 ethanol.

10.1002/anie.201806787 article EN Angewandte Chemie International Edition 2018-08-29

An efficiently siRNA transporting nanocarrier still remains to be developed. In this study, utilizing the dual stimulus of acid tumor extracellular environment and redox effect glutathione in cytosol, a new system combining triple effects folate targeting, sensitive polymer micelles, bio-reducible disulfide bond linked siRNA-cell penetrating peptides (CPPs) conjugate is developed suppress c-myc gene expression breast cancer (MCF-7 cells) both vitro vivo. Subsequent research demonstrates that...

10.1002/mabi.201500389 article EN Macromolecular Bioscience 2016-01-29

FR-1V, a fluorene-based aldehydic chromophore, binds its target protein as an imine to yield highly bathochromic pigment, CF-2, prototypic protein-dye tagging system whose NIR emission can be spatiotemporally switched ON by rapid UV-light activation. This is achieved through photoisomerization of the and subsequent protonation. We demonstrate no-wash protocol for live cell imaging subcellular compartments in variety mammalian lines with minimal fluorescence background.

10.1002/anie.201810065 article EN Angewandte Chemie International Edition 2018-10-12

Utilizing two robust C–C bond-forming reactions, the Baylis–Hillman reaction and Diels–Alder reaction, we report a highly enantio-, regio-, diastereoselective synthesis of hexahydro-2H-chromenes via sequential [4 + 2] cycloadditions. These tandem formal cycloadditions have also been performed as "one-pot" sequence to access corresponding heterocycles constituting up five contiguous stereocenters in excellent yields stereoselectivity.

10.1021/acs.orglett.6b01742 article EN Organic Letters 2016-08-03

Human cellular retinol binding protein II (hCRBPII) was used as a engineering platform to rationally regulate absorptive and emissive properties of covalently bound fluorogenic dye. We demonstrate the thio-dapoxyl analog via formation protonated imine between an active site lysine residue chromophore's aldehyde. Rational manipulation electrostatics pocket results in 204 nm shift absorption 131 emission. The is readily expressed mammalian systems binds with exogenously delivered fluorophore...

10.1021/acschembio.4c00125 article EN cc-by ACS Chemical Biology 2024-07-24

Abstract A reengineered human cellular retinol binding protein II (hCRBPII), a 15‐kDa belonging to the intracellular lipid (iLBP) family, generates highly fluorescent red pigment through covalent linkage of merocyanine aldehyde an active site lysine residue. The complex exhibits “turn‐on” fluorescence, due weakly that “lights up” with subsequent formation strongly dye within pocket protein. Cellular penetration is rapid, and fluorophore maturation nearly instantaneous. hCRBPII/merocyanine...

10.1002/cbic.201900428 article EN ChemBioChem 2019-09-04

Abstract Molecular reactivity can change dramatically with the absorption of a photon due to difference electronic configurations between excited and ground states. Here we report on discovery modular system (Schiff base formed from an aldehyde amine) that upon photoexcitation yields more basic imine capable intermolecular proton transfer protic solvents. Ultrafast dynamics state conjugated Schiff reveals pathway for transfer, culminating in 14‐unit increase p K give * >20 ethanol.

10.1002/ange.201806787 article EN Angewandte Chemie 2018-08-29

The absolute stereochemistry of chiral carboxylic acids is determined as a di(1-naphthyl)methanol ester derivative. Computational scoring conformations favoring either P or M helicity the naphthyl groups, capable exciton-coupled circular dichroic coupling, leads to predicted for derivatized acids.

10.1002/chir.22775 article EN publisher-specific-oa Chirality 2017-11-08

Visibly transparent luminescent solar concentrators (TLSCs) can optimize both power production and visible transparency by selectively harvesting the invisible portion of spectrum. Since primary applications TLSCs include building envelopes, greenhouses, automobiles, signage, mobile electronics, maintaining aesthetics functionalities is as important achieving high conversion efficiencies (PCEs) in practical deployment. In this work, we combine massive-downshifting phosphorescent nanoclusters...

10.2139/ssrn.3699147 article EN SSRN Electronic Journal 2020-01-01

An engineered hCRBPII protein binds a coumarin-based fluorophore to yield photoswitchable system via Michael/retro-Michael addition of cysteine residue. Alternate UV/visible light irradiation accesses the two optical states.

10.1039/d2an01395a article EN The Analyst 2023-01-01

10.1016/bs.mie.2020.04.058 article EN Methods in enzymology on CD-ROM/Methods in enzymology 2020-01-01

ZnS nanoparticles have been prepared by using 2, 3-dimercaptoethylthiopropanethiol (BES) as the coordinating modifier reagent to form Zn-thiol complex at low reaction temperatures. By controlling experimental conditions, diameter of nanopaticles can be tuned from 43 nm 115 nm. Systematic experiments were carried out investigate factors such amounts reagents (thiourea and BES) temperature, which great influence on sizes products. And when content BES is much higher, with mercapto surface...

10.4028/www.scientific.net/kem.575-576.24 article EN Key engineering materials 2013-09-01

A binary and ternary rare earth complexes were synthesized. The structure composition of the characterized by FT-IR Elemental Analyzer. It is found that have excellent fluorescence intensity thermal stability. Photoluminescent measurements show Phenanthroline (Phen) could efficiently transfer energy to Eu 3+ sensitize luminescence . copolymers complexes, methyl methacrylate (MMA) methacrylic acid (HMA) emit characteristic enhanced with content increasing. But apparent Eu(AA) 3 stronger...

10.4028/www.scientific.net/amr.284-286.1890 article EN Advanced materials research 2011-07-04

Abstract FR‐1V , a fluorene‐based aldehydic chromophore, binds its target protein as an imine to yield highly bathochromic pigment, CF‐2 prototypic protein–dye tagging system whose NIR emission can be spatiotemporally switched ON by rapid UV‐light activation. This is achieved through photoisomerization of the and subsequent protonation. We demonstrate no‐wash protocol for live cell imaging subcellular compartments in variety mammalian lines with minimal fluorescence background.

10.1002/ange.201810065 article EN Angewandte Chemie 2018-10-12

Visibly transparent luminescent solar concentrators (TLSCs) can optimize both power production and visible transparency by selectively harvesting the invisible portion of spectrum. Since primary applications TLSCs include building envelopes, greenhouses, automobiles, signage, mobile electronics, maintaining aesthetics functionalities is as important achieving high conversion efficiencies (PCEs) in practical deployment. In this work, we combine massive-downshifting phosphorescent nanoclusters...

10.48550/arxiv.2009.09542 preprint EN other-oa arXiv (Cornell University) 2020-01-01

Wet cleaning is very critical for technology nodes below 40&28nm in ULSI manufacturing. Better clean efficiency and less film damage becomes the main challenge WET processes advanced development. New chemicals were used this article to study BEOL post Etch 40nm node beyond. We compared performance of chemcial A chemical B through CD enlargement, kink profile, Cu loss, inline defect WAT. Experimental results indicated that copper loss better than B, even though defect, enlargement WAT comparable.

10.1109/cstic.2015.7153374 article EN China Semiconductor Technology International Conference 2015-03-01

The hybrid-photocatalyst was successfully prepared by compositing graphene and TiO 2 in this thesis. properties of the stydited XRD, SEM. hotocatalytic activity evaluated decolorization acid yellow dye solution under visible light irradiation. result shows that main phase is antase . effects different titanium carbon ratio, photocatalysis time, catalyst dosage pH on photocatalytic for are discussed. Under conditions ratio 100:50, time 120 min, dosing concentration 0.1g / L optimum 8,...

10.4028/www.scientific.net/amr.1092-1093.988 article EN Advanced materials research 2015-03-01
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