about
Stereochemical analysis of ferrocene and the uncertainty of fluorescence XAFS data.Methylation of zebularine: a quantum mechanical study incorporating interactive 3D pdf graphs.Differential attraction and repulsion of Staphylococcus aureus and Pseudomonas aeruginosa on molecularly smooth titanium films.Molecular dynamics studies on the NMR structures of rabbit prion protein wild type and mutants: surface electrostatic charge distributions.Correlation of electronic structures of three cyclic dipeptides with their photoemission spectra.Dynamical (e,2e) studies of tetrahydrofurfuryl alcohol.Density functional study of Cu(2+)-phenylalanine complex under micro-solvation environment.Norbornane: an investigation into its valence electronic structure using electron momentum spectroscopy, and density functional and Green's function theories.Electronic structure of the azide group in 3 cent-azido-3 cent-deoxythymidine (AZT) compared to small azide compounds.Impact of ketone and amino on the inner shell of guanine.A pH-induced conformational switch in a tyrosine kinase inhibitor identified by electronic spectroscopy and quantum chemical calculations.Inner-shell chemical shift of DNA/RNA bases and inheritance from their parent purine and pyrimidine.Reinterpretation of Dynamic Vibrational Spectroscopy to Determine the Molecular Structure and Dynamics of Ferrocene.The attachment of amino fragment to purine: inner-shell structures and spectra.Understanding glycine conformation through molecular orbitals.Coexistence of 1,3-butadiene conformers in ionization energies and Dyson orbitals.Orbital based electronic structural signatures of the guanine keto G-7H/G-9H tautomer pair as studied using dual space analysis.In silico design: extended molecular dynamic simulations of a new series of dually acting inhibitors against EGFR and HER2.Dominant Carbons in trans- and cis-Resveratrol Isomerization.First-principles study of Carbz-PAHTDDT dye sensitizer and two Carbz-derived dyes for dye sensitized solar cells.Resveratrol's Hidden Hand: A Route to Optical Detection of Biomolecular Binding.Valence structures of aromatic bioactive compounds: a combined theoretical and experimental study.Conformational Plasticity in Tyrosine Kinase Inhibitor-Kinase Interactions Revealed with Fluorescence Spectroscopy and Theoretical Calculations.Structures of cycloserine and 2-oxazolidinone probed by X-ray photoelectron spectroscopy: theory and experiment.Electronic structure and intramolecular interactions in three methoxyphenol isomersErratum to “Orbital based electronic structural signatures of the guanine keto G-7H/G-9H tautomer pair as studied using dual space analysis” [Biophys. Chem. 121 (2006) 105–120]An experimental and theoretical study into the valence electronic structure of bicyclo[2.2.1]hepta-2,5-dioneInvestigation into the Valence Electronic Structure of Norbornene Using Electron Momentum Spectroscopy, Green's Function, and Density Functional TheoriesStructural impact on the methano bridge in norbornadiene, norbornene and norbornaneAn electron momentum spectroscopy and density functional theory study of the outer valence electronic structure of stella-2,6-dioneExploring the electronic structure of 2,6-stelladione from momentum space I: the p-dominant molecular orbitals in the outer valence shellAdenine Tautomers: Relative Stabilities, Ionization Energies, and Mismatch with CytosineUnsaturated didehydrodeoxycytidine drugs. 1. Impact of C=C positions in the sugar ringPrediction of spectroscopic constants for diatomic molecules in the ground and excited states using time-dependent density functional theoryOrbital signatures of methyl in L-alaninePhotoelectron spectra and structures of three cyclic dipeptides: PhePhe, TyrPro, and HisGlyMethylation of zebularine investigated using density functional theory calculationsPhotoelectron spectra of some antibiotic building blocks: 2-azetidinone and thiazolidine-carboxylic acidEffects of alkyl side chains on properties of aliphatic amino acids probed using quantum chemical calculationsIntramolecular interactions of L-phenylalanine: Valence ionization spectra and orbital momentum distributions of its fragment molecules
P50
Q34160160-EC8F85AF-F31C-4BE5-BDCC-3211E82FAC65Q38435392-74C2FB8C-3ACB-4127-B2B4-B5828C66A150Q39872301-CB2CAFFE-D360-427A-A6AD-8F19C1760AB3Q42202651-69A4053B-1A49-4453-81D9-58B27FA51781Q42835588-A9DC2391-2975-4C77-9242-13B4054B1647Q43432129-E9C9CDE9-10F2-4E18-9C80-749CE5615881Q44272521-A79DF4EF-BC7A-4930-B669-495C4DF29F37Q45154360-825F76DE-B6C2-4C84-B3A1-97292AA5A66FQ45919332-1A034DAF-4940-4706-BC69-C042F912F44CQ45964784-8A033882-95A0-4192-9169-6C823F17C271Q46254098-3FF4D3B2-52FD-47C4-BA1B-03F58FC0D2C5Q46291253-F2D52D07-8B88-4266-B518-0AB267824AB3Q46478645-A186AB4A-646A-4856-976D-03AE6824F650Q46736263-9EC81CBF-167E-426C-A7C9-EB7679337722Q46852130-F3750333-1A31-4148-B9D1-70BBFA704321Q46879046-746C80C3-EB4F-4A78-88F6-DD25245B1B4CQ46932709-46F7A130-140B-4D6B-8D8E-38ABB7B5D0C5Q47868147-3901392D-76E8-461F-9B7E-2176CCEC6638Q48041599-076EBF45-6139-4319-8A17-335E736CD665Q48882759-447D3173-4E25-4055-ACAD-24B4D1961611Q49889353-79C9ECE0-E7A2-4C2C-B685-F226D0F932ABQ50492063-ABAC76A8-3BF2-4335-BD9A-6F6E31C7AA0DQ52328340-AB684C75-2EC3-42B3-A07C-43ABBA4ADCAEQ53552845-6A5D350C-A0A9-4C11-B245-99A45E3BE69FQ57182857-0791F8CE-E2A0-4FD3-99F0-1D010C55893BQ61925386-A3035EA7-07EF-46E3-8D17-8A50A40382B8Q61925388-721D1F9F-F882-4244-9A0D-95A3AE216DE4Q61925392-4153DD53-0519-4D0B-AE14-E7EB3297CBDAQ61925400-AB5C5A5D-F2BD-4344-B944-DAB5EECD166DQ61925402-3B713F8B-9489-4FB3-88DB-0BBFF730A764Q61925403-8F9F5EB4-E7F5-40E1-9904-63371646BBE6Q62109560-13A59E1F-B055-42EC-80BA-6F4021D91227Q80689413-8CBBEA65-576F-401A-85E5-4433E6CD7859Q81538955-C7DF49B0-1F23-4CD3-9917-FE220057C8FDQ83314119-A684E3E6-6AA8-40B8-A2C3-145A99345B4CQ83775082-139D4922-433A-45D0-84D8-19A39C2227B2Q84033010-1CFAF731-E2EB-40E0-BB78-88CCF9698967Q84576347-FAB345DC-40C0-4BD8-9ED1-411BB1198BC9Q84813769-2C4AD796-28F7-4D9B-8004-B31BDEBA565FQ84968781-9DC2F2CB-FDCF-4FDF-8E3A-29953CA7FCA3
P50
description
researcher ORCID ID = 0000-0002-6584-0516
@en
name
Feng Wang
@ast
Feng Wang
@en
Feng Wang
@es
Feng Wang
@nl
type
label
Feng Wang
@ast
Feng Wang
@en
Feng Wang
@es
Feng Wang
@nl
prefLabel
Feng Wang
@ast
Feng Wang
@en
Feng Wang
@es
Feng Wang
@nl
P2456
w/FengWang5
P31
P496
0000-0002-6584-0516