Nelson Rodrigo Vinueza Benitez

Quantification of docusate antimicrobial finishing after simulated landfill degradation via tandem mass spectrometry and QuEChERS extraction

Sui, X., Feng, C., Ankeny, M., & Vinueza, N. R. (2022, October 12). ANALYTICAL METHODS, Vol. 10.

Synthetic dyes: A mass spectrometry approach and applications

Millbern, Z., Trettin, A., Wu, R., Demmler, M., & Vinueza, N. R. (2022, November 10). MASS SPECTROMETRY REVIEWS, Vol. 11.

The characterization of disperse dyes in polyester fibers using DART mass spectrometry

Millbern, Z., & Vinueza, N. R. (2022, September 4). JOURNAL OF FORENSIC SCIENCES, Vol. 9.

A promising Ames battery for mutagenicity characterization of new dyes

ENVIRONMENTAL AND MOLECULAR MUTAGENESIS, 62(1), 52–65.

Are all charge-transfer parameters created equally? A study of functional dependence and excited-state charge-transfer quantification across two dye families

Marshburn, R. D., Ashley, D. C., Curtin, G. M., Sultana, N., Liu, C., Vinueza, N. R., … Jakubikova, E. (2021, August 30). PHYSICAL CHEMISTRY CHEMICAL PHYSICS, Vol. 8.

Identification and quantification of CI Reactive Blue 19 dye degradation product in soil

COLORATION TECHNOLOGY, 137(3), 251–258.

Molecular characterization and ecotoxicological evaluation of the natural dye madder and its chlorinated products

Freeman, H. S., Santos, T. C., Chen, Y., Vendemiatti, J. A. S., Oliveira, A. C., Vacchi, F. I., … Umbuzeiro, G. A. (2021, November 25). ENVIRONMENTAL SCIENCE AND POLLUTION RESEARCH, Vol. 11.

Separation and identification of commercial reactive dyes with hydrophilic interaction liquid chromatography and quadrupole time‐of‐flight mass spectrometry

Coloration Technology, 137(4), 407–417.

Characterization of synthetic dyes for environmental and forensic assessments: A chromatography and mass spectrometry approach

Journal of Separation Science, 44(1), 387–402.

Degradation studies of CI Reactive Blue 19 on biodegraded cellulosic fabrics via liquid chromatography-photodiode array detection coupled to high resolution mass spectrometry

COLORATION TECHNOLOGY, 135(6), 475–483.

Nanostructured GaOOH modified with reactive yellow, red and blue water-soluble dyes

AIP ADVANCES, 9(2).

Towards a reliable prediction of the aquatic toxicity of dyes

ENVIRONMENTAL SCIENCES EUROPE, 31(1).

Correlation between solubility parameters and recovery of phenolic compounds from fast pyrolysis bio-oil by diesel extraction

Carbon Resources Conversion, 1(3), 238–244.

Dimerised heterobifunctional reactive dyes. Part 1: characterisation using quadrupole time-of-flight mass spectrometry

Coloration Technology, 134(6), 470–477.

Direct analysis of textile dyes from trace fibers by automated microfluidics extraction system coupled with Q-TOF mass spectrometer for forensic applications

Forensic Science International, 289, 67–74.

Effects of hydrogen bonding on the gas-phase reactivity of didehydroisoquinolinium cation isomers

Physical Chemistry Chemical Physics, 20(33), 21567–21572.

Mass Spectrometry Exposes Undocumented Lignin-Carbohydrate Complexes in Biorefinery Pretreatment Stream

ACS Sustainable Chemistry & Engineering, 6(8), 10654–10659.

Rapid Quadrupole-Time-of-Flight Mass Spectrometry Method Quantifies Oxygen-Rich Lignin Compound in Complex Mixtures

JOURNAL OF THE AMERICAN SOCIETY FOR MASS SPECTROMETRY, 29(3), 535–542.

Characterization of biofuel refinery byproduct via selective electrospray ionization tandem mass spectrometry

FUEL, 188, 190–196.

Purification and characterization of three commercial phenylazoaniline disperse dyes

Coloration Technology, 133(6), 513–518.

Weaver's historic accessible collection of synthetic dyes: a cheminformatics analysis

CHEMICAL SCIENCE, 8(6), 4334–4339.

Microfluidic System for Automated Dye Molecule Extraction and Detection for Forensic Fiber Identification

[National Criminal Justice Report].

Reactivity Controlling Factors for an Aromatic Carbon-Centered sigma,sigma,sigma-Triradical: The 4,5,8-Tridehydroisoquinolinium Ion

CHEMISTRY-A EUROPEAN JOURNAL, 22(2), 809–815.

The Art of Color in Solving Mysteries and Crime

[National Chemistry Week brochure]. American Chemical Society.

Analysis of Sulfonated Anthraquinone Dyes by Electrospray Ionization Quadrupole Time-of-flight Tandem Mass Spectrometry

Journal of Textile Science & Engineering, 06(01).

Functional dye as a comonomer in a water-soluble polymer

Journal of Polymer Science Part A: Polymer Chemistry, 53(13), 1594–1599.

Tandem mass spectrometric characterization of the conversion of xylose to furfural

Biomass and Bioenergy, 74, 1–5.

Analysis of carbohydrates by atmospheric pressure chloride anion attachment tandem mass spectrometry

Fuel, 105, 235–246.

Analysis of xyloglucans by ambient chloride attachment ionization tandem mass spectrometry

Carbohydrate Polymers, 98(1), 1203–1213.

Does the 2,6-didehydropyridinium cation exist?

Journal of Physical Organic Chemistry, 26(9), 707–714.

Experimental and Computational Studies on the Formation of Threepara-Benzyne Analogues in the Gas Phase

Chemistry - A European Journal, 19(27), 9022–9033.

On-Line Mass Spectrometric Methods for the Determination of the Primary Products of Fast Pyrolysis of Carbohydrates and for Their Gas-Phase Manipulation

Analytical Chemistry, 85(22), 10927–10934.

Effects of a Hydroxyl Substituent on the Reactivity of the 2,4,6-Tridehydropyridinium Cation, an Aromatic σ,σ,σ-Triradical

Chemistry - A European Journal, 18(3), 969–974.

Identification and Counting of Oxygen Functionalities and Alkyl Groups of Aromatic Analytes in Mixtures by Positive-Mode Atmospheric Pressure Chemical Ionization Tandem Mass Spectrometry Coupled with High-Performance Liquid Chromatography

Energy & Fuels, 26(5), 2975–2989.

Reactivity of a σ,σ,σ,σ-Tetraradical: The 2,4,6-Tridehydropyridine Radical Cation

Journal of the American Chemical Society, 134(4), 1926–1929.

Reactivity of the 4,5-Didehydroisoquinolinium Cation

Chemistry - A European Journal, 18(28), 8692–8698.

Substituent Effects on the Nonradical Reactivity of 4-Dehydropyridinium Cation

The Journal of Physical Chemistry A, 116(12), 3089–3093.

Comparison of Functional Group Selective Ion–Molecule Reactions of Trimethyl Borate in Different Ion Trap Mass Spectrometers

Journal of The American Society for Mass Spectrometry, 22(3), 520–530.

Data-dependent neutral gain MS3: Toward automated identification of the N-Oxide functional group in drug metabolites

Journal of the American Society for Mass Spectrometry, 21(4), 559–563.

Laser-Induced Acoustic Desorption Coupled with a Linear Quadrupole Ion Trap Mass Spectrometer

Analytical Chemistry, 82(2), 608–614.

Liquid chromatography/tandem mass spectrometry utilizing ion-molecule reactions and collision-activated dissociation for the identification of N-oxide drug metabolites

Journal of Pharmaceutical and Biomedical Analysis, 51(4), 805–811.

Gas-Phase Reactivity of Aromatic σ,σ-Biradicals toward Dinucleoside Phosphates

Organic Letters, 10(10), 1889–1892.

Identification of the Carboxylic Acid Functionality by Using Electrospray Ionization and Ion−Molecule Reactions in a Modified Linear Quadrupole Ion Trap Mass Spectrometer

Analytical Chemistry, 80(9), 3416–3421.

Reactivity of the 3,4,5-Tridehydropyridinium Cation-An Aromatic σ,σ,σ-Triradical

Angewandte Chemie, 120(51), 10008–10013.

Reactivity of the 3,4,5-Tridehydropyridinium Cation-An Aromatic σ,σ,σ-Triradical

Angewandte Chemie International Edition, 47(51), 9860–9865.

Regioselective ion–molecule reactions for the mass spectrometric differentiation of protonated isomeric aromatic diamines

The Analyst, 133(4), 452.

Reactivity of an Aromatic σ,σ,σ-Triradical: The 2,4,6-Tridehydropyridinium Cation

Angewandte Chemie, 119(48), 9358–9361.

Reactivity of an Aromatic σ,σ,σ-Triradical: The 2,4,6-Tridehydropyridinium Cation

Angewandte Chemie International Edition, 46(48), 9198–9201.