World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
48
Citations
10451
World Ranking
15091
National Ranking
120

Nilo Zanatta publication distribution in Chemistry in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Chemistry in 2026. The highlighted bar marks where Nilo Zanatta sits on this spectrum.

61–80 publications: 66 scientists 81–100 publications: 302 scientists 101–120 publications: 623 scientists 121–140 publications: 918 scientists 141–160 publications: 1,218 scientists 161–180 publications: 1,350 scientists 181–200 publications: 1,344 scientists 201–220 publications: 1,281 scientists 221–240 publications: 1,216 scientists 241–260 publications: 1,100 scientists 261–280 publications: 979 scientists 281–300 publications: 939 scientists 301–320 publications: 764 scientists 321–340 publications: 643 scientists 341–360 publications: 628 scientists 361–380 publications: 522 scientists 381–400 publications: 459 scientists 401–420 publications: 397 scientists 421–440 publications: 327 scientists 441–460 publications: 270 scientists 461–480 publications: 265 scientists 481–500 publications: 252 scientists 501–520 publications: 201 scientists 521–540 publications: 185 scientists 541–560 publications: 148 scientists 561–580 publications: 148 scientists 581–600 publications: 132 scientists 601–620 publications: 114 scientists 621–640 publications: 104 scientists 641–660 publications: 91 scientists 661–680 publications: 92 scientists 681–700 publications: 73 scientists 701–720 publications: 57 scientists 721–740 publications: 54 scientists 741–760 publications: 67 scientists 761–780 publications: 45 scientists 781–800 publications: 46 scientists 801–820 publications: 39 scientists 821–840 publications: 32 scientists 841–860 publications: 36 scientists 861–880 publications: 29 scientists 881–900 publications: 26 scientists 901–920 publications: 24 scientists 921–940 publications: 14 scientists 941–960 publications: 23 scientists 961–980 publications: 28 scientists 981–1,000 publications: 15 scientists 1,001–1,020 publications: 29 scientists 1,021–1,040 publications: 12 scientists 1,041–1,060 publications: 19 scientists 1,061–1,080 publications: 12 scientists 1,081–1,100 publications: 6 scientists 1,101–1,120 publications: 8 scientists 1,121–1,140 publications: 12 scientists 1,141–1,160 publications: 5 scientists 1,161–1,180 publications: 6 scientists 1,181–1,200 publications: 14 scientists 1,201–1,220 publications: 7 scientists 1,221–1,240 publications: 2 scientists 1,241–1,260 publications: 6 scientists 1,261–1,280 publications: 4 scientists 1,281–1,294 publications: 6 scientists 1,295+ publications: 100 scientists
61 publications 1,295+

This scientist: 475 publications — 87th percentile

87% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 1,295 publications or more.

Nilo Zanatta D-index placement in Chemistry in 2026

The chart shows the D-index (discipline H-index) distribution of Chemistry scientists ranked by Research.com in 2026. The highlighted bar marks where Nilo Zanatta sits on this spectrum.

40–41 D-Index: 289 scientists 42–43 D-Index: 612 scientists 44–45 D-Index: 808 scientists 46–47 D-Index: 776 scientists 48–49 D-Index: 835 scientists 50–51 D-Index: 861 scientists 52–53 D-Index: 872 scientists 54–55 D-Index: 933 scientists 56–57 D-Index: 1,051 scientists 58–59 D-Index: 930 scientists 60–61 D-Index: 882 scientists 62–63 D-Index: 834 scientists 64–65 D-Index: 731 scientists 66–67 D-Index: 775 scientists 68–69 D-Index: 683 scientists 70–71 D-Index: 646 scientists 72–73 D-Index: 561 scientists 74–75 D-Index: 501 scientists 76–77 D-Index: 437 scientists 78–79 D-Index: 388 scientists 80–81 D-Index: 354 scientists 82–83 D-Index: 292 scientists 84–85 D-Index: 275 scientists 86–87 D-Index: 254 scientists 88–89 D-Index: 235 scientists 90–91 D-Index: 185 scientists 92–93 D-Index: 192 scientists 94–95 D-Index: 155 scientists 96–97 D-Index: 163 scientists 98–99 D-Index: 125 scientists 100–101 D-Index: 105 scientists 102–103 D-Index: 105 scientists 104–105 D-Index: 112 scientists 106–107 D-Index: 88 scientists 108–109 D-Index: 68 scientists 110–111 D-Index: 69 scientists 112–113 D-Index: 65 scientists 114–115 D-Index: 79 scientists 116–117 D-Index: 61 scientists 118–119 D-Index: 44 scientists 120–121 D-Index: 37 scientists 122–123 D-Index: 40 scientists 124–125 D-Index: 33 scientists 126–127 D-Index: 26 scientists 128–129 D-Index: 34 scientists 130–131 D-Index: 35 scientists 132–133 D-Index: 25 scientists 134–135 D-Index: 27 scientists 136–137 D-Index: 17 scientists 138–139 D-Index: 16 scientists 140–141 D-Index: 20 scientists 142–143 D-Index: 20 scientists 144–145 D-Index: 15 scientists 146–147 D-Index: 9 scientists 148–149 D-Index: 9 scientists 150–151 D-Index: 16 scientists 152–153 D-Index: 11 scientists 154–155 D-Index: 9 scientists 156–157 D-Index: 3 scientists 158 D-Index: 3 scientists 159+ D-Index: 98 scientists
40 D-Index 159+

This scientist: 48 D-Index — 16th percentile

16% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 159 D-Index or more.

Overview

Nilo Zanatta is affiliated with the Universidade Federal de Santa Maria in Brazil, focusing primarily on research within the fields of Materials Science and Chemistry. Their publication record includes 159 works in Materials Science and 130 in Chemistry, highlighting a research emphasis on the subfields of Materials Chemistry and Organic Chemistry.

Their research extends into specialized areas including Pharmaceutical Science, Physical and Theoretical Chemistry, and Molecular Biology. Central topics covered by Zanatta's work include Crystallization and Solubility Studies, with 148 publications related to this, and X-ray Diffraction in Crystallography, with 140 publications. Further investigations involve Synthesis and Biological Evaluation, Fluorine in Organic Chemistry, Click Chemistry and Applications, Crystallography and Molecular Interactions, as well as Synthesis and Reactions of Organic Compounds.

Frequent coauthors of Zanatta include Hélio G. Bonacorso with 140 joint publications, Marcos A. P. Martins (134 publications), Bernardo A. Iglesias (40), Mateus Mittersteiner (39), and Yuri G. Kappenberg (28). This collaboration network reflects an active involvement in multidisciplinary research teams.

Nilo Zanatta's work has appeared repeatedly in several scientific journals. The most common venues of publication are The Cambridge Structural Database with 71 publications, followed by the Journal of Molecular Structure (11), Synthesis (8), CrystEngComm (6), and the European Journal of Organic Chemistry (5).

Selected recent papers authored or coauthored by Nilo Zanatta include:

  • "Dicationic imidazolium-based dicarboxylate ionic liquids: Thermophysical properties and solubility" (2020) published in Journal of Molecular Liquids
  • "Ultrasound-assisted synthesis of pyrimidines and their fused derivatives: A review" (2021) published in Ultrasonics Sonochemistry
  • "Biological assays of BF2-naphthyridine compounds: Tyrosinase and acetylcholinesterase activity, CT-DNA and HSA binding property evaluations" (2020) published in International Journal of Biological Macromolecules
  • "D-dimer and reduced-dose apixaban for extended treatment after unprovoked venous thromboembolism: the Apidulcis study" (2022) published in Blood Advances
  • "New 1-(Spiro[chroman-2,1'-cycloalkan]-4-yl)-1H-1,2,3-Triazoles: Synthesis, QTAIM/MEP analyses, and DNA/HSA-binding assays" (2020) published in Journal of Molecular Liquids

Best Publications

  • Ionic liquids in heterocyclic synthesis.

    Marcos A. P. Martins;Clarissa P. Frizzo;Dayse N. Moreira;Nilo Zanatta

  • Hypothermic and antipyretic effects of 3-methyl- and 3-phenyl-5-hydroxy-5-trichloromethyl-4,5-dihydro-1H-pyrazole-1-carboxyamides in mice

    Fabiane R Souza;Vanessa T Souza;Viviane Ratzlaff;Lysandro P Borges

  • 4-Alkoxy-1,1,1-Trichloro-3-Alken-2-ones: Preparation and Applications in Heterocyclic Synthesis

    Marcos A. P. Martins;Wilson Cunico;Claudio M. P. Pereira;Adilson P. Sinhorin

  • Trifluoroacetylation of unsymmetrical ketone acetals. A convenient route to obtain alkyl side chain trifluoromethylated heterocycles

    Helio G Bonacorso;Marcos A.P Martins;Sandra R.T Bittencourt;Rogério V Lourega

  • Antimalarial activity of 4-(5-trifluoromethyl-1H-pyrazol-1-yl)-chloroquine analogues.

    Wilson Cunico;Cleber A. Cechinel;Cleber A. Cechinel;Helio G. Bonacorso;Helio G. Bonacorso;Marcos A.P. Martins;Marcos A.P. Martins

  • New Benzodiazepines Alter Acetylcholinesterase and ATPDase Activities

    M. R. C. Schetinger;N. M. Porto;M. B. Moretto;V. M. Morsch

  • Update 1 of: Ionic liquids in heterocyclic synthesis.

    Marcos A. P. Martins;Clarissa P. Frizzo;Aniele Z. Tier;Dayse N. Moreira

  • Baker yeast-induced fever in young rats: characterization and validation of an animal model for antipyretics screening.

    Jorgete Tomazetti;Daiana Silva Ávila;Ana Paula Oliveira Ferreira;Juliana Saibt Martins

  • Synthesis of 1,1,1-trihalo-4-methoxy-4-[2-heteroaryl]-3-buten-2-ones, the corresponding butan-1,3-dione and azole derivatives

    Alex F.C Flores;Sergio Brondani;Nilo Zanatta;Adriano Rosa

  • Design and microwave-assisted synthesis of 5-trifluoromethyl-4,5-dihydro-1H-pyrazoles: Novel agents with analgesic and anti-inflammatory properties

    Patricia D. Sauzem;Pablo Machado;Maribel A. Rubin;Gabriela da S. Sant'Anna

  • Antinociceptive effect of novel trihalomethyl-substituted pyrazoline methyl esters in formalin and hot-plate tests in mice.

    Julie Milano;Sara M. Oliveira;Mateus F. Rossato;Patricia D. Sauzem

  • Regiospecific acylation of acetals. A convenient method to obtain β-methoxyvinyl trichloromethyl ketones

    Marcos A.P. Martins;Giovani P. Bastos;Helio G. Bonacorso;Nilo Zanatta

  • 13C-NMR Relaxation in Three DNA Oligonucleotide Duplexes: Model-Free Analysis of Internal and Overall Motion

    Philip N. Borer;Steven R. LaPlante;Anil Kumar;Nilo Zanatta

  • Regiospecific Synthesis of 4-Alkoxy and 4-Amino Substituted 2-Trifluoromethyl Pyrroles

    Nilo Zanatta;Juliana M. F. M. Schneider;Paulo H. Schneider;Ana D. Wouters

  • Haloacetylated enol ethers: 12 [18]. Regiospecific synthesis and structural determination of stable 5-hydroxy-1H-pyrazolines

    Helio G. Bonacorso;MarlíR. Oliveira;Alexandre P. Wentz;Arci D. Wastowski

  • α2-Adrenoceptors and 5-HT receptors mediate the antinociceptive effect of new pyrazolines, but not of dipyrone

    Maria Celoni M Godoy;Michele R Fighera;Fabiane R Souza;Ariane E Flores

  • Haloacetylated enol ethers. 7 . Synthesis of 3-aryl-5-trihalomethylisoxazoles and 3-aryl-5-hydroxy-5-trihalomethyl-4,5-dihydroisoxazoles†

    Marcos A. P. Martins;Geonir M. Siqueira;Giovani P. Bastos;Helio G. Bonacorso

  • One-Pot Synthesis of 3(5)-Ethoxycarbonylpyrazoles

    Marcos A. P. Martins;Rogério Freitag;Alex F. C. Flores;Nilo Zanatta

  • A convenient one-pot synthesis of 5-carboxyisoxazoles: trichloromethyl group as a carboxyl group precursor

    Marcos A.P. Martins;Alex F.C. Flores;Giovani P. Bastos;Adilson Sinhorin

  • Antinociceptive effect of novel pyrazolines in mice.

    Z. Tabarelli;M. A. Rubin;D. B. Berlese;P. D. Sauzem

  • Haloacetylated enol ethers. 9. Synthesis of 4-trifluoromethyl-2-methyl[phenyl]pyrimidines and tetrahydro derivatives

    Nilo Zanatta;Madelon B. Fagundes;Ricardo Ellensohn;Marcelo Marques

Frequent Co-Authors

Helio G. Bonacorso
Helio G. Bonacorso Universidade Federal de Santa Maria
Marcos A. P. Martins
Marcos A. P. Martins Universidade Federal de Santa Maria
Carlos Fernando Mello
Carlos Fernando Mello Universidade Federal de Santa Maria
Juliano Ferreira
Juliano Ferreira Universidade Federal de Santa Maria
João Rocha
João Rocha Universidade Federal de Santa Maria
Maria Rosa Chitolina Schetinger
Maria Rosa Chitolina Schetinger Universidade Federal de Santa Maria
Ludger A. Wessjohann
Ludger A. Wessjohann Leibniz Association
Vera Maria Morsch
Vera Maria Morsch Universidade Federal de Santa Maria
Antoniana U. Krettli
Antoniana U. Krettli Oswaldo Cruz Foundation
Miguel Viveiros
Miguel Viveiros Universidade Nova de Lisboa

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