World's Best Scientists 2026 revealed!

D-Index & Metrics

Chemistry

D-Index
58
Citations
10910
World Ranking
10718
National Ranking
773

Dieter Schollmeyer 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 Dieter Schollmeyer 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: 572 publications — 92nd percentile

92% of scientists in this discipline score the same or lower.

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

Dieter Schollmeyer 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 Dieter Schollmeyer 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: 58 D-Index — 42nd percentile

42% of scientists in this discipline score the same or lower.

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

Overview

Dieter Schollmeyer is affiliated with Johannes Gutenberg University of Mainz in Germany. Their research spans primarily the fields of Materials Science and Chemistry, with a particular focus on subfields such as Materials Chemistry, Organic Chemistry, Inorganic Chemistry, Molecular Biology, and Physical and Theoretical Chemistry.

Their work covers several main scientific topics, including:

  • Crystallization and Solubility Studies
  • X-ray Diffraction in Crystallography
  • Radical Photochemical Reactions
  • Crystal structures of chemical compounds
  • Crystallography and molecular interactions
  • Sulfur-Based Synthesis Techniques
  • Catalytic C-H Functionalization Methods

Schollmeyer has contributed to a significant number of publications across various scientific journals and databases. Frequent publication venues for their work include:

  • The Cambridge Structural Database
  • IUCrData
  • Chemistry - A European Journal
  • Journal of the American Chemical Society
  • Molbank

Their notable recent papers include:

  • Amplification of Dissymmetry Factors in π-Extended [7]- and [9]Helicenes, 2021, Journal of the American Chemical Society
  • Negatively Curved Nanographene with Heptagonal and [5]Helicene Units, 2020, Journal of the American Chemical Society
  • Metal-Free Electrochemical Synthesis of Sulfonamides Directly from (Hetero)arenes, SO2, and Amines, 2020, Angewandte Chemie International Edition
  • Synthesis of Nonplanar Graphene Nanoribbon with Fjord Edges, 2021, Journal of the American Chemical Society
  • Electrochemical C−H Functionalization of (Hetero)Arenes-Optimized by DoE, 2020, Chemistry - A European Journal

These papers indicate a variety of research themes, from advanced molecular structures like helicenes and nanographenes to innovative synthesis methods involving electrochemical techniques and sulfur-based chemistry.

Schollmeyer frequently collaborates with other researchers. Key coauthors include:

  • Siegfried R. Waldvogel
  • Heiner Detert
  • Kläus Müllen
  • Akimitsu Narita
  • Zijie Qiu

This network of collaborators reflects interdisciplinary interactions spanning synthetic chemistry, materials science, and crystallography.

Best Publications

  • Metal‐ and Reagent‐Free Highly Selective Anodic Cross‐Coupling Reaction of Phenols

    Bernd Elsler;Dieter Schollmeyer;Katrin Marie Dyballa;Robert Franke;Robert Franke

  • Amplification of Dissymmetry Factors in π-Extended [7]- and [9]Helicenes.

    Zijie Qiu;Cheng-Wei Ju;Lucas Frédéric;Yunbin Hu;Yunbin Hu

  • Source of Selectivity in Oxidative Cross‐Coupling of Aryls by Solvent Effect of 1,1,1,3,3,3‐Hexafluoropropan‐2‐ol

    Bernd Elsler;Anton Wiebe;Dieter Schollmeyer;Katrin M. Dyballa

  • Reagent‐ and Metal‐Free Anodic C−C Cross‐Coupling of Aniline Derivatives

    Lara Schulz;Mathias Enders;Bernd Elsler;Dieter Schollmeyer

  • Insights into the Mechanism of Anodic N–N Bond Formation by Dehydrogenative Coupling

    Tile Gieshoff;Tile Gieshoff;Anton Kehl;Dieter Schollmeyer;Kevin D. Moeller

  • Taste, a new incentive to switch to (R)-praziquantel in schistosomiasis treatment.

    Thorsten Meyer;Harald Sekljic;Stefan Fuchs;Heiko Bothe

  • Selective Synthesis of Partially Protected Nonsymmetric Biphenols by Reagent- and Metal-Free Anodic Cross-Coupling Reaction.

    Anton Wiebe;Dieter Schollmeyer;Katrin M. Dyballa;Robert Franke

  • Synthesis of meta-Terphenyl-2,2''-diols by Anodic C-C Cross-Coupling Reactions.

    Sebastian Lips;Anton Wiebe;Anton Wiebe;Bernd Elsler;Dieter Schollmeyer

  • π-Extended Pyrene-Fused Double [7]Carbohelicene as a Chiral Polycyclic Aromatic Hydrocarbon

    Yunbin Hu;Yunbin Hu;Giuseppe M. Paternò;Xiao-Ye Wang;Xin-Chang Wang

  • Access to Pyrazolidin-3,5-diones through Anodic N-N Bond Formation.

    Tile Gieshoff;Dieter Schollmeyer;Siegfried R. Waldvogel

  • Syntheses, Structures, and Magnetic Properties of Diphenoxo-Bridged CuIILnIII and NiII(Low-Spin)LnIII Compounds Derived from a Compartmental Ligand (Ln = Ce−Yb)

    Arpita Jana;Samit Majumder;Luca Carrella;Malabika Nayak

  • Single and Twofold Metal- and Reagent-Free Anodic C-C Cross-Coupling of Phenols with Thiophenes.

    Anton Wiebe;Anton Wiebe;Sebastian Lips;Dieter Schollmeyer;Robert Franke

  • Flexible Minerals: Self-Assembled Calcite Spicules with Extreme Bending Strength

    Filipe Natalio;Filipe Natalio;Tomas P. Corrales;Martin Panthöfer;Dieter Schollmeyer

  • Design, Synthesis, and Biological Evaluation of Novel 3-Aryl-4-(1H-indole-3yl)-1,5-dihydro-2H-pyrrole-2-ones as Vascular Endothelial Growth Factor Receptor (VEGF-R) Inhibitors

    Christian Peifer;Roland Selig;Katrin Kinkel;Dimitri Ott

  • OH–π and halogen–π interactions as driving forces in the crystal organisations of tri-bromo and tri-iodo trityl alcohols

    Dieter Schollmeyer;Oleg V. Shishkin;Thomas Rühl;Myroslav O. Vysotsky

  • Design, synthesis, and biological evaluation of 3,4-diarylmaleimides as angiogenesis inhibitors.

    Christian Peifer;Thomas Stoiber;Eberhard Unger;Frank Totzke

  • Cover Picture: Metal‐ and Reagent‐Free Highly Selective Anodic Cross‐Coupling Reaction of Phenols (Angew. Chem. Int. Ed. 20/2014)

    Bernd Elsler;Dieter Schollmeyer;Katrin Marie Dyballa;Robert Franke;Robert Franke

  • Synthesis and Conformational Properties of Nonsymmetric Pillar[5]arenes and Their Acetonitrile Inclusion Compounds

    Yuhui Kou;Hongqi Tao;Derong Cao;Zhiyong Fu

  • Negatively Curved Nanographene with Heptagonal and [5]Helicene Units

    Zijie Qiu;Sobi Asako;Yunbin Hu;Cheng-Wei Ju;Cheng-Wei Ju

  • Metall‐ und reagensfreie hochselektive anodische Kreuzkupplung von Phenolen

    Bernd Elsler;Dieter Schollmeyer;Katrin Marie Dyballa;Robert Franke;Robert Franke

  • Unexpected Scholl Reaction of 6,7,13,14-Tetraarylbenzo[k]tetraphene: Selective Formation of Five-Membered Rings in Polycyclic Aromatic Hydrocarbons.

    Junzhi Liu;Akimitsu Narita;Silvio Osella;Wen Zhang

Frequent Co-Authors

Siegfried R. Waldvogel
Siegfried R. Waldvogel Johannes Gutenberg University of Mainz
Stefan Laufer
Stefan Laufer University of Tübingen
Robert Franke
Robert Franke Ruhr University Bochum
Klaus Müllen
Klaus Müllen Max Planck Institute for Polymer Research
Herbert Meier
Herbert Meier Johannes Gutenberg University of Mainz
Till Opatz
Till Opatz Johannes Gutenberg University of Mainz
Akimitsu Narita
Akimitsu Narita Okinawa Institute of Science and Technology
Martin Baumgarten
Martin Baumgarten Max Planck Society
Klaus Jurkschat
Klaus Jurkschat TU Dortmund University
George Floudas
George Floudas University of Ioannina

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