David Sigwalt

737 total citations
19 papers, 622 citations indexed

About

David Sigwalt is a scholar working on Organic Chemistry, Physical and Theoretical Chemistry and Materials Chemistry. According to data from OpenAlex, David Sigwalt has authored 19 papers receiving a total of 622 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 7 papers in Physical and Theoretical Chemistry and 6 papers in Materials Chemistry. Recurrent topics in David Sigwalt's work include Supramolecular Chemistry and Complexes (8 papers), Fullerene Chemistry and Applications (7 papers) and Crystallography and molecular interactions (7 papers). David Sigwalt is often cited by papers focused on Supramolecular Chemistry and Complexes (8 papers), Fullerene Chemistry and Applications (7 papers) and Crystallography and molecular interactions (7 papers). David Sigwalt collaborates with scholars based in France, United States and Czechia. David Sigwalt's co-authors include Jean‐François Nierengarten, Michel Holler, Jean-Serge Rémy, Iwona Nierengarten, Lyle Isaacs, Marc Nothisen, Laura Rodríguez‐Pérez, Rafaël Delgado, Antonio Muñoz and Joanna Luczkowiak and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Communications and Nature Chemistry.

In The Last Decade

David Sigwalt

18 papers receiving 620 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
David Sigwalt France 12 430 228 178 135 84 19 622
Felipe Reviriego Spain 13 503 1.2× 250 1.1× 117 0.7× 215 1.6× 100 1.2× 47 729
Kevin Buffet Belgium 9 570 1.3× 262 1.1× 380 2.1× 86 0.6× 29 0.3× 10 849
Caroline Clavel France 14 441 1.0× 191 0.8× 319 1.8× 174 1.3× 41 0.5× 25 682
Antonio Muñoz Spain 15 573 1.3× 380 1.7× 303 1.7× 74 0.5× 29 0.3× 27 1.0k
Viktoriia Postupalenko France 15 159 0.4× 193 0.8× 351 2.0× 79 0.6× 137 1.6× 23 636
Vincenzo Grande Germany 17 290 0.7× 361 1.6× 364 2.0× 108 0.8× 46 0.5× 19 867
W. Jesse Netherlands 14 178 0.4× 147 0.6× 190 1.1× 75 0.6× 175 2.1× 24 544
Edward J. Dale United States 18 799 1.9× 613 2.7× 163 0.9× 338 2.5× 165 2.0× 20 1.3k
Bo‐Liang Deng Belgium 10 398 0.9× 129 0.6× 189 1.1× 73 0.5× 28 0.3× 16 655
Sapna Ravindranathan India 17 203 0.5× 178 0.8× 529 3.0× 182 1.3× 19 0.2× 40 829

Countries citing papers authored by David Sigwalt

Since Specialization
Citations

This map shows the geographic impact of David Sigwalt's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by David Sigwalt with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites David Sigwalt more than expected).

Fields of papers citing papers by David Sigwalt

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by David Sigwalt. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by David Sigwalt. The network helps show where David Sigwalt may publish in the future.

Co-authorship network of co-authors of David Sigwalt

This figure shows the co-authorship network connecting the top 25 collaborators of David Sigwalt. A scholar is included among the top collaborators of David Sigwalt based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with David Sigwalt. David Sigwalt is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

19 of 19 papers shown
1.
Hahn, Uwe, Sebastiano Guerra, David Sigwalt, et al.. (2023). Si‐Tethered Bis‐ and Tris‐Malonates for the Regioselective Preparation of Fullerene Multi‐Adducts. Helvetica Chimica Acta. 106(6). 1 indexed citations
2.
Sigwalt, David, et al.. (2020). Conformationally mobile acyclic cucurbit[n]uril-type receptors derived from an S-shaped methylene bridged glycoluril pentamer. Supramolecular chemistry. 32(9). 479–494. 4 indexed citations
3.
Hostaš, Jiří, David Sigwalt, Marina Šekutor, et al.. (2018). A Nexus between Theory and Experiment: Non-empirical Quantum Mechanical Computational Methodology Applied to Cucurbit[n]uril•Guest Binding Interactions.
4.
Sigwalt, David, Marina Šekutor, Liping Cao, et al.. (2017). Unraveling the Structure–Affinity Relationship between Cucurbit[n]urils (n = 7, 8) and Cationic Diamondoids. Journal of the American Chemical Society. 139(8). 3249–3258. 77 indexed citations
5.
Sigwalt, David, Damien Moncelet, Shane D. Falcinelli, et al.. (2016). Acyclic Cucurbit[n]uril‐Type Molecular Containers: Influence of Linker Length on Their Function as Solubilizing Agents. ChemMedChem. 11(9). 980–989. 21 indexed citations
6.
Sigwalt, David, Peter Y. Zavalij, & Lyle Isaacs. (2016). Cationic acyclic cucurbit[n]uril-type containers: synthesis and molecular recognition toward nucleotides. Supramolecular chemistry. 28(9-10). 825–834. 11 indexed citations
7.
Sigwalt, David, Rubén Caballero, Michel Holler, et al.. (2016). Ultra‐Fast Dendritic Growth Based on the Grafting of Fullerene Hexa‐Adduct Macromonomers onto a Fullerene Core. European Journal of Organic Chemistry. 2016(16). 2882–2887. 15 indexed citations
8.
Hostaš, Jiří, David Sigwalt, Marina Šekutor, et al.. (2016). A Nexus between Theory and Experiment: Non‐Empirical Quantum Mechanical Computational Methodology Applied to Cucurbit[n]uril⋅Guest Binding Interactions. Chemistry - A European Journal. 22(48). 17226–17238. 30 indexed citations
9.
Sigwalt, David, et al.. (2015). Acyclic Cucurbit[n]uril Dendrimers. Organic Letters. 17(23). 5914–5917. 4 indexed citations
10.
Muñoz, Antonio, David Sigwalt, Beatriz M. Illescas, et al.. (2015). Synthesis of giant globular multivalent glycofullerenes as potent inhibitors in a model of Ebola virus infection. Nature Chemistry. 8(1). 50–57. 236 indexed citations
11.
Zhang, Mingming, David Sigwalt, & Lyle Isaacs. (2015). Differentially functionalized acyclic cucurbiturils: synthesis, self-assembly and CB[6]-induced allosteric guest binding. Chemical Communications. 51(78). 14620–14623. 21 indexed citations
12.
Flacher, Vincent, David Sigwalt, Jean‐Daniel Fauny, et al.. (2015). Mannoside Glycolipid Conjugates Display Anti-inflammatory Activity by Inhibition of Toll-like Receptor-4 Mediated Cell Activation. ACS Chemical Biology. 10(12). 2697–2705. 11 indexed citations
13.
Nierengarten, Iwona, Marc Nothisen, David Sigwalt, et al.. (2013). Polycationic Pillar[5]arene Derivatives: Interaction with DNA and Biological Applications. Chemistry - A European Journal. 19(51). 17552–17558. 67 indexed citations
14.
Guerra, Sebastiano, et al.. (2013). Synthesis of optically pure [60]fullerene e,e,e-tris adducts. Chemical Communications. 49(42). 4752–4752. 12 indexed citations
15.
16.
Sigwalt, David, Michel Holler, & Jean‐François Nierengarten. (2013). A rigid macrocyclic bis-malonate for the regioselective preparation of trans-1 and trans-3 fullerene bis-adducts. Tetrahedron Letters. 54(24). 3160–3163. 8 indexed citations
17.
Schaeffer, Evelyne, David Sigwalt, Vincent Flacher, et al.. (2013). Dynamic Micelles of Mannoside Glycolipids are more Efficient than Polymers for Inhibiting HIV-1 trans-Infection. Bioconjugate Chemistry. 24(11). 1813–1823. 16 indexed citations
18.
Sigwalt, David, et al.. (2013). An expeditious regioselective synthesis of [60]fullerene e,e,e tris-adduct building blocks. Tetrahedron Letters. 54(32). 4241–4244. 13 indexed citations
19.
Sigwalt, David, Michel Holler, Julien Iehl, et al.. (2011). Gene delivery with polycationic fullerene hexakis-adducts. Chemical Communications. 47(16). 4640–4640. 66 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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