Max M. Hansmann

4.1k total citations
81 papers, 3.4k citations indexed

About

Max M. Hansmann is a scholar working on Organic Chemistry, Inorganic Chemistry and Electrical and Electronic Engineering. According to data from OpenAlex, Max M. Hansmann has authored 81 papers receiving a total of 3.4k indexed citations (citations by other indexed papers that have themselves been cited), including 75 papers in Organic Chemistry, 22 papers in Inorganic Chemistry and 9 papers in Electrical and Electronic Engineering. Recurrent topics in Max M. Hansmann's work include N-Heterocyclic Carbenes in Organic and Inorganic Chemistry (25 papers), Catalytic Cross-Coupling Reactions (20 papers) and Catalytic Alkyne Reactions (20 papers). Max M. Hansmann is often cited by papers focused on N-Heterocyclic Carbenes in Organic and Inorganic Chemistry (25 papers), Catalytic Cross-Coupling Reactions (20 papers) and Catalytic Alkyne Reactions (20 papers). Max M. Hansmann collaborates with scholars based in Germany, Saudi Arabia and United States. Max M. Hansmann's co-authors include A. Stephen K. Hashmi, Guy Bertrand, Frank Röminger, Matthias Rudolph, Patrick W. Antoni, Mohand Melaïmi, Rodolphe Jazzar, Rebecca L. Melen, Douglas W. Stephan and David A. Thaisrivongs and has published in prestigious journals such as Science, Journal of the American Chemical Society and Angewandte Chemie International Edition.

In The Last Decade

Max M. Hansmann

77 papers receiving 3.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Max M. Hansmann Germany 36 3.1k 956 319 227 121 81 3.4k
Alain Igau France 23 2.0k 0.6× 1.0k 1.1× 220 0.7× 107 0.5× 125 1.0× 98 2.3k
Salvador Conejero Spain 31 2.4k 0.8× 958 1.0× 294 0.9× 60 0.3× 218 1.8× 75 2.7k
Tamás Bartik Germany 21 1.7k 0.6× 900 0.9× 267 0.8× 241 1.1× 156 1.3× 52 2.0k
Randy K. Hayashi United States 19 1.6k 0.5× 1.4k 1.5× 304 1.0× 143 0.6× 144 1.2× 39 2.0k
Take‐aki Koizumi Japan 25 1.1k 0.3× 620 0.6× 308 1.0× 170 0.7× 173 1.4× 84 1.5k
Ronan R. San Juan Canada 7 1.7k 0.5× 1.2k 1.2× 315 1.0× 85 0.4× 211 1.7× 8 1.9k
Rafael Gramage‐Doria France 22 1.7k 0.5× 808 0.8× 513 1.6× 83 0.4× 61 0.5× 72 2.1k
T. Keith Hollis United States 30 2.2k 0.7× 817 0.9× 262 0.8× 188 0.8× 202 1.7× 70 2.5k
Xiaolai Zheng United States 20 1.0k 0.3× 504 0.5× 358 1.1× 104 0.5× 133 1.1× 31 1.4k
M. Spiegler Germany 26 3.0k 1.0× 906 0.9× 333 1.0× 89 0.4× 262 2.2× 36 3.3k

Countries citing papers authored by Max M. Hansmann

Since Specialization
Citations

This map shows the geographic impact of Max M. Hansmann'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 Max M. Hansmann with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Max M. Hansmann more than expected).

Fields of papers citing papers by Max M. Hansmann

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Max M. Hansmann. 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 Max M. Hansmann. The network helps show where Max M. Hansmann may publish in the future.

Co-authorship network of co-authors of Max M. Hansmann

This figure shows the co-authorship network connecting the top 25 collaborators of Max M. Hansmann. A scholar is included among the top collaborators of Max M. Hansmann 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 Max M. Hansmann. Max M. Hansmann is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Sun, Qiu, et al.. (2025). Ph 2 SCCO: A New Versatile CCO‐Fragment Transfer Reagent. Angewandte Chemie International Edition. 64(47). e202518689–e202518689.
2.
Kutin, Yury, Μαρία Δρόσου, Patrick W. Antoni, et al.. (2025). Triplet Vinylidenes Based on (Benz)imidazole and 1,2,3-Triazole N-Heterocycles. JACS Au. 5(6). 2884–2897. 1 indexed citations
3.
Kutin, Yury, Μαρία Δρόσου, Alexander Schnegg, et al.. (2025). Ph 3 PC – A Monosubstituted C(0) Atom in Its Triplet State. Angewandte Chemie International Edition. 64(10). e202424166–e202424166. 2 indexed citations
4.
Antoni, Patrick W., et al.. (2025). Imidazo[1,5‐ a ]pyridines – A Versatile Platform for Structurally Distinct N ‐Heterocyclic Olefins and π‐Extended Heterocycles. Angewandte Chemie International Edition. 64(29). e202506305–e202506305. 2 indexed citations
5.
Sun, Qiu, et al.. (2025). Spiro-C(sp 3 )-atom transfer: Creating rigid three-dimensional structures with Ph 2 SCN 2. Science. 387(6736). 885–892. 11 indexed citations
6.
Hansmann, Max M., et al.. (2024). Cycloadditions of Diazoalkenes with P4 and tBuCP: Access to Diazaphospholes. Angewandte Chemie International Edition. 63(38). e202410107–e202410107. 6 indexed citations
7.
Nielsen, Mogens Brøndsted, et al.. (2024). para‐Aminoazobenzole – Bipolare Redoxaktive Verbindungen. Angewandte Chemie. 136(36).
8.
Antoni, Patrick W., et al.. (2024). Cleavage of Carbodicarbenes with N2O for Accessing Stable Diazoalkenes: Two‐Fold Ligand Exchange at a C(0)‐Atom. Angewandte Chemie International Edition. 64(3). e202415228–e202415228. 9 indexed citations
9.
Buchmeiser, Michael R., et al.. (2024). Mesoionic N‐Heterocyclic Olefins as Initiators for the Lewis Pair Polymerization of Epoxides. Macromolecular Rapid Communications. 45(12). e2300716–e2300716. 1 indexed citations
10.
Antoni, Patrick W., et al.. (2023). Pushing the Upper Limit of Nucleophilicity Scales by Mesoionic N‐Heterocyclic Olefins. Angewandte Chemie International Edition. 62(40). e202309790–e202309790. 18 indexed citations
11.
Sun, Qiu, et al.. (2023). Pyridinium‐Derived Mesoionic N‐Heterocyclic Olefins (py‐mNHOs). Angewandte Chemie International Edition. 63(10). e202318283–e202318283. 8 indexed citations
12.
Ullrich, Tobias, Piermaria Pinter, Philipp Haines, et al.. (2020). Singlet Fission in Carbene‐Derived Diradicaloids. Angewandte Chemie. 132(20). 7980–7988. 26 indexed citations
13.
Grünwald, Annette, Piermaria Pinter, Matthias E. Miehlich, et al.. (2020). Aromaticity and sterics control whether a cationic olefin radical is resistant to disproportionation. Chemical Science. 11(16). 4138–4149. 33 indexed citations
14.
Ullrich, Tobias, Piermaria Pinter, Philipp Haines, et al.. (2020). Singlet Fission in Carbene‐Derived Diradicaloids. Angewandte Chemie International Edition. 59(20). 7906–7914. 53 indexed citations
15.
Hansmann, Max M., Mohand Melaïmi, Dominik Munz, & Guy Bertrand. (2018). Modular Approach to Kekulé Diradicaloids Derived from Cyclic (Alkyl)(amino)carbenes. Journal of the American Chemical Society. 140(7). 2546–2554. 88 indexed citations
16.
Grünwald, Annette, et al.. (2018). Carbene derived diradicaloids – building blocks for singlet fission?. Chemical Science. 9(28). 6107–6117. 70 indexed citations
17.
18.
Hansmann, Max M., Matthias Rudolph, Frank Röminger, & A. Stephen K. Hashmi. (2013). Mechanistisches Umschalten bei der dualen Goldkatalyse von Diinen: C(sp3)‐H‐Aktivierung über Bifurkation – Vinyliden‐ versus Carbenreaktionswege. Angewandte Chemie. 125(9). 2653–2659. 94 indexed citations
19.
Hansmann, Max M., et al.. (2013). A Theoretical DFT‐Based and Experimental Study of the Transmetalation Step in Au/Pd‐Mediated Cross‐Coupling Reactions. Chemistry - A European Journal. 19(45). 15290–15303. 49 indexed citations
20.
Hashmi, A. Stephen K., Weibo Yang, Yang Yu, et al.. (2012). Gold‐Catalyzed Formal 1,6‐Acyloxy Migration Leading to 3,4‐Disubstituted Pyrrolidin‐2‐ones. Angewandte Chemie International Edition. 52(4). 1329–1332. 76 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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