Martin L. Kirk

8.4k total citations · 2 hit papers
173 papers, 6.7k citations indexed

About

Martin L. Kirk is a scholar working on Inorganic Chemistry, Renewable Energy, Sustainability and the Environment and Electronic, Optical and Magnetic Materials. According to data from OpenAlex, Martin L. Kirk has authored 173 papers receiving a total of 6.7k indexed citations (citations by other indexed papers that have themselves been cited), including 73 papers in Inorganic Chemistry, 66 papers in Renewable Energy, Sustainability and the Environment and 64 papers in Electronic, Optical and Magnetic Materials. Recurrent topics in Martin L. Kirk's work include Metalloenzymes and iron-sulfur proteins (65 papers), Magnetism in coordination complexes (61 papers) and Metal-Catalyzed Oxygenation Mechanisms (58 papers). Martin L. Kirk is often cited by papers focused on Metalloenzymes and iron-sulfur proteins (65 papers), Magnetism in coordination complexes (61 papers) and Metal-Catalyzed Oxygenation Mechanisms (58 papers). Martin L. Kirk collaborates with scholars based in United States, Canada and Germany. Martin L. Kirk's co-authors include Vincent L. Pecoraro, Jeff W. Kampf, Curtis M. Zaleski, Ezra C. Depperman, David A. Shultz, Benjamin W. Stein, Edward I. Solomon, Daniel R. Gamelin, Jing Yang and William E. Hatfield and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of the American Chemical Society and Journal of Biological Chemistry.

In The Last Decade

Martin L. Kirk

167 papers receiving 6.6k citations

Hit Papers

Synthesis, Structure, and Magnetic Properties of a Large ... 2004 2026 2011 2018 2004 2020 100 200 300 400 500

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Martin L. Kirk United States 43 3.0k 2.8k 2.8k 1.6k 1.2k 173 6.7k
Yasutaka Kitagawa Japan 39 2.7k 0.9× 3.3k 1.2× 2.1k 0.7× 1.0k 0.6× 563 0.5× 231 6.5k
Jordi Cirera Spain 32 2.8k 0.9× 2.9k 1.0× 2.6k 0.9× 418 0.3× 1.2k 1.0× 61 5.6k
Róbert K. Szilágyi United States 32 1.0k 0.3× 1.3k 0.5× 1.8k 0.7× 1.6k 1.0× 1.0k 0.8× 105 4.7k
Thomas C. Brunold United States 43 1.1k 0.4× 2.1k 0.8× 3.6k 1.3× 1.3k 0.8× 1.5k 1.2× 150 6.8k
Régis Guillot France 52 1.7k 0.6× 2.9k 1.1× 2.6k 0.9× 861 0.5× 1.0k 0.8× 393 9.6k
Andrew Ozarowski United States 43 3.1k 1.0× 2.6k 0.9× 2.2k 0.8× 283 0.2× 1.1k 0.9× 185 5.4k
Maren Pink United States 60 2.6k 0.9× 4.3k 1.5× 3.9k 1.4× 863 0.5× 773 0.6× 347 11.8k
Pierre Kennepohl Canada 28 969 0.3× 1.7k 0.6× 1.9k 0.7× 1.1k 0.7× 1.1k 0.9× 65 5.5k
B.C. Noll United States 54 1.7k 0.6× 5.0k 1.8× 3.5k 1.3× 1.3k 0.8× 808 0.7× 280 10.5k
Maylis Orio France 32 886 0.3× 1.2k 0.4× 1.3k 0.5× 1.5k 0.9× 866 0.7× 130 4.0k

Countries citing papers authored by Martin L. Kirk

Since Specialization
Citations

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

Fields of papers citing papers by Martin L. Kirk

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Martin L. Kirk. 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 Martin L. Kirk. The network helps show where Martin L. Kirk may publish in the future.

Co-authorship network of co-authors of Martin L. Kirk

This figure shows the co-authorship network connecting the top 25 collaborators of Martin L. Kirk. A scholar is included among the top collaborators of Martin L. Kirk 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 Martin L. Kirk. Martin L. Kirk 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.
Shultz, David A., et al.. (2025). Bridge connectivity effects on photoinduced ground-state electron spin polarization. The Journal of Chemical Physics. 162(8). 2 indexed citations
3.
Henderson, Ian, Curtis D. Mowry, John Watt, et al.. (2025). Precipitation of gadolinium from magnetic resonance imaging contrast agents may be the Brass tacks of toxicity. Magnetic Resonance Imaging. 119. 110383–110383. 1 indexed citations
4.
Kirk, Martin L., Emily Hong, Jing Yang, et al.. (2024). The safety of magnetic resonance imaging contrast agents. SHILAP Revista de lepidopterología. 6. 1376587–1376587. 4 indexed citations
5.
Shultz, David A., et al.. (2024). Metal–Ligand Exchange Coupling Alters the Open-Shell Ligand Electronic Structure in a Bis(semiquinone) Complex. Inorganic Chemistry. 63(14). 6493–6499. 3 indexed citations
6.
Belaj, Ferdinand, et al.. (2024). Understanding the Carbyne Formation from C2H2 Complexes. Journal of the American Chemical Society. 146(47). 32392–32402. 2 indexed citations
7.
Yang, Jing, et al.. (2024). Active Site Characterization of a Campylobacter jejuni Nitrate Reductase Variant Provides Insight into the Enzyme Mechanism. Inorganic Chemistry. 63(29). 13191–13196. 3 indexed citations
8.
Burgmayer, Sharon J. Nieter & Martin L. Kirk. (2023). Advancing Our Understanding of Pyranopterin-Dithiolene Contributions to Moco Enzyme Catalysis. Molecules. 28(22). 7456–7456. 9 indexed citations
9.
Kirk, Martin L., et al.. (2022). Resonance Raman spectroscopy of pyranopterin molybdenum enzymes. Journal of Inorganic Biochemistry. 235. 111907–111907. 3 indexed citations
10.
Yang, Jing, et al.. (2020). Addressing Ligand-Based Redox in Molybdenum-Dependent Methionine Sulfoxide Reductase. Journal of the American Chemical Society. 142(6). 2721–2725. 12 indexed citations
11.
Thomas, Alan K., Ryan S. Johnson, Benjamin W. Stein, et al.. (2017). Charge Transfer Doping Induced Conformational Ordering of a Non-Crystalline Conjugated Polymer. The Journal of Physical Chemistry C. 121(42). 23817–23826. 9 indexed citations
12.
Stein, Benjamin W. & Martin L. Kirk. (2013). Orbital contributions to CO oxidation in Mo–Cu carbon monoxide dehydrogenase. Chemical Communications. 50(9). 1104–1106. 24 indexed citations
13.
Kirk, Martin L. & David A. Shultz. (2012). Transition metal complexes of donor–acceptor biradicals. Coordination Chemistry Reviews. 257(1). 218–233. 60 indexed citations
14.
Rothery, Richard A., Benjamin W. Stein, Matthew Solomonson, Martin L. Kirk, & Joël H. Weiner. (2012). Pyranopterin conformation defines the function of molybdenum and tungsten enzymes. Proceedings of the National Academy of Sciences. 109(37). 14773–14778. 81 indexed citations
15.
Kirk, Martin L., et al.. (2011). Bridges, short and long term solutions for the London 2012 Games. 1. 2 indexed citations
16.
Perera, Eranda, et al.. (2011). A Valence Bond Description of Dizwitterionic Dithiolene Character in an Oxomolybdenum–Bis(dithione) Complex. European Journal of Inorganic Chemistry. 2011(36). 5467–5470. 22 indexed citations
17.
Kirk, Martin L.. (2005). Spin Crossover in Transition Metal Compounds II. Topics in Current Chemistry, 234. Journal of the American Chemical Society. 127(21). 7961. 19 indexed citations
18.
Shultz, David A., et al.. (2005). Valence tautomerization and exchange coupling in a cobalt–nitronylnitroxide–semiquinone complex. Polyhedron. 24(16-17). 2876–2879. 20 indexed citations
19.
Solomon, Edward I., Martin L. Kirk, Daniel R. Gamelin, & Sabine Coates Pulver. (1995). [5] Bioinorganic spectroscopy. Methods in enzymology on CD-ROM/Methods in enzymology. 246. 71–110. 171 indexed citations
20.

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.

Explore authors with similar magnitude of impact

Rankless by CCL
2026