Max Muir

585 total citations
12 papers, 452 citations indexed

About

Max Muir is a scholar working on Organic Chemistry, Atomic and Molecular Physics, and Optics and Pharmaceutical Science. According to data from OpenAlex, Max Muir has authored 12 papers receiving a total of 452 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Organic Chemistry, 7 papers in Atomic and Molecular Physics, and Optics and 5 papers in Pharmaceutical Science. Recurrent topics in Max Muir's work include Advanced Chemical Physics Studies (7 papers), Fluorine in Organic Chemistry (5 papers) and Spectroscopy and Quantum Chemical Studies (2 papers). Max Muir is often cited by papers focused on Advanced Chemical Physics Studies (7 papers), Fluorine in Organic Chemistry (5 papers) and Spectroscopy and Quantum Chemical Studies (2 papers). Max Muir collaborates with scholars based in United States, Russia and Puerto Rico. Max Muir's co-authors include Jon Baker, Jan Andzelm, Peter R. Taylor, Antonio Scala, John H. P. Tyman, Pierangela Ciuffreda, Mario Anastasia, Pietro Allevi, Alberto Fiecchi and Giuliana Cighetti and has published in prestigious journals such as The Journal of Chemical Physics, SHILAP Revista de lepidopterología and Chemical Physics Letters.

In The Last Decade

Max Muir

11 papers receiving 430 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 Muir United States 7 268 187 79 73 67 12 452
Grigoriy Vayner United States 8 297 1.1× 173 0.9× 58 0.7× 129 1.8× 68 1.0× 8 516
Georg Hornung Germany 8 259 1.0× 149 0.8× 54 0.7× 222 3.0× 91 1.4× 9 467
Jose A. Paulino United States 7 229 0.9× 234 1.3× 68 0.9× 109 1.5× 133 2.0× 7 433
Ambili S. Menon Australia 8 220 0.8× 217 1.2× 105 1.3× 66 0.9× 114 1.7× 8 411
Roustam Gareyev United States 13 174 0.6× 215 1.1× 54 0.7× 135 1.8× 77 1.1× 14 407
Frederic J. Dulles United States 7 236 0.9× 203 1.1× 72 0.9× 104 1.4× 158 2.4× 8 474
Colleen K. Regan United States 5 316 1.2× 161 0.9× 50 0.6× 168 2.3× 42 0.6× 5 453
Kathleen M. Morgan United States 12 77 0.3× 297 1.6× 65 0.8× 74 1.0× 62 0.9× 28 490
V. Güner Türkiye 8 193 0.7× 438 2.3× 87 1.1× 44 0.6× 88 1.3× 18 612
Kelli S. Khuong United States 11 218 0.8× 489 2.6× 151 1.9× 76 1.0× 106 1.6× 11 779

Countries citing papers authored by Max Muir

Since Specialization
Citations

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

Fields of papers citing papers by Max Muir

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Max Muir

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

All Works

12 of 12 papers shown
1.
Muir, Max, et al.. (2012). Further Successes of the Meisenheimer Model. SHILAP Revista de lepidopterología. 2(2). 443–452. 2 indexed citations
2.
3.
Сорокин, В. И., Valery A. Ozeryanskii, Г. С. Бородкин, et al.. (2006). Preparation of Dialkylamino-Substituted Benzenes and Naphthalenes by Nucleophilic Replacement of Fluorine in the Corresponding Perfluoroaromatic Compounds. Zeitschrift für Naturforschung B. 61(5). 615–625. 5 indexed citations
4.
Muir, Max & Jon Baker. (2005). A simple calculational model for predicting the site for nucleophilic substitution in aromatic perfluorocarbons. Journal of Fluorine Chemistry. 126(5). 727–738. 16 indexed citations
5.
Allevi, Pietro, Mario Anastasia, Pierangela Ciuffreda, et al.. (1998). Synthesis of carminic acid, the colourant principle of cochineal. Journal of the Chemical Society Perkin Transactions 1. 575–582. 30 indexed citations
6.
Baker, Jon & Max Muir. (1998). A density functional study of mono- and difluoropropenes. Journal of Fluorine Chemistry. 89(2). 145–166. 4 indexed citations
7.
Muir, Max. (1996). A systematic density functional study of fluorination in methane, ethane and ethylene. Molecular Physics. 89(1). 211–237. 32 indexed citations
8.
Baker, Jon, Jan Andzelm, Max Muir, & Peter R. Taylor. (1995). OH + H2 → H2O + H. The importance of ‘exact exchange’ in density functional theory. Chemical Physics Letters. 237(1-2). 53–60. 127 indexed citations
9.
Baker, Jon, Max Muir, & Jan Andzelm. (1995). A study of some organic reactions using density functional theory. The Journal of Chemical Physics. 102(5). 2063–2079. 198 indexed citations
10.
Allevi, Pietro, Mario Anastasia, Pierangela Ciuffreda, et al.. (1991). The first total synthesis of carminic acid. Journal of the Chemical Society Chemical Communications. 1319–1319. 13 indexed citations
11.
Muir, Max, et al.. (1988). Structure of cis-Pt(asb)2Cl2, a platinum(II) complex with a styrylbenzothiazole ligand. Acta Crystallographica Section C Crystal Structure Communications. 44(5). 803–806. 4 indexed citations
12.
King, Trevor J., J. A. H. MACBRIDE, Max Muir, & Peter M. Wright. (1983). Synthesis of hexahalogeno-1,8-diazabiphenylenes; separation of steric and electronic effects in extrusion of dinitrogen from benzo[c]cinnoline system, and the X-ray crystal structure of octachlorobenzo[c]cinnoline. Journal of the Chemical Society Chemical Communications. 425–425.

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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