M.R.J. Elsegood

13.6k total citations
530 papers, 11.6k citations indexed

About

M.R.J. Elsegood is a scholar working on Organic Chemistry, Inorganic Chemistry and Materials Chemistry. According to data from OpenAlex, M.R.J. Elsegood has authored 530 papers receiving a total of 11.6k indexed citations (citations by other indexed papers that have themselves been cited), including 395 papers in Organic Chemistry, 225 papers in Inorganic Chemistry and 113 papers in Materials Chemistry. Recurrent topics in M.R.J. Elsegood's work include Organometallic Complex Synthesis and Catalysis (186 papers), Metal complexes synthesis and properties (80 papers) and Asymmetric Hydrogenation and Catalysis (61 papers). M.R.J. Elsegood is often cited by papers focused on Organometallic Complex Synthesis and Catalysis (186 papers), Metal complexes synthesis and properties (80 papers) and Asymmetric Hydrogenation and Catalysis (61 papers). M.R.J. Elsegood collaborates with scholars based in United Kingdom, United States and Japan. M.R.J. Elsegood's co-authors include W. Clegg, Carl Redshaw, V.C. Gibson, Sophie H. Dale, Takehiko Yamato, Warren E. Piers, Martin B. Smith, Steven M. Allin, Xing Feng and Simon Doherty and has published in prestigious journals such as Journal of the American Chemical Society, Angewandte Chemie International Edition and Chemistry of Materials.

In The Last Decade

M.R.J. Elsegood

518 papers receiving 11.4k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
M.R.J. Elsegood United Kingdom 53 8.3k 4.1k 2.8k 1.7k 1.2k 530 11.6k
Gabriele Kociok‐Köhn United Kingdom 52 7.1k 0.8× 3.9k 1.0× 2.5k 0.9× 1.4k 0.8× 771 0.6× 435 10.6k
Jordi Benet‐Buchholz Spain 57 5.5k 0.7× 4.2k 1.0× 2.5k 0.9× 1.2k 0.7× 1.1k 0.9× 301 11.5k
Mary F. Mahon United Kingdom 64 12.7k 1.5× 7.9k 1.9× 3.0k 1.0× 2.5k 1.5× 1.1k 0.9× 543 17.4k
Eberhardt Herdtweck Germany 75 16.4k 2.0× 7.9k 1.9× 3.4k 1.2× 2.1k 1.2× 1.6k 1.3× 549 20.3k
Helmar Görls Germany 55 9.7k 1.2× 6.0k 1.5× 3.4k 1.2× 1.1k 0.6× 1.7k 1.4× 901 16.6k
Maren Pink United States 60 6.9k 0.8× 3.9k 1.0× 4.3k 1.5× 695 0.4× 777 0.6× 347 11.8k
Bas de Bruin Netherlands 64 12.5k 1.5× 7.3k 1.8× 2.5k 0.9× 1.6k 0.9× 833 0.7× 377 16.5k
Richard Goddard Germany 66 14.7k 1.8× 6.1k 1.5× 1.9k 0.7× 915 0.5× 1.9k 1.6× 433 17.2k
A.R. Cowley United Kingdom 53 5.1k 0.6× 2.8k 0.7× 2.2k 0.8× 578 0.3× 676 0.5× 235 8.0k
Lev N. Zakharov United States 62 8.3k 1.0× 4.3k 1.1× 5.1k 1.8× 423 0.3× 1.3k 1.0× 381 13.4k

Countries citing papers authored by M.R.J. Elsegood

Since Specialization
Citations

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

Fields of papers citing papers by M.R.J. Elsegood

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by M.R.J. Elsegood. 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 M.R.J. Elsegood. The network helps show where M.R.J. Elsegood may publish in the future.

Co-authorship network of co-authors of M.R.J. Elsegood

This figure shows the co-authorship network connecting the top 25 collaborators of M.R.J. Elsegood. A scholar is included among the top collaborators of M.R.J. Elsegood 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 M.R.J. Elsegood. M.R.J. Elsegood 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.
Sato, Shunsuke, et al.. (2025). Bi-Dentate Pyridyl Amine-Derived Complexes of Aluminium: Synthesis, Structure and ROP Capability. Catalysts. 15(12). 1119–1119.
2.
Song, Xinyi, Jun Zhang, Yue Zhang, et al.. (2025). A pyrene-based red-emissive AIEE fluorophore based on ICT and ESIPT effects for bioimaging. Dyes and Pigments. 244. 113111–113111.
3.
Elsegood, M.R.J., et al.. (2024). Reaction of Ph2C(X)(CO2H) (X = OH, NH2) with [VO(OR)3] (R = Et, nPr): structure, magnetic susceptibility and ROP capability. Dalton Transactions. 53(12). 5351–5355. 3 indexed citations
4.
Elsegood, M.R.J., et al.. (2024). Novel 4-[4-(4-methylpiperazin-1-yl)phenyl]-6-arylpyrimidine derivatives and their antitrypanosomal activities against T.brucei. Bioorganic & Medicinal Chemistry Letters. 109. 129825–129825. 1 indexed citations
6.
Pering, Samuel R., et al.. (2023). Band-gap engineering in methylammonium bismuth bromide perovskites for less-toxic perovskite solar cells. Materials Advances. 5(2). 625–631. 2 indexed citations
7.
Archer, Stuart A., et al.. (2023). An investigation into the adsorption mechanism of n-butanol by ZIF-8: a combined experimental and ab initio molecular dynamics approach. Physical Chemistry Chemical Physics. 25(29). 19911–19922. 7 indexed citations
8.
Elsegood, M.R.J., et al.. (2023). Transition-Metal-Free Continuous-Flow Synthesis of 2,5-Diaryl Furans: Access to Medicinal Building Blocks and Optoelectronic Materials. The Journal of Organic Chemistry. 89(1). 484–497. 3 indexed citations
9.
Dann, Sandra E., Jesús Ferrando‐Soria, Felix Plasser, et al.. (2022). Hierarchical Assembly of a Micro‐ and Macroporous Hydrogen‐Bonded Organic Framework with Tailored Single‐Crystal Size. Angewandte Chemie. 134(47). 6 indexed citations
10.
Montanaro, Stephanie, Piotr Pander, M.R.J. Elsegood, et al.. (2022). Simultaneous enhancement of thermally activated delayed fluorescence and photoluminescence quantum yield via homoconjugation. Journal of Materials Chemistry C. 10(16). 6306–6313. 14 indexed citations
11.
Dann, Sandra E., Jesús Ferrando‐Soria, Felix Plasser, et al.. (2022). Hierarchical Assembly of a Micro‐ and Macroporous Hydrogen‐Bonded Organic Framework with Tailored Single‐Crystal Size. Angewandte Chemie International Edition. 61(47). e202208677–e202208677. 15 indexed citations
12.
Feng, Xing, Jun Zhang, Zhen Hu, et al.. (2019). Pyrene-based aggregation-induced emission luminogens (AIEgen): structure correlated with particle size distribution and mechanochromism. Journal of Materials Chemistry C. 7(23). 6932–6940. 75 indexed citations
13.
Doan, Huan V., Fei Cheng, M.R.J. Elsegood, et al.. (2019). Using Supercritical CO2 in the Preparation of Metal-Organic Frameworks: Investigating Effects on Crystallisation. Crystals. 10(1). 17–17. 11 indexed citations
14.
Wang, Chuan‐Zeng, Xing Feng, Chong Wu, et al.. (2018). Pyrene-based color-tunable dipolar molecules: Synthesis, characterization and optical properties. Dyes and Pigments. 153. 125–131. 27 indexed citations
15.
Ignaszak, Anna, M.R.J. Elsegood, Takehiko Yamato, et al.. (2018). Vanadyl sulfates: molecular structure, magnetism and electrochemical activity. Dalton Transactions. 47(44). 15983–15993. 8 indexed citations
16.
Feng, Xing, Ying Li, Xuewen He, et al.. (2018). A Substitution‐Dependent Light‐Up Fluorescence Probe for Selectively Detecting Fe3+ Ions and Its Cell Imaging Application. Advanced Functional Materials. 28(35). 71 indexed citations
18.
Niu, Guangle, Ruoyao Zhang, Jacky W. Y. Lam, et al.. (2018). Specific Two-Photon Imaging of Live Cellular and Deep-Tissue Lipid Droplets by Lipophilic AIEgens at Ultralow Concentration. Chemistry of Materials. 30(14). 4778–4787. 165 indexed citations
19.
Ma, Jing, Ke‐Qing Zhao, Joseph A. Wright, et al.. (2014). Tri- and tetra-dentate imine vanadyl complexes: synthesis, structure and ethylene polymerization/ring opening polymerization capability. Dalton Transactions. 43(44). 16698–16706. 19 indexed citations
20.
Page, Philip C. Bulman, et al.. (2003). The Synthesis of Axially Chiral Resorcinarenes from Resorcinol Monoalkyl Ethers and Aldehyde Dimethylacetals.. ChemInform. 34(40). 1 indexed citations

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