F.J. Burgess

456 total citations
16 papers, 332 citations indexed

About

F.J. Burgess is a scholar working on Organic Chemistry, Industrial and Manufacturing Engineering and Materials Chemistry. According to data from OpenAlex, F.J. Burgess has authored 16 papers receiving a total of 332 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Organic Chemistry, 3 papers in Industrial and Manufacturing Engineering and 3 papers in Materials Chemistry. Recurrent topics in F.J. Burgess's work include Inorganic and Organometallic Chemistry (11 papers), Synthetic Organic Chemistry Methods (9 papers) and Organometallic Complex Synthesis and Catalysis (4 papers). F.J. Burgess is often cited by papers focused on Inorganic and Organometallic Chemistry (11 papers), Synthetic Organic Chemistry Methods (9 papers) and Organometallic Complex Synthesis and Catalysis (4 papers). F.J. Burgess collaborates with scholars based in India and United Kingdom. F.J. Burgess's co-authors include Duncan Richards, A.V. Cûnliffe, J.R. MacCallum, J. V. Dawkins, Damien Thompson, David C. Sherrington and Marc J.M. Abadie and has published in prestigious journals such as Polymer, European Polymer Journal and Die Makromolekulare Chemie.

In The Last Decade

F.J. Burgess

16 papers receiving 305 citations

Peers

F.J. Burgess
H. Schnecko Germany
Samuel F. Reed United States
B. C. Anderson United States
H. L. Hsieh United States
Robert Alan Smith United States
S. Cesca Italy
H. Schnecko Germany
F.J. Burgess
Citations per year, relative to F.J. Burgess F.J. Burgess (= 1×) peers H. Schnecko

Countries citing papers authored by F.J. Burgess

Since Specialization
Citations

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

Fields of papers citing papers by F.J. Burgess

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F.J. Burgess. 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 F.J. Burgess. The network helps show where F.J. Burgess may publish in the future.

Co-authorship network of co-authors of F.J. Burgess

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

All Works

16 of 16 papers shown
1.
Burgess, F.J., A.V. Cûnliffe, Duncan Richards, & Damien Thompson. (1978). Organic halides as cationic initiators. Polymer. 19(3). 334–340. 37 indexed citations
2.
Burgess, F.J., A.V. Cûnliffe, & Duncan Richards. (1978). The synthesis of diene and vinyl copolymers containing predetermined quantities of polynuclear hydrocarbon or heterocyclic adducts—VII. European Polymer Journal. 14(7). 509–515. 4 indexed citations
3.
Burgess, F.J., A.V. Cûnliffe, J.R. MacCallum, & Duncan Richards. (1977). Reaction to effect the transformation of anionic polymerization into cationic polymerization: 1. Synthesis and reactivities of anionically generated bromine terminated polymers. Polymer. 18(7). 719–725. 65 indexed citations
4.
Burgess, F.J., A.V. Cûnliffe, J. V. Dawkins, & Duncan Richards. (1977). Reaction to effect the transformation of anionic polymerization into cationic polymerization: 3. Analysis of block copolymer formation by gel permeation chromatography. Polymer. 18(7). 733–740. 48 indexed citations
5.
Burgess, F.J., A.V. Cûnliffe, J.R. MacCallum, & Duncan Richards. (1977). Reactions to effect the transformation of anionic polymerization into cationic polymerization: 2. Synthesis and reactivities of anionically generated xylelene bromide-terminated polymers. Polymer. 18(7). 726–732. 45 indexed citations
6.
Burgess, F.J. & Duncan Richards. (1976). Preparation and reactions of polymeric Grignard compounds. Polymer. 17(11). 1020–1023. 24 indexed citations
7.
Abadie, Marc J.M., F.J. Burgess, A.V. Cûnliffe, & Duncan Richards. (1976). Transformation reactions in polymerization systems. II. anionic polymerization to free‐radical polymerization by the use of lead salts. Journal of Polymer Science Polymer Letters Edition. 14(8). 477–482. 16 indexed citations
8.
Burgess, F.J., A.V. Cûnliffe, Duncan Richards, & David C. Sherrington. (1976). Transformation reactions in polymerization systems. I. Anionic polymerization to cationic polymerization. Journal of Polymer Science Polymer Letters Edition. 14(8). 471–476. 26 indexed citations
15.
Burgess, F.J., et al.. (1974). The synthesis of diene and of vinyl copolymers containing predetermined quantities of polynuclear hydrocarbons or heterocyclic adducts. European Polymer Journal. 10(2). 193–197. 13 indexed citations
16.
Burgess, F.J., A.V. Cûnliffe, & Duncan Richards. (1973). The synthesis of diols based on the dimer of butadiene. Die Makromolekulare Chemie. 165(1). 39–50. 1 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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