Roger Bishop

2.6k total citations
150 papers, 2.0k citations indexed

About

Roger Bishop is a scholar working on Organic Chemistry, Physical and Theoretical Chemistry and Inorganic Chemistry. According to data from OpenAlex, Roger Bishop has authored 150 papers receiving a total of 2.0k indexed citations (citations by other indexed papers that have themselves been cited), including 82 papers in Organic Chemistry, 79 papers in Physical and Theoretical Chemistry and 73 papers in Inorganic Chemistry. Recurrent topics in Roger Bishop's work include Crystallography and molecular interactions (77 papers), Crystal structures of chemical compounds (53 papers) and Crystallization and Solubility Studies (22 papers). Roger Bishop is often cited by papers focused on Crystallography and molecular interactions (77 papers), Crystal structures of chemical compounds (53 papers) and Crystallization and Solubility Studies (22 papers). Roger Bishop collaborates with scholars based in Australia, Singapore and United Kingdom. Roger Bishop's co-authors include M.L. Scudder, Donald C. Craig, Ian Dance, Solhe F. Alshahateet, Alison T. Ung, David D. MacNicol, Christopher E. Marjo, Stephen C. Hawkins, Mohan Bhadbhade and J. P. Ashmore and has published in prestigious journals such as Journal of the American Chemical Society, Chemical Society Reviews and Accounts of Chemical Research.

In The Last Decade

Roger Bishop

146 papers receiving 2.0k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Roger Bishop Australia 23 1.2k 1.0k 924 759 402 150 2.0k
B.R. Bhogala India 16 1.3k 1.0× 946 0.9× 496 0.5× 834 1.1× 255 0.6× 21 1.7k
R.K.R. Jetti India 24 798 0.6× 580 0.6× 537 0.6× 579 0.8× 271 0.7× 39 1.5k
Emmanuel Aubert France 27 804 0.7× 540 0.5× 725 0.8× 741 1.0× 520 1.3× 112 2.3k
N. Schultheiss United States 18 2.0k 1.6× 911 0.9× 750 0.8× 1.6k 2.1× 320 0.8× 32 2.6k
Dominik Cinčić Croatia 28 1.7k 1.4× 1.1k 1.1× 711 0.8× 972 1.3× 221 0.5× 82 2.4k
Hiroko Suezawa Japan 17 600 0.5× 441 0.4× 737 0.8× 309 0.4× 440 1.1× 51 1.5k
J.A. Bis United States 7 1.2k 1.0× 535 0.5× 349 0.4× 1.0k 1.3× 213 0.5× 9 1.5k
Amit Delori United Kingdom 16 1.3k 1.0× 418 0.4× 492 0.5× 1.5k 2.0× 333 0.8× 24 2.0k
Mátyás Czugler Hungary 27 442 0.4× 746 0.7× 1.6k 1.8× 494 0.7× 604 1.5× 161 2.4k
Κ. Ravikumar India 23 510 0.4× 566 0.5× 1.1k 1.2× 578 0.8× 255 0.6× 283 2.3k

Countries citing papers authored by Roger Bishop

Since Specialization
Citations

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

Fields of papers citing papers by Roger Bishop

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Roger Bishop

This figure shows the co-authorship network connecting the top 25 collaborators of Roger Bishop. A scholar is included among the top collaborators of Roger Bishop 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 Roger Bishop. Roger Bishop 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.
Williams, Steven G., Mohan Bhadbhade, Roger Bishop, & Alison T. Ung. (2017). Synthesis and Crystal Structure of Unexpected (1S,4R,5R,6S)-4-Cyano-2,2,6-trimethyl-3-azabicyclo[3.3.1]nonan-6-yl Acetate. Australian Journal of Chemistry. 70(12). 1269–1273. 1 indexed citations
2.
Bishop, Roger. (2015). Organic crystal engineering beyond the Pauling hydrogen bond. CrystEngComm. 17(39). 7448–7460. 32 indexed citations
3.
Bishop, Roger, et al.. (2009). A Metallocyclic Calixarene Wheel and Axle Inclusion Compound. Crystal Growth & Design. 9(3). 1334–1338. 10 indexed citations
4.
Bishop, Roger, et al.. (2008). 8-Methyl-5-methylene-2-oxotricyclo[5.3.1.13,9]dodecan-endo-8-ol. Acta Crystallographica Section E Structure Reports Online. 64(5). o841–o841.
5.
Bishop, Roger, et al.. (2008). Nodal equivalence of (O–H)6 and aromatic rings: a supramolecular cousin of Dianin's compound and β-hydroquinone1,2. CrystEngComm. 10(12). 1810–1810. 8 indexed citations
6.
Alshahateet, Solhe F., Roger Bishop, M.L. Scudder, et al.. (2005). New edge–edge packing motifs present in the crystal structures of a thia-bridged tetrabromo aryl host. CrystEngComm. 7(21). 139–142. 15 indexed citations
7.
Bishop, Roger, et al.. (2004). Pi–halogen dimer interactions and the inclusion chemistry of a new tetrahalo aryl host. Organic & Biomolecular Chemistry. 2(2). 175–182. 34 indexed citations
8.
Alshahateet, Solhe F., Roger Bishop, Donald C. Craig, & M.L. Scudder. (2004). Role of Double C−H···N Weak Hydrogen Bonding Motifs in N-Heteroaromatic Inclusion Chemistry. Crystal Growth & Design. 4(4). 837–844. 34 indexed citations
9.
Bishop, Roger, et al.. (2003). Analysis of pi–halogen dimer interactions present in a family of staircase inclusion compounds. CrystEngComm. 5(75). 422–428. 53 indexed citations
10.
Bishop, Roger, et al.. (2001). A New Lattice Inclusion Host Involving Double-stranded Columns of Diol Molecules [1]. Supramolecular chemistry. 13(1). 103–107. 3 indexed citations
11.
Alshahateet, Solhe F., Roger Bishop, Donald C. Craig, & M.L. Scudder. (2001). Dimeric C–H⋯N interactions and the crystal engineering of new inclusion host molecules. CrystEngComm. 3(48). 225–229. 26 indexed citations
12.
Bishop, Roger, et al.. (2000). Fine-control of Helical Tubuland Inclusion Properties through the Pendant Group Approach. Tetrahedron. 56(36). 6667–6673. 16 indexed citations
13.
Bishop, Roger, et al.. (1999). Complexation of Ethanol by a Helical Tubuland Diol Host. Structural Chemistry. 10(3). 169–176. 5 indexed citations
14.
Bishop, Roger, et al.. (1998). Systematic Structural Modification of a Pentacyclic Helical Tubuland Host Diol. Australian Journal of Chemistry. 50(11). 1053–1060. 3 indexed citations
15.
Bishop, Roger, et al.. (1997). Simple synthetic entries into the tricyclo[5.3.1.13,9]dodecane and 8-oxatetracyclo[5.4.1.13,10.05,9]tridecane ring systems. Journal of the Chemical Society Perkin Transactions 1. 2937–2937. 6 indexed citations
16.
Bishop, Roger, et al.. (1996). Ritter reactions. Part 11. The diverse reactivity of 5,10-(azenometheno)-5H-dibenzo[a,d]cyclohepten-11-yl amides with dimethyl acetylenedicarboxylate. Journal of the Chemical Society Perkin Transactions 1. 1859–1859. 6 indexed citations
17.
Bishop, Roger, Donald C. Craig, M.L. Scudder, Alan P. Marchand, & Zenghui Liu. (1995). Disorder versus symmetry in the helical tubuland inclusion host lattice—a successful trishomocubyl diol probe. Journal of the Chemical Society Perkin Transactions 2. 1295–1300. 9 indexed citations
18.
Bishop, Roger, et al.. (1994). Ritter reactions. X. Structure of a new multicyclic amide-benzene inclusion compound. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 20(4). 363–372. 3 indexed citations
19.
Bishop, Roger, et al.. (1993). Control of hydrogen bonding in the design of new diol lattice inclusion compounds. Supramolecular chemistry. 1(2). 171–178. 15 indexed citations
20.
Kim, Sungho, Roger Bishop, Donald C. Craig, Ian Dance, & M.L. Scudder. (1990). Formation and crystal structure of a novel azabishomotwistane. The Journal of Organic Chemistry. 55(1). 355–358. 3 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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