Nicholas M. Hext

641 total citations
11 papers, 549 citations indexed

About

Nicholas M. Hext is a scholar working on Physical and Theoretical Chemistry, Organic Chemistry and Molecular Biology. According to data from OpenAlex, Nicholas M. Hext has authored 11 papers receiving a total of 549 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Physical and Theoretical Chemistry, 3 papers in Organic Chemistry and 3 papers in Molecular Biology. Recurrent topics in Nicholas M. Hext's work include Molecular Sensors and Ion Detection (3 papers), DNA and Nucleic Acid Chemistry (3 papers) and Advanced Chemical Physics Studies (3 papers). Nicholas M. Hext is often cited by papers focused on Molecular Sensors and Ion Detection (3 papers), DNA and Nucleic Acid Chemistry (3 papers) and Advanced Chemical Physics Studies (3 papers). Nicholas M. Hext collaborates with scholars based in United Kingdom, United States and Switzerland. Nicholas M. Hext's co-authors include Thomas W. Bell, Mark Mascal, Ralf Warmuth, J.P. Turkenburg, M. H. Moore, Alisher Khasanov, Alexander J. Blake, Roger W. Alder, David E. Hibbs and Олег В. Шишкин and has published in prestigious journals such as Chemical Society Reviews, Chemical Communications and The Journal of Organic Chemistry.

In The Last Decade

Nicholas M. Hext

11 papers receiving 534 citations

Peers

Nicholas M. Hext
Vladimir Sidorov United States
Suk Kyu Chang South Korea
Andrei Andrievsky United States
M. Scott Goodman United States
Ana I. Oliva Spain
Sunggoo Yun South Korea
J.‐P. Desvergne France
Punidha Sokkalingam United States
Kyoung‐Jin Chang South Korea
Gosia M. Hübner Germany
Vladimir Sidorov United States
Nicholas M. Hext
Citations per year, relative to Nicholas M. Hext Nicholas M. Hext (= 1×) peers Vladimir Sidorov

Countries citing papers authored by Nicholas M. Hext

Since Specialization
Citations

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

Fields of papers citing papers by Nicholas M. Hext

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Nicholas M. Hext. 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 Nicholas M. Hext. The network helps show where Nicholas M. Hext may publish in the future.

Co-authorship network of co-authors of Nicholas M. Hext

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

All Works

11 of 11 papers shown
1.
Bell, Thomas W. & Nicholas M. Hext. (2005). Supramolecular Optical Chemosensors for Organic Analytes. ChemInform. 36(14). 34 indexed citations
2.
Bell, Thomas W. & Nicholas M. Hext. (2004). Supramolecular optical chemosensors for organic analytes. Chemical Society Reviews. 33(9). 589–98. 294 indexed citations
3.
Batsanov, Andrei S., Alexander J. Blake, Nicholas M. Hext, & Mark Mascal. (2001). Structure and polymorphism of the 10.10.10 Simmons and Park cryptand. Chemical Communications. 127–128. 4 indexed citations
4.
Mascal, Mark, et al.. (1999). The G−C DNA Base Hybrid:  Synthesis, Self-Organization and Structural Analysis. The Journal of Organic Chemistry. 64(23). 8479–8484. 34 indexed citations
5.
Hext, Nicholas M., Jens Hansen, Alexander J. Blake, et al.. (1998). Azatriquinanes:  Synthesis, Structure, and Reactivity. The Journal of Organic Chemistry. 63(17). 6016–6020. 29 indexed citations
6.
Bell, Thomas W., Nicholas M. Hext, & Alisher Khasanov. (1998). Binding biomolecules with designed, hydrogen-bonding receptors. Pure and Applied Chemistry. 70(12). 2371–2377. 22 indexed citations
7.
Gerson, Fabian, et al.. (1998). The Radical Cation of Azatriquinane: An ESR Study. Helvetica Chimica Acta. 81(10). 1749–1753. 5 indexed citations
8.
Mascal, Mark, et al.. (1996). Azatriquinane, azatriquinacene, and a remarkable dimerization product. Tetrahedron Letters. 37(1). 131–134. 13 indexed citations
9.
Mascal, Mark, Nicholas M. Hext, Ralf Warmuth, M. H. Moore, & J.P. Turkenburg. (1996). Programming a Hydrogen‐Bonding Code for the Specific Generation of a Supermacrocycle. Angewandte Chemie International Edition in English. 35(19). 2204–2206. 89 indexed citations
10.
Alder, Roger W., et al.. (1994). Intermediates for the synthesis of linear chains of 1,2:4,5-fused cyclohexa-1,4-diene rings and beltenes by repeated Diels–Alder reactions. Journal of the Chemical Society Perkin Transactions 1. 3071–3077. 9 indexed citations
11.
Alder, Roger W., et al.. (1988). Strongly basic medium-ring diamines which mimic gas phase behaviour in solution: 1,6-dimethyl-1,6-diazacyclodecane. Journal of the Chemical Society Chemical Communications. 1528–1528. 16 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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