Prince Ravat

2.0k total citations
56 papers, 1.7k citations indexed

About

Prince Ravat is a scholar working on Organic Chemistry, Materials Chemistry and Spectroscopy. According to data from OpenAlex, Prince Ravat has authored 56 papers receiving a total of 1.7k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Organic Chemistry, 36 papers in Materials Chemistry and 10 papers in Spectroscopy. Recurrent topics in Prince Ravat's work include Synthesis and Properties of Aromatic Compounds (41 papers), Photochromic and Fluorescence Chemistry (15 papers) and Luminescence and Fluorescent Materials (11 papers). Prince Ravat is often cited by papers focused on Synthesis and Properties of Aromatic Compounds (41 papers), Photochromic and Fluorescence Chemistry (15 papers) and Luminescence and Fluorescent Materials (11 papers). Prince Ravat collaborates with scholars based in Germany, India and Switzerland. Prince Ravat's co-authors include Martin Baumgarten, Michal Jurı́ček, Tomáš Šolomek, Kläus Müllen, Daniel Häußinger, Xinliang Feng, Fangyuan Zhang, Manfred Wagner, Olivier Blacque and Junzhi Liu and has published in prestigious journals such as Journal of the American Chemical Society, Advanced Materials and Angewandte Chemie International Edition.

In The Last Decade

Prince Ravat

51 papers receiving 1.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Prince Ravat Germany 24 1.4k 1.0k 317 211 182 56 1.7k
Gianluigi Albano Italy 21 1.1k 0.8× 751 0.7× 236 0.7× 229 1.1× 184 1.0× 52 1.7k
Martin D. Peeks United Kingdom 19 703 0.5× 857 0.8× 363 1.1× 122 0.6× 143 0.8× 39 1.4k
Chengshuo Shen China 24 1.4k 1.0× 1.0k 1.0× 234 0.7× 405 1.9× 136 0.7× 65 1.7k
Michel Rickhaus Switzerland 17 1.2k 0.9× 800 0.8× 216 0.7× 312 1.5× 77 0.4× 39 1.5k
Young Mo Sung South Korea 27 1.2k 0.9× 1.6k 1.6× 373 1.2× 182 0.9× 176 1.0× 64 2.1k
Hayato Sakai Japan 26 938 0.7× 1.3k 1.3× 601 1.9× 265 1.3× 120 0.7× 81 1.9k
Ana‐Maria Krause Germany 21 803 0.6× 1.1k 1.1× 768 2.4× 183 0.9× 122 0.7× 37 1.8k
Rosenildo Corrêa da Costa United Kingdom 18 1.5k 1.1× 1.1k 1.1× 598 1.9× 273 1.3× 283 1.6× 31 2.2k
Carlos M. Cruz Spain 18 1.2k 0.9× 1.1k 1.1× 237 0.7× 256 1.2× 141 0.8× 63 1.6k
Kais Dhbaibi France 14 993 0.7× 839 0.8× 150 0.5× 305 1.4× 194 1.1× 19 1.2k

Countries citing papers authored by Prince Ravat

Since Specialization
Citations

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

Fields of papers citing papers by Prince Ravat

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Prince Ravat

This figure shows the co-authorship network connecting the top 25 collaborators of Prince Ravat. A scholar is included among the top collaborators of Prince Ravat 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 Prince Ravat. Prince Ravat 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
2.
Saha, Priyanka, Nicolas Chrysochos, Ivo Krummenacher, et al.. (2025). Thienylene‐Based Diradicaloids: Electrochromic Ring‐Closing of Dithienylethene‐Based Bis‐Amidinium Cation. Chemistry - A European Journal. 31(72). e02914–e02914.
4.
Radacki, Krzysztof, et al.. (2024). Helically twisted nanoribbons via stereospecific annulative π-extension reaction employing [7]helicene as a molecular wrench. Chemical Science. 15(30). 11737–11747. 12 indexed citations
5.
Mehta, Sakshi, Ivo Krummenacher, Abhishake Mondal, et al.. (2023). Bis-[cyclic(alkyl)(amino)carbene]-derived diradicals. Chemical Communications. 60(13). 1739–1742. 2 indexed citations
6.
Blacque, Olivier, et al.. (2023). Dimethylnonacethrene – en route to a magnetic switch. Chemical Communications. 59(50). 7743–7746. 3 indexed citations
7.
Saha, Priyanka, Nicolas Chrysochos, Ivo Krummenacher, et al.. (2023). Bis‐Olefin Based Crystalline Schlenk Hydrocarbon Diradicals with a Triplet Ground State. Angewandte Chemie International Edition. 62(45). e202311868–e202311868. 13 indexed citations
8.
Chrysochos, Nicolas, Ivo Krummenacher, Ganesan Prabusankar, et al.. (2023). Introducing an orthogonally polarized electron-rich alkene: synthesis of a zwitterionic boron-containing π-conjugated system. Chemical Communications. 59(82). 12350–12353. 2 indexed citations
9.
Saha, Priyanka, Nicolas Chrysochos, Ivo Krummenacher, et al.. (2023). Von bis‐Olefin‐abgeleitete kristalline, diradikalische Schlenk‐Kohlenwasserstoffe mit einem Triplett‐Grundzustand. Angewandte Chemie. 135(45).
10.
Zhang, Fangyuan, et al.. (2023). Efficient Narrowband Circularly Polarized Light Emitters Based on 1,4‐B,N‐embedded Rigid Donor–Acceptor Helicenes. Angewandte Chemie. 135(16). 7 indexed citations
11.
Häußinger, Daniel, et al.. (2022). Nonacethrene Unchained: A Cascade to Chiral Contorted Conjugated Hydrocarbon with Two sp 3 -Defects. SHILAP Revista de lepidopterología. 2(7). 1616–1626. 10 indexed citations
12.
Mehta, Sakshi, Nicolas Chrysochos, Ivo Krummenacher, et al.. (2022). A bis-NHC–CAAC dimer derived dicationic diradical. Chemical Science. 13(42). 12533–12539. 10 indexed citations
13.
Zhang, Fangyuan, Ivo Krummenacher, Sakshi Mehta, et al.. (2021). Anionic Boron- and Carbon-Based Hetero-Diradicaloids Spanned by a p-Phenylene Bridge. Journal of the American Chemical Society. 143(10). 3687–3692. 49 indexed citations
14.
Ravat, Prince, Olivier Blacque, & Michal Jurı́ček. (2019). Benzo[cd]triangulene: A Spin 1/2 Graphene Fragment. The Journal of Organic Chemistry. 85(1). 92–100. 20 indexed citations
15.
Šolomek, Tomáš, Prince Ravat, & Michal Jurı́ček. (2019). ‘Forbidden’ Electrocyclizations of Diradicaloids. Trends in Chemistry. 1(7). 705–706. 6 indexed citations
16.
Ravat, Prince, Tomáš Šolomek, Daniel Häußinger, Olivier Blacque, & Michal Jurı́ček. (2018). Dimethylcethrene: A Chiroptical Diradicaloid Photoswitch. Journal of the American Chemical Society. 140(34). 10839–10847. 100 indexed citations
17.
Šolomek, Tomáš, Prince Ravat, Zhongyu Mou, Miklós Kertész, & Michal Jurı́ček. (2018). Cethrene: The Chameleon of Woodward–Hoffmann Rules. The Journal of Organic Chemistry. 83(8). 4769–4774. 41 indexed citations
18.
Ravat, Prince, et al.. (2017). Configurational Stability of [5]Helicenes. Organic Letters. 19(14). 3707–3710. 88 indexed citations
19.
Ravat, Prince, Tomáš Šolomek, Michel Rickhaus, et al.. (2015). Cethrene: A Helically Chiral Biradicaloid Isomer of Heptazethrene. Angewandte Chemie International Edition. 55(3). 1183–1186. 112 indexed citations
20.
Ravat, Prince, Tomáš Šolomek, Michel Rickhaus, et al.. (2015). Cethren: ein helikal‐chirales Biradikaloid‐Isomer von Heptazethren. Angewandte Chemie. 128(3). 1198–1202. 25 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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