Rui‐Lian Lin

830 total citations
53 papers, 666 citations indexed

About

Rui‐Lian Lin is a scholar working on Organic Chemistry, Spectroscopy and Physical and Theoretical Chemistry. According to data from OpenAlex, Rui‐Lian Lin has authored 53 papers receiving a total of 666 indexed citations (citations by other indexed papers that have themselves been cited), including 49 papers in Organic Chemistry, 37 papers in Spectroscopy and 33 papers in Physical and Theoretical Chemistry. Recurrent topics in Rui‐Lian Lin's work include Supramolecular Chemistry and Complexes (47 papers), Molecular Sensors and Ion Detection (35 papers) and Crystallography and molecular interactions (33 papers). Rui‐Lian Lin is often cited by papers focused on Supramolecular Chemistry and Complexes (47 papers), Molecular Sensors and Ion Detection (35 papers) and Crystallography and molecular interactions (33 papers). Rui‐Lian Lin collaborates with scholars based in China, United Kingdom and Australia. Rui‐Lian Lin's co-authors include Jing‐Xin Liu, Wen‐Qi Sun, Zhu Tao, Xin Xiao, Mingfu Ye, Wenrui Yao, Qian‐Jiang Zhu, Sai‐Feng Xue, Kai Chen and Xinhua Liu and has published in prestigious journals such as Journal of Agricultural and Food Chemistry, Scientific Reports and Chemical Engineering Journal.

In The Last Decade

Rui‐Lian Lin

52 papers receiving 662 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Rui‐Lian Lin China 17 479 337 281 257 159 53 666
Tomoaki Hinoue Japan 13 315 0.7× 239 0.7× 394 1.4× 161 0.6× 136 0.9× 22 687
Ronny Tepper Germany 8 286 0.6× 173 0.5× 161 0.6× 338 1.3× 180 1.1× 9 584
Yiliang Wang China 9 609 1.3× 367 1.1× 377 1.3× 125 0.5× 173 1.1× 12 833
Thanthapatra Bunchuay Thailand 15 240 0.5× 259 0.8× 236 0.8× 168 0.7× 131 0.8× 45 534
Matthew S. Vickers United Kingdom 6 366 0.8× 276 0.8× 284 1.0× 77 0.3× 111 0.7× 6 601
Rahul S. Patil United States 14 298 0.6× 123 0.4× 275 1.0× 88 0.3× 320 2.0× 24 555
Yang-Fan Guan China 12 460 1.0× 334 1.0× 300 1.1× 64 0.2× 129 0.8× 20 682
Guanfei Gong China 17 230 0.5× 364 1.1× 548 2.0× 94 0.4× 241 1.5× 36 772
Qian‐Shou Zong China 15 592 1.2× 393 1.2× 386 1.4× 54 0.2× 96 0.6× 34 841
Songhui Chen China 6 807 1.7× 552 1.6× 383 1.4× 144 0.6× 68 0.4× 7 911

Countries citing papers authored by Rui‐Lian Lin

Since Specialization
Citations

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

Fields of papers citing papers by Rui‐Lian Lin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Rui‐Lian Lin. 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 Rui‐Lian Lin. The network helps show where Rui‐Lian Lin may publish in the future.

Co-authorship network of co-authors of Rui‐Lian Lin

This figure shows the co-authorship network connecting the top 25 collaborators of Rui‐Lian Lin. A scholar is included among the top collaborators of Rui‐Lian Lin 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 Rui‐Lian Lin. Rui‐Lian Lin 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.
Wang, Xin, et al.. (2024). Chameleon-inspired supramolecular materials based on cucurbit[7]uril and viologens exhibiting full-color tunable photochromic behavior. Chemical Engineering Journal. 484. 149551–149551. 27 indexed citations
2.
Wang, Xiao‐Feng, Rui‐Lian Lin, Wen‐Qi Sun, et al.. (2024). Cucurbit[7]Uril‐Based Self‐Assembled Supramolecular Complex with Reversible Multistimuli‐Responsive Chromic Behavior and Controllable Fluorescence. Advanced Optical Materials. 12(23). 16 indexed citations
4.
Lin, Rui‐Lian, Lixia Chen, Zhu Tao, et al.. (2022). Encapsulation of l-valine, d-leucine and d-methionine by cucurbit[8]uril. CrystEngComm. 24(5). 1035–1040. 3 indexed citations
5.
Wang, Qin, Cheng Zhang, Wen‐Qi Sun, et al.. (2022). Inclusion Complexes of Cyclodextrins with 1-(4-Carboxybenzyl)-4-[2-(4-pyridyl)vinyl]pyridinium Chloride: Photochromism, Erasable Inkless Printing, and Color Tuning. The Journal of Physical Chemistry C. 126(44). 18900–18906. 12 indexed citations
6.
Wang, Qin, Kun Zhang, Rui‐Lian Lin, et al.. (2022). A light-responsive molecular switch based on cucurbit[7]uril and 1,1′-bis(benzyl)-4-[2-(4-pyridyl)-vinyl]-pyridinium dibromide displaying white light emission. Organic & Biomolecular Chemistry. 20(6). 1253–1259. 7 indexed citations
7.
Luo, Dan, Rong‐Guang Lin, Ningning Zhang, et al.. (2021). Chromic Properties of Carboxyphenyl Viologen Induced by Complexation in Cucurbit[7]uril. ChemistrySelect. 6(7). 1699–1704. 7 indexed citations
8.
Wang, Qin, et al.. (2021). Solid-State Supramolecular Inclusion Complexes of β-Cyclodextrin with Carboxyphenyl Viologens Showing Photochromic Properties. The Journal of Physical Chemistry C. 126(1). 844–850. 22 indexed citations
9.
Lin, Rui‐Lian, Yongping Dong, Min Tang, et al.. (2020). Selective Recovery and Detection of Gold with Cucurbit[n]urils (n = 5–7). Inorganic Chemistry. 59(6). 3850–3855. 34 indexed citations
10.
Zhao, Jie, Rui‐Lian Lin, Bing Bian, et al.. (2020). Selective recognition and determination of phenylalanine by a fluorescent probe based on cucurbit[8]uril and palmatine. Analytica Chimica Acta. 1104. 164–171. 22 indexed citations
12.
Zheng, Limei, et al.. (2019). Binding interactions of bisbenzimidazolyl derivatives with cyclohexanocucurbit[6]uril. Journal of Inclusion Phenomena and Macrocyclic Chemistry. 96(1-2). 125–135. 5 indexed citations
13.
Gao, Zhong‐Zheng, et al.. (2017). Host-guest complexation of cucurbit[8]uril with two enantiomers. Scientific Reports. 7(1). 44717–44717. 10 indexed citations
15.
Lin, Rui‐Lian, et al.. (2016). Aniline-containing guests recognized by α,α’,δ,δ’-tetramethyl-cucurbit[6]uril host. Scientific Reports. 6(1). 39057–39057. 23 indexed citations
16.
Sun, Wen‐Qi, et al.. (2015). Host–guest complexation of di-cyclohexanocucurbit[6]uril and hexa-cyclohexanocucurbit[6]uril with alkyldiammonium ions: a comparative study. Organic & Biomolecular Chemistry. 14(2). 674–679. 17 indexed citations
17.
Lin, Rui‐Lian, Wen‐Qi Sun, Wenrui Yao, Jing Zhu, & Jing‐Xin Liu. (2014). Anion concentration control in the self-assembly of symmetrical α,α′,δ,δ′-tetramethyl-cucurbit[6]uril-based tubular architectures. RSC Advances. 4(35). 18323–18323. 18 indexed citations
18.
Lin, Rui‐Lian, et al.. (2012). Inclusion of methylviologen in symmetrical α,α′,δ,δ′-tetramethyl-cucurbit[6]uril. RSC Advances. 2(20). 7754–7754. 14 indexed citations
19.
Chen, Kai, Rui‐Lian Lin, Wen‐Qi Sun, et al.. (2012). Ionic radius-dependent self-assembly of closed/opened molecular capsules based on pentacyclopentanocucurbit[5]uril. RSC Advances. 2(13). 5663–5663. 15 indexed citations
20.
Lin, Rui‐Lian, et al.. (2011). Acetate anion-selective encapsulation in the ellipsoidal cavity of symmetrical α,α′,δ,δ′-tetramethyl-cucurbit[6]uril. Supramolecular chemistry. 23(12). 829–834. 4 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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