The DOI matches its Crossref record.
Applications of Supramolecular Chemistry
Abstract
Applications of Supramolecular Chemistry introduces the use of non-covalent interactions and molecular recognition for many fields. Applications include the analysis of technically, medically, and environmentally important chemical compounds, their separation, purification and removal, and the design of new materials, including supramolecular elect
Overview
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Along with that, come stronger and more selective interactions, via a relationship between affinity and selectivity known to exist in ligand–target interactions in general [65,226].”
From Systems protobiology: origin of life in lipid catalytic networks (2018) · cites this paper as [226]
Citations
Cites
Still being checked.
Cited by
Sorted by citations
Review: A History of Cyclodextrins
Crini, G. (2014) · Chemical Reviews · doi:10.1021/cr500081p · Cited by 1,982
Biomedical Applications of Supramolecular Systems Based on Host–Guest Interactions
Ma, X., & Zhao, Y. (2014) · Chemical Reviews · doi:10.1021/cr500392w · Cited by 1,252
Photochromism into nanosystems: towards lighting up the future nanoworld.
Wang, L., & Li, Q. (2018) · Chemical Society Reviews · doi:10.1039/c7cs00630f · Cited by 407
Experimental Binding Energies in Supramolecular Complexes
Biedermann, F., & Schneider, H. (2016) · Chemical Reviews · doi:10.1021/acs.chemrev.5b00583 · Cited by 575
Self-citationRevisiting Fluorescent Calixarenes: From Molecular Sensors to Smart Materials
Kumar, R., Sharma, A. K., Singh, H., Suating, P., Kim, H. S., Sunwoo, K., Shim, I., Gibb, B. C., & Kim, J. S. (2019) · Chemical Reviews · doi:10.1021/acs.chemrev.8b00605 · Cited by 546
Cyclodextrins, from molecules to applications
Crini, G., Fourmentin, S., Fenyvesi, É., Torri, G., Fourmentin, M., & Morin‐Crini, N. (2018) · Environmental Chemistry Letters · doi:10.1007/s10311-018-0763-2 · Cited by 391
25th Anniversary Article: Supramolecular Materials for Regenerative Medicine
Boekhoven, J., & Stupp, S. I. (2014) · Advanced Materials · doi:10.1002/adma.201304606 · Cited by 328
Morin‐Crini, N., Winterton, P., Fourmentin, S., Wilson, L. D., Fenyvesi, É., & Crini, G. (2017) · Progress in Polymer Science · doi:10.1016/j.progpolymsci.2017.07.004 · Cited by 262
130 years of cyclodextrin discovery for health, food, agriculture, and the industry: a review
Morin‐Crini, N., Fourmentin, S., Fenyvesi, É., Lichtfouse, É., Torri, G., Fourmentin, M., & Crini, G. (2021) · Environmental Chemistry Letters · doi:10.1007/s10311-020-01156-w · Cited by 218
Nile Red Dye in Aqueous Surfactant and Micellar Solution
Kurniasih, I., Liang, H., Mohr, P. C., Khot, G., Rabe, J. P., & Mohr, A. (2015) · Langmuir · doi:10.1021/la504378m · Cited by 203
Systems protobiology: origin of life in lipid catalytic networks
Lancet, D., Zidovetzki, R., & Markovitch, O. (2018) · Journal of The Royal Society Interface · doi:10.1098/rsif.2018.0159 · Cited by 182
Lu, X., Li, X., Guo, K., Xie, T., Moorefield, C. N., Wesdemiotis, C., & Newkome, G. R. (2014) · Journal of the American Chemical Society · doi:10.1021/ja511341z · Cited by 122
Lindner, E., & Pendley, B. D. (2012) · Analytica Chimica Acta · doi:10.1016/j.aca.2012.11.022 · Cited by 119
Self-assembly of dynamic orthoester cryptates
Brachvogel, R., Hampel, F., & von Delius, M. (2015) · Nature Communications · doi:10.1038/ncomms8129 · Cited by 95
Hsu, S., Lin, Y., Chang, J., Liu, Y., & Lin, H. (2014) · Angewandte Chemie International Edition · doi:10.1002/anie.201307500 · Cited by 85
Recent advances and perspectives on supramolecular radical cages
Huang, B., Mao, L., Shi, X., & Yang, H. (2021) · Chemical Science · doi:10.1039/d1sc01618k · Cited by 84
Sayed, M., & Pal, H. (2015) · Journal of Materials Chemistry C · doi:10.1039/c5tc03321g · Cited by 83
Fu, J., Lee, Y., He, Y., & Chan, Y. (2015) · Angewandte Chemie International Edition · doi:10.1002/anie.201501507 · Cited by 82
Molecular Receptors for Recognition and Sensing of Nucleotides
Agafontsev, A. M., Ravi, A., Shumilova, T. A., Oshchepkov, A. S., & Kataev, E. A. (2018) · Chemistry - A European Journal · doi:10.1002/chem.201802978 · Cited by 70
Fundamentals and Applications of Cyclodextrins
Crini, G., Fourmentin, S., Fenyvesi, É., Torri, G., Fourmentin, M., & Morin‐Crini, N. (2018) · Environmental chemistry for a sustainable world · doi:10.1007/978-3-319-76159-6_1 · Cited by 59
Morin‐Crini, N., Fourmentin, S., Fenyvesi, É., Lichtfouse, É., Torri, G., Fourmentin, M., & Crini, G. (2020) · Environmental chemistry for a sustainable world · doi:10.1007/978-3-030-49308-0_1 · Cited by 51
Леонидович, П. П., Валерьевич, Г. В., & Stoikov, I. I. (2020) · International Journal of Molecular Sciences · doi:10.3390/ijms21041425 · Cited by 50
Structure elucidation of a complex CO 2 -based organic framework material by NMR crystallography
Leclaire, J., Poisson, G., Ziarelli, F., Pèpe, G., Fotiadu, F., Paruzzo, F. M., Rossini, A. J., Dumez, J., Elena‐Herrmann, B., & Emsley, L. (2016) · Chemical Science · doi:10.1039/c5sc03810c · Cited by 46
Zaitsev, S. Y. (2016) · Advances in Colloid and Interface Science · doi:10.1016/j.cis.2016.06.007 · Cited by 46
Fu, J., Lee, Y., He, Y., & Chan, Y. (2015) · Angewandte Chemie · doi:10.1002/ange.201501507 · Cited by 45
Selective recognition by novel calix system: ICT based chemosensor for metal ions
Bhatt, K., Makwana, B. A., Vyas, D. J., Mishra, D. R., & Jain, V. K. (2013) · Journal of Luminescence · doi:10.1016/j.jlumin.2013.10.004 · Cited by 42
Vertical Assembly of Giant Double‐ and Triple‐Decker Spoked Wheel Supramolecular Structures
Liu, D., Chen, M., Li, Y., Shen, Y., Huang, J. Y., Yang, X., Jiang, Z., Li, X., Newkome, G. R., & Wang, P. (2018) · Angewandte Chemie International Edition · doi:10.1002/anie.201809819 · Cited by 41
Hsu, S., Wu, F., Cheng, H., Huang, Y., Hsieh, Y., Tseng, D. T., Yeh, M., Hung, S., & Lin, H. (2016) · Advanced Healthcare Materials · doi:10.1002/adhm.201600342 · Cited by 40
Guest dependent dielectric properties of nickel( ii )-based supramolecular networks
Mendiratta, S., Usman, M., Luo, T., Lee, S., Lin, Y., & Lu, K. (2014) · CrystEngComm · doi:10.1039/c4ce00218k · Cited by 38
Ratiometric Detection of ATP by Fluorescent Cyclophanes with Bellows‐Type Sensing Mechanism
Agafontsev, A. M., Shumilova, T. A., Oshchepkov, A. S., Hampel, F., & Kataev, E. A. (2020) · Chemistry - A European Journal · doi:10.1002/chem.202001523 · Cited by 38
Li, Z., Leed, N. A., Dickson‐Karn, N. M., Dunbar, K. R., & Turró, C. (2013) · Chemical Science · doi:10.1039/c3sc52366g · Cited by 38
Ali, H., Alwan, B. A. M. A., Abdulrahman, A., Yue, D., & Hayat, A. (2025) · Materials Today · doi:10.1016/j.mattod.2025.06.016 · Cited by 32
Samoshin, A. V., Veselov, I. S., Chertkov, V. A., Yaroslavov, A. A., Grishina, G. V., Samoshina, N. M., & Samoshin, V. V. (2013) · Tetrahedron Letters · doi:10.1016/j.tetlet.2013.07.156 · Cited by 31
Adachi, K., Watanabe, K., & Yamazaki, S. (2014) · Industrial & Engineering Chemistry Research · doi:10.1021/ie5018817 · Cited by 31
Lascaux, A., Leener, G. D., Fusaro, L., Topić, F., Rissanen, K. T., Luhmer, M., & Jabin, I. (2015) · Organic & Biomolecular Chemistry · doi:10.1039/c5ob02067k · Cited by 31
Crini, G., Saintemarie, A. E., Rocchi, S., Fourmentin, M., Jeanvoine, A., Millon, L., & Morin‐Crini, N. (2017) · Heliyon · doi:10.1016/j.heliyon.2017.e00380 · Cited by 30
Analytical Applications of Transport Through Bulk Liquid Membranes
Diaconu, I., Ruse, E., Aboul-Enein, H. Y., & Bunaciu, A. A. (2015) · Critical Reviews in Analytical Chemistry · doi:10.1080/10408347.2015.1064759 · Cited by 28
Liu, X., Zheng, Y. F., Samoshina, N. M., Franz, A. H., Guo, X., & Samoshin, V. V. (2012) · Journal of Liposome Research · doi:10.3109/08982104.2012.698420 · Cited by 27
Chiral Supramolecular Selectors for Enantiomer Differentiation in Liquid Chromatography
Ciogli, A., Kotoni, D., Gasparrini, F., Pierini, M., & Villani, C. (2013) · Topics in current chemistry · doi:10.1007/128_2013_452 · Cited by 26
Gan, S., Zhong, L., Engelbrekt, C., Zhang, J., Han, D., Ulstrup, J., Chi, Q., & Niu, L. (2014) · Nanoscale · doi:10.1039/c4nr02308k · Cited by 26
Glucosamine-Based Supramolecular Nanotubes for Human Mesenchymal Cell Therapy
Talloj, S. K., Cheng, B., Weng, J.-P., & Lin, H. (2018) · ACS Applied Materials & Interfaces · doi:10.1021/acsami.8b03226 · Cited by 26
The Reciprocal Principle of Selectand-Selector-Systems in Supramolecular Chromatography †
Schurig, V. (2016) · Molecules · doi:10.3390/molecules21111535 · Cited by 25
Self-Assembly and Catalytic Reactivity of BINOL-Bridged Bis(phenanthroline) Metallocages
Cheng, K., Wang, S., Chen, Y.-S., & Chan, Y. (2017) · Inorganic Chemistry · doi:10.1021/acs.inorgchem.7b02540 · Cited by 23
Lu, X., Li, X., Guo, K., Wang, J., Huang, M., Wang, J., Xie, T., Moorefield, C. N., Cheng, S. Z. D., Wesdemiotis, C., et al. (2014) · Chemistry - A European Journal · doi:10.1002/chem.201404358 · Cited by 21
Nelli, S. R., Chakravarthy, R. D., Mohammed, M., & Lin, H. (2018) · RSC Advances · doi:10.1039/c8ra00929e · Cited by 20
Calixarene: a versatile scaffold for the development of highly sensitive biosensors
Quaglio, D., Polli, F., Plato, C. D., Cianfoni, G., Tortora, C., Mazzei, F., Botta, B., Calcaterra, A., & Ghirga, F. (2021) · Supramolecular chemistry · doi:10.1080/10610278.2021.2011283 · Cited by 20
Hazra, A., Gurunatha, K. L., & Maji, T. K. (2013) · Crystal Growth & Design · doi:10.1021/cg4009784 · Cited by 19
Liu, Y.-H., Hsu, S., Wu, F.-Y., Cheng, H., Yeh, M., & Lin, H. (2014) · Bioconjugate Chemistry · doi:10.1021/bc500299c · Cited by 19
Nandajan, P. C., Kim, H., Casado, S., Park, S. Y., & Gierschner, J. (2018) · The Journal of Physical Chemistry Letters · doi:10.1021/acs.jpclett.8b01562 · Cited by 19
Štimac, A., Tokić, M., Ljubetič, A., Vuletić, T., Šekutor, M., Požar, J., Leko, K., Hanževački, M., Frkanec, L., & Frkanec, R. (2019) · Organic & Biomolecular Chemistry · doi:10.1039/c9ob00488b · Cited by 19
A brief overview on supramolecular analytical chemistry of cucurbit[n]urils and hemicucurbit[n]urils
Mutihac, R., Bunaciu, A. A., Buschmann, H., & Mutihac, L. (2020) · Journal of Inclusion Phenomena and Macrocyclic Chemistry · doi:10.1007/s10847-020-01019-5 · Cited by 19
Smith, J. B., Camp, A. M., Farquhar, A. H., Kerr, S. H., Chen, C., & Miller, A. J. M. (2019) · Organometallics · doi:10.1021/acs.organomet.9b00462 · Cited by 17
Konter, A., Rostoll‐Berenguer, J., Besnard, C., Leforestier, B., & Mazet, C. (2025) · ACS Catalysis · doi:10.1021/acscatal.4c07646 · Cited by 16
Chakraborty, G., Ray, A. K., Singh, P. K., & Pal, H. (2020) · Photochemical & Photobiological Sciences · doi:10.1039/d0pp00103a · Cited by 16
Chakravarthy, R. D., Mohammed, M., & Lin, H. (2020) · Chemistry - An Asian Journal · doi:10.1002/asia.202000575 · Cited by 16
Reddersen, K., Finger, S., Zieger, M., Wiegand, C., Buschmann, H., Elsner, P. U., & Hipler, U. (2016) · Journal of Materials Science Materials in Medicine · doi:10.1007/s10856-016-5804-4 · Cited by 16
Separation of nitrophenols. Equilibriums in bi- and tri-phasic systems
Diaconu, I., Aboul-Enein, H. Y., Al-Omar, M. A., Nechifor, G., Ruse, E., Bunaciu, A. A., & Totu, E. E. (2010) · Arabian Journal of Chemistry · doi:10.1016/j.arabjc.2010.06.025 · Cited by 16
Ashwin, B. C. M. A., Vinothini, A., Thambusamy, S., & Mareeswaran, P. M. (2017) · ChemistrySelect · doi:10.1002/slct.201601939 · Cited by 15
Ali, S. M., & Shamim, S. (2015) · Magnetic Resonance in Chemistry · doi:10.1002/mrc.4250 · Cited by 15
Supramolecular and suprabiomolecular photochemistry: a perspective overview
Choudhury, S. D., & Pal, H. (2020) · Physical Chemistry Chemical Physics · doi:10.1039/d0cp03981k · Cited by 15
Supramolecular Membrane Chemistry
de Jesus, A. J., & Yin, H. H. (2016) · Elsevier eBooks · doi:10.1016/b978-0-12-409547-2.12572-7 · Cited by 14
Trans‐2‐Aminocyclohexanol derivatives as pH‐triggered conformational switches
Samoshin, V. V., Zheng, Y. F., & Liu, X. (2017) · Journal of Physical Organic Chemistry · doi:10.1002/poc.3689 · Cited by 12
Agafontsev, A. M., Oshchepkov, A. S., Shumilova, T. A., & Kataev, E. A. (2021) · Molecules · doi:10.3390/molecules26040980 · Cited by 12
Carboxylic decorated Schiff base complexes as metallotectons for hydrogen bonded 3D networks
Fondo, M., Doejo, J., García‐Deibe, A. M., Ocampo, N., & Sanmartín‐Matalobos, J. (2015) · Polyhedron · doi:10.1016/j.poly.2015.07.050 · Cited by 11
Dual photoreactivity of a new Rh2(II,II) complex for biological applications
Akhimie, R. N., White, J. K., & Turró, C. (2016) · Inorganica Chimica Acta · doi:10.1016/j.ica.2016.04.001 · Cited by 10
Chakraborty, G., Chattaraj, S., & Pal, H. (2022) · Journal of Photochemistry and Photobiology A Chemistry · doi:10.1016/j.jphotochem.2022.114266 · Cited by 9
Kashapov, R. R., Bekmukhametova, A., Zakharova, L. Y., Akhmetzyanova, Z. V., Popova, E. V., Solovieva, S. Е., Antipin, I. S., & Konovalov, A. I. (2017) · Macroheterocycles · doi:10.6060/mhc171146k · Cited by 9
Two sides to supramolecular drug delivery systems
Hu, X., & Wang, L. (2017) · Supramolecular chemistry · doi:10.1080/10610278.2017.1380280 · Cited by 9
Đaković, M. (2020) · Crystallography Reviews · doi:10.1080/0889311x.2020.1731803 · Cited by 8
The Analytical Separation of Enantiomers by Gas Chromatography on Chiral Stationary Phases
Juza, M., & Schurig, V. (2014) · Springer eBooks · doi:10.1007/978-3-642-54640-2_15 · Cited by 8
Hsu, S., Chakravarthy, R. D., Cheng, H., Wu, F.-Y., Lai, T.-S., & Lin, H. (2018) · New Journal of Chemistry · doi:10.1039/c7nj03565a · Cited by 7
Kuwabara, T., Tao, X., Guo, H., Katsumata, M., & Kurokawa, H. (2016) · Tetrahedron · doi:10.1016/j.tet.2016.01.001 · Cited by 6
Bayrakcı, M., & Yılmaz, B. (2018) · Journal of Inclusion Phenomena and Macrocyclic Chemistry · doi:10.1007/s10847-018-0786-0 · Cited by 6
Aakeröy, C. B., & Đaković, M. (2021) · Elsevier eBooks · doi:10.1016/b978-0-12-818192-8.00003-2 · Cited by 6
Metal Ion Sensing for Biomedical Uses
Magri, D. C., & Mallia, C. J. (2013) · Royal Society of Chemistry eBooks · doi:10.1039/9781849737821-00038 · Cited by 6
Hsu, S., Lin, Y., Chang, J., Liu, Y., & Lin, H. (2014) · Angewandte Chemie · doi:10.1002/ange.201307500 · Cited by 5
Biedermann, F. (2019) · Wiley eBooks · doi:10.1002/9783527814923.ch2 · Cited by 5
Molecular recognition for anion detection: Progress and environmental significance
Narkhede, H. I., Tupe, A. S., Kumbhare, M. N., Surana, A. R., & Khedkar, K. (2025) · Intelligent Pharmacy · doi:10.1016/j.ipha.2025.07.001 · Cited by 4
Vertical Assembly of Giant Double‐ and Triple‐Decker Spoked Wheel Supramolecular Structures
Liu, D., Chen, M., Li, Y., Shen, Y., Huang, J. Y., Yang, X., Jiang, Z., Li, X., Newkome, G. R., & Wang, P. (2018) · Angewandte Chemie · doi:10.1002/ange.201809819 · Cited by 4
Tar, A., Bãrboiu, M., Legrand, Y., & Luca, C. (2007) · Journal of Inclusion Phenomena and Macrocyclic Chemistry · doi:10.1007/s10847-007-9349-5 · Cited by 4
Ruminski, R. R., Malkan, R. M., Gonzalez, G. M., Powell, B. L., & Hiskey, M. A. (2016) · Inorganica Chimica Acta · doi:10.1016/j.ica.2016.07.002 · Cited by 4
(2012) · Egyptian Journal of Pure and Applied Science · doi:10.21608/ejaps.2012.186265 · Cited by 3
Polymer Families and Their Extended Activities
Gupta, T. K. (2017) · Springer eBooks · doi:10.1007/978-3-319-66405-7_4 · Cited by 3
Nanoparticles Based on Silver Chloride and Bambusuril[6] for the Fine-Tuning of Biological Activity
Turebayeva, P., Luchsheva, V., Fedorishin, D. A., Yerkassov, R., Бакибаев, А. А., Bolysbekova, S. M., Tugambayeva, T., Мубараковна, С. С., & Nurmukhanbetova, N. N. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms242216126 · Cited by 2
Ruminski, R. R., Canaria, J. A., & Padilla, R. (2013) · Inorganica Chimica Acta · doi:10.1016/j.ica.2013.03.016 · Cited by 2
A general informatic tool for treating solution equilibria in supramolecular chemistry
Salvio, R. (2026) · Journal of Mathematical Chemistry · doi:10.1007/s10910-026-01818-0 · Cited by 1
Supramolecular Metal Complexes for Imaging and Radiotherapy
Schatz, J., & Schühle, D. T. (2013) · Royal Society of Chemistry eBooks · doi:10.1039/9781849737821-00300 · Cited by 1
Ruminski, R. R., Kahrilas, G. A., & Schauer, B. M. (2015) · Inorganica Chimica Acta · doi:10.1016/j.ica.2015.03.001 · Cited by 1
Self-Assembled Nanomaterials Based on Perfluorophenyl-Capped Dipeptides
Lin, Y.-C., Shu-Min, H., Chang, J., Liu, Y., & Lin, H. (2014) · International Journal of Chemical Engineering and Applications · doi:10.7763/ijcea.2015.v6.456 · Cited by 1
Singh, H. K., & Sarma, M. (2023) · ChemPhysChem · doi:10.1002/cphc.202200928 · Cited by 1
Schurig, V. (2015) · Wiley eBooks · doi:10.1002/9783527678129.assep028 · Cited by 1
Alshahateet, S. F. (2016) · Molecular Crystals and Liquid Crystals · doi:10.1080/15421406.2015.1069445
Direct evidence of stress-induced chain proximity in a macromolecular complex
van Kesteren, S., Nikolaeva, T., As, H. V., & Dijksman, J. A. (2020) · Physical Review Materials · doi:10.1103/physrevmaterials.4.055603
Politi, A. T. (2021) · Liverpool John Moores University · doi:10.24377/ljmu.t.00014664
Agrawal, P. K., & Jacob, C. (2024) · Natural Product Communications · doi:10.1177/1934578x231219564
ElDin, N. B., Ali, N. M., El‐Rahman, M. K. A., & Shoeib, T. (2024) · Microchemical Journal · doi:10.1016/j.microc.2024.110727
Li, B., Li, Y., Shen, X. Y., Ge, Y., & Qi, Z. (2025) · ChemistrySelect · doi:10.1002/slct.202405879
Triazine‐Naphthalimide Cage for the Recognition of Nucleotides and Parallel G‐Quadruplex
Akhgar, M., & Kataev, E. A. (2026) · ChemistryEurope · doi:10.1002/ceur.202500198
Metadata
- Authors
- Schneider, H.
- Corresponding author
- Hans‐Jörg Schneider
- ORCID
- Hans‐Jörg Schneider
- Venue
- CRC Press eBooks
- Publisher
- CRC Press
- Published
- 2012-03-28
- OpenAlex
- W629465584
- Cited by
- 100
- References
- 0
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 2 · 2023: 2 · 2022: 1 · 2021: 6 · 2020: 9 · 2019: 4 · 2018: 12 · 2017: 10 · 2016: 11 · 2015: 11 · 2014: 13 · 2013: 8 · 2012: 3
- Type
- reference entry
- Language
- en
- Open access
- closed
- Locations
- CRC Press eBooks (publishedVersion)
- Topics
- Physical Sciences › Chemistry › Organic Chemistry › Supramolecular Chemistry and Complexes
- Physical Sciences › Materials Science › Biomaterials › Supramolecular Self-Assembly in Materials
- Physical Sciences › Chemistry › Physical and Theoretical Chemistry › Surface Chemistry and Catalysis
- Keywords
- supramolecular chemistry, non-covalent interactions, molecular recognition, chemical analysis, separation and purification, pollutant removal, supramolecular materials, supramolecular electronics
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review