Student or educator? Sign up with your school email and get 6 months of Pro free.
CoChat
Sign Up
Cited by 1,018

The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.

Supramolecular systems chemistry

Open access
Mattia, Elio, Otto, Sijbren·2015·Nature Nanotechnology
DOI 10.1038/nnano.2014.337
Open this paper in CoChat — free account

Overview

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1038/nnano.2014.337

Cites

8 of 8 references verified0 citation errors · 0 not checkable

Statistics

Verification

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Citations

Cites

Show all 8 references

Research works printed but not linked: 48

  1. Pross, A. Toward a general theory of evolution: extending Darwinian theory to inanimate matter. J. Syst. Chem. 2, 1 (2011). · DOI
  2. Pascal, R. & Pross, A. The nature and mathematical basis for material stability in the chemical and biological worlds. J. Syst. Chem. 5, 3 (2014). · DOI
  3. Newth, D. & Finnigan, J. Emergence and self-organization in chemistry and biology. Aust. J. Chem. 59, 841–848 (2006). · doi:10.1071/ch06292
  4. Ludlow, R. F. & Otto, S. Systems chemistry. Chem. Soc. Rev. 37, 101–108 (2008). · DOI · Paper page
  5. Peyralans, J. J. P. & Otto, S. Recent highlights in systems chemistry. Curr. Opin. Chem. Biol. 13, 705–713 (2009). · DOI
  6. Nitschke, J. R. Systems chemistry: molecular networks come of age. Nature 462, 736–738 (2009). · DOI · Paper page
  7. Gibb, B. C. Teetering towards chaos and complexity. Nature Chem. 1, 17–18 (2009). · DOI
  8. Chichak, K. S. et al. Molecular Borromean rings. Science 304, 1308–1312 (2004). · doi:10.1126/science.1096914
  9. De Greef, T. F. A. et al. Supramolecular polymerization. Chem. Rev. 109, 5687–5754 (2009). · DOI · Paper page
  10. Li, J., Nowak, P. & Otto, S. Dynamic combinatorial libraries: from exploring molecular recognition to systems chemistry. J. Am. Chem. Soc. 135, 9222–9239 (2013). · DOI · Paper page
  11. Hamieh, S. et al. A “dial-a-receptor” dynamic combinatorial library. Angew. Chem. Int. Ed. 52, 12368–12372 (2013). · doi:10.1002/anie.201305744
  12. Ponnuswamy, N., Cougnon, F. B. L., Clough, J. M., Dan Pantoş, G. & Sanders, J. K. M. Discovery of an organic trefoil knot. Science 338, 783–785 (2012). · DOI
  13. Du, G., Moulin, E., Jouault, N., Buhler, E. & Giuseppone, N. Muscle-like supramolecular polymers: integrated motion from thousands of molecular machines. Angew. Chem. Int. Ed. 51, 12504–12508 (2012). · doi:10.1002/anie.201206571
  14. Lasic, D. D. Kinetic and thermodynamic effects on the structure and formation of phosphatidylcholine vesicles. Hepatology 13, 1010–1013 (1991). · doi:10.1002/hep.1840130538
  15. Guida, V. Thermodynamics and kinetics of vesicles formation processes. Adv. Colloid Interface Sci. 161, 77–88 (2010). · DOI
  16. Tayebi, L., Vashaee, D. & Parikh, A. N. Stability of uni- and multillamellar spherical vesicles. ChemPhysChem 13, 314–322 (2011). · DOI
  17. Stano, P. & Luisi, P. L. Achievements and open questions in the self-reproduction of vesicles and synthetic minimal cells. Chem. Commun. 46, 3639–3653 (2010). · DOI · Paper page
  18. Hanczyc, H. H. & Szostak, J. W. Replicating vesicles as models of primitive cell growth and division. Curr. Opin. Chem. Biol. 8, 660–664 (2004). · DOI
  19. Zepik, H. H. & Walde, P. Achievements and challenges in generating protocell models. ChemBioChem 9, 2771–2772 (2008). · DOI
  20. Loakes, D. & Holliger, P. Darwinian chemistry: towards the synthesis of a simple cell. Mol. BioSyst. 5, 686–694 (2009). · DOI
  21. Takahashi, H. et al. Autocatalytic membrane-amplification on a pre-existing vesicular surface. Chem. Commun. 46, 8791–8793 (2010). · DOI
  22. Korevaar, P. A. et al. Pathway complexity in supramolecular polymerization. Nature 481, 492–496 (2012). · DOI · Paper page
  23. Ogi, S., Sugiyasu, K., Manna, S., Samitsu, S. & Takeuchi, M. Living supramolecular polymerization realized through a biomimetic approach. Nature Chem. 6, 188–195 (2014). · DOI · Paper page
  24. Tevis, I. D. et al. Self-assembly and orientation of hydrogen-bonded oligothiophene polymorphs at liquid-membrane-liquid interfaces. J. Am. Chem. Soc. 133, 16486–16494 (2011). · doi:10.1021/ja204811b
  25. Giri, G. et al. Tuning charge transport in solution-sheared organic semiconductors using lattice strain. Nature 480, 504–508 (2011). · DOI · Paper page
  26. Hill, J. P. et al. Self-assembled hexa-peri-hexabenzocoronene graphitic nanotube. Science 304, 1481–1483 (2004). · DOI · Paper page
  27. Würthner, F., Yao, S. & Beginn, U. Highly ordered merocyanine dye assemblies by supramolecular polymerization and hierarchical self-organization. Angew. Chem. Int. Ed. 42, 3247–3250 (2003). · DOI · Paper page
  28. Lohr, A., Lysetska, M. & Würthner, F. Supramolecular stereomutation in kinetic and thermodynamic self-assembly of helical merocyanine dye nanorods. Angew. Chem. Int. Ed. 44, 5071–5074 (2005). · DOI
  29. Hirst, A. R. et al. Biocatalytic induction of supramolecular order. Nature Chem. 2, 1089–1094 (2010). · doi:10.1038/nchem.861
  30. Wang, Q. G. et al. Enzymatic hydrogelation to immobilize an enzyme for high activity and stability. Soft Matter 4, 550–553 (2008). · doi:10.1039/b715439a
  31. Boekhoven, J. et al. Catalytic control over supramolecular gel formation. Nature Chem. 5, 433–437 (2013). · DOI · Paper page
  32. Lohr, A. & Würthner, F. Evolution of homochiral helical dye assemblies: involvement of autocatalysis in the “majority-rules” effect. Angew. Chem. Int. Ed. 47, 1232–1236 (2008). · DOI
  33. Rubinov, B. et al. Transient fibril structures facilitating nonenzymatic self-replication. ACS Nano 6, 7893–7901 (2012). · DOI
  34. Carnall, J. M. A. et al. Mechanosensitive self-replication driven by self-organization. Science 327, 1502–1506 (2010). · DOI · Paper page
  35. Fialkowski, M. et al. Principles and implementations of dissipative (dynamic) self-assembly. J. Phys. Chem. B 110, 2482–2496 (2006). · DOI · Paper page
  36. Klajn, R., Bishop, K. J. M. & Grzybowski, B. A. Light-controlled self-assembly of reversible and irreversible nanoparticle suprastructures. Proc. Natl Acad. Sci. USA 104, 10305–10309 (2007). · doi:10.1073/pnas.0611371104
  37. Boekhoven, J. et al. Dissipative self-assembly of a molecular gelator by using a chemical fuel. Angew. Chem. Int. Ed. 49, 4825–4828 (2010). · DOI · Paper page
  38. Debnath, S., Roy, S. & Ulijn, R. V. Peptide nanofibers with dynamic instability through nonequilibrium biocatalytic assembly. J. Am. Chem. Soc. 135, 16789–16792 (2013). · DOI · Paper page
  39. Emond, M. et al. Energy propagation through a protometabolism leading to the local emergence of singular stationary concentration profiles. Chem. Eur. J. 18, 14375–14383 (2012). · DOI
  40. Krabbenborg, S. O. Surface Gradients Under Electrochemical Control Ch. 7, PhD thesis, Univ. Twente (2014). · doi:10.3990/1.9789036535755
  41. Kudernac, T. et al. Electrically driven directional motion of a four-wheeled molecule on a metal surface. Nature 479, 208–211 (2011). · DOI · Paper page
  42. Ragazzon, G., Baroncini, M., Silvi, S., Venturi, M. & Credi, A. Light-powered autonomous and directional molecular motion of a dissipative self-assembling system. Nature Nanotech. 10, 70–75 (2015). · doi:10.1038/nnano.2014.260
  43. Gasparini, G., Dal Molin, M. & Prins, L. J. Dynamic approaches towards catalyst discovery. Eur. J. Org. Chem. 2010, 2429–2440 (2010). · DOI
  44. Fanlo-Virgós, H., Roig Alba, A.-N., Hamieh, S., Colomb-Delsuc, M. & Otto, S. Transient substrate-induced catalyst formation in a dynamic molecular network. Angew. Chem. Int. Ed. 53, 11346–11350 (2014). · doi:10.1002/anie.201403480
  45. Nguyen, R., Allouche, L., Buhler, E. & Giuseppone, N. Dynamic combinatorial evolution within self-replicating supramolecular assemblies. Angew. Chem. Int. Ed. 48, 1093–1096 (2009). · DOI · Paper page
  46. Del Amo, V. & Philp, D. Integrating replication-based selection strategies in dynamic covalent systems. Chem. Eur. J. 16, 13304–13318 (2010). · DOI
  47. de Greef, T. F. A. & Meijer, E. W. Materials science: Supramolecular polymers. Nature 453, 171–173 (2008). · DOI · Paper page
  48. Klajn, R., Wesson, P. J., Bishop, K. J. M. & Grzybowski, B. A. Writing self-erasing images using metastable nanoparticle “inks”. Angew. Chem. Int. Ed. 48, 7035–7039 (2009). · DOI · Paper page

Cited by

See all 1,018

Metadata

Authors
Mattia, E., & Otto, S.
Venue
Nature Nanotechnology
Publisher
Springer Science and Business Media LLC
Published
2015-02
Volume
10
Issue
2
Pages
111-119
ISSN
  • 1748-3387 (ISSN-L)
  • 1748-3395
DOI
10.1038/nnano.2014.337
OpenAlex
W1994222180
Cited by
1,018
References
8
FWCI
45.85
Type
journal article
Language
en
Open access
green
Licence
www.springer.com/tdm (tdm)

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

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Supramolecular systems chemistry. https://app.cochat.ai/papers/10.1038/nnano.2014.337
The paper
Mattia, E., & Otto, S. (2015). Supramolecular systems chemistry. Nature Nanotechnology. https://doi.org/10.1038/nnano.2014.337

Data sources

Bibliographic data: Semantic Scholar, OpenAlex, Crossref.

Contains information from the Semantic Scholar Academic Graph Datasets, made available under the ODC Attribution License (ODC-BY 1.0).

Semantic Scholar’s data is described in: Kinney, R., et al. (2023). The Semantic Scholar Open Data Platform. arXiv:2301.10140.