The DOI matches its Crossref record; 206 of the 206 references it cites were found in a registry or an index.
Self‐Assembly in Natural and Unnatural Systems
Abstract
Although there are no fundamental factors hindering the development of nanoscale structures, there is a growing realization that “engineering down” approaches, in other words a reduction in the size of structures generated by lithographic techniques below the present lower limit of roughly 1 μm, may become impractical. It has, therefore, become increasingly clear that only by the development of a fundamental understanding of the self‐assembly of large‐scale biological structures, which exist and function at and beyond the nanoscale, downwards, and the extension of our knowledge regarding the chemical syntheses of small‐scale structures upwards, can the gap between the promise and the reality of nanosystems be closed. This kind of construction of nanoscale structures and nanosystems represents the so‐called “bottom up” or “engineering up” approach to device fabrication. Significant progress can be made in the development of nanoscience by transferring concepts found in the biological world into the chemical arena. Central to this mission is the development of simple chemical systems capable of instructing their own organization into large aggregates of molecules through their mutual recognition properties. The precise programming of these recognition events, and hence the correct assembly of the growing superstructure, relies on a fundamental understanding and the practical exploitation of non‐covalent bonding interactions between and within molecules. The science of supramolecular chemistry—chemistry beyond the molecule in its very broadest sense—has started to bridge the yawning gap between molecular and macro‐molecular structures. By utilizing inter‐actions as diverse as aromatic π–π stacking and metal–ligand coordination for the information source for assembly processes, chemists have, in the last decade, begun to use biological concepts such as self‐assembly to construct nanoscale structures and superstructures with a variety of forms and functions. Here, we provide a flavor of how self‐assembly operates in natural systems and can be harnessed in unnatural ones.
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Cites
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Patterns in Hydrogen Bonding: Functionality and Graph Set Analysis in Crystals
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Molecular Self-Assembly and Nanochemistry: a Chemical Strategy for the Synthesis of Nanostructures
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Cited by
Molecular Materials by Self‐Assembly of Porphyrins, Phthalocyanines, and Perylenes
Elemans, J. A. A. W., van Hameren, R., Nolte, R. J. M., & Rowan, A. E. (2006) · Advanced Materials · doi:10.1002/adma.200502498 · Cited by 668
Einander durchdringende Netze: geordnete, periodische Verschlingung
Batten, S. R., & Robson, R. (1998) · Angewandte Chemie · doi:10.1002/(sici)1521-3757(19980605)110:11<1558::aid-ange1558>3.0.co;2-7 · Cited by 466
Chen, S., & Kimura, K. (1999) · Langmuir · doi:10.1021/la9812828 · Cited by 362
Metadata
- Authors
- Philp, D., & Stoddart, J. F.
- Venue
- Angewandte Chemie International Edition in English
- Publisher
- Wiley
- Published
- 1996-06-17
- Volume
- 35
- Issue
- 11
- Pages
- 1154-1196
- ISSN
- 0570-0833 (ISSN-L)
- OpenAlex
- W2147011143
- Cited by
- 2,115
- References
- 206
- FWCI
- 122.05
- Type
- journal article
- Language
- en
- Open access
- closed
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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.