File:Ligatio-covalens.jpg
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Ligatio-covalens.jpg (715 × 347 pixels, file size: 76 KB, MIME type: image/jpeg)
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Summary
[edit]DescriptionLigatio-covalens.jpg | Pictura ligationis covalentis duarum atomorum |
Date | |
Source | opera mea (own work) |
Author | Anselm H. C. Horn |
Permission (Reusing this file) |
opera mea -> vide licentiam (see license) |
Licensing
[edit]I, the copyright holder of this work, hereby publish it under the following license:
This file is licensed under the Creative Commons Attribution-Share Alike 2.5 Generic license.
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- to share – to copy, distribute and transmit the work
- to remix – to adapt the work
- Under the following conditions:
- attribution – You must give appropriate credit, provide a link to the license, and indicate if changes were made. You may do so in any reasonable manner, but not in any way that suggests the licensor endorses you or your use.
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Date/Time | Thumbnail | Dimensions | User | Comment | |
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current | 23:45, 25 September 2006 | 715 × 347 (76 KB) | Cornu (talk | contribs) | {{Information| |Description = Pictura ligationis covalentis duarum atomorum |Source = opera mea (own work) |Date = created 2006-09-25 |Author = Anselm H. C. Horn }} |
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- Amino acid
- Chemical bond
- Covalent bond
- Electron counting
- Hydrogen bond
- Ionic bonding
- Intermolecular force
- Metallic bonding
- Peptide bond
- Coordinate covalent bond
- Van der Waals force
- Glycosidic bond
- Conjugated system
- Aromaticity
- Double bond
- London dispersion force
- Chemical polarity
- Triple bond
- Electron deficiency
- Bound state
- Hückel's rule
- Hypervalent molecule
- Pi backbonding
- Single bond
- Homolysis (chemistry)
- Heterolysis (chemistry)
- Three-center two-electron bond
- Intercalation (chemistry)
- Dihydrogen bond
- Non-covalent interaction
- Bent bond
- Hyperconjugation
- Symmetric hydrogen bond
- Salt bridge (protein and supramolecular)
- Three-center four-electron bond
- Polyhedral skeletal electron pair theory
- Stacking (chemistry)
- Metal aromaticity
- Mechanically interlocked molecular architectures
- Homoaromaticity
- Hapticity
- Cation–π interaction
- Intramolecular force
- Aurophilicity
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