Talk:Supramolecular chemistry

Why supramolecular chemistry, not supramolecular science?

I wonder if the article can be more appropriately titled as 'Supramolecular Science' or just 'supramolecules' after all the subject is multidisciplinary and definitely not limited to conventional chemistry Hallenrm (talk) 08:54, 20 April 2010 (UTC)

Unverified Claims or Possible Original Research

The section I have marked does not cite sources which corroborate that those listed are, in fact, subsections of Supramolecular Chemistry. A source, such as one from Lehn or Cram or, well, anyone reputable, would help.  Jeremiah (talk·cont) 16:12, 26 December 2008 (UTC)

that tag is not helpful. The points you raise should be addressed on the specialist page with each segment (only the part on templated synthesis does not have a specialist page). I have seen a Lehn reference on at least three pages. No point in duplicating references V8rik (talk) 20:34, 26 December 2008 (UTC)

If there was a large banner that just said "Who says this?" I would have used it. Otherwise I would have to tag each paragraph with and it would make the whole section look like shit. If you'd like to avail yourself of something more useful than suggesting a tag is unhelpful, perhaps you could dig up that Lehn reference you seem to be aware of on at least 3 pages and posting it in the appropriate location.  Jeremiah (talk·cont) 18:48, 27 December 2008 (UTC)

• I apologize, my previous entry was unhelpful and brash. The tag does does necessarily describe each paragraph, but nevertheless there are several subsections (or paragraphs) within the section, thus I employ a full tag. The following sections do not contain references to supramolecular chemistry in them (if they contain any references at all). Resolve the reference issues therein or cite the appropriate reference in the paragraph and I'll consider the issue resolved.

Template-directed synthesis

Biomimetics

Molecular imprinting

 Jeremiah (talk·cont) 15:56, 29 December 2008 (UTC)

• Thanks for being considerate. Molecular imprinting appears to be a subset of molecular recognition. I still prefer you use

tags at the appropriate places instead of the current tag. That would be more to the point. V8rik (talk) 21:42, 29 December 2008 (UTC)

• If we can cut it back to just one paragraph, as opposed to three, I'd be happy to use as opposed to a full tag. As for molecular imprinting being a component of molecular recognition, it certainly is. The problem being, this is an article about supramolecular chemistry - which generally doesn't include (though it should) protein-substrate interactions -- this article presents it as an entirely synthetic concept. I would think that a reference could easily be found where synthetic molecular imprinting has been done under the penumbra of "supramolecular chemistry." Such a reference would be excellent.  Jeremiah (talk·cont) 16:27, 2 January 2009 (UTC)

Dumb Down

Think you could possibly dumb this down a bit. I understand it, but going on scienceforums.net and explaining it to someone is much of an annoyance. --Cyberman 08:24, 11 July 2005 (UTC)

I hope that my revisions helped. I attempted to remove content that simply described self-assembly and not the broader topic of supramolecular chemistry. There is a self-assembly topic for this content. I also tried to remove content that was repeated. --M_stone 19:14, 11 March 2006

Cycloaddition of trans-1,2-bis(4-pyridyl)ethylene (already in green chemistry)

this edit will have to go, it is also included in green chemistry. Try to limit specific content to just one page V8rik 15:21, 2 May 2006 (UTC)

Okay, I'm sorry. I just thought that it was applicable to both articles, but I'm still getting the hang of editing--thanks for the info. Mrestko 23:31, 2 May 2006 (UTC)

• First of all, welcome to Wiki! Also thanks for your consideration V8rik 19:06, 3 May 2006 (UTC)

• I think that this subject is too general to site specific examples. Instead I suggest linking it to another topic that is more specific to the example, such as green Chemistry perhaps. --M_stone 14:13, 4 May 2006

Definition of supramolecular chemistry

I wonder if the definition of supramolecular chemistry on this page is not broad enough. The IUPAC definition is rather narrow. A better definition might be found to include coordination complexes that still retain subunit function, but are definitely connected by covalent bonds. Polynuclear ruthenium and osmium complexes bridged by polyimine ligands require rather harsh conditions (refluxing DMF) to be broken, often resulting in decomposition, not reversible reaction behavior. There are other examples in the literature. For examples see: Balzani, V. et al. Chem. Rev. 1996, 96, 759. or Sauvage, J.-P. et al. Chem. Rev. 1994, 94, 993.

I think the definition is reasonably broad and well-supported. The non-covalent bonding requirement is crucial to avoid encompassing all areas of chemistry. M stone 22:26, 18 October 2006 (UTC)

New material and some organization.

I have added a lot of material in an attempt to cover more of the subject, since the article seemed to be rather focused on the synthetic chemical side of things. Other notable additions are a thermodynamics section (which is important since supramolecular thermodynamics has many differences to that of covalent chemistry), and a section listing important building blocks. I have tried to make this a better "jumping off" point for people looking for information.

It could still do with something about analytical techniques of particular interest to supramolecular chemistry (e.g. soft ionization MS methods, VT-NMR, UV-vis spectroscopy to measure CT complexes). Also, something about kinetics would be good, and although the pictures currently in are beautiful, it would be nice to have some that cover other aspects of the subject. I'm sure there are also a lot of details to add and copyedit to be done on my additions. Not to mention references to add (unfortunately I don't have easy access to a library and my old stuff is all boxed up so that's a bit of a PITA for me).

Any specific comments about my edit can be put here. I will check back. I think this is an extremely important article to have at a very high level, and I hope I've gone some of the way to make it so! • TheBendster (talk) 3 October 2007, 14:29 (UTC)

Overlap with Host-guest chemistrry

There is no obvious reason for this article and Host–guest chemistry being separate articles. I suggest that these two articles need to be replaced by a single article. A re-write rather than a merge is needed. Is anyone interesting in helping me to do this? Petergans (talk) 09:04, 17 April 2018 (UTC)

Help, please - nomenclature

The caption to the fifth figure from the left gives the included species as " p-xylylenediammonium ". This name comes from the original publication. Can someone please specify the IUPAC name. The chemical formula of the included compound is [H₃NCH₂(C₆H₄)CH₂NH₃]²⁺. Petergans (talk) 09:37, 13 May 2018 (UTC)

Gallery

If nobody objects, then I move the gallery to commons:Supramolecular chemistry. But some one image should remain here to illustrate the topic. Incnis Mrsi (talk) 20:35, 4 February 2019 (UTC)

Needs Examples

Many topics in the first half of the article do not mention any specific chemicals, reactions, or examples. It is hard to understand what the author really means. I am a person who thinks from concrete examples. Could someone just mention an example in each paragraph that does not have one? GoodExplainer (talk) 06:02, 6 October 2020 (UTC)

Merge and organization proposals

Two things are going on with this section: (i) an attempt to identify all articles that emphasize supramolecular chemistry and (ii) preparing to merge several.

Supramolecular chemistry is a large area as reflected in at least two books with that title, a journal, and a book series. The area is also somewhat vaguely defined.

Merge into supramolecular chemistry

• Non-covalent interaction (31 refs, most recent = 2016). To be merged with (redirected to) Supramolecular chemistry. Undefined by IUPAC.
• Molecular recognition (32, several >2020). How does this topic differ from Supramolecular chemistry? Undefined by IUPAC.
• Intermolecular force seems almost too broad. Redundant with many articles.

Merge into self-assembled monolayer

Parent: Self-assembled monolayer 45 refs, most recent 2012. We cannot merge this one but its interesting to see how this area has ceased to gain editing.

• • Coordination cage. 15 refs, some 2015. Fujita, Raymond. Seems to be a mature topic.
• Molecular self-assembly (23 refs, most recent = 2014). Focuses on surfaces, so maybe merge into Self-assembled monolayer. Undefined by IUPAC.
• Self-assembly. 50 refs. Some >2020. No IUPAC.

Components of supramolecular bonding

each to be mentioned in Supramolecular chemistry as well as H-bonding and coordination complexes

• • Cation–π interaction 34 refs, most recent = 2012. Probably cannot merge this one into the Borg, but again, notice that the editing stopped about the same as for others in this lot. Seems to be a mature topic.
  • Pi-stacking. 32 refs, one >2020. No IUPAC. Recently revised. Seems to be a mature topic.
  • van der Waals
    • Halogen bond. 38 refs, several >2020. A fairly popular topic (even if its not particularly useful, really just vdW's), so we dont merge this. Seems to be a mature topic.
    • Chalcogen bond. 16 refs, <2017. Student homework
    • Pnictogen bond. 10 refs, single author.
  • Salt bridge (protein and supramolecular). 26 refs, <2020.

Merge into supramolecular polymer

Parent: Supramolecular polymer. 50 refs, several >2020. Most of the article written by User:Injp20 in one edit. Their only contribution to Wikipedia.

• Macromolecular assembly. 18 refs, mostly 2016ish. Undefined by IUPAC. Merge into Supramolecular polymer.
• Two-dimensional polymer. 50 refs. Undefined by IUPAC. Merge into Supramolecular polymer. Imperfect fit.

Merge to Host-guest chemistry?

• Host-guest chemistry 45, several > 2020. Target of >100 links. Lead examples are crowns, calix's, cyclodextrins. Undefined by IUPAC. ChemRev 10.1021/cr5005315, 10.1021/cr200333h, 10.1021/acs.chemrev.9b00839, 10.1021/cr5006342, 10.1021/cr200213s
• Inclusion compound (also inclusion complex) (5 refs, most recent is 2010). Target of <50 links? How does this topic differ from Host-guest chemistry? Its lead examples are crowns, calix's, cyclodextrins. IUPAC def exists but not mentioned See "Supramolecular and molecular capsules, cages and containers" 10.1039/D4CS00761A
• Molecular encapsulation. 7 refs. Merge into Host-guest chemistry.
  • clathrate 12 refs, 2015 vintage. IUPAC def. Usually solids (zeolites, MOFs)
  • Cavitand 8 refs. = cyclodextrins + calixarenes + pillararenes + cucurbiturils.
    • Carcerand. 5 refs, <2000.
    • cyclodextrins
    • calixarenes. 24 refs, several >2020. IUPAC def
      • Resorcinarene. 12 refs <2015. Pyrogallolarenes. 4 refs
    • pillararenes. 24 refs, many primaries
    • cucurbiturils
    • Cryptophane. 4 refs.
    • cryptand 14 refs, most recent = 2001. Mature. Includes concept of "preorganization".
    • crown ethers. 18 refs, mostly pre 2000 it appears. Mature
  • Macromolecular cages. 11 refs. Pure homework assignment. Merge or redirect.
• addition compound, which redirects to Adduct, should be redirected to inclusion compound

Leave intact

• Supramolecular catalysis. 30 refs, most recent = 2013. A selective focus on a few results. Almost all enzyme-catalyzed reactions involve supramolecular aspects.
• Clathrate hydrate.

Peripheral

• Self-organization, a very broad topic including cosmology, physics...
• Mechanically interlocked molecular architectures. 13 refs (also see Rotaxane (see above), Catenane, Molecular knot, Molecular Borromean rings). Outside scope.
• Rotaxane. 24 refs, some 2015, most <2000. Many primaries. some supramolecular interactions involved in their formation but not particularly supramolecular.

--Smokefoot (talk) 19:21, 5 October 2024 (UTC)

I went ahead and merged Supramolecular assembly and supermolecule into this article.--Smokefoot (talk) 13:45, 9 October 2024 (UTC)