Author Archive

Forty (one) years on – The pico-mac-nano and Chemdraw.

Sunday, June 1st, 2025

Last year I reminisced on the occasion of the 40th Anniversary of the Macintosh computer.[1] Four decades of advances in technology now mean I can do a fair amount of computational quantum modelling on a recent Mac (one from 2022 with M1 processor), and since then they have only got even (~2 or 3 times) faster with the M4 processor. Many of the recent calculations done for these blogs have included at least one or two that were done on the Mac. So I was intrigued to find that a real working version of the original Mac is about to be released for sale, but with a twist. Its called the “Pico-mac-nano” and from its name it is truly diminutive, being only 6.2 cm high – half the height of a can of cola – and with a 2″ LCD display. It comes with a connector for a keyboard and mouse, although currently it has no sound.

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References

  1. H. Rzepa, "The Macintosh computer at 40.", 2024. https://doi.org/10.59350/f11dr-93t29

S7I1+: The largest anomeric effect exhibited by sulfur.

Wednesday, May 21st, 2025

In this series of posts about the electronic effects in small sulfur rings[1] I have explored increasingly large induced geometric effects. Here is the largest so far, for the compound S7I1+[2]

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References

  1. H. Rzepa, "5-Imino-5λ<sup>4</sup>-heptathiepane 3-oxide. More exuberent anomeric effects.", 2025. https://doi.org/10.59350/rzepa.28615
  2. J. Passmore, G. Sutherland, P. Taylor, T.K. Whidden, and P.S. White, "Preparations and x-ray crystal structures of iodo-cyclo-heptasulfur hexafluoroantimonate(V) and hexafluoroarsenate(V), S7ISbF6 and S7IAsF6", Inorganic Chemistry, vol. 20, pp. 3839-3845, 1981. https://doi.org/10.1021/ic50225a048

5-Imino-5λ4-heptathiepane 3-oxide. More exuberent anomeric effects.

Tuesday, May 20th, 2025

The two previous  posts[1],[2] on the topic of anomeric effects in 7-membered sulfur rings illustrated how orbital interactions between the lone pairs in the molecules and S-S bonds produced widely varying S-S bond lengths in the molecules, some are shorter than normal (which is ~2.05Å for e.g. the S8 ring) by ~ 0.1Å and some are longer by ~0.24Å. Here we extend this to the unknown molecule shown below.

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References

  1. H. Rzepa, "Cycloheptasulfur sulfoxide, S<sub>7</sub>O – Anomeric effects galore!", 2025. https://doi.org/10.59350/rzepa.28515
  2. H. Rzepa, "Cyclo-Heptasulfur, S<sub>7</sub> – a classic anomeric effect discovered during a pub lunch!", 2025. https://doi.org/10.59350/rzepa.28407

Cycloheptasulfur sulfoxide, S7O – Anomeric effects galore!

Monday, May 19th, 2025

The monosulfoxide of cyclo-heptasulfur was reported along with cycloheptasulfur itself in 1977,[1] along with the remarks that “The δ modification of S7 contains bonds of widely differing length: this has never been observed before in an unsubstituted molecule. and “the same effect having also been observed in other sulfur rings (S8O, S7I1+ and S7O).” Here I take a look at the last of these other molecules, the monosulfoxide of S7, as a follow up to the commentary on S7 itself.[2]

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References

  1. R. Steudel, R. Reinhardt, and T. Sandow, "Bond Interaction in Sulfur Rings: Crystal and Molecular Structure of <i>cyclo</i>‐Heptasulfur Oxide, S<sub>7</sub>O", Angewandte Chemie International Edition in English, vol. 16, pp. 716-716, 1977. https://doi.org/10.1002/anie.197707161
  2. H. Rzepa, "Cyclo-Heptasulfur, S<sub>7</sub> – a classic anomeric effect discovered during a pub lunch!", 2025. https://doi.org/10.59350/rzepa.28407

Cyclo-Heptasulfur, S7 – a classic anomeric effect discovered during a pub lunch!

Friday, May 16th, 2025

Way back in 1977, the crystal structure of the sulfur ring S7 was reported.[1] The authors noted that “The δ modification of S7 contains bonds of widely differing length: this has never been observed before in an unsubstituted molecule.” No explanation was offered, although they note that similar effects have been observed in S8O, S7I+ and S7O. The S7 molecule was yesterday brought to my attention (thanks Derek!) over a pub lunch and in the time honoured manner of scientists, sketched out on a napkin – with a pen obtained from the waitress!. As an “organic chemist”, I immediately thought “anomeric effects”. And so indeed it has proven. A calculation using the MN15L/Def2-TZVPP DFT method and analysis using the Weinhold NBO7 procedure[2] reveals the following structure (with Cs symmetry) and indeed the four unique S-S distances are all different (experimental values in parentheses). So how does this arise?

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References

  1. R. Steudel, R. Reinhardt, and F. Schuster, "Crystal and Molecular Structure of <i>cyclo</i>‐Heptasulfur (δ‐S<sub>7</sub>)", Angewandte Chemie International Edition in English, vol. 16, pp. 715-715, 1977. https://doi.org/10.1002/anie.197707151
  2. H. Rzepa, "Cyclo-Heptasulfur, S7 – a classic anomeric effect discovered during a pub lunch!", 2025. https://doi.org/10.14469/hpc/15228

Referencing and citing a science-based blog post.

Tuesday, April 8th, 2025

Back in early 2012, I pondered about the relationships between a science-based blog post and a science-based journal article[1]. This was in part induced by my discovering a blog plugin called Kcite, which allow a journal articles to be appended to the blog in the form of a numbered reference list. The only required input for Kcite was the DOI of the article (as you can see earlier in this paragraph). For around 500 posts after that moment, I always strove to add such references to my posts. Around 2016, I started including references to data in the form of repository DOIs to sit alongside the journal references, but this feature stopped working a year or two later because of changes in the metadata resolved by the DOI. Kcite itself lasted until January 2024 for this blog, when a required update to the software running the blog (WordPress) meant that it no longer worked and had to be removed as a plugin. Two years ago, Rogue Scholar (Science blogging on steroids) started coming along to the rescue.[2] ,[3] It provides some amazing automated features and infrastructure to blogs; I will illustrate from those listed on the top page of Rogue Scholar itself: (more…)

References

  1. H. Rzepa, "The blog post as a scientific article: citation management", 2012. https://doi.org/10.59350/3pbz1-vcd67
  2. M. Fenner, "Automatically list all your publications in your blog", 2013. https://doi.org/10.53731/axtz227-73n18e7
  3. M. Fenner, "Rogue Scholar now shows citations of science blog posts", 2025. https://doi.org/10.53731/4bvt3-hmd07

Crystallography meets DFT Quantum modelling.

Monday, March 17th, 2025

X-ray crystallography is the technique of using the diffraction of x-rays by the electrons in a molecule to determine the positions of all the atoms in that molecule. Quantum theory teaches us that the electrons are to be found in shells around the atomic nuclei. There are two broad types, the outermost shell (also called the valence shell) and all the inner or core shells. The density of the core electrons is much higher (more compact) than the more diffuse valence shell for all but the hydrogen atom, which only has valence electrons. How does this relate to x-ray diffraction by electrons? Well, core electrons, because of their relative compactness, diffract X-rays more strongly than the valence electrons. This compactness of the core also means that its electron density distribution can be well (but not exactly) approximated by a sphere, with the nucleus at the centre of that sphere. And from this it follows that the density for each atom can be treated independently, the so-called IAM or independent atom model. For example all the carbon atoms in a molecule are approximated as having the same value for the electron density of their core shell. But the IAM approximation is much less good for hydrogen atoms, especially when they are attached to very polar atoms (Li, O, F, etc) and even atoms such as carbon or oxygen have noticeable deviations as illustrated in  figure 1 below. [1]

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References

  1. F. Kleemiss, O.V. Dolomanov, M. Bodensteiner, N. Peyerimhoff, L. Midgley, L.J. Bourhis, A. Genoni, L.A. Malaspina, D. Jayatilaka, J.L. Spencer, F. White, B. Grundkötter-Stock, S. Steinhauer, D. Lentz, H. Puschmann, and S. Grabowsky, "Accurate crystal structures and chemical properties from NoSpherA2", Chemical Science, vol. 12, pp. 1675-1692, 2021. https://doi.org/10.1039/d0sc05526c

Finding and Discovery Aids as part of data availability statements for research articles.

Wednesday, February 19th, 2025

Starting around 2016, journal publishers started including mandatory “Data Availability” statements as part of research articles; a typical (dated) example is linked here, including guidelines for how to cite the data itself. I wrote about these aspects last year in a blog post for the RSC journal Digital Discovery[1] and here I follow up with more news.

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References

  1. H. Rzepa, "The evolving roles of data and citations in journal articles", 2024. https://doi.org/10.26434/chemrxiv-2024-dz2dv

Au-pseudocarbyne – a unusual example of a twelve coordination by carbon.

Saturday, February 1st, 2025

Derek Lowe tells the story of “carbyne”, a potential further allotrope of carbon, comprising linear chains of carbon atoms, C-C≡C-C≡C-C. Whether such a molecule can exist on its own has long been the the topic of speculation. Now a report has appeared of a “pseudocarbyne”, stabilised by gold atoms.[1]

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References

  1. J. Wu, P. Tarakeshwar, S.G. Sayres, M. Meneghetti, H. Kim, J. Barreto, and P.R. Buseck, "Crystal structure of Au-pseudocarbyne(C6)", Scientific Reports, vol. 15, 2025. https://doi.org/10.1038/s41598-024-80359-5

Molecules of the Year 2024: Molecular shuttle in a box.

Saturday, January 25th, 2025

This is another in the C&E News list of candidates for the Molecule of the Year, Molecular shuttle in a box [1] (more…)

References

  1. S. Ibáñez, P. Salvà, L.N. Dawe, and E. Peris, "Guest‐Shuttling in a Nanosized Metallobox", Angewandte Chemie International Edition, vol. 63, 2024. https://doi.org/10.1002/anie.202318829