Henry Rzepa's Blog

I have variously talked about persistent identifiers on this blog. These largely take the form of DOIs (Digital object identifiers), and here they relate to either journal articles or datasets associated with either the article or the blog post or both. Other disciplines, particularly the earth sciences, have long used persistent identifiers (PIDs) to identify physical objects rather than digital ones. One of my ambitions is to assign such identifiers to a small but highly historical collection of physical objects in my possession, as described at this post. As a prelude to this project, here I describe some ways of searching for physical objects that have been assigned a PID. Thanks Rorie for providing these! 

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Sometimes, the properties of a molecule are predicted long before it is synthesised. One such is diberyllocene. I first encountered a related molecule, beryllocene itself, many moons ago.[1] This was unusual because unlike the original metallocenes, the metal atom was not symmetrically disposed between the two cyclopentadienyl faces. Now diberyllocene is finally reported in which replacing one Be by Be-Be induces (according to calculation, D₂) symmetry[2]. I will not repeat the excellent analysis of the wavefunction reported in this article, but confine myself to showing two molecular orbitals which examplify its bonding.

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References

1. M.J.S. Dewar, and H.S. Rzepa, "Ground states of molecules. 45. MNDO results for molecules containing beryllium", Journal of the American Chemical Society, vol. 100, pp. 777-784, 1978. http://dx.doi.org/10.1021/ja00471a020
2. J.T. Boronski, A.E. Crumpton, L.L. Wales, and S. Aldridge, "Diberyllocene, a stable compound of Be(I) with a Be–Be bond", Science, vol. 380, pp. 1147-1149, 2023. http://dx.doi.org/10.1126/science.adh4419

This is a venerable organic reaction, which curiously I have not previously covered here. First described in 1859, its nature was only properly elucidated in 1873. It is a member of a class of reaction I have previously named “solvolytically assisted pericyclic”, or “perisolvolytic“. Here I explore some of the subtle stereoelectronic effects observed for this apparently simple reaction.

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This editorial from Nature[1] is a timely reminder of the importance of data. But also, not just any data, but “accurate and accessible training data“. Accessible of course is one of the attributes of FAIR (Findable, Accessible, Interoperable and Re-usable). The editorial also states “data need to be recorded in agreed and consistent formats, which they are not at present“. That is covered by the I and R of FAIR, often applied in conjunction with metadata recording the Media type that the data is held in (See DOI https://doi.org/jvk9 for examples of the use of Media types in chemical computation and chemical NMR). Again, “The best possible training sets would also include data on negative outcomes“. This relates to the separation of the two publication processes, namely the article itself (or the story behind the data) and the data itself as a first class scientific object. Thus when we publish FAIR data in association with articles, the data archive will often contain data that is not used in the article itself (perhaps because it led to a negative outcome), but is nevertheless part of the FAIR data collection for that topic. Even if the data does not lead to journal publication, publishing it in a data repository means it will not be lost. Somebody (or AI software) may still find it useful.

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References

1. "For chemists, the AI revolution has yet to happen", Nature, vol. 617, pp. 438-438, 2023. http://dx.doi.org/10.1038/d41586-023-01612-x