Science frequently works by people making connections between related (or even apparently unrelated) concepts or data. There are many ways of helping people make these connections – attending a conference or seminar, searching journals for published articles and nowadays also searching for data are just a few examples.
Nature has produced most natural molecules as chiral objects, which means the molecule can come in two enantiomeric forms, each being the mirror image of the other. When a natural product is synthesised in a laboratory, a chiral synthesis means just one form is made, and then is compared with the natural product to see if it matches.
I have previously looked at the pigments used to colour the Book of Kells, which dates from around 800 AD and which contained arsenic sulfide as the yellow colourant. The Bayeaux tapestry is a later embroidery dating probably from around 1077 and here the colours are based entirely on mordanted natural dyes.
In the previous post, I discussed how data associated with two of the candidates for molecules of the year – 2022 could be retrieved and then used to inspect their three dimensional structures.
The list of molecules of the year is out now at C&E News (but you have to have an account to view the list, unlike previous years). ♣ These three caught my eye: Electron in a cube: Synthesis and characterization of perfluorocubane as an electron acceptor ,[cite]10.1126/science.abq0516[/cite]. I have already written about this system and will not discuss it further, except to note this one topped the poll!
The topic of dicarbon, C 2 , has been discussed here for a few years now. It undoubtedly would be a gas!
What’s a Journal For? This debate has been raging ever since preprint servers were introduced as far back as 1991!
Sometimes you come across a reaction which is so simple in concept that you wonder why it took so long to be accomplished in practice.
The term bispericyclic reaction was famously coined by Caramella et a l in 2002[cite]10.1021/ja016622h[/cite] to describe the unusual features of the apparently innocuous dimerisation of cyclopentadiene. It shows features of two paths for different pericyclic reactions, comprising a 2+4 cycloaddition in the early stages, but evolving into a (degenerate) pair of [3,3] sigmatropic reactions in the latter stages.
In previously asking what the largest angle subtended at four-coordinate carbon might be, I noted that as the angle increases beyond 180°, the carbon becomes inverted, or hemispherical (all four ligands in one hemisphere). So what does a search for this situation reveal in the CSD?
