A periodic table for anomeric centres, this time with quantified interactions.

August 8th, 2016

The previous post contained an exploration of the anomeric effect as it occurs at an atom centre X for which the effect is manifest in crystal structures. Here I quantify the effect, by selecting the test molecule MeO-X-OMe, where X is of two types:

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A periodic table for anomeric centres.

August 6th, 2016

In the last few posts, I have explored the anomeric effect as it occurs at an atom centre X. Here I try to summarise the atoms for which the effect is manifest in crystal structures.

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Stereoelectronic effects galore: bis(trifluoromethyl)trioxide.

August 4th, 2016

Here is a little molecule that can be said to be pretty electron rich. There are lots of lone pairs present, and not a few electron-deficient σ-bonds. I thought it might be fun to look at the stereoelectronic interactions set up in this little system.

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Managing (open) NMR data: a working example using Mpublish.

August 1st, 2016

In March, I posted from the ACS meeting in San Diego on the topic of Research data: Managing spectroscopy-NMR, and noted a talk by MestreLab Research on how a tool called Mpublish in the forthcoming release of their NMR analysis software Mestrenova could help. With that release now out, the opportunity arose to test the system.

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Anomeric effects at carbon involving lone pairs originating from one or two nitrogens.

July 8th, 2016

The previous post looked at anomeric effects set up on centres such as B, Si or P, and involving two oxygen groups attached to these atoms. Here I vary the attached groups to include either one or two nitrogen atoms.[1]

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References

  1. H. Rzepa, "Anomeric effects at carbon, involving lone pairs originating from one or two nitrogens", 2016. https://doi.org/10.14469/hpc/936

Anomeric effects at boron, silicon and phosphorus.

July 1st, 2016

The anomeric effect occurs at 4-coordinate (sp3) carbon centres carrying two oxygen substituents and involves an alignment of a lone electron pair on one oxygen with the adjacent C-O σ*-bond of the other oxygen. Here I explore whether other centres can exhibit the phenomenon. I start with 4-coordinate boron, using the crystal structure search definition below (along with R < 0.1, no disorder, no errors).[1]anomeric-bo-sq

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References

  1. H. Rzepa, "Anomeric effects at boron, silicon and phosphorus.", 2016. https://doi.org/10.14469/hpc/696

How does an OH or NH group approach an aromatic ring to hydrogen bond with its π-face?

June 22nd, 2016

I previously used data mining of crystal structures to explore the directing influence of substituents on aromatic and heteroaromatic rings. Here I explore, quite literally, a different angle to the hydrogen bonding interactions between a benzene ring and OH or NH groups.

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Exploring the electrophilic directing influence of heteroaromatic rings using crystal structure data mining.

June 21st, 2016

This is a follow-up to the post on exploring the directing influence of (electron donating) substituents on benzene[1] with the focus on heteroaromatic rings such indoles, pyrroles and group 16 analogues (furans, thiophenes etc).

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References

  1. H.S. Rzepa, "Discovering More Chemical Concepts from 3D Chemical Information Searches of Crystal Structure Databases", Journal of Chemical Education, vol. 93, pp. 550-554, 2015. https://doi.org/10.1021/acs.jchemed.5b00346

Why is the carbonyl IR stretch in an ester higher than in a ketone: crystal structure data mining.

June 18th, 2016

In this post, I pondered upon the C=O infra-red spectroscopic properties of esters, and showed three possible electronic influences:

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A wider look at π-complex metal-alkene (and alkyne) compounds.

June 13th, 2016

Previously, I looked at the historic origins of the so-called π-complex theory of metal-alkene complexes. Here I follow this up with some data mining of the crystal structure database for such structures.

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