Archive for the ‘Interesting chemistry’ Category

The H4 (2+) dication and its bonding.

Wednesday, February 15th, 2017

This post arose from a comment attached to the post on Na2He and relating to peculiar and rare topological features of the electron density in molecules called non-nuclear attractors. This set me thinking about other molecules that might exhibit this and one of these is shown below.

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VSEPR Theory: A closer look at bromine trifluoride, BrF3.

Tuesday, February 14th, 2017

I analysed the bonding in chlorine trifluoride a few years back in terms of VSEPR theory. I noticed that several searches on this topic which led people to this post also included a query about the differences between it and the bromine analogue. For those who posed this question, here is an equivalent analysis.

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Na2He: a stable compound of helium and sodium at high pressure.

Saturday, February 11th, 2017

On February 6th I was alerted to this intriguing article[cite]10.1038/nchem.2716[/cite] by a phone call, made 55 minutes before the article embargo was due to be released. Gizmodo wanted to know if I could provide an (almost) instant quote. After a few days, this report of a stable compound of helium and sodium still seems impressive to me and I now impart a few more thoughts here.

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Forming a stabilized m-benzyne.

Friday, January 20th, 2017

The story so far. Inspired by the report of the most polar neutral compound yet made, I suggested some candidates based on the azulene ring system that if made might be even more polar. This then led to considering a smaller π-analogue of azulene, m-benzyne. Here I ponder how a derivative of this molecule might be made, using computational profiling as one reality check.

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Braiding a molecular knot with eight crossings.

Friday, January 20th, 2017

This is one of those posts of a molecule whose very structure is interesting enough to merit a picture and a 3D model. The study[cite]10.1126/science.aal1619[/cite] reports a molecular knot with the remarkable number of eight crossings.

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Ritonavir: a look at a famous example of conformational polymorphism.

Monday, January 2nd, 2017

Here is an inside peek at another one of Derek Lowe’s 250 milestones in chemistry, the polymorphism of Ritonavir.[cite]10.1023/A:1011052932607[/cite] The story in a nutshell concerns one of a pharma company’s worst nightmares; a drug which has been successfully brought to market unexpectedly “changes” after a few years on market to a less effective form (or to use the drug term, formulation). This can happen via a phenomenon known as polymorphism, where the crystalline structure of a molecule can have more than one form.[cite]10.1021/ar00052a005[/cite],[cite]10.1002/anie.201410356[/cite],[cite]10.1039/D1SC06074K[/cite] In this case, form I was formulated into soluble tablets for oral intake. During later manufacturing, a new less-soluble form appeared and “within weeks this new polymorph began to appear throughout both the bulk drug and formulation areas“[cite]10.1023/A:1011052932607[/cite]

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The dipole moments of highly polar molecules: glycine zwitterion.

Saturday, December 24th, 2016

The previous posts produced discussion about the dipole moments of highly polar molecules. Here to produce some reference points for further discussion I look at the dipole moment of glycine, the classic zwitterion (an internal ion-pair).

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Forking “The most polar neutral compound synthesized” into m-benzyne.

Wednesday, December 21st, 2016

A project fork is defined (in computing) as creating a distinct and separate strand from an existing (coding) project. Here I apply the principle to the polar azulene 4 explored in an earlier post, taking m-benzyne as a lower homologue of azulene as my starting point.

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Molecules of the year? Pnictogen chains and 16 coordinate Cs.

Monday, December 19th, 2016

I am completing my survey of the vote for molecule of the year candidates, which this year seems focused on chemical records of one type or another.

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Molecules of the year? The most polar neutral compound synthesized…

Sunday, December 18th, 2016

This, the fourth candidate provided by C&EN for a vote for the molecule of the year as discussed here, lays claim to the World’s most polar neutral molecule (system 1 shown below).[cite]10.1002/anie.201508249[/cite] Here I explore a strategy for extending that record.

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