Archive for the ‘Interesting chemistry’ Category
Friday, July 5th, 2013
A comment made on the previous post on the topic of hexa-coordinate carbon cited an article entitled “Observation of hypervalent CLi6 by Knudsen-effusion mass spectrometry“[cite]10.1038/355432a0[/cite] by Kudo as a amongst the earliest of evidence that such species can exist (in the gas phase). It was a spectacular vindication of the earlier theoretical prediction[cite]10.1021/ja00379a051[/cite],[cite]10.1021/ja00356a045[/cite] that such 6-coordinate species are stable with respect to dissociation to CLi4 and Li2.
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Tags:energy, gas phase, Knudsen, low energy 2s/2p carbon, metal-metal bonding, pence
Posted in Hypervalency, Interesting chemistry | 7 Comments »
Wednesday, July 3rd, 2013
C2 (dicarbon) is certainly interesting from a theoretical point of view. Whether or not it can be described as having a quadruple bond has induced much passionate discussion[cite]10.1038/nchem.1263[/cite],[cite]10.1002/anie.201208206[/cite],[cite]10.1002/anie.201301485[/cite],[cite]10.1002/anie.201302350[/cite]. Its occurrence in space and in flames is also well-known. But does it have what might be called a conventional chemistry? Other highly reactive species (cyclobutadiene is a well-known example) can often be tamed by trapping as a ligand coordinated to a metal and so one might speculate upon how C2 responds to the proximity of a metal. As is noted here[cite]10.1002/anie.201208206[/cite], dicarbon as a ligand has been known a long time as part of what is referred to as carbide chemistry. In this regard it is thought of as the di-anion, C22- (and isoelectronic therefore with dinitrogen). Thus calcium carbide, but in fact the degree to which the dicarbon can absorb electrons is thought to be wide (as judged by the resulting C-C bond length, see[cite]10.1002/anie.201208206[/cite]). Here I take a look at just one metal carbide[cite]10.1016/j.jssc.2008.08.005[/cite] that caught my eye (there are hundreds of others, many no doubt equally interesting!).
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Tags:metal, metal coordinating, Os-C
Posted in Interesting chemistry | 6 Comments »
Wednesday, June 26th, 2013
A reader asked me about the mechanism of the reaction of 2-picoline N-oxide with acetic anhydride to give 2-acetoxymethylpyridine (the Boekelheide Rearrangement[cite]10.1002/ejoc.201000936[/cite]). He wrote ” I don’t understand why the system should prefer to go via fragmentation-recombination (… the evidence being that oxygen labelling shows scrambling) when there is an easy concerted pathway available (… a [3,3]sigmatropic shift). Furthermore, is it possible for two pathways to co-exist?” Here is how computation might enlighten us.
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Tags:ATM, CF 3 CO, CH 3 CO, extraneous product, free energy, free energy barrier, recombination
Posted in Interesting chemistry, pericyclic, reaction mechanism | 3 Comments »
Friday, May 24th, 2013
The title of this post comes from a comment posted by Ryan, who asks about isocyanide’s role (in the form of the anion of tosyl isocyanide, or TosMIC) in two named reactions, Van Leusen and Ugi FCR. “In Van Leusen, it (the isocyanide) acts as an electrophile: however, in Ugi, it acts as a nucleophile”. Here are some valence bond forms for this species;
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Tags:Ugi, Van Leusen
Posted in Interesting chemistry | 2 Comments »
Wednesday, May 15th, 2013
In the preceding post, I introduced Dewar’s π-complex theory for alkene-metal compounds, outlining the molecular orbital analysis he presented, in which the filled π-MO of the alkene donates into a Ag+ empty metal orbital and back-donation occurs from a filled metal orbital into the alkene π* MO. Here I play a little “what if” game with this scenario to see what one can learn from doing so.
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Tags:African Union, alkene-metal compounds, empty metal orbital, energy, filled metal orbital, free energy, Historical, lower energy form, metal
Posted in Hypervalency, Interesting chemistry | 1 Comment »
Monday, May 13th, 2013
The period 1951–1954 was a golden one for structural chemistry; proteins, DNA, Ferrocene (1952) and the one I discuss here, a bonding model for Zeise’s salt (3).
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Tags:alkene-metal interaction, alkene-metal π-complex, cation Ag, Dewar, Dewar's Ag, Historical, metal, metal d-orbitals, naked metal cations, ZTE C79 Cellular Phone
Posted in Interesting chemistry | 1 Comment »
Saturday, May 11th, 2013
Lukas, who occasionally comments on this blog, sent me the following challenge. In a recent article[cite]10.1021/jo3021709[/cite] he had proposed that the stereochemical outcome (Z) of reaction between a butenal and thioacetic acid as shown below arose by an unusual concerted cycloaddtion involving an S-H bond. He wrote in the article “…this scheme … recommends itself for evaluation by in silico methods“. I asked if the answer could be posted here, and he agreed. So here it is.
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Tags:Reaction Mechanism
Posted in Interesting chemistry | 3 Comments »
Monday, April 29th, 2013
A few posts back, I explored the “benzidine rearrangement” of diphenyl hydrazine. This reaction requires diprotonation to proceed readily, but we then discovered that replacing one NH by an O as in N,O-diphenyl hydroxylamine required only monoprotonation to undergo an equivalent facile rearrangement. So replacing both NHs by O to form diphenyl peroxide (Ph-O-O-Ph) completes this homologous series. I had speculated that PhNHOPh might exist if all traces of catalytic acid were removed, but could the same be done to PhOOPh? Not if it continues the trend and requires no prior protonation at all!
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Tags:actual initial product, energy, energy transition state, Michael Dewar, New Hampshire, Reaction Mechanism
Posted in Interesting chemistry | 4 Comments »