Literature DB >> 20480465

The search for tricyanomethane (cyanoform).

Dubravka Sisak1, Lynne B McCusker, Andreas Buckl, Georg Wuitschik, Yi-Lin Wu, W Bernd Schweizer, Jack D Dunitz.   

Abstract

Although listed in organic chemistry textbooks as one of the strongest carbon acids, and in spite of more than a hundred years of attempts to prepare the compound, tricyanomethane (cyanoform) has resisted isolation and characterization, either as the carbon-acid 1 or as the dicyanoketenimine tautomer 2. Only in the vapor phase at very low pressure has the compound been identified from its microwave spectrum. Here we review and partially repeat the preparative work. With the aid of spectroscopic and diffraction methods (including powder diffraction) we have identified some of the products obtained as: hydronium tricyanomethanide (3), (Z)-3-amino-2-cyano-3-iminoacrylimide (4), a co-crystal of 4 with sulfuric acid (or corresponding iminium salt), and an addition product of 2 with hydrochloric acid (5/6). Quantum-mechanical calculations at the MP2/6-311++g(2d,2p) level have been made to assess the relative energies of some of the molecules involved.

Entities:  

Year:  2010        PMID: 20480465     DOI: 10.1002/chem.201000559

Source DB:  PubMed          Journal:  Chemistry        ISSN: 0947-6539            Impact factor:   5.236


  3 in total

1.  Differential hydration of tricyanomethanide observed by time resolved vibrational spectroscopy.

Authors:  Daniel G Kuroda; Prabhat K Singh; Robin M Hochstrasser
Journal:  J Phys Chem B       Date:  2012-09-25       Impact factor: 2.991

2.  Ring Enlargement of Three-Membered Heterocycles by Treatment with In Situ Formed Tricyanomethane.

Authors:  Klaus Banert; Madhu Chityala; Marcus Korb
Journal:  Chemistry       Date:  2020-04-30       Impact factor: 5.236

3.  Tautomerization, acidity, basicity, and stability of cyanoform: a computational study.

Authors:  Shaaban A Elroby
Journal:  Chem Cent J       Date:  2016-04-11       Impact factor: 4.215

  3 in total

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