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Very strong organosuperbases formed by combining imidazole and guanidine bases: synthesis, structure, and basicity.
| Content Provider | Semantic Scholar |
|---|---|
| Author | Vazdar, Katarina Kunetskiy, Roman A. Saame, Jaan Kaupmees, Karl Leito, Ivo Jahn, Ullrich |
| Copyright Year | 2014 |
| Abstract | New structural motives for organosuperbases, that are easy to prepare and highly basic are urgently required in many areas of chemistry. The synthesis of N,N'-bis(imidazolyl)guanidine bases (BIG bases) is reported. Their pKα values are determined as 26.1-29.3 in THF. They are thus probably the strongest known phosphorous-free organic bases both in solution and in the gas phase. Calculations help to determine the structural and electronic factors giving rise to the high basicity. |
| Starting Page | 101 |
| Ending Page | 106 |
| Page Count | 6 |
| File Format | PDF HTM / HTML |
| Alternate Webpage(s) | http://www.chtf.stuba.sk/~szolcsanyi/education/files/Chemia%20heterocyklickych%20zlucenin/Prednaska%203/Doplnkove%20studijne%20materialy/Di-Azoles/Very%20Strong%20Organosuperbases%20Formed%20by%20Combining%20Imidazole%20and%20Guanidine.pdf |
| PubMed reference number | 24339377v1 |
| Alternate Webpage(s) | https://doi.org/10.1002/anie.201307212 |
| DOI | 10.1002/anie.201307212 |
| Journal | Angewandte Chemie |
| Volume Number | 53 |
| Issue Number | 5 |
| Language | English |
| Access Restriction | Open |
| Subject Keyword | Base Chemical acidity/alkalinity Guanidine Imidazoles Phosphorus Schiff Bases Tetrahydrofolate |
| Content Type | Text |
| Resource Type | Article |