Resumen
Through structural modification of 2-anilinonicotinic acid by isomerization, a new synthon, acid-aminopyridine, is created, and the two original synthons, i.e., the acid-acid homosynthon and acid-pyridine heterosynthon are no longer observed in the newly designed 6-anilinonicotinic acids. The new synthon has a hydrogen-bond strength rivaling that of the acid-acid homosynthon and the acid-pyridine heterosynthon, as suggested by theoretical calculations, which explains its formation.
| Idioma original | English |
|---|---|
| Páginas (desde-hasta) | 4849-4859 |
| Número de páginas | 11 |
| Publicación | Crystal Growth and Design |
| Volumen | 18 |
| N.º | 9 |
| DOI | |
| Estado | Published - sept 5 2018 |
Nota bibliográfica
Publisher Copyright:Copyright © 2018 American Chemical Society.
Financiación
S.P. and S.L. thank Natural Science Foundation of Hubei Province (2014CFB787) and the President’s Fund of Wuhan Institute of Technology (CX2016075) for financial support.
| Financiadores | Número del financiador |
|---|---|
| Natural Science Foundation of Hubei Province | 2014CFB787 |
| Natural Science Foundation of Hubei Province | |
| Wuhan Institute of Technology | CX2016075 |
| Wuhan Institute of Technology |
ASJC Scopus subject areas
- General Chemistry
- General Materials Science
- Condensed Matter Physics
Huella
Profundice en los temas de investigación de 'Structural Isomerization of 2-Anilinonicotinic Acid Leads to a New Synthon in 6-Anilinonicotinic Acids'. En conjunto forman una huella única.Citar esto
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